Next Article in Journal
Sex-Based Evaluation of Lipid Profile in Postoperative Adjuvant Mitotane Treatment for Adrenocortical Carcinoma
Next Article in Special Issue
SAR296968, a Novel Selective Na+/Ca2+ Exchanger Inhibitor, Improves Ca2+ Handling and Contractile Function in Human Atrial Cardiomyocytes
Previous Article in Journal
G-Quadruplex Formed by the Promoter Region of the hTERT Gene: Structure-Driven Effects on DNA Mismatch Repair Functions
Previous Article in Special Issue
Novel Phenotyping for Acute Heart Failure—Unsupervised Machine Learning-Based Approach
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Biomedicines
Volume 10
Issue 8
10.3390/biomedicines10081874
biomedicines-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Soluble (Pro)Renin Receptor Levels Are Regulated by Plasma Renin Activity and Correlated with Edema in Mice and Humans with HFrEF

by
Inna P. Gladysheva
1,*,
Ryan D. Sullivan
1,
Kodangudi Ramanathan
2 and
Guy L. Reed
1
1
Department of Medicine, University of Arizona College of Medicine-Phoenix, Phoenix, AZ 85004, USA
2
Memphis Veterans Affairs Medical Center, Memphis, TN 38163, USA
*
Author to whom correspondence should be addressed.
Biomedicines 2022, 10(8), 1874; https://doi.org/10.3390/biomedicines10081874
Submission received: 8 June 2022 / Revised: 31 July 2022 / Accepted: 1 August 2022 / Published: 3 August 2022
(This article belongs to the Special Issue Advances in Therapy for Heart Failure)
Browse Figures
Versions Notes

Abstract

:
Symptomatic heart failure with reduced ejection fraction (HFrEF) is characterized by edema and chronic pathological activation of the classical renin–angiotensin–aldosterone system (RAAS). The soluble (pro)renin receptor (s(P)RR) is released into circulation by proteolytic cleavage of tissue expressed (P)RR and is a candidate biomarker of RAAS activation. However, previous studies linked elevated levels of s(P)RR in patients with HFrEF to renal dysfunction. Utilizing prospectively enrolled patients with comparable rEF, we show that increased plasma levels of s(P)RR are associated with symptomatic HF (characterized by edema), independent of chronic renal dysfunction. We also found that s(P)RR levels were positively correlated with patient plasma renin activity (PRA). Normotensive mice with dilated cardiomyopathy (DCM) and HFrEF, without renal dysfunction, showed plasma s(P)RR and PRA patterns similar to human HFrEF patients. Plasma s(P)RR levels positively correlated with PRA and systemic edema, but not with EF, resembling findings in patients with HFrEF without chronic kidney dysfunction. In female DCM mice with elevated PRA levels and plasma s(P)RR levels, a randomized, blinded trial comparing the direct renin inhibitor, aliskiren vs. vehicle control, showed that direct renin inhibition normalized PRA, lowered s(P)RR, and prevented symptomatic HFrEF. Considered in light of previous findings, these data suggest that, in HFrEF, in the absence of renal dysfunction, elevation of plasma s(P)RR levels is caused by increased PRA and associated with the development of systemic edema.

1. Introduction

Dilated cardiomyopathy (DCM), one major cause of heart failure (HF), is characterized by progressive heart enlargement with a reduced ejection fraction (rEF) [1,2,3]. Despite the best available therapies [4,5,6,7], for most patients, DCM progresses relentlessly from at-risk status (or stage A HF) to pre-HF (stage B HF) and then to symptomatic HF (sHF, stages C–D) with progressive fluid–salt retention (edema), cachexia/sarcopenia, disability, and a 50% mortality rate within 5 years of diagnosis [1,8,9,10]. New diagnostic and therapeutic strategies are needed to block the progression of DCM to sHF, prolong and improve the quality of life.
sHFrEF is characterized by the chronic pathological activation of the classical renin–angiotensin–aldosterone system (RAAS), dysregulation of the protective RAAS arm (Ang 1–7/MAS), and impairment of the natriuretic peptide (NP) system, which promotes salt and water retention leading to clinical HF signs and symptoms from edema, a decline in the quality of life, and premature death [9,11,12,13,14,15,16,17,18,19].
Systemic RAAS activation occurs with increased plasma renin activity (PRA), which initiates the first and rate-limiting step [18]. Circulating active renin and pro-renin bind to transmembrane (pro)renin receptor (P)RR to activate local tissue classical RAAS or initiate independent intracellular signaling [20]. The physiological role of (P)RR, among others, includes regulation of fluid balance; it is pathologically linked to renal and cardiovascular dysfunction including HF [21,22,23]. Cleavage of tissue expressed (P)RR by the serine protease furin [24] and/or metallopeptidase ADAM19 [25] leads to intercellular release of soluble (P)RR (s(P)RR) followed by its release into circulation. The circulating level of s(P)RR is suggested to be a surrogate biomarker of tissue RAAS activity [26] with a potential functional role in nonproteolytic pro-renin activation [27,28].
High serum s(P)RR levels were associated with HF progression in hemodialysis patients [29] and patients with chronic HF regardless of renal function [30]. In other studies, elevated circulating s(P)RR levels in patients with chronic HF were associated with renal dysfunction [31,32,33]. It remains unclear in HFrEF if s(P)RR levels reflect only renal dysfunction or the severity of systolic dysfunction and/or edema (a hallmark of sHF). A functional relationship between circulating s(P)RR and PRA levels in HFrEF also remains undetermined. Here, we report clinical and preclinical data demonstrating that, in DCM-HFrEF patients and mice with or without sHF, and without chronic kidney disease (CKD), elevated plasma levels of s(P)RR are associated with edema and potentially causally linked to increased PRA.

2. Materials and Methods

2.1. Study Population

Three groups of patients (n = 16 per group, ages 50–70) admitted to the medical service of the Memphis Veterans Affairs Medical Center (VAMC) were prospectively enrolled as previously described: (1) no HF and normal ejection fraction (healthy, mean EF: 63% ± 3%); (2) no HF and reduced EF (DCM, mean rEF: 27% ± 7%), and sHF with rEF (DCM-sHF, mean rEF: 24% ± 8%) [17]. The inclusion and exclusion criteria were previously described in detail [17]. Patient groups were comparable in terms of age, sex, and race. All patients were male, reflecting the VAMC patient population. The use of medications such as aspirin, clopidogrel, beta-blockers, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, warfarin, nitrates, statins, and antiarrhythmic agents were similar between the enrolled groups (p > 0.1). Patients with CKD (estimated glomerular filtration rate, eGFR < 60 mL/min/1.73 m2), pulmonary hypertension, myocardial infarction within the last 6 weeks, critical valvular heart disease, metastatic or terminal cancer, morbid obesity (BMI > 35), and cardiopulmonary support were excluded from the study. sHF was defined by abbreviated Framingham criteria, including peripheral edema, and by plasma level of a B-type natriuretic peptide, BNP > 400 pg/mL. There was no significant difference in EF between groups with rEF regardless of sHF status. The selected group sample size (based on our previous study [13]) allowed us to detect the difference in targeted plasma markers levels between enrolled groups of patients with statistical power >90%. The study was approved by the Institutional Review Board of the Memphis VAMC and conformed to the principles and ethical guidelines of the Declaration of Helsinki (1964). All enrolled patients provided their signed informed consent to participate in the study [17].

2.2. Mouse Model of DCM-HFrEF

This study utilized the previously established preclinical normotensive mouse model of progressive DCM with preserved kidney function (on C57BL/6J background), generated by cardiac-specific, dominant negative, transgenic suppression of CREB phosphorylation driven by the alpha myosin heavy chain promoter [19,34,35,36,37,38,39,40,41,42]. DCM progression in this model is not associated with cardiac arrhythmias, blood pressure alteration, or kidney failure [19,39].
Experimental mouse studies were conducted in accordance with National Institute of Health (NIH) Guide for the Care and Use of Laboratory Animals and with the Animal Research: Reporting In Vivo Experiments (ARRIVE) guidelines. Mice were housed in an individually ventilated caging system and fed an ad libitum maintenance diet (Envigo Tekland 7912, Madison, WI, USA) within AAALACi accredited facilities under a 12 h/12 h light/dark cycle. Mouse health, behavioral changes including loss of ambulatory activity (fatigue, lethargy, dyspnea, body tremors, and self-isolation), and death records were monitored by investigators or animal care staff daily as we previously reported [19]. Female mice with DCM were randomly and blindly treated with DRI aliskiren hemifumarate (100 mg/kg/day in drinking water; BOC Sciences, Shirley, NY, USA) or vehicle starting from the stage B HF corresponding to 7 weeks of age [40]), and characterized by pathologically elevated PRA levels as we previously reported [39]. Groups were analyzed at the point when vehicle-treated DCM mice progressed to stage D HF, corresponding to ~13 weeks of age [39]. The physiological outcomes were analyzed using clinically relevant diagnostic modalities for translational relevance. The subgroups of mice were sacrificed at 13 weeks of age for organ and plasma collection after systolic function (EF) and systemic edema (extracellular water, ECW) assessed by quantitative magnetic resonance (QMR) were recorded.
Studies were approved by the Institutional Animal Care and Use Committees at the University of Arizona College of Medicine–Phoenix (Protocol 17-303, approved 11 December 2017) or the University of Tennessee Health Science Center (Protocol 15-050.0, approved 9 July 2015; Protocol 17-059.0, approved 26 July 2017).

2.3. Blood Sample Collection

Venous blood samples of enrolled VAMC patients were collected in standard EDTA-aprotinin tubes to prevent coagulation and proteolysis of targeted proteins and immediately stored on ice [17]. Mouse blood samples were collected by cardiocentesis with syringes supplied with EDTA (Sigma-Aldrich, MO, USA) and aprotinin (Sigma-Aldrich, MO, USA) as previously described [40]. The blood samples were centrifuged at 4 °C, 3000× g for 20 min, and the plasma samples were aliquoted and stored at −80 °C until analyzed.

2.4. Plasma Biomarker Measurements

Plasma levels of s(P)RR were measured by solid-phase sandwich enzyme-linked immunosorbent assay (ELISA) using IBL Immuno-Biological Labs Co. Ltd., Fujioka-Shi, Japan kit (Code number 27782) for human and mouse plasma samples. The proper dilution factors and the optimum incubation time with test samples were determined in the laboratory.
Renin enzymatic activity in plasma samples (or plasma renin activity, PRA) was measured and quantified by cleavage of the fluorescence resonance transfer (FRET) peptide substrates optimized for human renin or mouse renin with minimal background autofluorescence, FRET-QXL™520/5-FAM, using the SensoLyte 520 renin assay kits (AnaSpec, Fremont, CA, USA) as previously reported [18,19,39,40,41].

2.5. Extracellular Water Analysis

Systemic extracellular water (ECW) or free water, was objectively recorded by the QMR system (EchoMRI 4-in-1 Analyzer, Echo Medical Systems, Houston, TX, USA) as we previously described [19,40,41]. The fully conscious mice (after urination) were noninvasively examined (~1.5 min recording time) at 13 weeks, prior to necropsy.

2.6. Echocardiography

Systolic function and heart rate were assessed in anesthetized mice by transthoracic echocardiography (Vevo 2100/3100 Imaging Systems, VisualSonics, Toronto, ON, Canada) as we described [19,38,39,40,41,42]. Mice were maintained at an anesthetized heart rate of 450 ± 50 beats per minute and 37 ± 1 °C rectal temperature. Data were blindly analyzed by Vevo LAB 3.1.0 software using company standard protocols for systolic function.

2.7. Statistical Analysis

Data were analyzed with appropriate parametric or nonparametric methods with GraphPad Prism 9.0 software (GraphPad Software, San Diego, CA, USA) using Mann–Whitney multiple comparison between groups, one-way ANOVA, or two-way ANOVA with Tukey’s multiple comparison test and Pearson or Spearman correlations. Data are presented as the mean ± SE. A two-tailed p-value < 0.05 was considered statistically significant and denoted in the figure legends as * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001.

3. Results

3.1. Plasma s(P)RR Levels Elevate as Clinical HFrEF Progress and Positively Correlate with PRA

We measured plasma s(P)RR levels and correlated them with PRA levels (Figure 1) in three groups of prospectively enrolled VMAC patients without CKD (eGFR > 60 mL/min/1.73 m2; n = 16/group) [17]. The groups included patients without systolic dysfunction and HF (healthy group), no HF with rEF (DCM group), and sHF with rEF (DCM + sHF group). Systolic dysfunction (rEF) was comparable between DCM groups. This experimental clinical setting allowed us to investigate whether systolic dysfunction and HF signs, including edema, modulate s(P)RR independently from kidney dysfunction. Both PRA and s(P)RR plasma levels were significantly increased in clinical pre-symptomatic HF with rEF (DCM group) vs. the healthy group. Both levels were further elevated in the DCM + sHF group, which was characterized by the onset of edema and other Framingham HF diagnostic criteria, (Figure 1a,b). Spearman’s analysis demonstrated that s(P)RR levels are positively correlated with PRA levels (rs = 0.59, p < 0.0001; Figure 1c). Collectively, these data illustrate that, in DCM patients without CKD, the positive association between s(P)RR and PRA levels positively aligned with the presence of edema, thus reflecting the degree of sHF.

3.2. Association between Plasma s(P)RR and PRA Levels in DCM-HFrEF Mouse Model

We and others have extensively characterized a mouse model of DCM-HFrEF, without kidney dysfunction, with high translational relevance to human DCM-HFrEF [19,34,35,36,37,38,39,40,41,42]. In these mice, we described the longitudinal progression of HF stages according to systolic dysfunction, cardiac remodeling and fibrosis, edema, visible HF signs (fatigue, dyspnea, etc.), cachexia/sarcopenia, well-defined HF biomarker profiles, and premature death [19,38,39,40]. The DCM-HFrEF mice recapitulate human HF progressive stages [8,9] in an age- and sex-related manner, from at risk for HF (stage A) to pre-HF (stage B: to progressive decline in contractile function (rEF) and increasing heart dilation), HF (stage C: systemic and pulmonary edema with increases in HF biomarkers (NT-pro-ANP and BNP/NT-pro-BNP, etc.) and cardiac fibrosis), and advanced HF (stage D: edema, pulmonary effusion, visible HF signs, decreased muscle/fat mass (cachexia/sarcopenia), with a median survival age of 13–14 weeks in females and 20 weeks in males) (Figure 2).
Like humans with DCM-HFrEF, both sexes of mice with DCM-HFrEF have progressive pathologically elevated PRA levels, activation of classical RAAS, and an impaired protective RAAS arm [19,39,40]. We analyzed plasma levels of PRA and s(P)RR in female and male DCM mice at the age corresponding to advanced HF (stage D HF) vs. congenic WT mice (Figure 3 a,b). Data demonstrate that advanced HF is characterized by significant elevation of both PRA and s(P)RR levels in both sexes. Spearman’s analysis of combined male and female mouse groups demonstrated that plasma s(P)RR levels are positively correlated with PRA levels (rs = 0.57, p < 0.004) signifying a significant association of s(P)RR with HF (Figure 3c).

3.3. Normalization of PRA with Direct Renin Inhibitor Normalizes Plasma s(P)RR Levels in DCM-HFrEF Mice

To examine the functional relationship between plasma s(P)RR and PRA during DCM progression to symptomatic HFrEF, we analyzed and correlated their levels in groups of DCM female littermate mice enrolled in a randomized, blinded preclinical trial that compared outcomes of treatments with DRI aliskiren vs. vehicle control [40]; the wildtype (WT) congenic group was used for control (Figure 4a). We reported that normalization of PRA levels (equivalent to WT group) in DCM mice treated with aliskiren, in comparison to control DCM mice treated with vehicle (Figure 4b), improved systolic function (EF, p < 0.05; cardiac output, p < 0.01), reduced systemic edema (ECW levels, p < 0.0001), and prolonged life (p < 0.05) [40]. Treatment with the DRI vs. vehicle significantly reduced plasma s(P)RR to levels detected in the WT control group (p < 0.0001, Figure 4c). Plasma s(P)RR and PRA levels were significantly correlated (rs = 0.73, p < 0.0001; Figure 4d). The levels were higher in the DCM group of mice treated with vehicle (red dots) that progressed to HF at 13 weeks of age (defined by systemic edema assessed by QMR) than in the DCM group treated with DRI (blue dots) and characterized by the absence of HF [40]. Consistently, s(P)RR levels were positively correlated with ECW (Figure 4e), indicating that s(P)RR levels are associated with systemic edema. The plasma levels of s(P)RR were not associated with EF (Figure 4f), suggesting that systolic function does not affect receptor levels in circulation.

4. Discussion

Chronic renal dysfunction (eGFR ≤ 60 mL/min/1.73 m2) accelerates HFrEF decompensation and mortality [43,44,45]. In patients with sHF with rEF, the elevation of circulating s(P)RR levels was associated with renal dysfunction [31,32,33]. In contrast, in this study, we demonstrated that an elevation in the circulating level of s(P)RR in DCM patients reflected the progression of systolic dysfunction to symptomatic HFrEF, characterized by edema independent of CKD. Moreover, s(P)RR levels are positively correlated with PRA levels. The limited patient group size may have reduced our power to detect a linkage between the presence of HF-related edema and plasma s(P)RR levels or a s(P)RR level correlation with PRA. Normotensive DCM mice of both sexes, which mirror human DCM progression and transition to symptomatic HfrEF without kidney dysfunction [19,36,38,39,40], demonstrated the same patterns of circulating s(P)RR and PRA. Our data showed that, in female mice with DCM, treatment with direct renin inhibitor (DRI), aliskiren, not only normalized the elevated pathological PRA and attenuated progression to HFrEF [40], but also simultaneously reduced plasma s(P)RR levels to that of WT congenic mice.
Classical RAAS activation is thought to compensate for impaired cardiac function through increased salt and water retention and other actions. Yet, chronic overactivation of RAAS by PRA has deleterious effects on cardiac structure and performance, leading to symptomatic HFrEF characterized by edema [16,18]. Translational and clinical evidence suggests that as DCM progresses, pathologically elevated PRA enhances systolic dysfunction, promotes edema, and accelerates the development of symptomatic HFrEF [39,40,46]. The presented data demonstrate that in humans and mice with DCM-HFrEF without renal impairment, a significant rise in plasma s(P)RR is associated with the presence of edema and positively correlated with PRA levels. The correlation between circulating levels of s(P)RR and PRA may be unique for HFrEF without CKD, as it has not been observed in patients without HF or those with CKD. Thus, there was no correlation between s(P)RR and active renin or pro-renin in healthy subjects and non-HF patients with an overactivated RAAS [47]. s(P)RR levels were not correlated with PRA and HF stage in patients with severe HFrEF and kidney failure (eGFR in a range of about 60–15 mL/min/1.73 m2) [33]. Additionally, there was no correlation between s(P)RR and PRA serum levels in patients with autosomal dominant polycystic kidney disease without HF [48].
Furthermore, we investigated the functional association between circulating s(P)RR and PRA in DCM mice as they progress from pre-symptomatic stage B HF to advanced symptomatic HFrEF (stage D), characterized, as we previously reported [39,40], by systemic edema, cachexia/sarcopenia, and premature mortality. These mice are normotensive and have preserved renal function, eliminating confounding outcomes from these variables. The randomized, blinded trial demonstrated improvement of systolic function, prevention of systemic edema (symptomatic HFrEF), and improved survival in the DCM mouse group treated with DRI aliskiren vs. DCM littermate control mice treated with vehicle [40,49]. DRI treatment normalized pathologically elevated PRA and plasma s(P)RR levels to levels detected in the congenic mouse group without DCM. The positive association of plasma s(P)RR levels with systemic edema agrees with the previously reported antidiuretic role of urine s(P)RR in regulating fluid homeostasis and urine concentrating capability in rodents [50,51]. Nevertheless, it remains to be investigated whether, in DCM-HFrEF without CKD, elevated circulating s(P)RR has a causative effect or is simply correlated with HF and edema.
Little is known about the role of circulating s(P)RR in pro-renin activation in physiological and pathological conditions [18,27,28]. As DCM progressed to sHF, circulating s(P)RR might bind and nonproteolytically activate pro-renin, similar to tissue-expressed (P)RR [20], contributing to pathologically increased PRA levels directly associated with edema [40] and conversion of angiotensinogen to angiotensin I.
Cardiac (P)RR transcript (ATP6AP2 gene) and protein expression were significantly elevated in patients with idiopathic DCM and NYHA class II–IV compared to healthy donor hearts [52] and in rodent models of HFrEF [52,53,54]. Preclinical studies in mice demonstrated that pathologically expressed (P)RR contributed to developing DCM and HFrEF [55,56,57,58,59,60]. Aliskiren treatment, at a dose of 10 mg/kg per day via osmotic mini-pump for 6 weeks, reduced cardiac transcripts and protein levels of (P)RR in TGR(mRen2)-27 rats with streptozotocin-induced diabetic cardiomyopathy with diastolic dysfunction in the absence of edema [61]. In this rat model, aliskiren treatment (10 or 30 mg/kg per day, 10 weeks i.v.) also reduced (P)RR expression in the renal compartments [62]. These data support the finding of our study that lowering PRA affects circulating levels of sP(RR). The reduced plasma levels of s(P)RR in DRI-treated DCM mice may be due in part to the diminished gene and protein expression or altered processing/cleavage of (P)RR.

5. Conclusions

Taken together, these DCM-HFrEF clinical and preclinical results indicate that plasma s(P)RR levels are significantly correlated with PRA and the presence of edema/congestion or symptomatic HF. In both humans and mice, elevated levels of circulating s(P)RR may be a biomarker (and potential regulator) of pathological fluid retention of HF origin, in the absence of chronic kidney dysfunction. Experimental normalization of PRA by the DRI, aliskiren, in normotensive mice with DCM without renal dysfunction attenuates progression to HFrEF and decreases levels of circulating s(P)RR. This may be due to downregulation of tissue expression, as well as other mechanisms that are yet to be investigated. Further research into the functional role of circulating s(P)RR in DCM and HFrEF is needed to support its role as a potential therapeutic target. Clinical studies are required to confirm that DRIs reduce s(P)RR circulating levels in patients with HFrEF without CKD. The potential mechanisms through which DRI might affect s(P)RR levels in circulation and circulating s(P)RR might contribute to edema promotion in HFrEF are schematically summarized in Figure 5.

6. Patents

UA Tech Launch, along with the authors, have filed USA patents application related to (1) the methods of personalized treatment for cardiomyopathy and heart failure and other related diseases by measuring renin activity, pro-renin and (pro)renin receptor levels in blood (Pub. No.: 20210262008, 26 August 2021), and (2) extracellular water analysis as a measure of edema (Pub. No.: US 20210263120, 26 August 2021).

Author Contributions

I.P.G. designed and supervised the study, performed the experiments, analyzed and interpreted the data, prepared the figures, and wrote the original manuscript; R.D.S. performed the experiments, analyzed the data, and reviewed and edited the manuscript; K.R. enrolled the patient population and edited the manuscript; G.L.R. interpreted the data, reviewed the statistical analyses, and critically edited the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This study was supported by research funds from the University of Arizona, College of Medicine-Phoenix and, in part, by the National Institute of Health (Grant HL115036 to I.P.G. and NS89707 to G.R.).

Institutional Review Board Statement

The study was a part of our previously reported study [17]; it was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board and Ethical Committee of Memphis VA Center, TN, USA. All experimental animal studies were reviewed and approved by the Institutional Animal Care and Use Committees at the University of Tennessee Health Science Center (15–050; approved 9 July 2015 and 17–059; approved 26 July 2017) and the University of Arizona College of Medicine–Phoenix (17–303; approved 11 December 2017 and 12 December 2020), and they were conducted within AAALACi accredited facilities in accordance with the National Institutes of Health (NIH) Guide for the Care and Use of Laboratory Animals.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Data generated for this study are available upon reasonable request to the corresponding author I.P.G.

Acknowledgments

The authors gratefully acknowledge the technical assistance of Radhika M. Mehta.

Conflicts of Interest

A patent application has been filed on the basis of this study, as indicated above.

References

  1. Weintraub, R.G.; Semsarian, C.; Macdonald, P. Dilated Cardiomyopathy. Lancet 2017, 390, 400–414. [Google Scholar] [CrossRef]
  2. Schultheiss, H.P.; Fairweather, D.; Caforio, A.L.P.; Escher, F.; Hershberger, R.E.; Lipshultz, S.E.; Liu, P.P.; Matsumori, A.; Mazzanti, A.; McMurray, J.; et al. Dilated Cardiomyopathy. Nat. Rev. Dis. Primers 2019, 5, 32. [Google Scholar] [CrossRef] [PubMed]
  3. Rosenbaum, A.N.; Agre, K.E.; Pereira, N.L. Genetics of Dilated Cardiomyopathy: Practical Implications for Heart Failure Management. Nat. Rev. Cardiol. 2020, 17, 286–297. [Google Scholar] [CrossRef] [PubMed]
  4. Vaduganathan, M.; Claggett, B.L.; Jhund, P.S.; Cunningham, J.W.; Pedro Ferreira, J.; Zannad, F.; Packer, M.; Fonarow, G.C.; McMurray, J.J.V.; Solomon, S.D. Estimating Lifetime Benefits of Comprehensive Disease-Modifying Pharmacological Therapies in Patients with Heart Failure with Reduced Ejection Fraction: A Comparative Analysis of Three Randomised Controlled Trials. Lancet 2020, 396, 121–128. [Google Scholar] [CrossRef]
  5. McMurray, J.J.V.; Packer, M. How Should We Sequence the Treatments for Heart Failure and a Reduced Ejection Fraction? A Redefinition of Evidence-Based Medicine. Circulation 2021, 143, 875–877. [Google Scholar] [CrossRef] [PubMed]
  6. McDonagh, T.A.; Metra, M.; Adamo, M.; Gardner, R.S.; Baumbach, A.; Bohm, M.; Burri, H.; Butler, J.; Celutkiene, J.; Chioncel, O.; et al. 2021 Esc Guidelines for the Diagnosis and Treatment of Acute and Chronic Heart Failure. Eur. Heart J. 2021, 42, 3599–3726. [Google Scholar] [CrossRef] [PubMed]
  7. Hernandez, M.; Sullivan, R.D.; McCune, M.E.; Reed, G.L.; Gladysheva, I.P. Sodium-Glucose Cotransporter-2 Inhibitors Improve Heart Failure with Reduced Ejection Fraction Outcomes by Reducing Edema and Congestion. Diagnostics 2022, 12, 989. [Google Scholar] [CrossRef]
  8. Yancy, C.W.; Jessup, M.; Bozkurt, B.; Butler, J.; Casey, D.E., Jr.; Drazner, M.H.; Fonarow, G.C.; Geraci, S.A.; Horwich, T.; Januzzi, J.L.; et al. 2013 Accf/Aha Guideline for the Management of Heart Failure: Executive Summary: A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation 2013, 128, 1810–1852. [Google Scholar] [CrossRef] [PubMed]
  9. Bozkurt, B.; Coats, A.J.S.; Tsutsui, H.; Abdelhamid, C.M.; Adamopoulos, S.; Albert, N.; Anker, S.D.; Atherton, J.; Bohm, M.; Butler, J.; et al. Universal Definition and Classification of Heart Failure: A Report of the Heart Failure Society of America, Heart Failure Association of the European Society of Cardiology, Japanese Heart Failure Society and Writing Committee of the Universal Definition of Heart Failure: Endorsed by the Canadian Heart Failure Society, Heart Failure Association of India, Cardiac Society of Australia and New Zealand, and Chinese Heart Failure Association. Eur. J. Heart Fail. 2021, 23, 352–380. [Google Scholar] [CrossRef]
  10. Heidenreich, P.A.; Bozkurt, B.; Aguilar, D.; Allen, L.A.; Byun, J.J.; Colvin, M.M.; Deswal, A.; Drazner, M.H.; Dunlay, S.M.; Evers, L.R.; et al. 2022 Aha/Acc/Hfsa Guideline for the Management of Heart Failure: Executive Summary: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation 2022, 79, 1757–1780. [Google Scholar] [CrossRef] [PubMed]
  11. Dzau, V.J.; Colucci, W.S.; Hollenberg, N.K.; Williams, G.H. Relation of the Renin-Angiotensin-Aldosterone System to Clinical State in Congestive Heart Failure. Circulation 1981, 63, 645–651. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Schrier, R.W.; Abraham, W.T. Hormones and Hemodynamics in Heart Failure. N. Engl. J. Med. 1999, 341, 577–585. [Google Scholar] [CrossRef] [PubMed]
  13. Ibebuogu, U.N.; Gladysheva, I.P.; Houng, A.K.; Reed, G.L. Decompensated Heart Failure Is Associated with Reduced Corin Levels and Decreased Cleavage of Pro-Atrial Natriuretic Peptide. Cardiocirc. Heart Fail. 2011, 4, 114–120. [Google Scholar] [CrossRef] [Green Version]
  14. Dries, D.L. Process Matters: Emerging Concepts Underlying Impaired Natriuretic Peptide System Function in Heart Failure. Cardiocirc. Heart Fail. 2011, 4, 107–110. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Patel, V.B.; Zhong, J.C.; Grant, M.B.; Oudit, G.Y. Role of the Ace2/Angiotensin 1-7 Axis of the Renin-Angiotensin System in Heart Failure. Cardiocirc. Res. 2016, 118, 1313–1326. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Hartupee, J.; Mann, D.L. Neurohormonal Activation in Heart Failure with Reduced Ejection Fraction. Nat. Rev. Cardiol. 2017, 14, 30–38. [Google Scholar] [CrossRef] [Green Version]
  17. Zaidi, S.S.; Ward, R.D.; Ramanathan, K.; Yu, X.; Gladysheva, I.P.; Reed, G.L. Possible Enzymatic Downregulation of the Natriuretic Peptide System in Patients with Reduced Systolic Function and Heart Failure: A Pilot Study. BioMed Res. Int. 2018, 2018, 7279036. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  18. Sullivan, R.D.; Mehta, R.M.; Tripathi, R.; Reed, G.L.; Gladysheva, I.P. Renin Activity in Heart Failure with Reduced Systolic Function-New Insights. Int. J. Mol. Sci. 2019, 20, 3182. [Google Scholar] [CrossRef] [Green Version]
  19. Tripathi, R.; Sullivan, R.D.; Fan, T.M.; Mehta, R.M.; Gladysheva, I.P.; Reed, G.L. A Low-Sodium Diet Boosts Ang (1-7) Production and No-Cgmp Bioavailability to Reduce Edema and Enhance Survival in Experimental Heart Failure. Int. J. Mol. Sci. 2021, 22, 4035. [Google Scholar] [CrossRef] [PubMed]
  20. Nguyen, G.; Delarue, F.; Burckle, C.; Bouzhir, L.; Giller, T.; Sraer, J.D. Pivotal Role of the Renin/Prorenin Receptor in Angiotensin Ii Production and Cellular Responses to Renin. J. Clin. Investig. 2002, 109, 1417–1427. [Google Scholar] [CrossRef] [PubMed]
  21. Ichihara, A.; Yatabe, M.S. The (Pro)Renin Receptor in Health and Disease. Nat. Rev. Nephrol. 2019, 15, 693–712. [Google Scholar] [CrossRef] [PubMed]
  22. Quadri, S.S.; Cooper, C.; Ghaffar, D.; Vaishnav, H.; Nahar, L. The Pathological Role of Pro(Renin) Receptor in Renal Inflammation. J. Exp. Pharmacol. 2021, 13, 339–344. [Google Scholar] [CrossRef] [PubMed]
  23. Xu, C.; Liu, C.; Xiong, J.; Yu, J. Cardiovascular Aspects of the (Pro)Renin Receptor: Function and Significance. FASEB J. 2022, 36, e22237. [Google Scholar] [CrossRef] [PubMed]
  24. Cousin, C.; Bracquart, D.; Contrepas, A.; Corvol, P.; Muller, L.; Nguyen, G. Soluble Form of the (Pro)Renin Receptor Generated by Intracellular Cleavage by Furin Is Secreted in Plasma. Hypertension 2009, 53, 1077–1082. [Google Scholar] [CrossRef] [Green Version]
  25. Yoshikawa, A.; Aizaki, Y.; Kusano, K.; Kishi, F.; Susumu, T.; Iida, S.; Ishiura, S.; Nishimura, S.; Shichiri, M.; Senbonmatsu, T. The (Pro)Renin Receptor Is Cleaved by Adam19 in the Golgi Leading to Its Secretion into Extracellular Space. Hypertens. Res. 2011, 34, 599–605. [Google Scholar] [CrossRef] [Green Version]
  26. Morimoto, S.; Ando, T.; Niiyama, M.; Seki, Y.; Yoshida, N.; Watanabe, D.; Kawakami-Mori, F.; Kobori, H.; Nishiyama, A.; Ichihara, A. Serum Soluble (Pro)Renin Receptor Levels in Patients with Essential Hypertension. Hypertens. Res. 2014, 37, 642–648. [Google Scholar] [CrossRef] [Green Version]
  27. Gonzalez, A.A.; Lara, L.S.; Luffman, C.; Seth, D.M.; Prieto, M.C. Soluble Form of the (Pro)Renin Receptor Is Augmented in the Collecting Duct and Urine of Chronic Angiotensin Ii-Dependent Hypertensive Rats. Hypertension 2011, 57, 859–864. [Google Scholar] [CrossRef] [Green Version]
  28. Biswas, K.B.; Nabi, A.H.; Arai, Y.; Nakagawa, T.; Ebihara, A.; Ichihara, A.; Watanabe, T.; Inagami, T.; Suzuki, F. Aliskiren Binds to Renin and Prorenin Bound to (Pro)Renin Receptor in Vitro. Hypertens. Res. 2010, 33, 1053–1059. [Google Scholar] [CrossRef] [Green Version]
  29. Amari, Y.; Morimoto, S.; Iida, T.; Takimoto, H.; Okuda, H.; Yurugi, T.; Oyama, Y.; Aoyama, N.; Nakajima, F.; Ichihara, A. Association between Serum Soluble (Pro)Renin Receptor Level and Worsening of Cardiac Function in Hemodialysis Patients: A Prospective Observational Study. PLoS ONE 2020, 15, e0233312. [Google Scholar] [CrossRef]
  30. Obradovic, D.; Loncar, G.; Radenovic, S.; Tahirovic, E.; Heidecke, H.; Schulze-Forster, K.; Muller, D.; Busjahn, A.; Buttner, P.; Veskovic, J.; et al. Soluble (Pro)Renin Receptor in Elderly Chronic Heart Failure Patients. Front. Biosci. (Landmark Ed) 2020, 25, 1839–1853. [Google Scholar] [CrossRef]
  31. Fukushima, A.; Kinugawa, S.; Homma, T.; Masaki, Y.; Furihata, T.; Abe, T.; Suga, T.; Takada, S.; Kadoguchi, T.; Okita, K.; et al. Increased Plasma Soluble (Pro)Renin Receptor Levels Are Correlated with Renal Dysfunction in Patients with Heart Failure. Int. J. Cardiol. 2013, 168, 4313–4314. [Google Scholar] [CrossRef] [PubMed]
  32. Gong, L.; Zhang, S.; Li, L.; Gao, X.; Wang, D.; Wu, D.; Wang, K.; Liu, Y. Elevated Plasma Soluble (Pro)Renin Receptor Levels Are Associated with Left Ventricular Remodeling and Renal Function in Chronic Heart Failure Patients with Reduced Ejection Fraction. Peptides 2019, 111, 152–157. [Google Scholar] [CrossRef]
  33. Ikeda, Y.; Tsutsui, K.; Yamada, Y.; Kato, R.; Muramatsu, T.; Senbonmatsu, T. Relationship between Soluble (Pro)Renin Receptor and Renin Activity in Patients with Severe Heart Failure. J. Clin. Med. 2020, 9, 4110. [Google Scholar] [CrossRef] [PubMed]
  34. Fentzke, R.C.; Korcarz, C.E.; Lang, R.M.; Lin, H.; Leiden, J.M. Dilated Cardiomyopathy in Transgenic Mice Expressing a Dominant-Negative Creb Transcription Factor in the Heart. J. Clin. Investig. 1998, 101, 2415–2426. [Google Scholar] [CrossRef] [PubMed]
  35. Watson, P.A.; Birdsey, N.; Huggins, G.S.; Svensson, E.; Heppe, D.; Knaub, L. Cardiac-Specific Overexpression of Dominant-Negative Creb Leads to Increased Mortality and Mitochondrial Dysfunction in Female Mice. Am. J. Physiol. Heart Circ. Physiol. 2010, 299, H2056–H2068. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Gladysheva, I.P.; Wang, D.; McNamee, R.A.; Houng, A.K.; Mohamad, A.A.; Fan, T.M.; Reed, G.L. Corin Overexpression Improves Cardiac Function, Heart Failure, and Survival in Mice with Dilated Cardiomyopathy. Hypertension 2013, 61, 327–332. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Wang, D.; Gladysheva, I.P.; Fan, T.H.; Sullivan, R.; Houng, A.K.; Reed, G.L. Atrial Natriuretic Peptide Affects Cardiac Remodeling, Function, Heart Failure, and Survival in a Mouse Model of Dilated Cardiomyopathy. Hypertension 2014, 63, 514–519. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Tripathi, R.; Wang, D.; Sullivan, R.; Fan, T.H.; Gladysheva, I.P.; Reed, G.L. Depressed Corin Levels Indicate Early Systolic Dysfunction before Increases of Atrial Natriuretic Peptide/B-Type Natriuretic Peptide and Heart Failure Development. Hypertension 2016, 67, 362–367. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Tripathi, R.; Sullivan, R.; Fan, T.M.; Wang, D.; Sun, Y.; Reed, G.L.; Gladysheva, I.P. Enhanced Heart Failure, Mortality and Renin Activation in Female Mice with Experimental Dilated Cardiomyopathy. PLoS ONE 2017, 12, e0189315. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Sullivan, R.D.; Mehta, R.M.; Tripathi, R.; Gladysheva, I.P.; Reed, G.L. Normalizing Plasma Renin Activity in Experimental Dilated Cardiomyopathy: Effects on Edema, Cachexia, and Survival. Int. J. Mol. Sci. 2019, 20, 3886. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Tripathi, R.; Sullivan, R.D.; Fan, T.M.; Houng, A.K.; Mehta, R.M.; Reed, G.L.; Gladysheva, I.P. Cardiac-Specific Overexpression of Catalytically Inactive Corin Reduces Edema, Contractile Dysfunction, and Death in Mice with Dilated Cardiomyopathy. Int. J. Mol. Sci. 2020, 21, 203. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Tripathi, R.; Sullivan, R.D.; Fan, T.M.; Mehta, R.M.; Gladysheva, I.P.; Reed, G.L. In Experimental Dilated Cardiomyopathy Heart Failure and Survival Are Adversely Affected by a Lack of Sexual Interactions. Int. J. Mol. Sci. 2020, 21, 5450. [Google Scholar] [CrossRef] [PubMed]
  43. Schefold, J.C.; Filippatos, G.; Hasenfuss, G.; Anker, S.D.; von Haehling, S. Heart Failure and Kidney Dysfunction: Epidemiology, Mechanisms and Management. Nat. Rev. Nephrol. 2016, 12, 610–623. [Google Scholar] [CrossRef] [PubMed]
  44. Damman, K.; Masson, S.; Lucci, D.; Gorini, M.; Urso, R.; Maggioni, A.P.; Tavazzi, L.; Tarantini, L.; Tognoni, G.; Voors, A.; et al. Progression of Renal Impairment and Chronic Kidney Disease in Chronic Heart Failure: An Analysis from Gissi-Hf. J. Card. Fail. 2017, 23, 2–9. [Google Scholar] [CrossRef] [Green Version]
  45. Adamska-Welnicka, A.; Welnicki, M.; Mamcarz, A.; Gellert, R. Chronic Kidney Disease and Heart Failure-Everyday Diagnostic Challenges. Diagnostics 2021, 11, 2164. [Google Scholar] [CrossRef] [PubMed]
  46. Rachwan, R.J.; Butler, J.; Collins, S.P.; Cotter, G.; Davison, B.A.; Senger, S.; Ezekowitz, J.A.; Filippatos, G.; Levy, P.D.; Metra, M.; et al. Is Plasma Renin Activity Associated with Worse Outcomes in Acute Heart Failure? A Secondary Analysis from the Blast-Ahf Trial. Eur. J. Heart Fail. 2019, 21, 1561–1570. [Google Scholar] [CrossRef] [PubMed]
  47. Nguyen, G.; Blanchard, A.; Curis, E.; Bergerot, D.; Chambon, Y.; Hirose, T.; Caumont-Prim, A.; Tabard, S.B.; Baron, S.; Frank, M.; et al. Plasma Soluble (Pro)Renin Receptor Is Independent of Plasma Renin, Prorenin, and Aldosterone Concentrations but Is Affected by Ethnicity. Hypertension 2014, 63, 297–302. [Google Scholar] [CrossRef] [Green Version]
  48. Miyaoka, T.; Morimoto, S.; Kataoka, H.; Mochizuki, T.; Tsuchiya, K.; Ichihara, A.; Nitta, K. Serum Soluble (Pro) Renin Receptor Level Is Increased in Association with.Impaired Renal Function in Patients with Autosomal Dominant Polcystic Kidney.Disease. J. Clin. Exp. Nephrol. 2018, 3, 2. [Google Scholar] [CrossRef]
  49. Sullivan, R.D.; Mehta, R.M.; Tripathi, R.; Gladysheva, I.P.; Reed, G.L. Targeting Renin Activity in Heart Failure: Precision Therapy with Aliskiren Improves Systolic Function and Prolongs Survival in Female Experimental Dilated Cardiomyopathy. Circulation 2018, 138, A16743. [Google Scholar]
  50. Lu, X.; Wang, F.; Xu, C.; Soodvilai, S.; Peng, K.; Su, J.; Zhao, L.; Yang, K.T.; Feng, Y.; Zhou, S.F.; et al. Soluble (Pro)Renin Receptor Via Beta-Catenin Enhances Urine Concentration Capability as a Target of Liver X Receptor. Proc. Natl. Acad. Sci. USA 2016, 113, E1898–E1906. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  51. Wang, F.; Xu, C.; Luo, R.; Peng, K.; Ramkumar, N.; Xie, S.; Lu, X.; Zhao, L.; Zuo, C.J.; Kohan, D.E.; et al. Site-1 Protease-Derived Soluble (Pro)Renin Receptor Targets Vasopressin Receptor 2 to Enhance Urine Concentrating Capability. JCI Insight 2019, 4, e124174. [Google Scholar] [CrossRef] [PubMed]
  52. Mahmud, H.; Sillje, H.H.; Cannon, M.V.; van Gilst, W.H.; de Boer, R.A. Regulation of the (Pro)Renin-Renin Receptor in Cardiac Remodelling. J. Cell Mol. Med. 2012, 16, 722–729. [Google Scholar] [CrossRef] [Green Version]
  53. Hirose, T.; Mori, N.; Totsune, K.; Morimoto, R.; Maejima, T.; Kawamura, T.; Metoki, H.; Asayama, K.; Kikuya, M.; Ohkubo, T.; et al. Gene Expression of (Pro)Renin Receptor Is Upregulated in Hearts and Kidneys of Rats with Congestive Heart Failure. Peptides 2009, 30, 2316–2322. [Google Scholar] [CrossRef]
  54. Peng, H.; Wu, Z.B.; Kong, S.S.; Li, L. Role of (Pro)Rennin Receptor in Cardiomyocytes of Heart Failure Rat Model. J. Huazhong Univ. Sci. Technol. Med. Sci. 2013, 33, 640–643. [Google Scholar] [CrossRef] [PubMed]
  55. Kinouchi, K.; Ichihara, A.; Sano, M.; Sun-Wada, G.H.; Wada, Y.; Kurauchi-Mito, A.; Bokuda, K.; Narita, T.; Oshima, Y.; Sakoda, M.; et al. The (Pro)Renin Receptor/Atp6ap2 Is Essential for Vacuolar H+-Atpase Assembly in Murine Cardiomyocytes. Circ. Res. 2010, 107, 30–34. [Google Scholar] [CrossRef] [Green Version]
  56. Moilanen, A.M.; Rysa, J.; Serpi, R.; Mustonen, E.; Szabo, Z.; Aro, J.; Napankangas, J.; Tenhunen, O.; Sutinen, M.; Salo, T.; et al. (Pro)Renin Receptor Triggers Distinct Angiotensin Ii-Independent Extracellular Matrix Remodeling and Deterioration of Cardiac Function. PLoS ONE 2012, 7, e41404. [Google Scholar] [CrossRef]
  57. Cao, X.; Yu, S.; Wang, Y.; Yang, M.; Xiong, J.; Yuan, H.; Dong, B. Effects of the (Pro)Renin Receptor on Cardiac Remodeling and Function in a Rat Alcoholic Cardiomyopathy Model Via the Prr-Erk1/2-Nox4 Pathway. Oxidative Med. Cell. Longev. 2019, 2019, 4546975. [Google Scholar] [CrossRef]
  58. Xiong, J.; Cao, X.; Qiao, S.; Yu, S.; Li, L.; Yu, Y.; Fu, C.; Jiang, F.; Dong, B.; Su, Q. (Pro)Renin Receptor Is Involved in Myocardial Damage in Alcoholic Cardiomyopathy. Alcohol Clin. Exp. Res. 2019, 43, 2344–2353. [Google Scholar] [CrossRef] [PubMed]
  59. Xiong, J.; Dong, X.; Li, S.; Jiang, F.; Chen, J.; Yu, S.; Dong, B.; Su, Q. Effects of (Pro)Renin Receptor on Diabetic Cardiomyopathy Pathological Processes in Rats Via the Prr-Ampk-Yap Pathway. Front. Physiol. 2021, 12, 657378. [Google Scholar] [CrossRef] [PubMed]
  60. Yu, S.; Dong, X.; Yang, M.; Yu, Q.; Xiong, J.; Chen, J.; Dong, B.; Su, Q. (Pro)Renin Receptor Involves in Myocardial Fibrosis and Oxidative Stress in Diabetic Cardiomyopathy Via the Prr-Yap Pathway. Sci. Rep. 2021, 11, 3259. [Google Scholar] [CrossRef] [PubMed]
  61. Connelly, K.A.; Advani, A.; Kim, S.; Advani, S.L.; Zhang, M.; White, K.E.; Kim, Y.M.; Parker, C.; Thai, K.; Krum, H.; et al. The Cardiac (Pro)Renin Receptor Is Primarily Expressed in Myocyte Transverse Tubules and Is Increased in Experimental Diabetic Cardiomyopathy. J. Hypertens. 2011, 29, 1175–1184. [Google Scholar] [CrossRef]
  62. Feldman, D.L.; Jin, L.; Xuan, H.; Contrepas, A.; Zhou, Y.; Webb, R.L.; Mueller, D.N.; Feldt, S.; Cumin, F.; Maniara, W.; et al. Effects of Aliskiren on Blood Pressure, Albuminuria, and (Pro)Renin Receptor Expression in Diabetic Tg(Mren-2)27 Rats. Hypertension 2008, 52, 130–136. [Google Scholar] [CrossRef] [Green Version]
Biomedicines 10 01874 g001 550
Figure 1. Plasma renin activity (PRA) [18] (a) and soluble (pro)renin receptor, s(P)RR (b) levels alteration in clinical DCM and symptomatic HFrEF. (c) Spearman correlation of PRA vs. s(P)RR. Arbitrary units (AU). Comparisons between groups were analyzed with Mann–Whitney multiple comparison; * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. Black: healthy—no HF and normal EF; Blue: DCM (dilated cardiomyopathy)—pre-symptomatic HFrEF; Red: DCM + sHF (HF symptoms)—symptomatic HFrEF.
Figure 1. Plasma renin activity (PRA) [18] (a) and soluble (pro)renin receptor, s(P)RR (b) levels alteration in clinical DCM and symptomatic HFrEF. (c) Spearman correlation of PRA vs. s(P)RR. Arbitrary units (AU). Comparisons between groups were analyzed with Mann–Whitney multiple comparison; * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. Black: healthy—no HF and normal EF; Blue: DCM (dilated cardiomyopathy)—pre-symptomatic HFrEF; Red: DCM + sHF (HF symptoms)—symptomatic HFrEF.
Biomedicines 10 01874 g001
Biomedicines 10 01874 g002 550
Figure 2. Schematic presentation of established progressive mouse model of dilated cardiomyopathy heart failure with reduced ejection fraction (DCM-HFrEF).
Figure 2. Schematic presentation of established progressive mouse model of dilated cardiomyopathy heart failure with reduced ejection fraction (DCM-HFrEF).
Biomedicines 10 01874 g002
Biomedicines 10 01874 g003 550
Figure 3. Levels of plasma renin activity (PRA) and soluble (pro)renin receptor (s(P)RR in male and female control mice vs. DCM mice with stage D heart failure: (a) levels of PRA; (b) plasma levels of (s(P)RR; (c) Spearman correlation analysis of combined s(P)RR (c) vs. combined PRA. Groups represent female mice with DCM (13 weeks of age, corresponding stage D HF, DCM + HF) and congenic wild-type (WT) mice at 13 weeks of age, and male mice with DCM (20 weeks of age corresponding to stage D HF) and congenic WT at 20 weeks of age. Arbitrary units (AU). Data were analyzed with two-way ANOVA with Tukey’s multiple comparison; * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001; ns—not significant. HF—heart failure; DCM—dilated cardiomyopathy.
Figure 3. Levels of plasma renin activity (PRA) and soluble (pro)renin receptor (s(P)RR in male and female control mice vs. DCM mice with stage D heart failure: (a) levels of PRA; (b) plasma levels of (s(P)RR; (c) Spearman correlation analysis of combined s(P)RR (c) vs. combined PRA. Groups represent female mice with DCM (13 weeks of age, corresponding stage D HF, DCM + HF) and congenic wild-type (WT) mice at 13 weeks of age, and male mice with DCM (20 weeks of age corresponding to stage D HF) and congenic WT at 20 weeks of age. Arbitrary units (AU). Data were analyzed with two-way ANOVA with Tukey’s multiple comparison; * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001; ns—not significant. HF—heart failure; DCM—dilated cardiomyopathy.
Biomedicines 10 01874 g003
Biomedicines 10 01874 g004 550
Figure 4. Plasma soluble (pro)renin receptor (s(P)RR) levels are correlated with plasma renin activity (PRA) and edema and suppressed by direct inhibition of renin activity in mice with DCM. (a) Experimental design: female mice with DCM (7 weeks of age corresponding stage B HF) were randomly assigned to treatment with direct renin inhibitor (DRI) aliskiren (DRI) in drinking water or vehicle (control, plain drinking water). PRA [40] (b) and s(P)RR (c) level alterations in mice with DCM at 13 weeks of age after treatment with vehicle (control) or DRI. Arbitrary units (AU). Data were analyzed with one-way ANOVA with Tukey’s multiple comparison. (d) Spearman correlation analysis of s(P)RR (b) vs. PRA (a). The values for the wildtype (WT, n = 4 or 7) are shown as a black dotted line for reference. Association of s(P)RR plasma levels with systemic edema assessed by ECW (e) or EF (f) by Pearson’s correlation analysis. QMR—quantitative magnetic resonance for the extracellular water retention (ECW) monitoring; EF—ejection fraction. Data are presented as the mean ± SE; * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001 for control vs. DRI; ++ p < 0.01 and ++++ p < 0.0001 for control vs. WT; ns—not significant.
Figure 4. Plasma soluble (pro)renin receptor (s(P)RR) levels are correlated with plasma renin activity (PRA) and edema and suppressed by direct inhibition of renin activity in mice with DCM. (a) Experimental design: female mice with DCM (7 weeks of age corresponding stage B HF) were randomly assigned to treatment with direct renin inhibitor (DRI) aliskiren (DRI) in drinking water or vehicle (control, plain drinking water). PRA [40] (b) and s(P)RR (c) level alterations in mice with DCM at 13 weeks of age after treatment with vehicle (control) or DRI. Arbitrary units (AU). Data were analyzed with one-way ANOVA with Tukey’s multiple comparison. (d) Spearman correlation analysis of s(P)RR (b) vs. PRA (a). The values for the wildtype (WT, n = 4 or 7) are shown as a black dotted line for reference. Association of s(P)RR plasma levels with systemic edema assessed by ECW (e) or EF (f) by Pearson’s correlation analysis. QMR—quantitative magnetic resonance for the extracellular water retention (ECW) monitoring; EF—ejection fraction. Data are presented as the mean ± SE; * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001 for control vs. DRI; ++ p < 0.01 and ++++ p < 0.0001 for control vs. WT; ns—not significant.
Biomedicines 10 01874 g004
Biomedicines 10 01874 g005 550
Figure 5. Simplified schematic summary. Levels of PRA, s(P)RR, and edema increase in worsening dilated cardiomyopathy (DCM) with HF without renal impairment. Levels of PRA and s(P)RR are closely correlated. Increased PRA activates the RAAS to enhance edema formation and worsen DCM. Normalization of PRA level with a direct renin inhibitor (DRI) suppresses s(P)RR, edema, and progression of cardiomyopathy to HFrEF. Increased levels of s(P)RR may worsen DCM and promote edema through direct effects or through indirect effects, by increasing PRA. In HFrEF without chronic kidney disease, the protective effects of DRI may be mediated in part through suppression of s(P)RR.
Figure 5. Simplified schematic summary. Levels of PRA, s(P)RR, and edema increase in worsening dilated cardiomyopathy (DCM) with HF without renal impairment. Levels of PRA and s(P)RR are closely correlated. Increased PRA activates the RAAS to enhance edema formation and worsen DCM. Normalization of PRA level with a direct renin inhibitor (DRI) suppresses s(P)RR, edema, and progression of cardiomyopathy to HFrEF. Increased levels of s(P)RR may worsen DCM and promote edema through direct effects or through indirect effects, by increasing PRA. In HFrEF without chronic kidney disease, the protective effects of DRI may be mediated in part through suppression of s(P)RR.
Biomedicines 10 01874 g005
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Gladysheva, I.P.; Sullivan, R.D.; Ramanathan, K.; Reed, G.L. Soluble (Pro)Renin Receptor Levels Are Regulated by Plasma Renin Activity and Correlated with Edema in Mice and Humans with HFrEF. Biomedicines 2022, 10, 1874. https://doi.org/10.3390/biomedicines10081874

AMA Style

Gladysheva IP, Sullivan RD, Ramanathan K, Reed GL. Soluble (Pro)Renin Receptor Levels Are Regulated by Plasma Renin Activity and Correlated with Edema in Mice and Humans with HFrEF. Biomedicines. 2022; 10(8):1874. https://doi.org/10.3390/biomedicines10081874

Chicago/Turabian Style

Gladysheva, Inna P., Ryan D. Sullivan, Kodangudi Ramanathan, and Guy L. Reed. 2022. "Soluble (Pro)Renin Receptor Levels Are Regulated by Plasma Renin Activity and Correlated with Edema in Mice and Humans with HFrEF" Biomedicines 10, no. 8: 1874. https://doi.org/10.3390/biomedicines10081874

APA Style

Gladysheva, I. P., Sullivan, R. D., Ramanathan, K., & Reed, G. L. (2022). Soluble (Pro)Renin Receptor Levels Are Regulated by Plasma Renin Activity and Correlated with Edema in Mice and Humans with HFrEF. Biomedicines, 10(8), 1874. https://doi.org/10.3390/biomedicines10081874

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop