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Review

p-Cresyl Sulfate

by
Tessa Gryp
1,2,
Raymond Vanholder
1,
Mario Vaneechoutte
2 and
Griet Glorieux
1,*
1
Department of Internal Medicine, Nephrology Division, Ghent University Hospital, 9000 Ghent, Belgium
2
Laboratory for Bacteriology Research, Department of Clinical Chemistry, Microbiology & Immunology, Ghent University, 9000 Ghent, Belgium
*
Author to whom correspondence should be addressed.
Toxins 2017, 9(2), 52; https://doi.org/10.3390/toxins9020052
Submission received: 23 November 2016 / Revised: 12 January 2017 / Accepted: 23 January 2017 / Published: 29 January 2017
(This article belongs to the Special Issue Novel Issues in Uremic Toxicity)
Browse Figure
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Abstract

:
If chronic kidney disease (CKD) is associated with an impairment of kidney function, several uremic solutes are retained. Some of these exert toxic effects, which are called uremic toxins. p-Cresyl sulfate (pCS) is a prototype protein-bound uremic toxin to which many biological and biochemical (toxic) effects have been attributed. In addition, increased levels of pCS have been associated with worsening outcomes in CKD patients. pCS finds its origin in the intestine where gut bacteria metabolize aromatic amino acids, such as tyrosine and phenylalanine, leading to phenolic end products, of which pCS is one of the components. In this review we summarize the biological effects of pCS and its metabolic origin in the intestine. It appears that, according to in vitro studies, the intestinal bacteria generating phenolic compounds mainly belong to the families Bacteroidaceae, Bifidobacteriaceae, Clostridiaceae, Enterobacteriaceae, Enterococcaceae, Eubacteriaceae, Fusobacteriaceae, Lachnospiraceae, Lactobacillaceae, Porphyromonadaceae, Staphylococcaceae, Ruminococcaceae, and Veillonellaceae. Since pCS remains difficult to remove by dialysis, the gut microbiota could be a future target to decrease pCS levels and its toxicity, even at earlier stages of CKD, aiming at slowing down the progression of the disease and decreasing the cardiovascular burden.

1. Introduction

When kidney function deteriorates, a myriad of compounds, the so-called uremic retention solutes, accumulate in the circulation and tissues [1,2,3]. As a consequence, progression of kidney dysfunction is paralleled with the development of complications, affecting both the quality of life and survival of patients with chronic kidney disease (CKD) [4,5,6,7]. Uremic retention solutes are, conventionally, classified into three groups based on their physicochemical characteristics [2]. Next to the small water-soluble compounds (<500 Da) and the larger middle molecules (mostly peptidic compounds with molecular weight >500 Da) the protein-bound compounds form a third group. Many of these compounds, amongst which the phenols and indoles, originate from the intestinal microbial metabolism of dietary amino acids [8]. Whereas in the healthy kidney, removal of protein-bound solutes largely depends on tubular secretion, removal by dialysis, primarily replacing the filtration capacity of the kidney, is limited to the unbound fraction and is not affected by dialyzer pore size [9], and only marginally by convection [10]. Hence, dialysis removal is unsatisfactory, compared to, e.g., the low molecular weight compounds which are not bound to protein. For the protein-bound compounds alternative measures, preferably preventive (such as decreasing generation, adsorption, and preserving kidney function), will be necessary to keep concentrations low. In this review, p-cresyl sulfate (pCS), a prototype protein-bound molecule, to which many biological and biochemical (toxic) actions have been attributed, and for which increased concentrations have been associated with worsening outcomes (see below), will be discussed in depth. We will especially focus on the intestinal origin of pCS and the contributing bacterial species which could be a future target to decrease levels and hence toxicity, even at earlier stages of CKD, aiming at slowing down the progression of the disease and decreasing the cardiovascular burden.

2. Characteristics of p-Cresyl Sulfate

2.1. Chemical Structure and Molecular Weight

The aromatic pCS originates from sulfation (para-) of the intestinally generated p-cresol (MW: 108.1 g/mol). pCS (C7H8O4S) (Figure 1) has a molecular weight of 188.2 g/mol and in the circulation (plasma) it is bound for approximately 95% to the protein albumin in healthy controls, as well as in CKD patients [11].

2.2. Normal and Uremic Serum/Plasma Concentrations

Normal total average serum/plasma concentrations of pCS reported, vary between 2.8 ± 1.7 mg/L (14.9 ± 9.0 µM) [12] and 6.6 ± 3.7 mg/L (35.1 ± 19.7 µM) [13] as determined in serum by ultra-performance liquid chromatography (UPLC) and UPLC-mass spectrometry (MS)-MS, respectively. In end-stage kidney disease (ESKD), concentrations of pCS are significantly increased with total average concentrations varying from 21.8 ± 12.4 mg/L (115.8 ± 65.9 µM) [14] to 106.9 ± 44.6 mg/L (568.0 ± 237.0 µM) [15], as quantified by UPLC in serum and LC-MS-MS in plasma, respectively.

3. Metabolism

3.1. p-Cresyl Sulfate, a Colon-Derived Solute

The gut microbiota plays an important role in human health and disease [16,17], with alterations of the intestinal microbiota linked to the development of different diseases, such as inflammatory bowel disease [18], cancer [19], obesity [20], diabetes [21,22], cardiovascular disease [23], and kidney disease [24]. Next to protection against invading pathogens and differentiation of the human immune system, the microbiota contributes to various metabolic functions, such as fermentation of non-digestible dietary compounds in the large intestine [17,25,26]. Approximately 6–18 g of proteins and peptides enters the large intestine every day, mostly from diet, and to a lesser extent from endogenous sources, such as host tissues, pancreatic enzymes, and other secretions [27,28,29]. Entering the large bowel, these substances undergo depolymerization by host- and bacteria-derived proteases and peptidases into small oligopeptides and amino acids. These small oligopeptides and amino acids are then available for assimilation by colon microbiota or can be further metabolized by host enzymes [30,31]. Predominantly in the distal part of the colon, the aromatic amino acids tyrosine and phenylalanine are converted into phenolic compounds, such as phenol and p-cresol, through a series of deamination, transamination, and decarboxylation reactions by bacterial fermentation [29,32] (Figure 1). Detoxification of phenols occurs in the mucosa of the colon [33] and in the liver [34], where, e.g., p-cresol is sulfated into pCS and a small fraction is glucuronated into p-cresyl glucuronide (pCG) [35,36]. When entering the circulation these solutes bind to plasma albumin in a reversible manner, such that a rapid equilibrium between the bound and free fraction is established [37]. Finally, under normal conditions, the free fraction of these compounds is filtered at the site of the glomerulus and the bound fraction is secreted at the site of the tubular epithelial cells and both end up in the urine. In CKD patients, excretion of these solutes is impaired, resulting in their accumulation. Of note, in CKD estimates of proximal tubular secretion function and glomerular filtration of pCS correlate to each other to a certain extent, but that substantial variability in the change of net secretion vs. normal by the two components of the kidney remains [38]. In many studies plasma/serum and urine levels of p-cresol are reported. It is of note that these levels reflect the sum of both conjugates, pCS and pCG, since p-cresol is not present at detectable levels in the circulation [39].
The degradation routes by the gut microbiota of the aromatic amino acids tyrosine and phenylalanine are known to a large extent. As shown in Figure 1, several phenolic compounds and intermediates are generated from tyrosine and phenylalanine through intestinal bacterial fermentation [40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57].
Smith et al. demonstrated that, in the large intestine, bacterial fermentation of proteins mainly occurs in the distal part of the colon, since they found a four-fold higher concentration of phenolic compounds in that section of the intestine compared to the proximal bowel. In the distal colon, phenol and p-cresol account for 70% of all products of the dissimilatory aromatic amino acid metabolism [29]. Accordingly, in batch culture incubations with human faecal slurries, phenol and p-cresol are the predominant end products of tyrosine fermentation [29,32], whereas the predominant end products of phenylalanine are phenylacetate and phenylpropionate [29].

3.2. Disturbed Protein Assimilation in CKD

Assimilation of protein (digestion, metabolism, and absorption) in the small intestine is impaired in both non-dialyzed and dialyzed CKD patients [58,59] which might contribute to protein malnutrition, a well-known problem in CKD patients [60,61]. The 13C protein breath test is used to measure the impairment of protein assimilation in CKD, which worsens as kidney function declines. Proteins which are not absorbed or digested in the small intestine are further metabolized in the colon, by the gut proteolytic bacteria, which will cause an increase of urinary p-cresol concentration [58,59], an indicator of colonic p-cresol generation [62,63]. In the small intestine, protein absorption and digestion are also dependent on the degree of dietary protein intake, which is decreased in many malnourished uremic patients. This should have a lowering effect on urinary p-cresol [62,64]. However, in the study of Bammens et al., urinary p-cresol levels were still more pronounced as kidney function declined in CKD patients, after normalisation for dietary protein intake [58]. Gastro-intestinal motility disorders and dysbiosis in the gut should also be taken into account when evaluating protein assimilation [58,59]. Conditions that can interfere with protein assimilation are hepatic failure [65], diabetes mellitus [66], and metabolic acidosis [67]. Whereas hepatic failure and especially diabetes mellitus are frequent causes of CKD, acidosis is a frequent complication in uremia, accelerating amino acid and protein catabolism by, e.g., increasing muscle protein breakdown [67,68]. Correction of metabolic acidosis in CKD patients results in a normalization of the catabolic response to a low-protein diet by reducing amino acid oxidation and protein degradation, and stimulating protein synthesis to normal levels [68].

4. Gut Microbiota

4.1. Intestinal Phenolic Compounds Generating Microbiota

In general, the most abundant bacterial phyla among the human adult gut microbiota are Firmicutes, Bacteroidetes, Actinobacteria, Proteobacteria, and Verrucomicrobia and, to a lesser extent, Cyanobacteria, Fusobacteria, Lentisphaerae, Spirochaetes, and TM7 [69]. Obligate anaerobic bacterial genera such as Bacteroides, Bifidobacterium, and Eubacterium predominantly inhabit the human colon, while bacterial species of the genera Clostridium, Enterococcus, and Lactobacillus are present to a lesser extent [70,71]. Macfarlane et al., found in 1986 that proteolytic bacterial species in faeces are predominantly Bacteroides spp. and Propionibacterium spp. and belong, in a lesser proportion, to the genera Bacillus, Clostridium, Staphylococcus, and Streptococcus [30]. Gut microbiota are known to be the source of phenolic compounds, generated in the colon from tyrosine and phenylalanine, as demonstrated in hemodialysis (HD) patients without colon who have the same plasma pCS levels as healthy subjects [72]. This was also demonstrated by Wikoff et al., who could not detect pCS in plasma of germ-free mice [73] and by Kikuchi et al., who observed a non-significant downward trend in urinary pCS levels in cecectomized rats [74]. Two operational taxonomic units (OTUs), belonging to the genus Oscillospira and the family Ruminococcaceae, are associated with urinary pCS levels and one OTU, belonging to the family Ruminococcaceae, is associated with levels of pCG in healthy subjects [75]. In vitro studies have been carried out to identify the microbiota generating phenolic compounds. Table 1 gives an overview of culturable phenolic compound generating bacteria with predominant phenol-producing bacteria belonging to the Enterococcaceae, Clostridiaceae, Staphylococcaceae, and Enterobacteriaceae, of which the latter group is known to produce the enzyme tyrosine phenol-lyase [40,43]. Most studied proteolytic bacteria are of the genus Clostridium [76,77,78,79], of which some can use amino acids as their sole carbon and energy source [76,77]. Additionally, Bifidobacterium strains are known to ferment aromatic amino acids in the absence of other energy sources such as carbohydrates [70]. Next to phenol, the main tyrosine end products of several Clostridium species are p-cresol and 4-hydroxyphenylacetate, the precursor of p-cresol. Additionally, Bacteroidaceae, Bifidobacteriaceae, Eubacteriaceae, Lachnospiraceae, Porphyromonadaceae, Ruminococcaceae, and Veillonellaceae have the property to ferment tyrosine to p-cresol and to 4-hydroxyphenylacetate, while Fusobacteriaceae only generate p-cresol (Table 1). Bone et al. hypothesized that in the large intestine, phenol-forming bacteria are mainly facultative anaerobes, while p-cresol-forming bacteria are obligate anaerobes [80]. This hypothesis largely corresponds to the data presented in Table 1. The kind of phenolic compounds that are generated by gut bacteria can depend on the bacterial strain under study, but also largely on the carbon and energy source, whereby in vitro study of external factors, such as medium composition and incubation conditions, can have a large impact on protein dissimilation [70]. Since only a small fraction of the bacterial gut community is culturable [81], it can be suspected that the aromatic amino acid fermenting bacteria listed are only the tip of the iceberg. For future directions, culture conditions will have to be optimized in order to increase the identification yield of these phenolic compound generating bacteria.

4.2. Gut Dysbiosis in CKD

It has been shown that the composition of the gastro-intestinal microbiota of CKD patients is altered [82]. More specifically, CKD patients suffer from bacterial overgrowth in the small intestine [83] with elevated levels of aerobic (106 cells/mL) and anaerobic (107 cells/mL) bacteria in the duodenum and jejunum [84] and overgrowth of aerobic bacteria in the colon [85,86]. Alterations in the gut microbiota composition are also observed in nephrectomized rats, who have an increase of Bacteroides species and a decrease of Lactobacillus species compared with sham-operated rats [87]. Changes in the gut bacterial species composition may even begin in early stages of CKD, as increased levels of pCS are associated with an increase of an OTU belonging to the Ruminococcus genus in the early stages of CKD [88]. Vaziri et al. demonstrated that the relative abundance of 190 bacterial OTUs differed between controls and ESKD patients, whereby ESKD patients had higher amounts of aerobic and facultative anaerobic bacteria, with the largest increases in the Clostridia, Actinobacteria, and Gammaproteobacteria [82]. To distinguish the effect of uremia, per se, from inter-individual variations, Vaziri et al. investigated the gut microbial composition in nephrectomized rats. Differences in 175 bacterial OTUs were found with, more specifically, a decrease in the Lactobacillaceae and Prevotellaceae families in uremic rats. The total richness was significantly higher in control rats than in the nephrectomized rats [82]. Additionally, in HD patients, analysis of the faecal microbial composition by culturing techniques revealed an approximately 100 times higher abundance of aerobes, such as Enterobacteriaceae and Enterococcaceae, compared to healthy individuals. Of the anaerobes in HD patients, bifidobacteria were decreased while the number of Clostridium perfringens increased [85]. These findings are consistent with the results of Fukuuchi et al., studying the faecal microbial composition by traditional plating methods in CKD, HD, and control patients. However in this study, the total amount of bacteria was decreased in the HD and CKD groups [86], while Hida et al. found no differences [85]. Among the Enterobacteriaceae, the level of Escherichia coli was significantly increased in both patient groups compared to the control group [86]. However, when using real-time polymerase chain reaction (PCR) analysis on faecal samples, no difference was observed in the E. coli level between peritoneal dialysis (PD) patients and controls, while the Bifidobacterium species decreased [89]. According to Table 1, these studies indicate a higher prevalence of phenol-producing bacteria belonging to the Enterobacteriaceae and Enterococcaceae families and of p-cresol-producing bacteria, like C. perfringens in CKD patients. This has been confirmed by the quantification of the faecal and serum levels of phenol and p-cresol, which are higher in HD and CKD patients than in controls [85,86]. The lowered levels of bifidobacteria in CKD, HD and PD [85,86,89] indicate that these bacterial species are probably not responsible for the increased production of phenol and p-cresol in these patients, although bifidobacteria have been found to generate phenolic compounds in in vitro studies (Table 1). From the section above, it becomes clear that the information in this field of research is still scattered and incomplete, underscoring that the characterization of the uremic intestinal microbiota will require further investigation before the composition of the responsible bacterial species, contributing to the increased pCS and phenyl sulfate levels in CKD patients has been unraveled completely.
Next to the gut microbiota composition, also its functional characteristics play a role in determining the gut levels of p-cresol. The altered composition of the gastro-intestinal microbiota in CKD [82] is probably due to bacteria-derived hydrolysis of increased concentrations of urea entering the intestine via the entero-hepatic cycle, resulting in high levels of ammonia, which elevates the faecal pH value [90]. Wong et al. demonstrated that 19 microbial families were dominant in ESKD compared to controls, and that 63% of these dominant microbial families possessed urease-forming enzymes, needed to convert urea in ammonia. Other dominant families in ESKD (i.e., Clostridiaceae and Enterobacteriaceae) possess uricase- and p-cresol-forming enzymes, while a lowered family abundance was found for Lactobacillaceae and Prevotellaceae, producing butyrate-forming enzymes [91] which can further influence the butyrate production, knowing that this short chain fatty acid has a beneficial effect on the gastro-intestinal health [69]. Thus, uremia can modify the biochemical milieu of the gastro-intestinal tract. In addition to uremia itself, therapeutic interventions and dietary restrictions will also contribute to an altered gut microbiota composition and function [82].

5. Toxicity

5.1. Biological Effects

Literature reports on biological activity of pCS only emerged during the last decade, as until 2005, due to a preparative artefact caused by using acidification for deproteinization of plasma, its intestinally-generated precursor, p-cresol, was thought to be retained in the circulation [39]. Shortly after de Loor et al. [36] and Martinez et al. [103] reported this phenomenon independently from each other by using alternative deproteinization protocols (acetone and methanol, respectively), a first in vitro study by Schepers et al. pointed to a role of pCS in causing increased oxidative stress in leukocytes [104]. In vivo intravital microscopy in rat peritoneal capillary venules confirmed the stimulatory effect of pCS on leukocytes showing an increase in the number of rolling leukocytes along the vascular endothelium after superfusion of the peritoneal membrane with a solution containing pCS at uremic concentration [105]. Furthermore, pCS stimulated endothelial microparticle release, a marker of endothelial damage [106], and induced oxidative stress in both human umbilical vein endothelial cells (HUVECs) and human vascular smooth muscle cells (HVSMCs) [107]. Ex vivo, pCS induced contraction of mouse thoracic aorta, through direct activation of rho-kinase, independently of oxidative stress induction, as well as inward eutrophic vascular remodelling [107]. Furthermore, pCS induced NADPH oxidase activity and reactive oxygen species (ROS) production in cardiomyocytes facilitating cardiac apoptosis and resulting in diastolic dysfunction in nephrectomized mice [108]. These data suggest that pCS might contribute to cardiovascular morbidity and mortality in CKD.
In addition, toxic effects on renal tubular cells have also been reported. pCS increased expression of DNA methyltransferases 1, 3a, and 3b isoforms which suppressed Klotho expression in HK2 cells and injection of pCS in uninephrectomized B-6 mice caused kidney fibrosis, CpG hypermethylation of the klotho gene, and decreased klotho expression in the renal tubular cells [109]. Sun et al. also demonstrated that pCS activated the renal renin angiotensin aldosterone system/transforming growth factor-beta pathway and induced epithelial-to-mesenchymal transition-like transition contributing to kidney injury and fibrosis [110]. In parallel to what is observed at the cardiovascular level, pCS also induces NADPH oxidase driven production of ROS next to expression of inflammatory cytokines in renal tubular cells, a process involved in kidney fibrosis [111]. This pro-inflammatory, but also pro-apoptotic, effect of pCS on human proximal tubular epithelial cells (PTEC) was confirmed by Poveda et al. [112]. Interestingly, pCS was shown to inhibit the activity of the human conditionally immortalized PTEC efflux transporters Multidrug Resistance Protein 4 (MRP4) and Breast Cancer Resistance Protein (BCRP), by 40% and 25%, respectively. These are two efflux transporters involved in pumping solutes out of the tubular cell, of which inhibition may possibly lead to intracellular accumulation and increased toxicity of the substrates of those transporters which are various organic acids amongst which pCS, which may contribute to progression of CKD [113].
Finally, pCS was shown to play a role in insulin resistance, in aberrant adipose tissue metabolism, and reallocation of fat in the body [114], in hampering calcium deposition and osteoprotegrin expression in human mesenchymal stem cells and in suppressing the immune response by Th1-cells [115] and macrophages [116].
Hence, pCS contributes to many mechanisms that are involved in cardiovascular and renal damage. The question is whether these experimental findings are corroborated in clinical studies.

5.2. Clinical Associations

As summarized in Table 2, both increasing levels of total and free pCS [117,118,119,120,121,122,123,124,125,126,127,128], as well as its urinary excretion [129], have been repeatedly associated with cardiovascular complications and mortality in patients with CKD whether or not on dialysis [130]. In addition, total pCS has been linked to progression of renal failure [131]. Recently, total pCS also has been associated with pruritus in CKD [132].

6. Therapeutic Methods for Reducing p-Cresyl Sulfate Concentration

6.1. Affecting the Generation of pCS

Most strategies to lower plasma pCS levels (summarized in Table 3) are based on solute removal by dialysis (see below) and are, to a lesser extent, focused on suppressing solute production.

6.1.1. Diet

Diet has a major effect on the gut microbial composition, considering that healthy colon microbiota is primarily composed by saccharolytic bacteria whereas, in CKD, proteolytic bacteria predominate. Saccharolytic bacterial species mainly ferment carbohydrates, which yields short chain fatty acids, such as acetate, butyrate, and propionate, which are beneficial to the host [17]. Proteolytic bacterial species, on the other hand, predominantly metabolize proteins resulting in the generation of a variety of end products including short or branched chain fatty acids, ammonia, amines, thiols, phenols, and indoles, some of which have toxic properties [134]. Thus, a potential way to lower the generation of proteolysis-derived microbial metabolites such as phenol and p-cresol is trying to alter the gut metabolism in favour of a saccharolytic profile by increasing the dietary intake of complex carbohydrates and fibers while decreasing dietary protein intake [29,134], and some data indeed suggest that this is the case [17,135]. Exclusion of dietary protein intake by adhering to a vegan diet was shown to decrease bacterial urease activity by 66% [136], and also to cause a decline of serum and urinary p-cresol and phenol levels [136]. Patel et al. demonstrated a decrease of urinary pCS levels by 62% in healthy vegetarians, who consume 25% less protein and 69% more fibre than individuals consuming an unrestricted diet [137]. To the contrary, when protein intake was enriched by 8.4% in healthy humans, urinary p-cresol levels increased from a mean concentration of 7.71 ± 2.47 mg/g creatinine in the control period to 17.59 ± 4.58 mg/g creatinine in the protein rich period [64]. This is in agreement with a study in healthy subjects on a controlled diet, whereby increasing the protein intake by 73.3 g/day, mainly by increasing meat intake, resulted in a an elevation of the level of total urinary volatile phenol from a concentration of 74 ± 14.5 mg/day in the low protein diet period to 108 ± 14.6 mg/day in the high protein diet period. On other hand, addition of 29.8 g of wheat fibre per day to the high protein diet induced a non-significant downward trend in total urinary phenol levels [138]. However, for some bacterial species the presence of carbohydrates also stimulates the dissimilation of aromatic amino acids [29] or is needed for activating the aromatic amino acid metabolism because of their inability to use amino acids as their sole carbon and energy source [93]. Birkett et al. demonstrated in healthy volunteers that a diet consisting of high resistant starch decreased faecal p-cresol and phenol concentrations by about 29 ± 2 µg/g and 1.0 ± 0.1 µg/g, respectively, however without a significant effect on urinary p-cresol concentrations [139]. Rossi et al. showed that carbohydrates are an important factor in reducing free and total pCS levels in non-dialyzed CKD patients, with total dietary fibre, negatively, and protein-fibre index, positively associated with total serum pCS [140]. Additionally, in HD patients, increased dietary fibre intake resulted in a lower free plasma pCS [141]. An animal study in uremic rats ingesting fermentable dietary fibre high amylose maize resistant starch type 2 (HAMRS2) resulted in a decrease of cecal pH and urinary p-cresol by 47%. The microbial diversity was also decreased in this group while the Bacteroidetes-to-Firmicutes ratio increased. The latter is considered to be an indicator of a healthy gut [142]. It is of note a rigid dietary protein restriction in CKD/HD patients is not a good solution to diminish uremic toxins level because inadequate dietary protein intake contributes to malnutrition [58]. According to the British diabetic association evidence-based guidelines, a minimum protein intake of 1.1 g/kg ideal body weight (IBW)/day and 1.0–1.2 g/kg IBW/day is required for HD and PD patients, respectively [143]. Irrespective of protein intake, patients with CKD are in addition often prescribed a combined diet to prevent fluid overload, hyperphosphatemia and hyperkalemia, with restrictive intake of fruits, vegetables, and high-fibre products [82], which is likely to alter the fermentation in favour of a proteolytic profile, increasing the generation of the unwanted phenolic compounds. In a meta-analysis, supplementation of a restricted protein diet with ketoacid analogues of essential amino acids has been suggested to delay the progression of CKD effectively without causing malnutrition [144]. In addition, this therapy has been shown to improve the native arteriovenous fistula maturation, to decrease the initial vascular stiffness and to limit inflammatory response in CKD patients [145]. However, the effects of keto-analogues on intestinal microbiota and on levels of intestinally-generated uremic toxins has to our knowledge as yet not been evaluated.

6.1.2. Probiotics, Prebiotics, and Synbiotics

Several studies demonstrated favourable effects on p-cresol metabolism due to the administration of probiotics, prebiotics, and synbiotics [85,146,147,148,149,150,151,152,153,154,155,156,157]. In general, pre- and probiotics aim to increase the saccharolytic activity of colonic bacteria because of the beneficial effects attributed to the end products of carbohydrate fermentation and to decrease the generation of the proteolytic fermentation end products of which some have toxic effects [146]. Administration of the probiotic Lactobacillus acidophilus (1 × 1010 CFU/kg/day) mitigated urinary protein excretion in nephrectomised rats and lowered serum pCS levels. However, administration of L. acidophilus had no effect on faecal p-cresol and phenol levels. This suggests that the reduced serum pCS levels are primarly due to blocking of p-cresol entry from the intestine into the circulation through restoring the intestinal tight junction protein expression by L. acidophilus [87]. With regard to the effect of probiotics on the pCS levels in healthy humans, as reviewed by Rossi et al. [147], it has been shown that probiotic Lactobacillus strains are associated with a decreased urinary p-cresol excretion [148] along with decreased faecal bacterial β-glucuronidase, nitroreductase and glycocholic acid hydrolase enzyme activities [158]. At least one strain of Lactobacillus gasseri has the ability to decrease faecal p-cresol levels in healthy subjects and to lower the number of cells of Staphylococcus [149], a proteolytic bacterium [30]. Also dietary addition of the probiotic Lactobacillus casei Shirota strain or the probiotic Bifidobacterium breve Yakult strain resulted in a decrease of urinary p-cresol in healthy volunteers [146]. Furthermore, Lebenin, an oral preparation of lactic acid bacteria containing Bifidobacterium infantis, Enterococcus faecalis, and L. acidophilus decreased faecal p-cresol levels in healthy persons [85]. In contrast, in pediatric HD and PD patients, a high concentration of a probiotic preparation, containing Lactobacillus spp., Bifidobacterium spp., and Streptococcus salivarius subsp. thermophilus, had no effect on the serum pCS levels [159]. Lowering the pH value by lactic acid producing bacteria, such as Lactobacillus and Streptococcus spp., reduced the dissimilatory metabolism of aromatic amino acids [29] and suppressed aerobic bacterial overgrowth [85], which in its turn reduces the accumulation of pCS.
Administration of prebiotics, such as lactulose or oligofructose-enriched inulin (OF-IN) to healthy humans, resulted in a significant reduction of p-cresol in the urine for both substrates, with OF-IN having the largest effect (from 27.7 ± 15.3 mg/day to 17.8 ± 10.8 mg/day) compared to the lactulose group (from 20.7 ± 11.6 mg/day to 12.7 ± 8.9 mg/day) [150]. Using real-time PCR, it was shown that the total number of bifidobacteria in faeces were elevated after administration of both prebiotics [146,150]. Davis et al. demonstrated that administration of the prebiotic galacto-oligosaccharide (GOS) during 12 weeks to healthy humans resulted in a dose-dependent increased abundance of actinobacteria with specific enrichment of bifidobacteria at the expense of the Bacteroides group [151]. In HD patients, OF-IN decreased the pCS generation rate and serum pCS concentrations by 20% [152]. Acarbose, a small intestinal α-glucosidase inhibitor, is another prebiotic that is administered to increase undigested carbohydrate levels in the colon. Acarbose was shown to lower serum p-cresol concentration and urinary p-cresol excretion, the latter reflecting its colonic generation rate [153]. However, Poesen et al. could not establish any effect of the prebiotic arabinoxylan oligosaccharide on serum and 24 h urinary excretion pCS and pCG levels in CKD patients [154].
Finally, the combination of pre- and probiotics, the so-called synbiotics, more recently gained interest. In healthy humans, long-term administration of the L. casei Shirota strain in association with OF-IN resulted in a significant urinary p-cresol reduction [146]. Similar effects were shown in HD patients, in who synbiotic administration, consisting of the L. casei Shirota strain, the B. breve Yakult strain, and GOS, decreased serum p-cresol levels [155]. Additionally, Probinul-neutro, a synbiotic containing Lactobacillaceae, Bifidobactericeae, S. thermophilus, inulin, and tapioca-resistant starch, reduced total plasma p-cresol concentrations in non-dialyzed CKD patient stages 3–4 [156]. In a randomized controlled trial (RCT), Rossi et al. recently demonstrated a significant reduction of serum pCS in CKD patients administered a combination of inulin, fructo-oligosaccharides, GOS, and different strains belonging to the genera Lactobacillus, Bifidobacteria, and Streptococcus. This decrease was even more marked if the patients who had received antibiotics in this study (about 1/3 of the enrolled subjects) were excluded [157].

6.1.3. Laxatives

In CKD patients, the colonic transit time is prolonged mainly in the colon ascendens and in the recto-sigmoid segment [160]. Constipation was documented to occur more frequently in HD patients (63.1% of 268 patients) compared to continuous ambulatory peritoneal dialysis (CAPD) patients (28.9% of 204 patients) [161]. The higher frequency of constipation, in general, is due to several factors, such as dietary restrictions, medication, lifestyle, low fluid intake, and comorbidity [8]. Longer colonic transit time results in an elevated bacterial fermentation of amino acids [75,138] and may subsequently induce an overgrowth of proteolytic bacteria in the human colon. In a study of Roager et al., urinary pCS and pCG correlated positively with colonic transit time [75]. A consecutive stepwise three-stage in vitro culture model mimicking the colon with fresh faecal slurries as initial substrate entered into the system showed a higher p-cresol and phenol concentration with longer transit time [29]. From this point of view it might be interesting to study in future whether administration of laxatives might decrease pCS levels.

6.2. Adsorption

6.2.1. AST-120

Decreasing the uptake of colon-derived solutes by administering oral adsorbents, such as AST-120, might be another option to lower pCS levels. Administration of AST-120 in CKD rats resulted in a decrease of serum pCS [162] and of p-cresol levels and a reduction of p-cresol urinary excretion [163]. This is in agreement with a recent study of Velenosi et al., demonstrating a significant reduction of pCS and pCG in plasma, heart, kidney, and liver of uremic rats after AST-120 administration [164]. Next to decreasing serum and urinary pCS levels, AST-120 also changed overall gut microbiota composition in uremic rats [74]. In dialyzed patients, treatment with AST-120 resulted in a decrease of total and free pCS plasma levels [165,166]. Thus, AST-120 is a potential treatment to lower pCS and even pCG levels in CKD patients, but this treatment does not have a lasting effect after intake discontinuation [165]. Two recent RCTs in CKD patients, in which plasma levels of pCS were not reported, showed no beneficial effect of AST-120 on the progression of CKD [167,168]. In one of these studies, however, the evolution of the concentration of another protein-bound compound, indoxyl sulfate (IxS), was followed, without changing a change in concentration in the group on AST-120 [168].

6.3. Preserving Kidney Function

In healthy kidneys, urinary excretion of protein-bound metabolites like pCS is, in large part, determined by tubular secretion rather than filtration, which shifts the binding and allows active secretion of these solutes. To mediate urinary solute excretion, renal proximal tubules are equipped with a range of transporters that cooperate in basolateral uptake (e.g., organic anion transporter (OAT)-1 and OAT-3) and luminal excretion, such as multidrug resistance protein (MRP)-4 and breast cancer resistance protein (BCRP). It is conceivable that these functions are lost as kidney failure progresses and that any intervention to prevent this progression will also result in less retention of uremic solutes, including pCS.

6.4. Dialysis and Renal Transplantation

6.4.1. Dialysis

Due to their binding, protein-bound uremic toxins, such as pCS, are poorly filtered across dialysis membranes. Pre-and post-dilution hemodiafiltration (HDF) increased the reduction ratios of pCS when compared to high flux hemodialysis (HFHD) [169] and when compared to pre-dilution hemofiltration [170]. Thus, combining convective with diffusive removal seems to improve removal of protein-bound toxins during dialysis. However, these results were not confirmed in a study by Krieter et al. [171], who did not find superior reduction ratios for pCS with post-dilution HDF compared to HFHD. In a longitudinal setting, after six months of treatment with pre-dilution hemofiltration, the concentrations of total and free p-cresol, representing the combination of pCS and pCG, were reduced compared to low-flux dialysis used before the start of the study [10]. Similarly, a decrease in the predialysis concentration of total pCS was observed after nine weeks of post-dilution HDF compared to high-flux dialysis before the start of the study [172]. Even if reductions with convective strategies are significant, the question is whether these changes are clinically relevant. Increase in dialysate flow (QD) and dialyzer surface (KoA) is another way to increase the clearance of pCS [173]. The same group pointed to the fact that in dialysis patients, a notable fraction of the weekly solute removal of protein-bound toxins is accomplished by residual renal function (RRF) [174].
A possible promising strategy to optimize the removal of protein-bound toxins could be the use of sorbent technology in dialysis. Using fractional plasma separation and absorption (FPAD), the reduction ratios of p-cresol were doubled in comparison to HFHD. This study however, was discontinued due to serious clotting problems [175]. In a more recent study, removal rates of FPAD treatment in comparison to HFHD were 127% for p-cresol [176]. In an in vitro setting, pCS was fully absorbed from dialysate by a commercially available activated carbon sorber [177]. In pilot in vitro experiments, mixed matrix membranes, that contained incorporated activated carbon, adsorbed on average 2.27 mg pCS/g membrane in 4 h in diffusion experiments and 2.68 mg pCS/g membrane in convection experiments. It was estimated that the membranes would suffice to remove the daily production of pCS [178]. Recently, alternative sorbents were proposed. A nanoporous activated carbon monolith prototype designed for direct blood contact was shown to almost completely remove pCS in vitro [179] and highly porous microparticles prepared from poly(etherimide) were also able to highly absorb pCS with high affinity [180]. In an in vitro hemodiafiltration setting aiming to interfere with protein binding by increasing plasma ion strength (IPIS; hypertonic NaCl solution), the clearance of pCS was increased by 53.6% ± 10.2% [181]. In a pilot RCT comparing HDF-IPIS to HD and HDF only an increase in dialytic clearance of free IxS, but not of pCS was observed [182].
In PD, the total clearance, dialysis plus RRF, of p-cresol as surrogate for pCS was markedly lower compared to HFHD, in spite of less removal per unit of time with PD [183]. In contrast to the water-soluble compounds, PD clearance of pCS did not increase when RRF was lost, but nevertheless no rise in their plasma concentration occurred [184]. In a more recent prospective observational cohort of incident PD patients, PD clearance tended to increase, but did not compensate for the declining renal clearance, with as a consequence that serum pCS concentrations increased in parallel with loss of RRF [185]. The importance of RRF in removal of pCS in PD patients was recently confirmed by Huang et al. [186]. The fact that, despite the lower removal rate, the plasma concentration of protein-bound compounds is lower in PD patients that in HD patients [183,184], is suggesting that other, possibly metabolic, factors are determining pCS concentrations [187]. Additionally, in HD patients, concentrations of pCS seem dependent on protein equivalent of nitrogen appearance and not on dialysis adequacy as assessed by Kt/V (urea) [188].

6.4.2. Renal Transplantation

Finally, with renal transplantation, decreases of serum pCS (and pCG) were observed at each of the analysed time points post-transplantation (day 7 and three and 12 months) [189]. Levels were significantly lower in transplant recipients when compared with CKD control patients with the same kidney function. Further analysis demonstrated significantly lower 24 h urinary excretion of these solutes in transplant recipients in spite of virtually identical glomerular filtration rates (GFR) [190]. Thus, differences in GFR do not seem to play a major role in this lower concentration of pCS among renal transplants. These changes may be due to immunosuppressive agents, antibiotics, other drugs, the transplantation procedure itself [191].

7. Conclusions and Future Perspectives

The protein-bound uremic toxin, p-cresyl sulfate, originates from the bacterial metabolism in the intestine and several phenolic compound-generating bacteria have been identified. Circulating levels of pCS are increased in CKD and increased levels have been associated with worse outcome of CKD patients. The currently available therapeutic methods trying to decrease levels of pCS, among other protein-bound uremic toxins, still remain inadequate. Targeting its generation seems an attractive measure, which could not only be applied as a preventive measure at earlier stages of CKD, but also in addition to dialysis at the end stage. Development of intervention strategies at the level of the intestinal microbiota first needs a thorough characterization of the uremic microbiome and its functional capacity.

Acknowledgments

The first author is supported by The Research Foundation Flanders (FWO Vlaanderen) grant No. G017815N.

Author Contributions

All authors contributed substantially to the writing of review.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Duranton, F.; Cohen, G.; de Smet, R.; Rodriguez, M.; Jankowski, J.; Vanholder, R.; Argiles, A. Normal and pathologic concentrations of uremic toxins. J. Am. Soc. Nephrol. 2012, 23, 1258–1270. [Google Scholar] [CrossRef] [PubMed]
  2. Vanholder, R.; de Smet, R.; Glorieux, G.; Argiles, A.; Baurmeister, U.; Brunet, P.; Clark, W.; Cohen, G.; de Deyn, P.P.; Deppisch, R.; et al. Review on uremic toxins: Classification, concentration, and interindividual variability. Kidney Int. 2003, 63, 1934–1943. [Google Scholar] [CrossRef] [PubMed]
  3. Vanholder, R.; Glorieux, G.; de Smet, R.; Lameire, N. New insights in uremic toxins. Kidney Int. Suppl. 2003, S6–S10. [Google Scholar] [CrossRef] [PubMed]
  4. Meyer, T.W.; Hostetter, T.H. Uremia. N. Engl. J. Med. 2007, 357, 1316–1325. [Google Scholar] [CrossRef] [PubMed]
  5. Vanholder, R.; de Smet, R. Pathophysiologic effects of uremic retention solutes. J. Am. Soc. Nephrol. 1999, 10, 1815–1823. [Google Scholar] [PubMed]
  6. Vanholder, R.; Massy, Z.; Argiles, A.; Spasovski, G.; Verbeke, F.; Lameire, N. Chronic kidney disease as cause of cardiovascular morbidity and mortality. Nephrol. Dial. Transplant. 2005, 20, 1048–1056. [Google Scholar] [CrossRef] [PubMed]
  7. Vanholder, R.; Baurmeister, U.; Brunet, P.; Cohen, G.; Glorieux, G.; Jankowski, J. A bench to bedside view of uremic toxins. J. Am. Soc. Nephrol. 2008, 19, 863–870. [Google Scholar] [CrossRef] [PubMed]
  8. Evenepoel, P.; Meijers, B.K.; Bammens, B.R.; Verbeke, K. Uremic toxins originating from colonic microbial metabolism. Kidney Int. Suppl. 2009, S12–S19. [Google Scholar] [CrossRef] [PubMed]
  9. Lesaffer, G.; de Smet, R.; Lameire, N.; Dhondt, A.; Duym, P.; Vanholder, R. Intradialytic removal of protein-bound uraemic toxins: Role of solute characteristics and of dialyser membrane. Nephrol. Dial. Transplant. 2000, 15, 50–57. [Google Scholar] [CrossRef] [PubMed]
  10. Meert, N.; Beerenhout, C.; Schepers, E.; Glorieux, G.; Kooman, J.; Vanholder, R. Evolution of protein-bound uraemic solutes during predilution haemofiltration. J. Nephrol. 2009, 22, 352–357. [Google Scholar] [PubMed]
  11. Deltombe, O.; Van Biesen, W.; Glorieux, G.; Massy, Z.; Dhondt, A.; Eloot, S. Exploring protein binding of uremic toxins in patients with different stages of chronic kidney disease and during hemodialysis. Toxins (Basel) 2015, 7, 3933–3946. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Pretorius, C.J.; McWhinney, B.C.; Sipinkoski, B.; Johnson, L.A.; Rossi, M.; Campbell, K.L.; Ungerer, J.P. Reference ranges and biological variation of free and total serum indoxyl- and p-cresyl sulphate measured with a rapid UPLC fluorescence detection method. Clin. Chim. Acta 2013, 419, 122–126. [Google Scholar] [CrossRef] [PubMed]
  13. Boelaert, J.; Lynen, F.; Glorieux, G.; Eloot, S.; Van Landschoot, M.; Waterloos, M.A.; Sandra, P.; Vanholder, R. A novel UPLC-MS-MS method for simultaneous determination of seven uremic retention toxins with cardiovascular relevance in chronic kidney disease patients. Anal. Bioanal. Chem. 2013, 405, 1937–1947. [Google Scholar] [CrossRef] [PubMed]
  14. Lin, C.J.; Chen, H.H.; Pan, C.F.; Chuang, C.K.; Wang, T.J.; Sun, F.J.; Wu, C.J. p-Cresylsulfate and indoxyl sulfate level at different stages of chronic kidney disease. J. Clin. Lab. Anal. 2011, 25, 191–197. [Google Scholar] [CrossRef] [PubMed]
  15. Cuoghi, A.; Caiazzo, M.; Bellei, E.; Monari, E.; Bergamini, S.; Palladino, G.; Ozben, T.; Tomasi, A. Quantification of p-cresol sulphate in human plasma by selected reaction monitoring. Anal. Bioanal. Chem. 2012, 404, 2097–2104. [Google Scholar] [CrossRef] [PubMed]
  16. Hooper, L.V.; Gordon, J.I. Commensal host-bacterial relationships in the gut. Science 2001, 292, 1115–1118. [Google Scholar] [CrossRef] [PubMed]
  17. Flint, H.J.; Scott, K.P.; Louis, P.; Duncan, S.H. The role of the gut microbiota in nutrition and health. Nat. Rev. Gastroenterol. Hepatol. 2012, 9, 577–589. [Google Scholar] [CrossRef] [PubMed]
  18. Frank, D.N.; St Amand, A.L.; Feldman, R.A.; Boedeker, E.C.; Harpaz, N.; Pace, N.R. Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases. Proc. Natl. Acad. Sci. USA 2007, 104, 13780–13785. [Google Scholar] [CrossRef] [PubMed]
  19. Francescone, R.; Hou, V.; Grivennikov, S.I. Microbiome, inflammation, and cancer. Cancer J. 2014, 20, 181–189. [Google Scholar] [CrossRef] [PubMed]
  20. Ley, R.E.; Turnbaugh, P.J.; Klein, S.; Gordon, J.I. Microbial ecology: Human gut microbes associated with obesity. Nature 2006, 444, 1022–1023. [Google Scholar] [CrossRef] [PubMed]
  21. Dunne, J.L.; Triplett, E.W.; Gevers, D.; Xavier, R.; Insel, R.; Danska, J.; Atkinson, M.A. The intestinal microbiome in type 1 diabetes. Clin. Exp. Immunol. 2014, 177, 30–37. [Google Scholar] [CrossRef] [PubMed]
  22. Qin, J.; Li, Y.; Cai, Z.; Li, S.; Zhu, J.; Zhang, F.; Liang, S.; Zhang, W.; Guan, Y.; Shen, D.; et al. A metagenome-wide association study of gut microbiota in type 2 diabetes. Nature 2012, 490, 55–60. [Google Scholar] [CrossRef] [PubMed]
  23. Rajendhran, J.; Shankar, M.; Dinakaran, V.; Rathinavel, A.; Gunasekaran, P. Contrasting circulating microbiome in cardiovascular disease patients and healthy individuals. Int. J. Cardiol. 2013, 168, 5118–5120. [Google Scholar] [CrossRef] [PubMed]
  24. Ramezani, A.; Raj, D.S. The gut microbiome, kidney disease, and targeted interventions. J. Am. Soc. Nephrol. 2014, 25, 657–670. [Google Scholar] [CrossRef] [PubMed]
  25. Backhed, F.; Ley, R.E.; Sonnenburg, J.L.; Peterson, D.A.; Gordon, J.I. Host-bacterial mutualism in the human intestine. Science 2005, 307, 1915–1920. [Google Scholar] [CrossRef] [PubMed]
  26. Guarner, F. Enteric flora in health and disease. Digestion 2006, 73 (Suppl. 1), 5–12. [Google Scholar] [CrossRef] [PubMed]
  27. Yao, C.K.; Muir, J.G.; Gibson, P.R. Review article: Insights into colonic protein fermentation, its modulation and potential health implications. Aliment. Pharmacol. Ther. 2016, 43, 181–196. [Google Scholar] [CrossRef] [PubMed]
  28. Chacko, A.; Cummings, J.H. Nitrogen losses from the human small bowel: Obligatory losses and the effect of physical form of food. Gut 1988, 29, 809–815. [Google Scholar] [CrossRef] [PubMed]
  29. Smith, E.A.; Macfarlane, G.T. Enumeration of human colonic bacteria producing phenolic and indolic compounds: Effects of pH, carbohydrate availability and retention time on dissimilatory aromatic amino acid metabolism. J. Appl. Bacteriol. 1996, 81, 288–302. [Google Scholar] [CrossRef] [PubMed]
  30. Macfarlane, G.T.; Cummings, J.H.; Allison, C. Protein degradation by human intestinal bacteria. J. Gen. Microbiol. 1986, 132, 1647–1656. [Google Scholar] [CrossRef] [PubMed]
  31. Gibson, S.A.; McFarlan, C.; Hay, S.; MacFarlane, G.T. Significance of microflora in proteolysis in the colon. Appl. Environ. Microbiol. 1989, 55, 679–683. [Google Scholar] [PubMed]
  32. Smith, E.A.; Macfarlane, G.T. Dissimilatory amino Acid metabolism in human colonic bacteria. Anaerobe 1997, 3, 327–337. [Google Scholar] [CrossRef] [PubMed]
  33. Ramakrishna, B.S.; Gee, D.; Weiss, A.; Pannall, P.; Roberts-Thomson, I.C.; Roediger, W.E. Estimation of phenolic conjugation by colonic mucosa. J. Clin. Pathol. 1989, 42, 620–623. [Google Scholar] [CrossRef] [PubMed]
  34. Schepers, E.; Glorieux, G.; Vanholder, R. The gut: The forgotten organ in uremia? Blood Purif. 2010, 29, 130–136. [Google Scholar] [CrossRef] [PubMed]
  35. Poesen, R.; Evenepoel, P.; de Loor, H.; Kuypers, D.; Augustijns, P.; Meijers, B. Metabolism, protein binding, and renal clearance of microbiota-derived p-cresol in patients with CKD. Clin. J. Am. Soc. Nephrol. 2016, 11, 1136–1144. [Google Scholar] [CrossRef] [PubMed]
  36. de Loor, H.; Bammens, B.; Evenepoel, P.; de Preter, V.; Verbeke, K. Gas chromatographic-mass spectrometric analysis for measurement of p-cresol and its conjugated metabolites in uremic and normal serum. Clin. Chem. 2005, 51, 1535–1538. [Google Scholar] [CrossRef] [PubMed]
  37. Meyer, T.W.; Hostetter, T.H. Uremic solutes from colon microbes. Kidney Int. 2012, 81, 949–954. [Google Scholar] [CrossRef] [PubMed]
  38. Suchy-Dicey, A.M.; Laha, T.; Hoofnagle, A.; Newitt, R.; Sirich, T.L.; Meyer, T.W.; Thummel, K.E.; Yanez, N.D.; Himmelfarb, J.; Weiss, N.S.; et al. Tubular secretion in CKD. J. Am. Soc. Nephrol. 2016, 27, 2148–2155. [Google Scholar] [CrossRef] [PubMed]
  39. Vanholder, R.; Bammens, B.; de Loor, H.; Glorieux, G.; Meijers, B.; Schepers, E.; Massy, Z.; Evenepoel, P. Warning: The unfortunate end of p-cresol as a uraemic toxin. Nephrol. Dial. Transplant. 2011, 26, 1464–1467. [Google Scholar] [CrossRef] [PubMed]
  40. Kumagai, H.; Matsui, H.; Yamada, H. Formation of tyrosine phenol-lyase by bacteria. Agric. Biol. Chem. 1970, 34, 1259–1261. [Google Scholar] [CrossRef]
  41. Brot, N.; Smit, Z.; Weissbach, H. Conversion of l-tyrosine to phenol by Clostridium tetanomorphum. Arch. Biochem. Biophys. 1965, 112, 1–6. [Google Scholar] [CrossRef]
  42. Chandel, M.; Azmi, W. Optimization of process parameters for the production of tyrosine phenol lyase by Citrobacter freundii MTCC 2424. Bioresour. Technol. 2009, 100, 1840–1846. [Google Scholar] [CrossRef] [PubMed]
  43. Enei, H.; Matsui, H.; Yamashita, K. Distribution of tyrosine phenol lyase in microorganisms. Agric. Biol. Chem. 1972, 36, 1861–1868. [Google Scholar] [CrossRef]
  44. Blakley, E.R. The catabolism of l-tyrosine by an Arthrobacter sp. Can. J. Microbiol. 1977, 23, 1128–1139. [Google Scholar] [CrossRef] [PubMed]
  45. Powell, J.T.; Morrison, J.F. The purification and properties of the aspartate aminotransferase and aromatic-amino-acid aminotransferase from Escherichia coli. Eur. J. Biochem. 1978, 87, 391–400. [Google Scholar] [CrossRef] [PubMed]
  46. Gummalla, S.; Broadbent, J.R. Tyrosine and phenylalanine catabolism by Lactobacillus cheese flavor adjuncts. J. Dairy Sci. 2001, 84, 1011–1019. [Google Scholar] [CrossRef]
  47. Seah, S.Y.; Britton, K.L.; Rice, D.W.; Asano, Y.; Engel, P.C. Single amino acid substitution in Bacillus sphaericus phenylalanine dehydrogenase dramatically increases its discrimination between phenylalanine and tyrosine substrates. Biochemistry 2002, 41, 11390–11397. [Google Scholar] [CrossRef] [PubMed]
  48. Selmer, T.; Andrei, P.I. p-Hydroxyphenylacetate decarboxylase from Clostridium difficile. A novel glycyl radical enzyme catalysing the formation of p-cresol. Eur. J. Biochem. 2001, 268, 1363–1372. [Google Scholar] [CrossRef] [PubMed]
  49. Yokoyama, M.T.; Carlson, J.R. Production of skatole and para-cresol by a rumen Lactobacillus sp. Appl. Environ. Microbiol. 1981, 41, 71–76. [Google Scholar] [PubMed]
  50. Brix, L.A.; Barnett, A.C.; Duggleby, R.G.; Leggett, B.; McManus, M.E. Analysis of the substrate specificity of human sulfotransferases SULT1A1 and SULT1A3: Site-directed mutagenesis and kinetic studies. Biochemistry 1999, 38, 10474–10479. [Google Scholar] [CrossRef] [PubMed]
  51. King, C.D.; Rios, G.R.; Green, M.D.; Tephly, T.R. UDP-glucuronosyltransferases. Curr. Drug Metab. 2000, 1, 143–161. [Google Scholar] [CrossRef] [PubMed]
  52. Erlandsen, H.; Kim, J.Y.; Patch, M.G.; Han, A.; Volner, A.; Abu-Omar, M.M.; Stevens, R.C. Structural comparison of bacterial and human iron-dependent phenylalanine hydroxylases: Similar fold, different stability and reaction rates. J. Mol. Biol. 2002, 320, 645–661. [Google Scholar] [CrossRef]
  53. Fitzpatrick, P.F. Mechanism of aromatic amino acid hydroxylation. Biochemistry 2003, 42, 14083–14091. [Google Scholar] [CrossRef] [PubMed]
  54. Asano, Y.; Nakazawa, A.; Endo, K.; Hibino, Y.; Ohmori, M.; Numao, N.; Kondo, K. Phenylalanine dehydrogenase of Bacillus badius. Purification, characterization and gene cloning. Eur. J. Biochem. 1987, 168, 153–159. [Google Scholar] [CrossRef] [PubMed]
  55. Lee-Peng, F.C.; Hermodson, M.A.; Kohlhaw, G.B. Transaminase B from Escherichia coli: Quaternary structure, amino-terminal sequence, substrate specificity, and absence of a separate valine-alpha-ketoglutarate activity. J. Bacteriol. 1979, 139, 339–345. [Google Scholar] [PubMed]
  56. Asakawa, T.; Wada, H.; Yamano, T. Enzymatic conversion of phenylpyruvate to phenylacetate. Biochim. Biophys. Acta 1968, 170, 375–391. [Google Scholar] [CrossRef]
  57. Ferrandez, A.; Prieto, M.A.; Garcia, J.L.; Diaz, E. Molecular characterization of PadA, a phenylacetaldehyde dehydrogenase from Escherichia coli. FEBS Lett. 1997, 406, 23–27. [Google Scholar] [CrossRef]
  58. Bammens, B.; Verbeke, K.; Vanrenterghem, Y.; Evenepoel, P. Evidence for impaired assimilation of protein in chronic renal failure. Kidney Int. 2003, 64, 2196–2203. [Google Scholar] [CrossRef] [PubMed]
  59. Bammens, B.; Evenepoel, P.; Verbeke, K.; Vanrenterghem, Y. Impairment of small intestinal protein assimilation in patients with end-stage renal disease: Extending the malnutrition-inflammation-atherosclerosis concept. Am. J. Clin. Nutr. 2004, 80, 1536–1543. [Google Scholar] [PubMed]
  60. Qureshi, A.R.; Alvestrand, A.; Danielsson, A.; Divino-Filho, J.C.; Gutierrez, A.; Lindholm, B.; Bergstrom, J. Factors predicting malnutrition in hemodialysis patients: A cross-sectional study. Kidney Int. 1998, 53, 773–782. [Google Scholar] [CrossRef] [PubMed]
  61. Cianciaruso, B.; Brunori, G.; Kopple, J.D.; Traverso, G.; Panarello, G.; Enia, G.; Strippoli, P.; de Vecchi, A.; Querques, M.; Viglino, G.; et al. Cross-sectional comparison of malnutrition in continuous ambulatory peritoneal dialysis and hemodialysis patients. Am. J. Kidney Dis. 1995, 26, 475–486. [Google Scholar] [CrossRef]
  62. Evenepoel, P.; Claus, D.; Geypens, B.; Hiele, M.; Geboes, K.; Rutgeerts, P.; Ghoos, Y. Amount and fate of egg protein escaping assimilation in the small intestine of humans. Am. J. Physiol. 1999, 277, G935–G943. [Google Scholar] [PubMed]
  63. Evenepoel, P.; Claus, D.; Geypens, B.; Maes, B.; Hiele, M.; Rutgeerts, P.; Ghoos, Y. Evidence for impaired assimilation and increased colonic fermentation of protein, related to gastric acid suppression therapy. Aliment. Pharmacol. Ther. 1998, 12, 1011–1019. [Google Scholar] [CrossRef] [PubMed]
  64. Geypens, B.; Claus, D.; Evenepoel, P.; Hiele, M.; Maes, B.; Peeters, M.; Rutgeerts, P.; Ghoos, Y. Influence of dietary protein supplements on the formation of bacterial metabolites in the colon. Gut 1997, 41, 70–76. [Google Scholar] [CrossRef] [PubMed]
  65. McCullough, A.J.; Mullen, K.D.; Tavill, A.S.; Kalhan, S.C. In vivo differences between the turnover rates of leucine and leucine’s ketoacid in stable cirrhosis. Gastroenterology 1992, 103, 571–578. [Google Scholar] [CrossRef]
  66. Halvatsiotis, P.G.; Turk, D.; Alzaid, A.; Dinneen, S.; Rizza, R.A.; Nair, K.S. Insulin effect on leucine kinetics in type 2 diabetes mellitus. Diabetes Nutr. Metab. 2002, 15, 136–142. [Google Scholar] [PubMed]
  67. Mitch, W.E.; Price, S.R.; May, R.C.; Jurkovitz, C.; England, B.K. Metabolic consequences of uremia: Extending the concept of adaptive responses to protein metabolism. Am. J. Kidney Dis. 1994, 23, 224–228. [Google Scholar] [CrossRef]
  68. Lim, V.S.; Yarasheski, K.E.; Flanigan, M.J. The effect of uraemia, acidosis, and dialysis treatment on protein metabolism: A longitudinal leucine kinetic study. Nephrol. Dial. Transplant. 1998, 13, 1723–1730. [Google Scholar] [CrossRef] [PubMed]
  69. Tremaroli, V.; Backhed, F. Functional interactions between the gut microbiota and host metabolism. Nature 2012, 489, 242–249. [Google Scholar] [CrossRef] [PubMed]
  70. Van der Meulen, R.; Camu, N.; Van Vooren, T.; Heymans, C.; de Vuyst, L. In vitro kinetic analysis of carbohydrate and aromatic amino acid metabolism of different members of the human colon. Int. J. Food Microbiol. 2008, 124, 27–33. [Google Scholar] [CrossRef] [PubMed]
  71. Ikeda, N.; Saito, Y.; Shimizu, J.; Ochi, A.; Mizutani, J.; Watabe, J. Variations in concentrations of bacterial metabolites, enzyme activities, moisture, pH and bacterial composition between and within individuals in faeces of seven healthy adults. J. Appl. Bacteriol. 1994, 77, 185–194. [Google Scholar] [CrossRef] [PubMed]
  72. Aronov, P.A.; Luo, F.J.; Plummer, N.S.; Quan, Z.; Holmes, S.; Hostetter, T.H.; Meyer, T.W. Colonic contribution to uremic solutes. J. Am. Soc. Nephrol. 2011, 22, 1769–1776. [Google Scholar] [CrossRef] [PubMed]
  73. Wikoff, W.R.; Anfora, A.T.; Liu, J.; Schultz, P.G.; Lesley, S.A.; Peters, E.C.; Siuzdak, G. Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites. Proc. Natl. Acad. Sci. USA 2009, 106, 3698–3703. [Google Scholar] [CrossRef] [PubMed]
  74. Kikuchi, M.; Ueno, M.; Itoh, Y.; Suda, W.; Hattori, M. Uremic toxin-producing gut microbiota in rats with chronic kidney disease. Nephron 2017, 135, 51–60. [Google Scholar] [CrossRef] [PubMed]
  75. Roager, H.M.; Hansen, L.B.; Bahl, M.I.; Frandsen, H.L.; Carvalho, V.; Gobel, R.J.; Dalgaard, M.D.; Plichta, D.R.; Sparholt, M.H.; Vestergaard, H.; et al. Colonic transit time is related to bacterial metabolism and mucosal turnover in the gut. Nat. Microbiol. 2016, 1, 16093. [Google Scholar] [CrossRef] [PubMed]
  76. Elsden, S.R.; Hilton, M.G.; Waller, J.M. The end products of the metabolism of aromatic amino acids by Clostridia. Arch. Microbiol. 1976, 107, 283–288. [Google Scholar] [CrossRef] [PubMed]
  77. Mead, G.C. The amino acid-fermenting Clostridia. J. Gen. Microbiol. 1971, 67, 47–56. [Google Scholar] [CrossRef] [PubMed]
  78. Giesel, H.; Simon, H. On the occurrence of enoate reductase and 2-oxo-carboxylate reductase in clostridia and some observations on the amino acid fermentation by Peptostreptococcus anaerobius. Arch. Microbiol. 1983, 135, 51–57. [Google Scholar] [CrossRef] [PubMed]
  79. Moss, C.W.; Lambert, M.A.; Goldsmith, D.J. Production of hydrocinnamic acid by Clostridia. Appl. Microbiol. 1970, 19, 375–378. [Google Scholar] [PubMed]
  80. Bone, E.; Tamm, A.; Hill, M. The production of urinary phenols by gut bacteria and their possible role in the causation of large bowel cancer. Am. J. Clin. Nutr. 1976, 29, 1448–1454. [Google Scholar] [PubMed]
  81. Walker, A.W.; Duncan, S.H.; Louis, P.; Flint, H.J. Phylogeny, culturing, and metagenomics of the human gut microbiota. Trends Microbiol. 2014, 22, 267–274. [Google Scholar] [CrossRef] [PubMed]
  82. Vaziri, N.D.; Wong, J.; Pahl, M.; Piceno, Y.M.; Yuan, J.; DeSantis, T.Z.; Ni, Z.; Nguyen, T.H.; Andersen, G.L. Chronic kidney disease alters intestinal microbial flora. Kidney Int. 2013, 83, 308–315. [Google Scholar] [CrossRef] [PubMed]
  83. Strid, H.; Simren, M.; Stotzer, P.O.; Ringstrom, G.; Abrahamsson, H.; Bjornsson, E.S. Patients with chronic renal failure have abnormal small intestinal motility and a high prevalence of small intestinal bacterial overgrowth. Digestion 2003, 67, 129–137. [Google Scholar] [CrossRef] [PubMed]
  84. Simenhoff, M.L.; Saukkonen, J.J.; Burke, J.F.; Wesson, L.G., Jr.; Schaedler, R.W.; Gordon, S.J. Bacterial populations of the small intestine in uremia. Nephron 1978, 22, 63–68. [Google Scholar] [CrossRef] [PubMed]
  85. Hida, M.; Aiba, Y.; Sawamura, S.; Suzuki, N.; Satoh, T.; Koga, Y. Inhibition of the accumulation of uremic toxins in the blood and their precursors in the feces after oral administration of Lebenin, a lactic acid bacteria preparation, to uremic patients undergoing hemodialysis. Nephron 1996, 74, 349–355. [Google Scholar] [CrossRef] [PubMed]
  86. Fukuuchi, F.; Hida, M.; Aiba, Y.; Koga, Y.; Endoh, M.; Kurokawa, K.; Sakai, H. Intestinal bacteria-derived putrefactants in chronic renal failure. Clin. Exp. Nephrol. 2002, 6, 99–104. [Google Scholar] [CrossRef]
  87. Yoshifuji, A.; Wakino, S.; Irie, J.; Tajima, T.; Hasegawa, K.; Kanda, T.; Tokuyama, H.; Hayashi, K.; Itoh, H. Gut Lactobacillus protects against the progression of renal damage by modulating the gut environment in rats. Nephrol. Dial. Transplant. 2016, 31, 401–412. [Google Scholar] [CrossRef] [PubMed]
  88. Barrios, C.; Beaumont, M.; Pallister, T.; Villar, J.; Goodrich, J.K.; Clark, A.; Pascual, J.; Ley, R.E.; Spector, T.D.; Bell, J.T.; et al. Gut-microbiota-metabolite axis in early renal function decline. PLoS ONE 2015, 10, e0134311. [Google Scholar] [CrossRef] [PubMed]
  89. Wang, I.K.; Lai, H.C.; Yu, C.J.; Liang, C.C.; Chang, C.T.; Kuo, H.L.; Yang, Y.F.; Lin, C.C.; Lin, H.H.; Liu, Y.L.; et al. Real-time PCR analysis of the intestinal microbiotas in peritoneal dialysis patients. Appl. Environ. Microbiol. 2012, 78, 1107–1112. [Google Scholar] [CrossRef] [PubMed]
  90. Bourke, E.; Milne, M.D.; Stokes, G.S. Caecal pH and ammonia in experimental uraemia. Gut 1966, 7, 558–561. [Google Scholar] [CrossRef] [PubMed]
  91. Wong, J.; Piceno, Y.M.; Desantis, T.Z.; Pahl, M.; Andersen, G.L.; Vaziri, N.D. Expansion of urease- and uricase-containing, indole- and p-cresol-forming and contraction of short-chain fatty acid-producing intestinal microbiota in ESRD. Am. J. Nephrol. 2014, 39, 230–237. [Google Scholar] [CrossRef] [PubMed]
  92. Mayrand, D.; Bourgeau, G. Production of phenylacetic acid by anaerobes. J. Clin. Microbiol. 1982, 16, 747–750. [Google Scholar] [PubMed]
  93. Russell, W.R.; Duncan, S.H.; Scobbie, L.; Duncan, G.; Cantlay, L.; Calder, A.G.; Anderson, S.E.; Flint, H.J. Major phenylpropanoid-derived metabolites in the human gut can arise from microbial fermentation of protein. Mol. Nutr. Food Res. 2013, 57, 523–535. [Google Scholar] [CrossRef] [PubMed]
  94. Elsden, S.R.; Hilton, M.G. Amino acid utilization patterns in clostridial taxonomy. Arch. Microbiol. 1979, 123, 137–141. [Google Scholar] [CrossRef] [PubMed]
  95. Giesel, H.; Machacek, G.; Bayerl, J.; Simon, H. On the formation of 3-phenylpropionate and the different stereo-chemical course of the reduction of cinnamate by Clostridium sporogenes and Peptostreptococcus anaerobius. FEBS Lett. 1981, 123, 107–110. [Google Scholar] [CrossRef]
  96. Ohhiral, I.; Kuwaki, S.; Morita, H.; Suzuki, T.; Tomita, S.; Hisamatsu, S.; Sonoki, S.; Shinoda, S. Identification of 3-phenyllactic acid as a possible antibacterial substance produced by Enterococcus faecalis TH10. Biocontrol Sci. 2004, 9, 77–81. [Google Scholar] [CrossRef]
  97. Valerio, F.; Lavermicocca, P.; Pascale, M.; Visconti, A. Production of phenyllactic acid by lactic acid bacteria: An approach to the selection of strains contributing to food quality and preservation. FEMS Microbiol. Lett. 2004, 233, 289–295. [Google Scholar] [CrossRef] [PubMed]
  98. Makras, L.; Triantafyllou, V.; Fayol-Messaoudi, D.; Adriany, T.; Zoumpopoulou, G.; Tsakalidou, E.; Servin, A.; de Vuyst, L. Kinetic analysis of the antibacterial activity of probiotic lactobacilli towards Salmonella enterica serovar Typhimurium reveals a role for lactic acid and other inhibitory compounds. Res. Microbiol. 2006, 157, 241–247. [Google Scholar] [CrossRef] [PubMed]
  99. Magnusson, J.; Strom, K.; Roos, S.; Sjogren, J.; Schnurer, J. Broad and complex antifungal activity among environmental isolates of lactic acid bacteria. FEMS Microbiol. Lett. 2003, 219, 129–135. [Google Scholar] [CrossRef]
  100. Li, X.; Jiang, B.; Pan, B.; Mu, W.; Zhang, T. Purification and partial characterization of Lactobacillus species SK007 lactate dehydrogenase (LDH) catalyzing phenylpyruvic acid (PPA) conversion into phenyllactic acid (PLA). J. Agric. Food Chem. 2008, 56, 2392–2399. [Google Scholar] [CrossRef] [PubMed]
  101. Vermeulen, N.; Ganzle, M.G.; Vogel, R.F. Influence of peptide supply and cosubstrates on phenylalanine metabolism of Lactobacillus sanfranciscensis DSM20451(T) and Lactobacillus plantarum TMW1.468. J. Agric. Food Chem. 2006, 54, 3832–3839. [Google Scholar] [CrossRef] [PubMed]
  102. Armaforte, E.; Carri, S.; Ferri, G.; Caboni, M.F. High-performance liquid chromatography determination of phenyllactic acid in MRS broth. J. Chromatogr. A 2006, 1131, 281–284. [Google Scholar] [CrossRef] [PubMed]
  103. Martinez, A.W.; Recht, N.S.; Hostetter, T.H.; Meyer, T.W. Removal of P-cresol sulfate by hemodialysis. J. Am. Soc. Nephrol. 2005, 16, 3430–3436. [Google Scholar] [CrossRef] [PubMed]
  104. Schepers, E.; Meert, N.; Glorieux, G.; Goeman, J.; Van der Eycken, J.; Vanholder, R. P-cresylsulphate, the main in vivo metabolite of p-cresol, activates leucocyte free radical production. Nephrol. Dial. Transplant. 2007, 22, 592–596. [Google Scholar] [CrossRef] [PubMed]
  105. Pletinck, A.; Glorieux, G.; Schepers, E.; Cohen, G.; Gondouin, B.; Van Landschoot, M.; Eloot, S.; Rops, A.; Van de Voorde, J.; de Vriese, A.; et al. Protein-bound uremic toxins stimulate crosstalk between leukocytes and vessel wall. J. Am. Soc. Nephrol. 2013, 24, 1981–1994. [Google Scholar] [CrossRef] [PubMed]
  106. Meijers, B.K.; Van Kerckhoven, S.; Verbeke, K.; Dehaen, W.; Vanrenterghem, Y.; Hoylaerts, M.F.; Evenepoel, P. The uremic retention solute p-cresyl sulfate and markers of endothelial damage. Am. J. Kidney Dis. 2009, 54, 891–901. [Google Scholar] [CrossRef] [PubMed]
  107. Gross, P.; Massy, Z.A.; Henaut, L.; Boudot, C.; Cagnard, J.; March, C.; Kamel, S.; Drueke, T.B.; Six, I. Para-cresyl sulfate acutely impairs vascular reactivity and induces vascular remodeling. J. Cell. Physiol. 2015, 230, 2927–2935. [Google Scholar] [CrossRef] [PubMed]
  108. Han, H.; Zhu, J.; Zhu, Z.; Ni, J.; Du, R.; Dai, Y.; Chen, Y.; Wu, Z.; Lu, L.; Zhang, R. p-Cresyl sulfate aggravates cardiac dysfunction associated with chronic kidney disease by enhancing apoptosis of cardiomyocytes. J. Am. Heart Assoc. 2015, 4, e001852. [Google Scholar] [CrossRef] [PubMed]
  109. Sun, C.Y.; Chang, S.C.; Wu, M.S. Suppression of Klotho expression by protein-bound uremic toxins is associated with increased DNA methyltransferase expression and DNA hypermethylation. Kidney Int. 2012, 81, 640–650. [Google Scholar] [CrossRef] [PubMed]
  110. Sun, C.Y.; Chang, S.C.; Wu, M.S. Uremic toxins induce kidney fibrosis by activating intrarenal renin-angiotensin-aldosterone system associated epithelial-to-mesenchymal transition. PLoS ONE 2012, 7, e34026. [Google Scholar] [CrossRef] [PubMed]
  111. Watanabe, H.; Miyamoto, Y.; Honda, D.; Tanaka, H.; Wu, Q.; Endo, M.; Noguchi, T.; Kadowaki, D.; Ishima, Y.; Kotani, S.; et al. p-Cresyl sulfate causes renal tubular cell damage by inducing oxidative stress by activation of NADPH oxidase. Kidney Int. 2013, 83, 582–592. [Google Scholar] [CrossRef] [PubMed]
  112. Poveda, J.; Sanchez-Nino, M.D.; Glorieux, G.; Sanz, A.B.; Egido, J.; Vanholder, R.; Ortiz, A. p-Cresyl sulphate has pro-inflammatory and cytotoxic actions on human proximal tubular epithelial cells. Nephrol. Dial. Transplant. 2014, 29, 56–64. [Google Scholar] [CrossRef] [PubMed]
  113. Mutsaers, H.A.; Caetano-Pinto, P.; Seegers, A.E.; Dankers, A.C.; van den Broek, P.H.; Wetzels, J.F.; van den Brand, J.A.; van den Heuvel, L.P.; Hoenderop, J.G.; Wilmer, M.J.; et al. Proximal tubular efflux transporters involved in renal excretion of p-cresyl sulfate and p-cresyl glucuronide: Implications for chronic kidney disease pathophysiology. Toxicol. In Vitro 2015, 29, 1868–1877. [Google Scholar] [CrossRef] [PubMed]
  114. Koppe, L.; Pillon, N.J.; Vella, R.E.; Croze, M.L.; Pelletier, C.C.; Chambert, S.; Massy, Z.; Glorieux, G.; Vanholder, R.; Dugenet, Y.; et al. p-Cresyl sulfate promotes insulin resistance associated with CKD. J. Am. Soc. Nephrol. 2013, 24, 88–99. [Google Scholar] [CrossRef] [PubMed]
  115. Shiba, T.; Kawakami, K.; Sasaki, T.; Makino, I.; Kato, I.; Kobayashi, T.; Uchida, K.; Kaneko, K. Effects of intestinal bacteria-derived p-cresyl sulfate on Th1-type immune response in vivo and in vitro. Toxicol. Appl. Pharmacol. 2014, 274, 191–199. [Google Scholar] [CrossRef] [PubMed]
  116. Shiba, T.; Makino, I.; Kawakami, K.; Kato, I.; Kobayashi, T.; Kaneko, K. p-Cresyl sulfate suppresses lipopolysaccharide-induced anti-bacterial immune responses in murine macrophages in vitro. Toxicol. Lett. 2016, 245, 24–30. [Google Scholar] [CrossRef] [PubMed]
  117. Chen, T.C.; Wang, C.Y.; Hsu, C.Y.; Wu, C.H.; Kuo, C.C.; Wang, K.C.; Yang, C.C.; Wu, M.T.; Chuang, F.R.; Lee, C.T. Free p-cresol sulfate is associated with survival and function of vascular access in chronic hemodialysis patients. Kidney Blood Press. Res. 2012, 35, 583–588. [Google Scholar] [CrossRef] [PubMed]
  118. Chiu, C.A.; Lu, L.F.; Yu, T.H.; Hung, W.C.; Chung, F.M.; Tsai, I.T.; Yang, C.Y.; Hsu, C.C.; Lu, Y.C.; Wang, C.P.; et al. Increased levels of total p-Cresylsulphate and indoxyl sulphate are associated with coronary artery disease in patients with diabetic nephropathy. Rev. Diabet. Stud. 2010, 7, 275–284. [Google Scholar] [CrossRef] [PubMed]
  119. Hsu, H.J.; Yen, C.H.; Wu, I.W.; Hsu, K.H.; Chen, C.K.; Sun, C.Y.; Chou, C.C.; Chen, C.Y.; Tsai, C.J.; Wu, M.S.; et al. The association of uremic toxins and inflammation in hemodialysis patients. PLoS ONE 2014, 9, e102691. [Google Scholar] [CrossRef] [PubMed]
  120. Lin, C.J.; Pan, C.F.; Liu, H.L.; Chuang, C.K.; Jayakumar, T.; Wang, T.J.; Chen, H.H.; Wu, C.J. The role of protein-bound uremic toxins on peripheral artery disease and vascular access failure in patients on hemodialysis. Atherosclerosis 2012, 225, 173–179. [Google Scholar] [CrossRef] [PubMed]
  121. Lin, C.J.; Pan, C.F.; Chuang, C.K.; Sun, F.J.; Wang, D.J.; Chen, H.H.; Liu, H.L.; Wu, C.J. p-cresyl sulfate is a valuable predictor of clinical outcomes in pre-ESRD patients. BioMed Res. Int. 2014, 2014, 526932. [Google Scholar] [CrossRef] [PubMed]
  122. Lu, L.F.; Tang, W.H.; Hsu, C.C.; Tsai, I.T.; Hung, W.C.; Yu, T.H.; Wu, C.C.; Chung, F.M.; Lu, Y.C.; Lee, Y.J.; et al. Associations among chronic kidney disease, high total p-cresylsulfate and left ventricular systolic dysfunction. Clin. Chim. Acta 2016, 457, 63–68. [Google Scholar] [CrossRef] [PubMed]
  123. Rossi, M.; Campbell, K.L.; Johnson, D.W.; Stanton, T.; Vesey, D.A.; Coombes, J.S.; Weston, K.S.; Hawley, C.M.; McWhinney, B.C.; Ungerer, J.P.; et al. Protein-bound uremic toxins, inflammation and oxidative stress: A cross-sectional study in stage 3–4 chronic kidney disease. Arch. Med. Res. 2014, 45, 309–317. [Google Scholar] [CrossRef] [PubMed]
  124. Shafi, T.; Meyer, T.W.; Hostetter, T.H.; Melamed, M.L.; Parekh, R.S.; Hwang, S.; Banerjee, T.; Coresh, J.; Powe, N.R. Free levels of selected organic solutes and cardiovascular morbidity and mortality in hemodialysis patients: Results from the Retained Organic Solutes and Clinical Outcomes (ROSCO) investigators. PLoS ONE 2015, 10, e0126048. [Google Scholar] [CrossRef] [PubMed]
  125. Tang, W.H.; Wang, C.P.; Yu, T.H.; Hung, W.C.; Chung, F.M.; Lu, Y.C.; Hsu, C.C.; Lu, L.F.; Huang, L.L.; Lee, Y.J.; et al. Serum total p-cresylsulfate level is associated with abnormal QTc interval in stable angina patients with early stage of renal failure. Clin. Chim. Acta 2014, 437, 25–30. [Google Scholar] [CrossRef] [PubMed]
  126. Wang, C.P.; Lu, L.F.; Yu, T.H.; Hung, W.C.; Chiu, C.A.; Chung, F.M.; Yeh, L.R.; Chen, H.J.; Lee, Y.J.; Houng, J.Y. Serum levels of total p-cresylsulphate are associated with angiographic coronary atherosclerosis severity in stable angina patients with early stage of renal failure. Atherosclerosis 2010, 211, 579–583. [Google Scholar] [CrossRef] [PubMed]
  127. Wang, C.P.; Lu, L.F.; Yu, T.H.; Hung, W.C.; Chiu, C.A.; Chung, F.M.; Hsu, C.C.; Lu, Y.C.; Lee, Y.J.; Houng, J.Y. Associations among chronic kidney disease, high total p-cresylsulfate and major adverse cardiac events. J. Nephrol. 2013, 26, 111–118. [Google Scholar] [CrossRef] [PubMed]
  128. Wu, I.W.; Hsu, K.H.; Hsu, H.J.; Lee, C.C.; Sun, C.Y.; Tsai, C.J.; Wu, M.S. Serum free p-cresyl sulfate levels predict cardiovascular and all-cause mortality in elderly hemodialysis patients—a prospective cohort study. Nephrol. Dial. Transplant. 2012, 27, 1169–1175. [Google Scholar] [CrossRef] [PubMed]
  129. Poesen, R.; Viaene, L.; Verbeke, K.; Augustijns, P.; Bammens, B.; Claes, K.; Kuypers, D.; Evenepoel, P.; Meijers, B. Cardiovascular disease relates to intestinal uptake of p-cresol in patients with chronic kidney disease. BMC Nephrol. 2014, 15, 87. [Google Scholar] [CrossRef] [PubMed]
  130. Lin, C.J.; Wu, V.; Wu, P.C.; Wu, C.J. Meta-Analysis of the Associations of p-Cresyl Sulfate (PCS) and Indoxyl Sulfate (IS) with Cardiovascular Events and All-Cause Mortality in Patients with Chronic Renal Failure. PLoS ONE 2015, 10, e0132589. [Google Scholar] [CrossRef] [PubMed]
  131. Wu, I.W.; Hsu, K.H.; Lee, C.C.; Sun, C.Y.; Hsu, H.J.; Tsai, C.J.; Tzen, C.Y.; Wang, Y.C.; Lin, C.Y.; Wu, M.S. p-Cresyl sulphate and indoxyl sulphate predict progression of chronic kidney disease. Nephrol. Dial. Transplant. 2011, 26, 938–947. [Google Scholar] [CrossRef] [PubMed]
  132. Wang, C.P.; Lu, Y.C.; Tsai, I.T.; Tang, W.H.; Hsu, C.C.; Hung, W.C.; Yu, T.H.; Chen, S.C.; Chung, F.M.; Lee, Y.J.; et al. Increased Levels of Total p-Cresylsulfate Are Associated with Pruritus in Patients with Chronic Kidney Disease. Dermatology 2016, 232, 363–370. [Google Scholar] [CrossRef] [PubMed]
  133. Liabeuf, S.; Barreto, D.V.; Barreto, F.C.; Meert, N.; Glorieux, G.; Schepers, E.; Temmar, M.; Choukroun, G.; Vanholder, R.; Massy, Z.A. Free p-cresylsulphate is a predictor of mortality in patients at different stages of chronic kidney disease. Nephrol. Dial. Transplant. 2010, 25, 1183–1191. [Google Scholar] [CrossRef] [PubMed]
  134. Montemurno, E.; Cosola, C.; Dalfino, G.; Daidone, G.; de Angelis, M.; Gobbetti, M.; Gesualdo, L. What would you like to eat, Mr CKD Microbiota? A Mediterranean Diet, please! Kidney Blood Press. Res. 2014, 39, 114–123. [Google Scholar] [CrossRef] [PubMed]
  135. Walker, A.W.; Ince, J.; Duncan, S.H.; Webster, L.M.; Holtrop, G.; Ze, X.; Brown, D.; Stares, M.D.; Scott, P.; Bergerat, A.; et al. Dominant and diet-responsive groups of bacteria within the human colonic microbiota. ISME J. 2011, 5, 220–230. [Google Scholar] [CrossRef] [PubMed]
  136. Ling, W.H.; Hanninen, O. Shifting from a conventional diet to an uncooked vegan diet reversibly alters fecal hydrolytic activities in humans. J. Nutr. 1992, 122, 924–930. [Google Scholar] [PubMed]
  137. Patel, K.P.; Luo, F.J.; Plummer, N.S.; Hostetter, T.H.; Meyer, T.W. The production of p-cresol sulfate and indoxyl sulfate in vegetarians versus omnivores. Clin. J. Am. Soc. Nephrol. 2012, 7, 982–988. [Google Scholar] [CrossRef] [PubMed]
  138. Cummings, J.H.; Hill, M.J.; Bone, E.S.; Branch, W.J.; Jenkins, D.J. The effect of meat protein and dietary fiber on colonic function and metabolism. II. Bacterial metabolites in feces and urine. Am. J. Clin. Nutr. 1979, 32, 2094–2101. [Google Scholar] [PubMed]
  139. Birkett, A.; Muir, J.; Phillips, J.; Jones, G.; O’Dea, K. Resistant starch lowers fecal concentrations of ammonia and phenols in humans. Am. J. Clin. Nutr. 1996, 63, 766–772. [Google Scholar] [PubMed]
  140. Rossi, M.; Johnson, D.W.; Xu, H.; Carrero, J.J.; Pascoe, E.; French, C.; Campbell, K.L. Dietary protein-fiber ratio associates with circulating levels of indoxyl sulfate and p-cresyl sulfate in chronic kidney disease patients. Nutr. Metab. Cardiovasc. Dis. 2015, 25, 860–865. [Google Scholar] [CrossRef] [PubMed]
  141. Sirich, T.L.; Plummer, N.S.; Gardner, C.D.; Hostetter, T.H.; Meyer, T.W. Effect of increasing dietary fiber on plasma levels of colon-derived solutes in hemodialysis patients. Clin. J. Am. Soc. Nephrol. 2014, 9, 1603–1610. [Google Scholar] [CrossRef] [PubMed]
  142. Kieffer, D.A.; Piccolo, B.D.; Vaziri, N.D.; Liu, S.; Lau, W.L.; Khazaeli, M.; Nazertehrani, S.; Moore, M.E.; Marco, M.L.; Martin, R.J.; et al. Resistant starch alters gut microbiome and metabolomic profiles concurrent with amelioration of chronic kidney disease in rats. Am. J. Physiol. Ren. Physiol. 2016, 310, F857–F871. [Google Scholar] [CrossRef] [PubMed]
  143. Naylor, H.L.; Jackson, H.; Walker, G.H.; Macafee, S.; Magee, K.; Hooper, L.; Stewart, L.; MacLaughlin, H.L. British Dietetic Association evidence-based guidelines for the protein requirements of adults undergoing maintenance haemodialysis or peritoneal dialysis. J. Hum. Nutr. Diet. 2013, 26, 315–328. [Google Scholar] [CrossRef] [PubMed]
  144. Jiang, Z.; Zhang, X.; Yang, L.; Li, Z.; Qin, W. Effect of restricted protein diet supplemented with keto analogues in chronic kidney disease: A systematic review and meta-analysis. Int. Urol. Nephrol. 2016, 48, 409–418. [Google Scholar] [CrossRef] [PubMed]
  145. David, C.; Peride, I.; Niculae, A.; Constantin, A.M.; Checherita, I.A. Very low protein diets supplemented with keto-analogues in ESRD predialysis patients and its effect on vascular stiffness and AVF Maturation. BMC Nephrol. 2016, 17, 131. [Google Scholar] [CrossRef] [PubMed]
  146. De Preter, V.; Vanhoutte, T.; Huys, G.; Swings, J.; de Vuyst, L.; Rutgeerts, P.; Verbeke, K. Effects of Lactobacillus casei Shirota, Bifidobacterium breve, and oligofructose-enriched inulin on colonic nitrogen-protein metabolism in healthy humans. Am. J. Physiol. Gastrointest. Liver Physiol. 2007, 292, G358–G368. [Google Scholar] [CrossRef] [PubMed]
  147. Rossi, M.; Klein, K.; Johnson, D.W.; Campbell, K.L. Pre-, pro-, and synbiotics: Do they have a role in reducing uremic toxins? A systematic review and meta-analysis. Int. J. Nephrol. 2012, 673631. [Google Scholar] [CrossRef] [PubMed]
  148. Tohyama, K.; Kobayashi, Y.; Kan, T.; Yazawa, K.; Terashima, T.; Mutai, M. Effect of lactobacilli on urinary indican excretion in gnotobiotic rats and in man. Microbiol. Immunol. 1981, 25, 101–112. [Google Scholar] [CrossRef] [PubMed]
  149. Fujiwara, S.; Seto, Y.; Kimura, A.; Hashiba, H. Establishment of orally-administered Lactobacillus gasseri SBT2055SR in the gastrointestinal tract of humans and its influence on intestinal microflora and metabolism. J. Appl. Microbiol. 2001, 90, 343–352. [Google Scholar] [CrossRef] [PubMed]
  150. de Preter, V.; Vanhoutte, T.; Huys, G.; Swings, J.; Rutgeerts, P.; Verbeke, K. Baseline microbiota activity and initial bifidobacteria counts influence responses to prebiotic dosing in healthy subjects. Aliment. Pharmacol. Ther. 2008, 27, 504–513. [Google Scholar] [CrossRef] [PubMed]
  151. Davis, L.M.; Martinez, I.; Walter, J.; Goin, C.; Hutkins, R.W. Barcoded pyrosequencing reveals that consumption of galactooligosaccharides results in a highly specific bifidogenic response in humans. PLoS ONE 2011, 6, e25200. [Google Scholar] [CrossRef] [PubMed]
  152. Meijers, B.K.; de Preter, V.; Verbeke, K.; Vanrenterghem, Y.; Evenepoel, P. p-Cresyl sulfate serum concentrations in haemodialysis patients are reduced by the prebiotic oligofructose-enriched inulin. Nephrol. Dial. Transplant. 2010, 25, 219–224. [Google Scholar] [CrossRef] [PubMed]
  153. Evenepoel, P.; Bammens, B.; Verbeke, K.; Vanrenterghem, Y. Acarbose treatment lowers generation and serum concentrations of the protein-bound solute p-cresol: A pilot study. Kidney Int. 2006, 70, 192–198. [Google Scholar] [CrossRef] [PubMed]
  154. Poesen, R.; Evenepoel, P.; de Loor, H.; Delcour, J.A.; Courtin, C.M.; Kuypers, D.; Augustijns, P.; Verbeke, K.; Meijers, B. The influence of prebiotic arabinoxylan oligosaccharides on microbiota derived uremic retention solutes in patients with chronic kidney disease: A randomized controlled trial. PLoS ONE 2016, 11, e0153893. [Google Scholar] [CrossRef] [PubMed]
  155. Nakabayashi, I.; Nakamura, M.; Kawakami, K.; Ohta, T.; Kato, I.; Uchida, K.; Yoshida, M. Effects of synbiotic treatment on serum level of p-cresol in haemodialysis patients: A preliminary study. Nephrol. Dial. Transplant. 2011, 26, 1094–1098. [Google Scholar] [CrossRef] [PubMed]
  156. Guida, B.; Germano, R.; Trio, R.; Russo, D.; Memoli, B.; Grumetto, L.; Barbato, F.; Cataldi, M. Effect of short-term synbiotic treatment on plasma p-cresol levels in patients with chronic renal failure: A randomized clinical trial. Nutr. Metab. Cardiovasc. Dis. 2014, 24, 1043–1049. [Google Scholar] [CrossRef] [PubMed]
  157. Rossi, M.; Johnson, D.W.; Morrison, M.; Pascoe, E.M.; Coombes, J.S.; Forbes, J.M.; Szeto, C.C.; McWhinney, B.C.; Ungerer, J.P.; Campbell, K.L. Synbiotics Easing Renal failure by improving Gut microbiology (SYNERGY): A randomized trial. Clin. J. Am. Soc. Nephrol. 2016, 11, 223–231. [Google Scholar] [CrossRef] [PubMed]
  158. Ling, W.H.; Korpela, R.; Mykkanen, H.; Salminen, S.; Hanninen, O. Lactobacillus strain GG supplementation decreases colonic hydrolytic and reductive enzyme activities in healthy female adults. J. Nutr. 1994, 124, 18–23. [Google Scholar] [PubMed]
  159. Hyun, H.S.; Paik, K.H.; Cho, H.Y. p-Cresyl sulfate and indoxyl sulfate in pediatric patients on chronic dialysis. Korean J. Pediatr. 2013, 56, 159–164. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  160. Wu, M.J.; Chang, C.S.; Cheng, C.H.; Chen, C.H.; Lee, W.C.; Hsu, Y.H.; Shu, K.H.; Tang, M.J. Colonic transit time in long-term dialysis patients. Am. J. Kidney Dis. 2004, 44, 322–327. [Google Scholar] [CrossRef] [PubMed]
  161. Yasuda, G.; Shibata, K.; Takizawa, T.; Ikeda, Y.; Tokita, Y.; Umemura, S.; Tochikubo, O. Prevalence of constipation in continuous ambulatory peritoneal dialysis patients and comparison with hemodialysis patients. Am. J. Kidney Dis. 2002, 39, 1292–1299. [Google Scholar] [CrossRef] [PubMed]
  162. Kikuchi, K.; Itoh, Y.; Tateoka, R.; Ezawa, A.; Murakami, K.; Niwa, T. Metabolomic search for uremic toxins as indicators of the effect of an oral sorbent AST-120 by liquid chromatography/tandem mass spectrometry. J. Chromatogr. B Anal. Technol. Biomed. Life Sci. 2010, 878, 2997–3002. [Google Scholar] [CrossRef] [PubMed]
  163. Niwa, T.; Ise, M.; Miyazaki, T.; Meada, K. Suppressive effect of an oral sorbent on the accumulation of p-cresol in the serum of experimental uremic rats. Nephron 1993, 65, 82–87. [Google Scholar] [CrossRef] [PubMed]
  164. Velenosi, T.J.; Hennop, A.; Feere, D.A.; Tieu, A.; Kucey, A.S.; Kyriacou, P.; McCuaig, L.E.; Nevison, S.E.; Kerr, M.A.; Urquhart, B.L. Untargeted plasma and tissue metabolomics in rats with chronic kidney disease given AST-120. Sci. Rep. 2016, 6, 22526. [Google Scholar] [CrossRef] [PubMed]
  165. Yamamoto, S.; Kazama, J.J.; Omori, K.; Matsuo, K.; Takahashi, Y.; Kawamura, K.; Matsuto, T.; Watanabe, H.; Maruyama, T.; Narita, I. Continuous reduction of protein-bound uraemic toxins with improved oxidative stress by using the oral charcoal adsorbent AST-120 in haemodialysis patients. Sci. Rep. 2015, 5, 14381. [Google Scholar] [CrossRef] [PubMed]
  166. Lee, C.T.; Hsu, C.Y.; Tain, Y.L.; Ng, H.Y.; Cheng, B.C.; Yang, C.C.; Wu, C.H.; Chiou, T.T.; Lee, Y.T.; Liao, S.C. Effects of AST-120 on blood concentrations of protein-bound uremic toxins and biomarkers of cardiovascular risk in chronic dialysis patients. Blood Purif. 2014, 37, 76–83. [Google Scholar] [CrossRef] [PubMed]
  167. Schulman, G.; Berl, T.; Beck, G.J.; Remuzzi, G.; Ritz, E.; Arita, K.; Kato, A.; Shimizu, M. Randomized placebo-controlled EPPIC trials of AST-120 in CKD. J. Am. Soc. Nephrol. 2015, 26, 1732–1746. [Google Scholar] [CrossRef] [PubMed]
  168. Cha, R.H.; Kang, S.W.; Park, C.W.; Cha, D.R.; Na, K.Y.; Kim, S.G.; Yoon, S.A.; Han, S.Y.; Chang, J.H.; Park, S.K.; et al. A Randomized, Controlled trial of oral intestinal sorbent AST-120 on Renal function deterioration in patients with advanced renal dysfunction. Clin. J. Am. Soc. Nephrol. 2016, 11, 559–567. [Google Scholar] [CrossRef] [PubMed]
  169. Meert, N.; Eloot, S.; Schepers, E.; Lemke, H.D.; Dhondt, A.; Glorieux, G.; Van Landschoot, M.; Waterloos, M.A.; Vanholder, R. Comparison of removal capacity of two consecutive generations of high-flux dialysers during different treatment modalities. Nephrol. Dial. Transplant. 2011, 26, 2624–2630. [Google Scholar] [CrossRef] [PubMed]
  170. Meert, N.; Eloot, S.; Waterloos, M.A.; Van Landschoot, M.; Dhondt, A.; Glorieux, G.; Ledebo, I.; Vanholder, R. Effective removal of protein-bound uraemic solutes by different convective strategies: A prospective trial. Nephrol. Dial. Transplant. 2009, 24, 562–570. [Google Scholar] [CrossRef] [PubMed]
  171. Krieter, D.H.; Hackl, A.; Rodriguez, A.; Chenine, L.; Moragues, H.L.; Lemke, H.D.; Wanner, C.; Canaud, B. Protein-bound uraemic toxin removal in haemodialysis and post-dilution haemodiafiltration. Nephrol. Dial. Transplant. 2010, 25, 212–218. [Google Scholar] [CrossRef] [PubMed]
  172. Meert, N.; Waterloos, M.A.; Van Landschoot, M.; Dhondt, A.; Ledebo, I.; Glorieux, G.; Goeman, J.; Van der Eycken, J.; Vanholder, R. Prospective evaluation of the change of predialysis protein-bound uremic solute concentration with postdilution online hemodiafiltration. Artif. Organs 2010, 34, 580–585. [Google Scholar] [CrossRef] [PubMed]
  173. Sirich, T.L.; Luo, F.J.; Plummer, N.S.; Hostetter, T.H.; Meyer, T.W. Selectively increasing the clearance of protein-bound uremic solutes. Nephrol. Dial. Transplant. 2012, 27, 1574–1579. [Google Scholar] [CrossRef] [PubMed]
  174. Marquez, I.O.; Tambra, S.; Luo, F.Y.; Li, Y.; Plummer, N.S.; Hostetter, T.H.; Meyer, T.W. Contribution of residual function to removal of protein-bound solutes in hemodialysis. Clin. J. Am. Soc. Nephrol. 2011, 6, 290–296. [Google Scholar] [CrossRef] [PubMed]
  175. Meijers, B.K.; Weber, V.; Bammens, B.; Dehaen, W.; Verbeke, K.; Falkenhagen, D.; Evenepoel, P. Removal of the uremic retention solute p-cresol using fractionated plasma separation and adsorption. Artif. Organs 2008, 32, 214–219. [Google Scholar] [CrossRef] [PubMed]
  176. Brettschneider, F.; Tolle, M.; von der Giet, M.; Passlick-Deetjen, J.; Steppan, S.; Peter, M.; Jankowski, V.; Krause, A.; Kuhne, S.; Zidek, W.; et al. Removal of protein-bound, hydrophobic uremic toxins by a combined fractionated plasma separation and adsorption technique. Artif. Organs 2013, 37, 409–416. [Google Scholar] [CrossRef] [PubMed]
  177. Kruse, A.; Tao, X.; Bhalani, V.; Handelman, G.; Levin, N.W.; Kotanko, P.; Thijssen, S. Clearance of p-cresol sulfate and β-2-microglobulin from dialysate by commercially available sorbent technology. ASAIO J. 2011, 57, 219–224. [Google Scholar] [CrossRef] [PubMed]
  178. Tijink, M.S.; Wester, M.; Glorieux, G.; Gerritsen, K.G.; Sun, J.; Swart, P.C.; Borneman, Z.; Wessling, M.; Vanholder, R.; Joles, J.A.; et al. Mixed matrix hollow fiber membranes for removal of protein-bound toxins from human plasma. Biomaterials 2013, 34, 7819–7828. [Google Scholar] [CrossRef] [PubMed]
  179. Sandeman, S.R.; Howell, C.A.; Phillips, G.J.; Zheng, Y.; Standen, G.; Pletzenauer, R.; Davenport, A.; Basnayake, K.; Boyd, O.; Holt, S.; et al. An adsorbent monolith device to augment the removal of uraemic toxins during haemodialysis. J. Mater. Sci. Mater. Med. 2014, 25, 1589–1597. [Google Scholar] [CrossRef] [PubMed]
  180. Tetali, S.D.; Jankowski, V.; Luetzow, K.; Kratz, K.; Lendlein, A.; Jankowski, J. Adsorption capacity of poly(ether imide) microparticles to uremic toxins. Clin. Hemorheol. Microcirc. 2016, 61, 657–665. [Google Scholar] [CrossRef] [PubMed]
  181. Bohringer, F.; Jankowski, V.; Gajjala, P.R.; Zidek, W.; Jankowski, J. Release of uremic retention solutes from protein binding by hypertonic predilution hemodiafiltration. ASAIO J. 2015, 61, 55–60. [Google Scholar] [CrossRef] [PubMed]
  182. Krieter, D.H.; Devine, E.; Korner, T.; Ruth, M.; Wanner, C.; Raine, M.; Jankowski, J.; Lemke, H.D. Haemodiafiltration at Increased Plasma Ionic Strength for Improved Protein-Bound Toxin Removal. Acta Physiol. (Oxf.) 2016. [Google Scholar] [CrossRef] [PubMed]
  183. Evenepoel, P.; Bammens, B.; Verbeke, K.; Vanrenterghem, Y. Superior dialytic clearance of beta(2)-microglobulin and p-cresol by high-flux hemodialysis as compared to peritoneal dialysis. Kidney Int. 2006, 70, 794–799. [Google Scholar] [CrossRef] [PubMed]
  184. Pham, N.M.; Recht, N.S.; Hostetter, T.H.; Meyer, T.W. Removal of the protein-bound solutes indican and p-cresol sulfate by peritoneal dialysis. Clin. J. Am. Soc. Nephrol. 2008, 3, 85–90. [Google Scholar] [CrossRef] [PubMed]
  185. Viaene, L.; Meijers, B.K.; Bammens, B.; Vanrenterghem, Y.; Evenepoel, P. Serum concentrations of p-cresyl sulfate and indoxyl sulfate, but not inflammatory markers, increase in incident peritoneal dialysis patients in parallel with loss of residual renal function. Perit. Dial. Int. 2014, 34, 71–78. [Google Scholar] [CrossRef] [PubMed]
  186. Huang, W.H.; Hung, C.C.; Yang, C.W.; Huang, J.Y. High correlation between clearance of renal protein-bound uremic toxins (indoxyl sulfate and p-cresyl sulfate) and renal water-soluble toxins in peritoneal dialysis patients. Ther. Apher. Dial. 2012, 16, 361–367. [Google Scholar] [CrossRef] [PubMed]
  187. Vanholder, R.; Meert, N.; Van Biesen, W.; Meyer, T.; Hostetter, T.; Dhondt, A.; Eloot, S. Why do patients on peritoneal dialysis have low blood levels of protein-bound solutes? Nat. Clin. Pract. Nephrol. 2009, 5, 130–131. [Google Scholar] [CrossRef] [PubMed]
  188. Eloot, S.; Van Biesen, W.; Glorieux, G.; Neirynck, N.; Dhondt, A.; Vanholder, R. Does the adequacy parameter Kt/V(urea) reflect uremic toxin concentrations in hemodialysis patients? PLoS ONE 2013, 8, e76838. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  189. Liabeuf, S.; Desjardins, L.; Massy, Z.A.; Brazier, F.; Westeel, P.F.; Mazouz, H.; Titeca-Beauport, D.; Diouf, M.; Glorieux, G.; Vanholder, R.; et al. Levels of indoxyl sulfate in kidney transplant patients, and the relationship with hard outcomes. Circ. J. 2016, 80, 722–730. [Google Scholar] [CrossRef] [PubMed]
  190. Poesen, R.; Evenepoel, P.; de Loor, H.; Bammens, B.; Claes, K.; Sprangers, B.; Naesens, M.; Kuypers, D.; Augustijns, P.; Meijers, B. The influence of renal transplantation on retained microbial-human co-metabolites. Nephrol. Dial. Transplant. 2016, 31, 1721–1729. [Google Scholar] [CrossRef] [PubMed]
  191. Vanholder, R.; Glorieux, G.; Massy, Z.A. Intestinal metabolites, chronic kidney disease and renal transplantation: Enigma Variations? Nephrol. Dial. Transplant. 2016, 31, 1547–1551. [Google Scholar] [CrossRef] [PubMed]
Toxins 09 00052 g001 550
Figure 1. Conversion pathway of tyrosine and phenylalanine into p-cresyl sulfate. Full arrows: process through bacterial fermentation; dotted arrows: process through enzymatic reactions of the host; EC: enzyme commission number. l-tyrosine, derived from diet and endogenous proteins and peptides, can be converted to phenol and 4-hydroxyphenylpyruvate. Tyrosine phenol-lyase (EC 4.1.99.2.), previously named β–tyrosinase, is responsible for the reversible deamination of l-tyrosine, requiring pyridoxyl phosphate as a cofactor, into phenol ammonia and pyruvate [40,41,42]. This reaction is also reversible by the same enzyme using l-serine and phenol as substrates [43]. In addition, the reversible reaction of l-tyrosine with 2-oxoglutarate in 4-hydroxyphenylpyruvate and L-glutamate is catalysed by tyrosine transaminase (EC 2.6.1.5.) or by aromatic-amino-acid transaminase (EC 2.6.1.57.) [44,45,46]. To a small extent, 4-hydroxyphenylpyruvate and ammonia can also be formed by the enzyme phenylalanine dehydrogenase (EC 1.4.1.20.) from l-tyrosine [47]. 4-Hydroxyphenylpyruvate is the precursor of 4-hydroxyphenylacetate, catalysed by p-hydroxyphenylpyruvate oxidase (EC 1.2.3.13.) [44,46], and can subsequently lead to the formation of p-cresol by p-hydroxyphenylacetate decarboxylase (EC 4.1.1.83.) [48,49]. In the gut mucosa and in the liver, the majority of p-cresol will be conjugated into the uremic toxin p-cresyl sulfate by aryl sulfotransferases (EC 2.8.2.1.) [50] and a small fraction will be metabolized to p-cresyl glucuronide by UDP-glucuronyltransferases (EC 2.4.1.17.) [51]. Another aromatic amino acid, phenylalanine, also plays a role in the production of p-cresyl sulfate through the hydroxylation reaction to tyrosine by phenylalanine 4-monooxygenase, also referred as phenylalanine hydroxylase (EC 1.14.16.1.) [52]. This metabolic process is carried out by bacteria as well by liver cells, transforming excess diet phenylalanine to tyrosine [53]. In addition, phenylalanine is converted into 3-phenylpyruvate by either phenylalanine dehydrogenase (EC 1.4.1.20.) [47,54], branched-chain-amino-acid transaminase (EC 2.6.1.42.) [55] or by aromatic-amino-acid transaminase (EC 2.6.1.57.) [45]. Then 3-phenylpyruvate can be transformed in 3-phenylacetaldehyde by phenylpyruvate decarboxylase (EC 4.1.1.43.) [56] or in 3-phenyllactate by l-lactate dehydrogenase (EC 1.1.1.27.) [46]. Finally, 3-phenylacetaldehyde can be converted to 3-phenylacetate by phenylacetaldehyde dehydrogenase (EC 1.2.1.39.) [56,57]. All of these reactions of the phenylalanine metabolic pathway are reversible, which can lead, in the end, to p-cresyl sulfate generation.
Figure 1. Conversion pathway of tyrosine and phenylalanine into p-cresyl sulfate. Full arrows: process through bacterial fermentation; dotted arrows: process through enzymatic reactions of the host; EC: enzyme commission number. l-tyrosine, derived from diet and endogenous proteins and peptides, can be converted to phenol and 4-hydroxyphenylpyruvate. Tyrosine phenol-lyase (EC 4.1.99.2.), previously named β–tyrosinase, is responsible for the reversible deamination of l-tyrosine, requiring pyridoxyl phosphate as a cofactor, into phenol ammonia and pyruvate [40,41,42]. This reaction is also reversible by the same enzyme using l-serine and phenol as substrates [43]. In addition, the reversible reaction of l-tyrosine with 2-oxoglutarate in 4-hydroxyphenylpyruvate and L-glutamate is catalysed by tyrosine transaminase (EC 2.6.1.5.) or by aromatic-amino-acid transaminase (EC 2.6.1.57.) [44,45,46]. To a small extent, 4-hydroxyphenylpyruvate and ammonia can also be formed by the enzyme phenylalanine dehydrogenase (EC 1.4.1.20.) from l-tyrosine [47]. 4-Hydroxyphenylpyruvate is the precursor of 4-hydroxyphenylacetate, catalysed by p-hydroxyphenylpyruvate oxidase (EC 1.2.3.13.) [44,46], and can subsequently lead to the formation of p-cresol by p-hydroxyphenylacetate decarboxylase (EC 4.1.1.83.) [48,49]. In the gut mucosa and in the liver, the majority of p-cresol will be conjugated into the uremic toxin p-cresyl sulfate by aryl sulfotransferases (EC 2.8.2.1.) [50] and a small fraction will be metabolized to p-cresyl glucuronide by UDP-glucuronyltransferases (EC 2.4.1.17.) [51]. Another aromatic amino acid, phenylalanine, also plays a role in the production of p-cresyl sulfate through the hydroxylation reaction to tyrosine by phenylalanine 4-monooxygenase, also referred as phenylalanine hydroxylase (EC 1.14.16.1.) [52]. This metabolic process is carried out by bacteria as well by liver cells, transforming excess diet phenylalanine to tyrosine [53]. In addition, phenylalanine is converted into 3-phenylpyruvate by either phenylalanine dehydrogenase (EC 1.4.1.20.) [47,54], branched-chain-amino-acid transaminase (EC 2.6.1.42.) [55] or by aromatic-amino-acid transaminase (EC 2.6.1.57.) [45]. Then 3-phenylpyruvate can be transformed in 3-phenylacetaldehyde by phenylpyruvate decarboxylase (EC 4.1.1.43.) [56] or in 3-phenyllactate by l-lactate dehydrogenase (EC 1.1.1.27.) [46]. Finally, 3-phenylacetaldehyde can be converted to 3-phenylacetate by phenylacetaldehyde dehydrogenase (EC 1.2.1.39.) [56,57]. All of these reactions of the phenylalanine metabolic pathway are reversible, which can lead, in the end, to p-cresyl sulfate generation.
Toxins 09 00052 g001
Table
Table 1. Overview of the phenolic compound generating bacterial species (in vitro literature data).
Table 1. Overview of the phenolic compound generating bacterial species (in vitro literature data).
Bacterial SpeciesTyrosine End ProductsPhenylalanine End Products
Phenolp-Cresol4-Hydroxy-Phenyl-AcetatePhenyl-AcetatePhenyl-Lactate
FIRMICUTES
Clostridiaceae
 Clostridium aminovalericum [92]
 Clostridium bartletti [93][93][93][93]
 Clostridium bifermentans[29] [76,92][29,76]
 Clostridium botulinum type G [94][94]
 Clostridium butyricum [80]
 Clostridium clostridioforme [70][70][70][70]
 Clostridium cochlearium[76]
 Clostridium difficile [29,48,76][29,76][29,76,92]
 Clostridium ghoni [76]
 Clostridium lentoputrescens[76] [92]
 Clostridium limosum[76]
 Clostridium lituseburense [76][76]
 Clostridium malenomenatum[76]
 Clostridium mangenoti [76]
 Clostridium paraperfringens [92]
 Clostridium paraputrificum [29,80]
 Clostridium perfringens [29,70] [92][29]
 Clostridium propionicum [76][76]
 Clostridium putrefaciens [76][76]
 Clostridium saccharolyticum [93][93][93]
 Clostridium septicum [29,80]
 Clostridium sordellii [76,92][76]
 Clostridium sporogenes [80] [95][95]
 Clostridium sticklandii [76,94][76,94]
 Clostridium subterminale [76][76]
 Clostridium tetani[76]
 Clostridium tetanomorphum[41,76]
 Faecalibacterium prausnitzii [93][93][93][93]
 Peptostreptococcus anaerobius [95]
 Peptostreptococcus asaccharolyticus[29]
Enterococcaceae
 Enterococcus faecalis[80] a [96]
 Enterococcus faecium [97]
Eubacteriaceae
 Eubacterium cylindroides [93][93][93]
 Eubacterium hallii [93][93]
 Eubacterium rectale [93][93][93][93]
Lactobacillaceae
 Lactobacillus acidophilus [97,98]
 Lactobacillus alimentarius [97]
 Lactobacillus brevis [97]
 Lactobacillus casei [46][46][76]
 Lactobacillus casei Shirota [70]
 Lactobacillus confusus [97] b
 Lactobacillus coryniformis [99]
 Lactobacillus fermentum [97]
 Lactobacillus helveticus [46][46][46]
 Lactobacillus hilgardii [97]
 Lactobacillus johnsonii [98]
 Lactobacillus pentosus [100]
 Lactobacillus plantarum [97,100,101,102]
 Lactobacillus rhamnosus [97,98]
 Lactobacillus sanfranciscencis [97,101]
Lachnospiraceae
 Anaerostipes caccae [93][93][93]
 Anaerostipes hadrus [93][93][93]
 Butyrivibrio fibrisolvens [93][93][93]
 Roseburia intestinalis [93][93][93][93]
 Roseburia inulinovorans [93][93][93]
Ruminococcaceae
 Ruminococcus obeum [93][93][93][93]
 Ruminococcus sp. [93][93][93]
 Ruminooccus torques [93][93][93]
Staphylococcaceae
 Staphylococcus epidermidis[80] c[80] c
Veillonellaceae
 Megamonas hypermegale [93][93][93][93]
BACTEROIDETES
Bacteroidaceae
 Bacteroides distasonis [92]
 Bacteroides eggerthii [93][93]
 Bacteroides fragilis[29][29,80,93][92,93][29,70,92,93]
 Bacteroides gingivalis [92]
 Bacteroides ovatus [29,93][29,92,93][29]
 Bacteroidesruminicola subsp. brevis [92]
 subsp. Ruminicola [92]
 Bacteroides thetaiotaomicron [29,70][70,93][29,70,92,93]
 Bacteroides uniformis [93][93][93]
 Bacteroides vulgatus [93][93]
Porphyromonadaceae
 Parabacteroides distasonis [93][93][93]
ACTINOBACTERIA
Bifidobacteriaceae
 Bifidobacterium adolescentis [29,93][29,93][93]
 Bifidobacteriumanimalis subsp. Lactis [70] [70]
 Bifidobacterium bifidum [29][29]
 Bifidobacterium infantis [29,93][29,93][93][93]
 Bifidobacterium longum[29] [29] [29,70]
 Bifidobacterium pseudolongum [29][29]
 Bifidobacterium sp. [80]
PROTEOBACTERIA
Enterobacteriaceae
 Citrobacter freundii[40] d, [42]
 Citrobacter intermedius[40] e
 Enterobacter aerogenes[40] f
 Escherichia coli[29,40,80]
 Morganella morganii[40] g
 Proteus sp.[80]
FUSOBACTERIA
Fusobacteriaceaea
 Fusobacterium sp. [80]
a mentioned in original paper as Streptococcus faecalis; b mentioned in original paper as Weisella confusa; c mentioned in original paper as Staphylococcus albus; d mentioned in original paper as Escherichia freundii; e mentioned in original paper as Escherichia intermedia; f mentioned in original paper as Aerobacter aerogenes; gmentioned in original paper as Proteus morganii.
Table
Table 2. Studies describing associations between p-cresyl sulfate concentrations and clinical parameters and outcomes of patients with chronic kidney disease.
Table 2. Studies describing associations between p-cresyl sulfate concentrations and clinical parameters and outcomes of patients with chronic kidney disease.
Patient TypePatient NumberTotal or Free pCS ConcentrationAssociationRef.
Diabetic nephropathy209totalCAD[118]
Stable angina202totalSeverity of CAD[126]
Stable angina with early CKD154totalQTc prolongation[125]
CKD and stable angina403totalLV systolic function[122]
CKD72totalCV and dialysis event (progression)[121]
149free and total freeIL-6 and PWV Plasma glutathione peroxidase[123]
200urinary excretionCV event[129]
268totalRenal progression and all-cause mortality[131]
320totalPruritus[132]
CKD and CAD340totalMACE[127]
CKD and HD (32%)139freeSurvival[133]
HD91freeSurvival and function of vascular access[117]
100totalAnkle Brachial index, AV-shunt failure and vascular access failure event[120]
209totalCo-morbidity of CAD and DM *[119]
394totalCV mortality and first CV event[124]
Elderly HD112freeAll-cause and CV mortality[128]
AV: arterio-venous; CAD: coronary artery disease; CKD: chronic kidney disease; CV: cardiovascular; DM: diabetes mellitus; HD: hemodialysis; IL-6: interleukin-6; LV: left ventricle; MACE: major cardiovascular events; pCS: p-cresyl sulfate; PWV: pulse wave velocity; QTc: heart-rate corrected QT interval; * not with pro-inflammatory markers.
Table
Table 3. Targets and methods to reduce p-cresyl sulfate concentrations.
Table 3. Targets and methods to reduce p-cresyl sulfate concentrations.
TargetMethod
Toxins 09 00052 i0011. Affecting the generation of pCS
Diet:
↑ Carbohydrate/fiber (risk for hyperphosphatemia, hyperkalemia in CKD) versus
↓ Protein intake (risk for malnutrition in HD)
Pro-, pre-, synbiotics:
↑ Saccharolytic activity of bacteria
Laxatives
↓ Colonic transit time
2. Adsorption
Oral sorbent AST-120
Toxins 09 00052 i0023. Preserving kidney function
Preserving tubular secretion (transporter expression)
4. Renal replacement therapy
Dialysis: combining convective and diffusive removal
Renal transplantation

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Gryp, T.; Vanholder, R.; Vaneechoutte, M.; Glorieux, G. p-Cresyl Sulfate. Toxins 2017, 9, 52. https://doi.org/10.3390/toxins9020052

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Gryp T, Vanholder R, Vaneechoutte M, Glorieux G. p-Cresyl Sulfate. Toxins. 2017; 9(2):52. https://doi.org/10.3390/toxins9020052

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Gryp, Tessa, Raymond Vanholder, Mario Vaneechoutte, and Griet Glorieux. 2017. "p-Cresyl Sulfate" Toxins 9, no. 2: 52. https://doi.org/10.3390/toxins9020052

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Gryp, T., Vanholder, R., Vaneechoutte, M., & Glorieux, G. (2017). p-Cresyl Sulfate. Toxins, 9(2), 52. https://doi.org/10.3390/toxins9020052

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