Next Article in Journal
Influence of Storage Time on the DNA Integrity and Viability of Spermatozoa of the Spider Crab Maja brachydactyla
Previous Article in Journal
Modeling Paratuberculosis in Laboratory Animals, Cells, or Tissues: A Focus on Their Applications for Pathogenesis, Diagnosis, Vaccines, and Therapy Studies
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

From Metabolism to Vitality: Uncovering Riboflavin’s Importance in Poultry Nutrition

Nutrition & Health Division, BASF SE, 67063 Ludwigshafen am Rhein, Germany
*
Author to whom correspondence should be addressed.
Animals 2023, 13(22), 3554; https://doi.org/10.3390/ani13223554
Submission received: 26 October 2023 / Revised: 10 November 2023 / Accepted: 14 November 2023 / Published: 17 November 2023
(This article belongs to the Section Poultry)

Abstract

:

Simple Summary

Riboflavin, an essential B-vitamin, plays a crucial role in poultry metabolism, impacting energy production, growth, and immune regulation. Its role in redox reactions and energy metabolism is vital for optimal growth and development. Riboflavin is essential for ATP production and the conversion of tryptophan into niacin. Deficiency can lead to skeletal deformities, impaired growth, and compromised immune function. Dietary riboflavin supplementation is necessary due to variable bioavailability in plant-derived sources. The vitamin is absorbed through specialized transport proteins, and its cellular uptake is facilitated by specific receptors. Riboflavin’s role in protein synthesis and its antioxidant properties influence poultry growth and defense against oxidative stress. Its impact on reproductive performance, hatchability, and overall poultry health underscores its significance in poultry nutrition. Future research should focus on its interactions with other nutrients, exploring analogs, and integrating advanced technologies like precision nutrition and nanotechnology for enhanced delivery.

Abstract

Riboflavin, or vitamin B2, is indispensable for poultry, profoundly impacting their metabolic equilibrium, growth, and overall health. In a climate of increasing demand for poultry products and heightened production intensity, grasping the multifaceted roles of riboflavin in domestic fowl nutrition becomes paramount. This essential vitamin serves as a precursor to two vital coenzymes, flavin mononucleotide and flavin adenine dinucleotide, integral players in pivotal redox reactions and energy metabolism. Inadequate riboflavin levels translate into stunted growth, skeletal deformities, and compromised feed conversion efficiency, thereby adversely affecting poultry performance and bottom-line profitability. Riboflavin goes beyond its fundamental role, ameliorating nutrient utilization, facilitating protein synthesis, and augmenting enzyme activity, rightfully earning its epithet as the “growth-promoting vitamin”. Poultry’s reproductive success intricately hinges on riboflavin levels, dictating egg production and hatchability. It is imperative to note that riboflavin requirements exhibit variations among poultry species and distinct production phases, emphasizing the importance of judicious and balanced supplementation strategies. Aligning dietary recommendations with genetic advancements holds the promise of fostering sustainable growth within the poultry sector. Exploring the multifaceted aspects of riboflavin empowers researchers, nutritionists, and producers to elevate poultry nutrition and overall well-being, harmonizing with the industry’s evolving demands.

1. Introduction

In the ever-evolving landscape of poultry farming, the critical role of nutrition in maximizing productivity and promoting avian health has gained significant attention. Domestic fowl, specifically chickens, turkeys, geese, and ducks, hold a paramount position in the global animal protein industry, meeting the rising demand for affordable and nutritious protein sources. Forecasts indicate that by 2031, approximately 47% of the protein sourced from meat will stem from poultry, overshadowing pig, sheep, and bovine meat consumption [1]. Within the intricate web of micronutrients necessary for poultry well-being, the B-vitamins, a group of water-soluble compounds, play a vital role in various physiological processes [2,3]. Among these, riboflavin, also known as vitamin B2, emerges as a pivotal player in maintaining metabolic equilibrium, ensuring optimal growth and safeguarding the health of poultry [4,5,6,7]. The recognized nomenclature by the International Union of Pure and Applied Chemistry (IUPAC) for riboflavin is 6,7-dimethyl-9-(D-ribityl)isoalloxazine.
Riboflavin, standing prominently as one of the eight essential B-vitamins, assumes an unparalleled role due to its involvement in an extensive array of metabolic reactions that constitute the foundation of life [8,9]. Functioning as a critical coenzyme precursor, vitamin B2 orchestrates pivotal redox reactions, contributing indispensably to the intricate processes of energy production, growth facilitation, and the coordination of immune responses [10,11]. As modern poultry production systems witness an intensification in their practices and the demand for poultry-derived products continues its upward trajectory, the imperative for an all-encompassing grasp of micronutrient prerequisites amplifies manifold. In this context, riboflavin emerges as a linchpin micronutrient, capable of exerting far-reaching impacts on poultry performance and holistic well-being [12,13].
Central to the matter lies the astounding metabolic demands of poultry, characterized by rapid growth kinetics and inherent production prowess, necessitating substantial nutritional resources [14]. Vitamin B2 is a precursor for two important coenzymes: flavin mononucleotide (FMN), involved in the mitochondrial electron system, and flavin adenine dinucleotide (FAD), associated with various proteins in redox reactions [15]. These redox reactions are pivotal for the breakdown of carbohydrates, fats, and proteins, culminating in the production of adenosine triphosphate (ATP), the cell’s primary energy currency [16]. Deficiency in this essential micronutrient could disrupt balanced metabolic functioning in poultry, resulting in delayed growth, skeletal deformities, and worsened feed conversion efficiency, a critical metric in poultry farming [8,17]. Frequent clinical indications encompass limping, paralysis, toes curling inward, and elevated culling rates [17]. As riboflavin insufficiency reverberates through metabolic pathways, its consequences extend even to immunity [18,19].
This escalating complexity propels riboflavin to the forefront of nutritional concerns in the poultry sector. The intricate interplay between this seemingly unremarkable vitamin and the complex pathways of metabolism surpasses mere scientific curiosity, holding direct economic implications for poultry production [13,20,21,22,23,24,25,26]. Riboflavin’s dual role as a conductor of energy dynamics and an architect of growth processes underscores the delicate equilibrium underlying poultry nutrition. By elucidating how vitamin B2 shapes metabolic landscapes and influences avian health, nutritionists, researchers, and poultry producers can advance towards enhanced sustainability and efficiency in the industry’s landscape. As the poultry industry continues its ascendancy [27], riboflavin’s centrality as a cornerstone of avian nourishment becomes increasingly pronounced [9]. Table 1 provides a summary of the primary functions of vitamin B2.
While plants may contain significant amounts of vitamin B2 synthesized through biochemical pathways [34], animal tissues and by-products generally exhibit comparatively lower riboflavin concentrations [35]. The riboflavin content in plant-based feedstuffs can substantially vary due to factors like soil quality, climate, and agricultural practices [36]. Given this variability, supplementing animal diets with riboflavin-containing additives or vitamin mixes becomes crucial for meeting optimal requirements in livestock growth, development, and overall performance. Maintaining a balanced and sufficient vitamin B2 intake is vital for bolstering the health of both animals and humans [10].
This review seeks to unravel the multifaceted roles of vitamin B2 in metabolism, growth, and health within poultry populations. Our concentration will be on the following key facets:
  • Biochemical Fundamentals of Riboflavin;
  • Riboflavin Metabolism in Poultry;
  • Riboflavin and Poultry Growth;
  • Oxidative Stress Defense;
  • Reproductive Performance and Hatchability;
  • Riboflavin Requirements for Poultry;
  • Future Prospects and Research Avenues.
By comprehending riboflavin’s intricate interplay with poultry physiology, nutritionists, researchers, and poultry producers can collaboratively pave the way for innovative nutritional strategies that sustainably advance the poultry industry.

2. Biochemical Fundamentals of Riboflavin

Riboflavin plays a key role in the fundamental biochemical processes that sustain avian life. Its significance arises from its multifaceted functions as a coenzyme in a variety of metabolic reactions, notably those involving redox reactions and energy metabolism [15,26]. To grasp the biochemical underpinnings of riboflavin’s role in poultry health, it is imperative to delve into the intricate details of its molecular structure and its coenzyme derivatives, namely FMN and FAD. Furthermore, comprehending its key functions within the avian system, encompassing its involvement in redox reactions and facilitation of energy metabolism, illuminates its indispensability for optimal growth and development.
At its core, riboflavin comprises a heterocyclic ring system, consisting of a central isoalloxazine ring intricately linked to a ribitol side chain [10,37]. This distinctive chemical arrangement enables riboflavin to serve as a precursor to its coenzyme derivatives, FMN and FAD [38] (Figure 1). FMN is synthesized through the phosphorylation of riboflavin catalyzed by riboflavin kinase in the presence of ATP:Mg2+. This conversion represents a major rate-limiting step in FAD biosynthesis [39]. FAD formation occurs as FMN:ATP adenylyl transferase catalytically adenylylates FMN to produce FAD [40]. FMN and FAD are tightly associated with enzyme cofactors that can either accept or donate two electrons and two protons to achieve full reduction or a single electron and proton to form the semiquinone intermediate [41]. This coenzyme system facilitates electron transfer during biochemical reactions, establishing riboflavin as an indispensable component in enzyme-catalyzed oxidation reduction processes in avian species as well as mammals [26,42].
Fundamentally, the biochemical functions of riboflavin in poultry are intricately linked to its role as a coenzyme in redox reactions [29]. These reactions play a crucial role in maintaining the delicate equilibrium between the oxidized and reduced states of molecules within the cellular environment. The coenzymes of riboflavin, namely FMN and FAD, play an active role in these reactions by functioning as carriers of electrons [41]. When enzymes facilitate reactions involving electron transfer, the coenzymes FMN and FAD alternate between their oxidized and reduced states, effectively shuttling electrons to and from the reaction site [43,44].
This unique ability to mediate electron transfer is particularly crucial in enzymatic reactions taking place within the mitochondria—the cellular powerhouses. This is where oxidative phosphorylation occurs [45,46]. Given this backdrop, riboflavin’s coenzymes serve a vital role in the electron transport chain, an integral process for generating ATP [28]. In its inherent capacity, riboflavin functions as a cofactor for multiple enzymes, playing a crucial role in the synthesis of prosthetic groups within them. Illustrative examples encompass cytochrome reductase, lipoamide dehydrogenase, xanthine oxidase, L- and D-amino acid oxidase, as well as histaminase [47]. The pivotal function of these enzymes lies in facilitating the indispensable redox reactions that underlie cellular respiration.
In the context of energy metabolism, riboflavin’s significance cannot be overstated. Poultry, like all living organisms, requires energy for various physiological processes, including growth, maintenance, and reproduction. Riboflavin’s involvement in energy metabolism primarily stems from its participation in the electron transport chain [26,28] (Figure 2). During this process, electrons are shuttled through a series of protein complexes, leading to the pumping of protons across the membrane [48,49]. The resulting proton gradient is then used to drive the synthesis of ATP, which serves as the energy reservoir for cellular activities [50].
Moreover, riboflavin’s influence on energy metabolism extends beyond its impact on mitochondria; it assumes a central role in the intricate processing of macronutrients such as carbohydrates, lipids, and proteins [51]. Notably, riboflavin-dependent enzymes referred to as dehydrogenases actively participate in the oxidation of glucose and fatty acids [52,53]. This oxidative process stands as a pivotal stage in harnessing energy from these substrates. Furthermore, riboflavin is a key player in the conversion of the amino acid tryptophan into niacin, an essential B-vitamin [54,55]. Although the efficiency of this conversion, as illustrated in turkey poults, may be limited, it nevertheless contributes to the provision of niacin—an indispensable element for diverse metabolic mechanisms in poultry [54].
In the domain of poultry well-being, insufficiency in vitamin B2 can yield deleterious repercussions [6,8]. Avians lacking in riboflavin may manifest various clinical indications, encompassing diminished growth rates, musculoskeletal abnormalities, peripheral nervous system impairment, and compromised reproductive capabilities [4,12,17,56]. These manifestations trace their origins to the disruption of energy metabolism and redox reactions, both of which are indispensable for sustaining the heightened metabolic requisites of fast-growing poultry [57]. Riboflavin deficiency can lead to a curtailed capacity in ATP generation, culminating in reduced energy availability for growth and maintenance [7]. Furthermore, the disruption of redox reactions can compromise the cell’s proficiency in fending off oxidative stress, consequently precipitating cellular damage and compromised immune functionality [58].

3. Riboflavin Metabolism in Poultry

Understanding the metabolism of riboflavin in domestic fowl is vital for ensuring optimal health, growth, and production in these birds. The journey of vitamin B2 in poultry begins with its absorption, transport, and subsequent tissue distribution.
The absorption mechanism of riboflavin predominantly takes place within the small intestine of domestic fowl [59]. This intricate process commences with the liberation of riboflavin from dietary sources. Common constituents of poultry diets, such as grains and protein-rich meals, contain varying concentrations of vitamin B2 [60,61,62]. As elucidated by Merrill et al. [63], the major portion of riboflavin in feed materials exists in the form of free coenzymes—FMN and FAD—the predominant being FAD. The availability of riboflavin to the avian system necessitates its prior release from these coenzymes, which is facilitated by gut pyrophosphatases and phosphatases [64]. This step is crucial for the subsequent absorption of riboflavin.
Due to the inherent variability in the vitamin B2 content of plant-derived ingredients, coupled with factors leading to variable bioavailability and occasional degradation, the supplementation of fermentation-synthesized riboflavin via premixes becomes essential to fulfill the vitamin’s requirements in animal nutrition [35,36,64,65,66]. Industrially produced riboflavin, being in a non-esterified form, can be directly absorbed without the need for a hydrolysis step, which is necessary for plant-derived native vitamin B2. However, even in this case, the liberation of riboflavin from the feed matrix post-ingestion remains a prerequisite, achieved through mechanical breakdown and enzymatic activity along the avian digestive tract [67]. This liberation phase precedes absorption since riboflavin must be in its unbound form to be effectively taken up by the system [64].
Following liberation from feed particles, riboflavin emerges into an aqueous environment within the digestive tract, undergoing solubilization to facilitate subsequent absorption. The loss of biosynthetic pathways for most vitamins in the ancestors of vertebrates led to the development of mechanisms such as specialized transport proteins [68]. These proteins aid in the uptake of dietary vitamins from both the intestine and serum [69]. In the case of vitamin B2, a crucial step in its intestinal absorption involves active transportation across epithelial cells via specialized riboflavin transporters, ensuring the efficient flux of the vitamin into the bloodstream [19]. Under physiological concentrations, riboflavin is taken up through an active and saturable transport mechanism [70]. Although Cordona and Payne’s [59] study did not discern significant differences in riboflavin absorption across various segments of the small intestine in chickens, it is conceivable that vitamin B2 is predominantly absorbed in the proximal section of the small intestine, similar to the absorption pattern observed for other vitamins [71]. This proposition finds support in human studies, which indicate that riboflavin is primarily absorbed in the proximal small intestine [72].
Vitamin B2 transportation within poultry species is facilitated by its association with specialized transport proteins, ensuring its equitable dispersion throughout the avian organism [73,74]. In these species, riboflavin is conveyed via the circulatory system, serving as the conduit for its movement. An instrumental component in this mechanism is the chicken riboflavin-binding protein (RBP), a phosphoglycoprotein weighing 29.4 kDa [75,76,77]. The pivotal role of RBPs lies in safeguarding riboflavin from degradation, facilitating its secure transfer to diverse tissues [69]. By means of the RBP-mediated process, a consistent supply of vitamin B2 is assured to organs and tissues reliant on this vital micronutrient for optimal functioning.
The gene responsible for producing egg white, yolk, and serum RBPs is shared, exhibiting slight tissue-specific disparities in post-translational modifications [68]. RBPs are synthesized by the liver or oviduct in poultry and subsequently released into the bloodstream or eggs [26,78]. The mature and functional form of RBP (depicted in Figure 3) undergoes initial post-translational modifications [73]. This entails cleavage of an unidentified signal peptide, blockade of its amino terminus with pyroglutamic acid, and excision of an 11-13-residue acidic carboxyl-terminal peptide during or after transportation [79]. Additionally, nine disulfide bonds have been identified, along with two N-linked oligosaccharides whose composition varies based on the synthesizing tissue, and a serine-rich region bearing eight phosphoryl groups [73,80,81]. Notably, these phosphoryl groups play a critical role in facilitating the transportation of serum RBP into diverse tissues [75].
The cellular uptake process of riboflavin involves the transport of the vitamin across the plasma membrane via specific receptors called riboflavin transporters, following its release from the plasma through the RBP [78]. This mechanism relies on a calcium-ion-dependent RBP receptor, situated within clathrin-coated pits on the phospholipid bilayer [82]. This receptor serves as a catalyst for the endocytosis of the vitamin B2, enabling its subsequent internalization and release [78]. Subsequently, the receptor and RBP undergo recycling, while catabolic processes occur within endosomes.
The distribution of vitamin B2 in various tissues provides valuable insights into its significance in avian metabolism, particularly its involvement in enzymatic reactions. Riboflavin plays a critical role as a precursor to two essential coenzyme forms: FMN and FAD [38]. Tissues with elevated energy demands, such as muscle and liver, exhibit higher concentrations of riboflavin due to their reliance on FMN and FAD [83,84,85]. Moreover, tissues engaged in redox reactions, including the heart and kidney, maintain substantial riboflavin levels due to the participation of FAD-dependent enzymes in these processes [70,72]. When an abundant quantity of riboflavin is absorbed by the small intestine, surpassing the body’s current needs, the excess riboflavin is efficiently eliminated from the bloodstream and excreted through urine without undergoing significant alteration [86]. Nonetheless, a portion of vitamin B2 is excreted through the renal route in the form of metabolites. These metabolites result from oxidative cleavage in the ribityl side chain and subsequent conversion of the ring methyl functions to hydroxymethyl groups [87].
The enzymatic pathways responsible for the conversion of riboflavin into its active coenzyme forms, FMN and FAD, represent a pivotal facet of riboflavin metabolism in poultry. These conversions occur through a series of enzymatic reactions collectively referred to as the riboflavin kinase pathway [88]. The initial step involves the phosphorylation of riboflavin, catalyzed by riboflavin kinase, resulting in the formation of riboflavin 5′-phosphate [42,89]. This phosphorylation step is crucial for the subsequent transformations. The final conversion entails the synthesis of FAD from FMN (i.e., riboflavin 5′-phosphate) and ATP, facilitated by FAD synthetase [78]. These coenzyme derivatives, FMN and FAD, become indispensable participants in a range of redox reactions, spanning from the electron transport chain to various dehydrogenase reactions [29,41].

4. Riboflavin and Poultry Growth

An important observation from the first half of the 20th century is that riboflavin was designated as the “growth-promoting vitamin G” [90,91,92,93,94,95]. This recognition is rooted in riboflavin’s involvement in a multitude of physiological processes intricately linked to the overall growth performance of domestic fowl species. Within this complex web of biological interactions, vitamin B2 significantly influences pivotal factors that contribute to poultry growth, including nutrient utilization, protein synthesis, and enzyme activity [7,30,93,96].
The interrelation between vitamin B2 and nutrient utilization constitutes a fundamental aspect in comprehending its influence on poultry growth. Riboflavin serves as a cofactor for enzymes engaged in the metabolic pathways responsible for the degradation of carbohydrates, lipids, and proteins [10,97]. Through facilitation of these enzymatic reactions, riboflavin indirectly enhances the efficacy of nutrient breakdown and absorption within the avian gastrointestinal tract [26]. This, in turn, culminates in a heightened extraction of energy and nutrients from the ingested feed, thereby furnishing the essential foundational components required for optimal growth. The amelioration in nutrient utilization serves as a principal catalyst underpinning the growth-promoting ramifications of riboflavin across diverse poultry species [25,30,91,98].
Chou et al. [98] initially underscored that a reduction in energy or protein intake possesses the potential to curtail the riboflavin necessity in juvenile chickens. Significantly, their investigation unveiled that a marked deficiency of riboflavin (2.26 mg/kg diet) elicited a substantial regression (p < 0.01) in both energy and protein utilization among ad libitum-fed chicks. Analogously, a marginal insufficiency of riboflavin (3.02 mg/kg diet) was found to diminish energy utilization (p < 0.01) in chicks subjected to unrestricted feeding. Furthermore, the severe dearth of riboflavin was noted to engender diminished protein utilization (p < 0.05) in chicks exposed to energy-restricted diets (ranging from 80% to 60% of controls).
The Tricarboxylic Acid cycle (TCA) holds pivotal significance in the growth of living organisms, as it induces energy production, furnishes foundational constituents, and upholds redox equilibrium [99]. FAD and FADH2, integral to the TCA cycle, assume a pivotal role by engaging in redox reactions that contribute to energy synthesis and streamlined growth processes [100]. Dysfunction within this cycle or disruptions in FAD/FADH2 participation can impede growth-associated pathways and cellular functionality.
Shifting focus beyond nutrient utilization, the significance of riboflavin in protein synthesis emerges as a pivotal factor in promoting poultry growth. The process of protein biosynthesis, fundamental to the development of muscles, tissues, and bodily structures in both mammals and avian species, involves riboflavin. Specifically, vitamin B2 plays a role in the folding of newly synthesized proteins within the endoplasmic reticulum, facilitated by an FAD-dependent enzyme called endoplasmic reticulum oxidoreductase 1 [101,102]. Hypovitaminosis B2 can potentially disrupt this protein folding process due to diminished flavoproteins and an imbalanced redox state, triggering a stress response within the endoplasmic reticulum [102]. Research has also indicated that insufficiency of vitamin B2 significantly reduces glutathione reductase activity and glutathione content, while downregulating the expressions of endoplasmic reticulum oxidoreductase 1 and protein disulfide isomerase, as observed in poultry and other species [12,26,103,104,105].
Empirical evidence supporting the influence of riboflavin on domestic fowl growth is substantial and compelling. Diverse experiments across various poultry species have been conducted to explore the impact of vitamin B2 supplementation on growth performance [4,5,8,13,17,25,33,90,91,92,93,94,95,98]. For example, in broiler chickens, the consistent outcome of dietary riboflavin supplementation has been linked to improvements in growth rate, feed conversion efficiency, and carcass yield [24,60,106]. These growth-promoting effects are attributed to riboflavin’s contributions to nutrient utilization, as its involvement in metabolism clearly correlates with improved growth metrics.
Likewise, investigations centered on turkey poults have substantiated the favorable impact of vitamin B2 on their growth and developmental processes [61,107,108]. Supplementation of riboflavin in the diets of turkeys, ducks, and chickens has also been linked to enhanced feather development. Moreover, insufficient levels of vitamin B2 have been associated with conditions like the “clubbed down syndrome” or the twisting of feather follicles, alongside instances of dermatitis [26,109,110,111,112]. The “clubbed down syndrome” refers to the failure of down feather follicles to rupture their surrounding sheaths, causing feathers to coil and take on the appearance of a French knot [113]. This link underscores the interrelation between riboflavin and protein synthesis, as the synthesis of specialized proteins is crucial for proper feather and skin development [114]. Riboflavin’s role in providing essential coenzymes for protein synthesis and proper folding contributes significantly to the production of these proteins, consequently fostering feather growth [102,115].
The growth of ducklings also offers a pertinent illustration of riboflavin’s influence on growth. Analogous to observations in chickens and turkeys, studies conducted on ducks have indicated that a deficiency in vitamin B2 leads to diminished growth rates and compromised overall health [116]. Researchers in the study assessed specific proteins in the liver through Western blotting techniques. The reduced presence of certain proteins in the tissue was primarily associated with fatty acid β-oxidation and the mitochondrial electron transport chain (ETC), implying that hypovitaminosis B2 may contribute to liver lipid accumulation and growth impediment by hampering fatty acid β-oxidation and the ETC process. Table 2 summarizes the impact of riboflavin supplementation on the performance of poultry.

5. Oxidative Stress Defense

Oxidative stress, characterized by an imbalance between the production of reactive oxygen species (ROS) and cellular detoxification mechanisms, presents a significant challenge to domestic fowl health and productivity [58]. Avian cells have developed an intricate defense network to counter this threat, with riboflavin emerging as a pivotal component in this system [11]. Recent investigations have unveiled an additional dimension to riboflavin’s role—its function as a potent antioxidant within animal cells [30]. This discovery underscores its critical contribution to ROS neutralization and cellular protection, rendering it indispensable in poultry’s defense against redox imbalance [26].
The complex metabolic processes inherent to avian cells inevitably lead to the generation of ROS as natural by-products. While ROS serve important physiological roles, their excessive accumulation triggers oxidative stress, inducing damage to lipids, proteins, and nucleic acids [119]. Such cellular damage disrupts vital functions, compromises immune responses, and fosters the onset of diverse poultry ailments [58]. Herein lies the significance of riboflavin’s role as an antioxidant. Riboflavin partakes in various enzymatic reactions, particularly within the mitochondria’s electron transport chain [26,28], aiding in nutrient conversion for energy production. Yet, its fundamental antioxidant capabilities stem from its role as a precursor for two crucial coenzymes, FMN and FAD. These coenzymes play a central role in the activity of key antioxidant enzymes, including glutathione reductase and lactate dehydrogenase, indispensable for cellular defense against oxidative stress in animal cells, including domestic fowl [23,30,120,121].
Central to riboflavin’s role as an antioxidant is its active involvement in the glutathione redox cycle. Glutathione, a robust tripeptide antioxidant, plays a pivotal role in defending against damage induced by ROS. Vitamin B2 contributes to this cycle by facilitating the activity of glutathione reductase. This enzymatic action promotes the regeneration of reduced glutathione from its oxidized state, as detailed by Suwannasom et al. [10] (Figure 4). This dynamic process is crucial for maintaining cellular redox equilibrium, a fundamental factor in mitigating oxidative stress.
Zhang et al. [11] conducted a study centered around White Pekin duck breeders to investigate the impact of varying dietary riboflavin levels (ranging from 0 to 15 mg/kg) on oxidative status. The results demonstrated that duck breeders deprived of vitamin B2 supplementation experienced a significant decrease in their antioxidant capacity. This was evident from elevated plasma malondialdehyde levels and diminished glutathione levels. These findings underscore the pivotal role of riboflavin in fortifying the oxidative defense mechanisms of duck breeders via the glutathione pathway.
Furthermore, in vitro experiments revealed that an oxidized form of riboflavin engages in redox reactions with organic radicals and superoxide anions. This interaction results in the formation of a leuko form, which can be further oxidized by oxygen or iron-containing proteins [122]. As a consequence, riboflavin generates hydrogen peroxide or ferro forms of heme-containing proteins, underlining its potential as an antioxidant. Its interplay with superoxide anions may also contribute to stabilizing nitric oxide levels, further highlighting its significance in mitigating oxidative stress and sustaining cellular well-being [122].
The significance of riboflavin’s robust antioxidant capabilities becomes notably more conspicuous when contextualized within the contemporary landscape of poultry farming. Modern techniques of poultry production expose avian species to an assortment of stress-inducing factors, encompassing elevated temperatures, pathogenic microorganisms, and environmental pollutants. These factors collectively contribute to an exacerbation of oxidative stress conditions [58,123]. Moreover, the deliberate genetic selection aimed at promoting accelerated growth rates and heightened egg production imposes supplementary metabolic burdens on the avian cells, potentially leading to an amplification of the production of ROS [124].
In such intricate scenarios, the availability of riboflavin and other vital antioxidant vitamins, including retinol, α-tocopherol, L-ascorbic acid, and calciferol, assumes utmost importance [58,125]. The introduction of riboflavin through dietary supplementation has demonstrated its capacity to fortify the poultry’s antioxidant defense mechanisms, thereby engendering an ameliorated state of overall health and performance [11,23,120,121]. The beneficial impacts extend beyond a mere enhancement in antioxidant potential and growth facilitation; riboflavin supplementation additionally exerts a constructive influence on immune functions [126] (Figure 5), culminating in an elevated state of avian well-being and concurrently fostering favorable economic outcomes [7,9,13].

6. Reproductive Performance and Hatchability

Reproductive performance and hatchability constitute pivotal determinants within the poultry industry, wielding substantial influence over egg production efficiency and the overall triumph of poultry farming [127]. One elemental factor that has been extensively scrutinized in relation to these parameters is riboflavin. The impact of vitamin B2 on reproductive variables such as egg production, egg quality, and hatchability has elicited considerable attention from both researchers and poultry producers [11,12,26,56,109,118,128,129,130]. Through an array of studies, it has been unequivocally demonstrated that a dearth of riboflavin can exert a substantial impact on poultry reproductive success, carrying profound ramifications for both economic and bird welfare considerations.
A comprehensive exploration of the ramifications of vitamin B2 on reproductive parameters reveals its integral role in sustaining optimal egg production rate [26,56,128]. Riboflavin’s involvement in energy metabolism and cellular function is directly tethered to the energy-intensive process of egg production [11]. A sufficiency of vitamin B2 is imperative for supporting the heightened metabolic activity requisite during follicle development and yolk formation [111,118,131]. Research has substantiated that supplementation of riboflavin can culminate in improved egg production rates, yielding a heightened output of superior-quality eggs [118].
Hatchability, a critical parameter in poultry farming, is significantly influenced by riboflavin status [132,133,134,135]. In fact, hypovitaminosis B2 emerges as one of the prevalent nutritional insufficiencies capable of influencing the hatching process [136]. The various developmental stages of an embryo within an egg demand a consistent supply of nutrients and energy. Riboflavin’s role in cellular energy generation through its participation in the electron transport chain bears a direct connection to embryonic development and viability [137,138]. A lack of riboflavin during incubation can lead to impaired growth and development of the embryo, ultimately resulting in reduced hatchability rates [139]. Furthermore, the antioxidant properties of vitamin B2 play a pivotal role in safeguarding the nascent embryo from oxidative stress, a factor with potential to imperil embryonic viability [12,26,140,141].
The mechanisms through which riboflavin deficiency might impact reproductive success are multifaceted and involve intricate physiological processes. One primary mechanism is tied to riboflavin’s role in energy metabolism, where hypovitaminosis B2 can lead to a metabolic crisis [26]. As previously mentioned, riboflavin, in its coenzyme forms FMN and FAD, participates in oxidative phosphorylation, a process critical for ATP production, the primary energy currency of cells [28]. Inadequate vitamin B2 levels could lead to impaired energy production, affecting the high energy demands of reproductive processes such as follicle development, egg formation, ovulation, and embryo development and viability [128,139,142]. Hatchability is primarily affected by hypovitaminosis B2, followed by a decrease in egg production [143]. Additionally, evidence suggests a direct correlation between the amount of riboflavin in the hen’s diet and the vigor and viability of the baby chick [144].
Moreover, riboflavin’s impact on reproductive success can also be attributed to its involvement in cellular growth and differentiation. Vitamin B2 plays a crucial role in maintaining the integrity of cell membranes through its participation in lipid metabolism and the regulation of oxidative stress [11,102,145]. Riboflavin deficiency can disrupt cellular membrane structure and function, affecting the development and viability of reproductive cells [145]. This disruption may potentially yield impaired follicle development, disrupted ovulation, and compromised sperm and oocyte quality, ultimately influencing hatchability rates. The summary in Table 3 presents the effects of riboflavin supplementation on poultry reproductive performance and hatchability.

7. Riboflavin Requirements for Poultry

The recommended dietary requirements for vitamin B2 vary among different poultry species and at different stages of their production cycle, reflecting the dynamic nature of avian growth and development. In broiler chickens, for instance, riboflavin needs are influenced by their rapid growth during the fattening phase [25]. This phase, characterized by rapid muscle and skeletal development, necessitates increased riboflavin intake, along with other essential vitamins, to support energy metabolism and tissue repair [148]. Conversely, when considering laying hens during their peak egg production phase, distinct vitamin B2 requirements emerge [11,56]. Turkeys, with their unique growth characteristics and reproductive patterns, differ from both meat-type and laying-type chickens, resulting in varying nutritional needs, including specific considerations for riboflavin, when compared to broilers and layers (Table 4).
Beyond species and production stages, riboflavin requirements are intricately tied to feed composition [13]. The delicate interplay between vitamin B2 and other nutrients underscores the importance of a balanced diet [64]. Poor-quality feeds can hinder riboflavin absorption and utilization, leading to deficiencies despite adequate dietary levels. Additionally, stressors, drug usage, and disease challenges amplify avian metabolic demands, prompting heightened vitamin requirements [35]. In stressful conditions, be they environmental, physiological, or pathogenic, riboflavin’s role in antioxidant defense systems becomes increasingly vital, aiding in the preservation of cellular integrity and resilience in adverse conditions [165].
It is crucial to distinguish between vitamin B2 requirement estimates and allowances as determined by scientific committees such as the National Academies of Sciences, Engineering, and Medicine [149] (formerly known as the National Research Council), the Gesellschaft für Ernährungsphysiologie (GfE) [150], and recommendations from poultry breeding companies like Aviagen, Cobb-Vantress, and Lohmann [153,154,155,158]. Poultry producers often refer to both sources to strike a balance between scientific knowledge and the specific genetic potential of their flocks. However, there is a pressing need for an update of the NASEM requirement estimates, given that their last revision dates back to 1994, and substantial genetic advancements have been made in broilers, turkeys, and laying hens.
In contemporary times, there is a growing acknowledgment that the vitamin requirements for commercial poultry production may surpass the previously established levels for healthy birds in controlled research settings, as outlined by organizations like NASEM [71]. Stress, infections, and illnesses can substantially elevate the vitamin needs of birds, factors that must be taken into account in real-world farming scenarios [166]. For example, the most recent recommendations from Aviagen and Cobb [153,154], dated 2022, are designed to ensure adequate vitamin levels in commercial farming operations, probably factoring in potential vitamin losses during storage and processing by incorporating a safety margin (see Table 4).
Understanding the complex roles of riboflavin requires a comprehensive perspective. From an energy standpoint, vitamin B2 plays a pivotal role in metabolic pathways that extract energy from nutrients [100]. By facilitating the conversion of carbohydrates, fats, and proteins into usable energy units, riboflavin contributes to poultry’s overall vigor and vitality [26,28]. This function is especially critical during the brooding period, as young chicks transition from yolk-derived sustenance to external feed sources. Special attention to breeder requirements for vitamin B2 is necessary. Riboflavin’s role as a coenzyme in key enzymatic reactions orchestrates this metabolic shift, ensuring efficient nutrient utilization and sustained growth [38].
Riboflavin’s involvement in cellular growth and repair mechanisms underscores its significance during the rapid growth phase of poultry. Skeletal development, a complex process of bone formation and remodeling, relies heavily on vitamin B2-mediated energy transactions. As chicks develop their skeletal framework at a rapid pace, the mineralization process depends on the energy generated through riboflavin-supported metabolic pathways [167]. This not only influences bone strength but also contributes to the overall structural robustness of growing birds. Hypovitaminosis B2 can lead to an increase in deformed legs and poor mobility in broilers [117]. Citrate, which comprises approximately 1.6% of bone content and about 80% of total body citrate residing in bones, plays a crucial role in bone stability, strength, and resistance to fracture [168]. Riboflavin in its coenzyme form FAD is critical for the normal functioning of the citric acid cycle, which is presumed to be a key supplier of citrate for the bone’s apatite nanocrystal structure [168]. This occurs through the prevention of citrate oxidation via the Krebs cycle in some bone cells, maximizing citrate accumulation [168].
However, the intricate tapestry of riboflavin’s functions is interwoven with feed composition. Common feed ingredients like corn, wheat, soybean meal, and oilseed meals can contribute to riboflavin content [36]. Nevertheless, the intrinsic levels of vitamin B2 are insufficient to meet the requirements of poultry on a commercial scale in most cases [17,24,25,169]. Therefore, premixes used in poultry feeding are universally supplemented with vitamin B2 and other vitamins. Yet, inconsistencies or imbalances in premix and feed formulation can potentially lead to riboflavin and other vitamin B group deficiencies [12,170,171]. This underscores the importance of quality control in premix and feed production and the judicious selection of feed ingredients to ensure optimal riboflavin provision.

8. Future Prospects and Research Avenues

As we venture into the future of riboflavin research in poultry, it becomes evident that there is a wealth of untapped potential waiting to be explored. Among the most promising directions for research in this field is the investigation of how vitamin B2 interacts with other essential nutrients, such as vitamins, minerals, and amino acids. Understanding these interactions can yield valuable insights into optimizing poultry diets for improved growth and performance. For instance, delving into the synergy between riboflavin and other B vitamins could lead to more efficient nutrient utilization, ultimately benefiting poultry health and productivity. It is well-documented in mammalian studies that riboflavin plays a role in the metabolism of other B-vitamins, including vitamin B3 (niacin), vitamin B6 (pyridoxine), and vitamin B9 (folate) [172]. It facilitates the conversion of these vitamins into their active forms, enabling them to fulfill their respective functions in the body. While the impact of riboflavin on niacin synthesis has been demonstrated in turkey poults [54], further research in this area is warranted in domestic fowl.
Another intriguing avenue for exploration in avian health lies in the examination of riboflavin analogs [173]. These analogs have shown promise in offering anti-infective benefits in poultry, as demonstrated in both in vivo and in vitro studies in mammalian and bacterial cells [174]. Investigating this area could shed light on novel compounds that may be incorporated into poultry diets to achieve improved outcomes, including their potential as anticoccidial, antibacterial, and antiviral agents [175,176]. Several studies have already illustrated the therapeutic efficacy of photoactivated riboflavin against nosocomial infections, multidrug-resistant bacterial infections, and microbial-associated biofilm infections. This highlights the potential of riboflavin as a promising antimicrobial candidate, which could play a role in addressing the global crisis of emerging antimicrobial resistance among various pathogenic microbes [177].
In addition to studying riboflavin’s interactions with other nutrients and exploring analogs, integrating advanced technologies holds significant promise for enhancing vitamin B2 delivery in poultry diets. One such technology is precision nutrition, which involves customizing poultry diets based on individual bird characteristics and daily nutritional requirements [178]. By leveraging techniques like artificial intelligence and machine learning, researchers can develop predictive models that optimize riboflavin and other vitamin supplementation, potentially tailoring diets for each bird in a flock [179]. This approach can reduce waste, lower production costs, and enhance overall flock performance.
Furthermore, the utilization of nanotechnology in riboflavin delivery to poultry presents another exciting avenue for future research. Nanoencapsulation of riboflavin can enhance its stability and bioavailability, ensuring a consistent and effective supply of this essential micronutrient to poultry [180]. Nanoparticles can protect riboflavin from degradation in the proximal part of the gastrointestinal tract, facilitating more efficient intestinal absorption [181].
Moreover, exploring the potential role of vitamin B2 in mitigating the adverse effects of stressors on poultry health is a compelling area of research. Stressors such as heat stress, disease outbreaks, and transportation can negatively impact poultry well-being and productivity [182]. Investigating how riboflavin supplementation can alleviate the detrimental effects of these stressors is a critical research avenue, as already evaluated in humans [183,184]. Understanding the mechanisms by which riboflavin and other vitamins contribute to stress resilience in poultry can lead to innovative solutions for maintaining poultry health and welfare under challenging conditions.

9. Conclusions

Riboflavin plays a crucial role in the field of poultry nutrition and health. Its diverse functions as a coenzyme in various metabolic reactions, particularly in redox reactions and energy metabolism, emphasize its indispensability in avian physiology. Vitamin B2 significantly contributes to enhancing nutrient utilization, facilitating protein synthesis and folding, and promoting enzyme activity. These roles collectively support optimal growth and performance in domestic fowl. Moreover, the impact of riboflavin on reproductive parameters, such as egg production, egg quality, and hatchability, cannot be overstated. Its involvement in energy metabolism and antioxidant defense mechanisms directly influences the reproductive success of avian species, with far-reaching implications for both economic viability and animal welfare considerations.
Exploring riboflavin’s interactions with other essential nutrients, investigating the potential of riboflavin analogs as antimicrobial agents, and embracing advanced technologies like precision nutrition and nanotechnology for improved riboflavin delivery represent promising avenues for future research in poultry nutrition.
In essence, vitamin B2 emerges as a pivotal micronutrient within the intricate web of poultry nutrition, exerting profound effects on growth, health, and reproductive performance. As the poultry industry continues to advance, a deeper understanding of riboflavin’s roles and innovative approaches to its supplementation will prove essential in sustaining and furthering this vital sector.

Author Contributions

Conceptualization, Y.S.; methodology, Y.S. and W.P.; software, Y.S.; validation, W.P.; formal analysis, W.P.; investigation, Y.S.; resources, Y.S. and W.P.; data curation, Y.S.; writing—original draft preparation, Y.S.; writing—review and editing, W.P.; visualization, Y.S.; supervision, W.P.; project administration, Y.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

Not applicable. No new data were created or analyzed in this study.

Conflicts of Interest

Both authors of this work are affiliated with BASF, a manufacturer of vitamins and carotenoids, including vitamin B2. Nevertheless, it is crucial to underscore that the content of this manuscript has been sourced exclusively from scientific peer-reviewed data. Our unwavering commitment lies in upholding transparency and adhering to ethical research principles.

Abbreviations

AMPAdenosine monophosphate
ATPAdenosine triphosphate
COXCytochrome c oxidase
ETCElectron transport chain
FADFlavin adenine dinucleotide
FADH2Dinucleotide adenine flavine molecule
FAOThe Food and Agriculture Organization of the United Nations
FCRFeed conversion ratio
FMNFlavin mononucleotide
G-6P-DGlucose-6-phosphate dehydrogenase
GSHReduced form of glutathione
GSSGOxidized glutathione
Irg1The immune responsive gene 1 protein
IUPACThe International Union of Pure and Applied Chemistry
NADHDinucleotide nicotinamide molecules
NADPHNicotinamide adenine dinucleotide phosphate
Nox2NADPH oxidase 2
PDHPyruvate dehydrogenase
QCoenzyme Q10
RBPRiboflavin-binding protein
RFRiboflavin
RFKRiboflavin kinase
ROSReactive oxygen species
TCATricarboxylic Acid cycle
TNFTumor necrosis factor
TNFR1Tumor necrosis factor receptor 1

References

  1. FAO (The Food and Agriculture Organization of the United Nations). OECD-FAO Agricultural Outlook 2022–2031: 6. Meat. 2022. Available online: https://www.oecd-ilibrary.org/sites/ab129327-en/index.html?itemId=/content/component/ab129327-en#:~:text=Poultry%20meat%20is%20projected%20to,by%20pig%2C%20sheep%20and%20bovine (accessed on 23 August 2023).
  2. Roth-Maier, D.A.; Paulicks, B.R. Effects of a suboptimal dietary intake of particular B-vitamins on the growth of fattening chicken. Arch. Geflügelkunde 2002, 66, 201–205. [Google Scholar]
  3. McDowell, L.R. Vitamin nutrition of livestock animals: Overview from vitamin discovery to today. Can. J. Anim. Sci. 2006, 86, 171–179. [Google Scholar] [CrossRef]
  4. Jortner, B.S.; Cherry, J.; Lidsky, T.I.; Manetto, C.; Shell, L. Peripheral Neuropathy of Dietary Riboflavin Deficiency in Chickens. J. Neuropathol. Exp. Neurol. 1987, 46, 544–555. [Google Scholar] [CrossRef] [PubMed]
  5. Johnson, W.D.; Storts, R.W. Peripheral Neuropathy Associated with Dietary Riboflavin Deficiency in the Chicken I. Light Microscopic Study. Vet. Pathol. 1988, 25, 9–16. [Google Scholar] [CrossRef]
  6. Cai, Z.; Finnie, J.W.; Blumbergs, P.C. Avian Riboflavin Deficiency: An Acquired Tomaculous Neuropathy. Vet. Pathol. 2006, 43, 780–781. [Google Scholar] [CrossRef]
  7. Leiber, F.; Amsler, Z.; Bieber, A.; Quander-Stoll, N.; Maurer, V.; Lambertz, C.; Früh, B.; Ayrle, H. Effects of riboflavin supplementation level on health, performance, and fertility of organic broiler parent stock and their chicks. Animal 2022, 16, 100433. [Google Scholar] [CrossRef]
  8. Asplin, F. Riboflavin Deficiency in Poultry. Vet. J. 1941, 97, 16–26. [Google Scholar] [CrossRef]
  9. Cai, Z.; Finnie, J.; Manavis, J.; Blumbergs, P. Avian riboflavin deficiency causes reliably reproducible peripheral nerve demyelination and, with vitamin supplementation, rapid remyelination. Hum. Exp. Toxicol. 2023, 42. [Google Scholar] [CrossRef]
  10. Suwannasom, N.; Kao, I.; Pruß, A.; Georgieva, R.; Bäumler, H. Riboflavin: The Health Benefits of a Forgotten Natural Vitamin. Int. J. Mol. Sci. 2020, 21, 950. [Google Scholar] [CrossRef]
  11. Zhang, B.; Zhao, R.; Fouad, A.; Wu, Y.; Sun, P.; Wei, J.; Huang, W.; Xie, M.; Tang, J.; Hou, S. Research Note: Effects of riboflavin on reproductive performance and antioxidant status of duck breeders. Poult. Sci. 2020, 99, 1564–1570. [Google Scholar] [CrossRef]
  12. Tang, J.; Hu, J.; Xue, M.; Guo, Z.; Xie, M.; Zhang, B.; Zhou, Z.; Huang, W.; Hou, S. Maternal diet deficient in riboflavin induces embryonic death associated with alterations in the hepatic proteome of duck embryos. Nutr. Metab. 2019, 16, 19. [Google Scholar] [CrossRef]
  13. Lambertz, C.; Leopold, J.; Damme, K.; Vogt-Kaute, W.; Ammer, S.; Leiber, F. Effects of a riboflavin source suitable for use in organic broiler diets on performance traits and health indicators. Animal 2020, 14, 716–724. [Google Scholar] [CrossRef] [PubMed]
  14. Cherian, G. Nutrition and metabolism in poultry: Role of lipids in early diet. J. Anim. Sci. Biotechnol. 2015, 6, 28. [Google Scholar] [CrossRef] [PubMed]
  15. Abbas, C.A.; Sibirny, A.A. Genetic Control of Biosynthesis and Transport of Riboflavin and Flavin Nucleotides and Construction of Robust Biotechnological Producers. Microbiol. Mol. Biol. Rev. 2011, 75, 321–360. [Google Scholar] [CrossRef] [PubMed]
  16. Udhayabanu, T.; Manole, A.; Rajeshwari, M.; Varalakshmi, P.; Houlden, H.; Ashokkumar, B. Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases. J. Clin. Med. 2017, 6, 52. [Google Scholar] [CrossRef] [PubMed]
  17. Brooks, A.; Martin, E. Riboflavin Deficiency in Broiler Chickens. AHL Newsletter 27(1):20 (Animal Health Laboratory, University of Guelph, Ontario, Canada). Available online: https://www.uoguelph.ca/ahl/riboflavin-deficiency-broiler-chickens (accessed on 23 August 2023).
  18. Cook, M.E.; Springer, W.T. Effect of Reovirus Infection and Dietary Levels of Selected Vitamins on Immunocompetence of Chickens. Avian Dis. 1983, 27, 367–377. [Google Scholar] [CrossRef]
  19. Yoshii, K.; Hosomi, K.; Sawane, K.; Kunisawa, J. Metabolism of Dietary and Microbial Vitamin B Family in the Regulation of Host Immunity. Front. Nutr. 2019, 6, 48. [Google Scholar] [CrossRef]
  20. Scott, M.L.; Holm, E.R.; Reynolds, R.E. Studies on the Niacin, Riboflavin, Choline, Manganese and Zinc Requirements of Young Ringnecked Pheasants for Growth, Feathering and Prevention of Leg Disorders. Poult. Sci. 1959, 38, 1344–1350. [Google Scholar] [CrossRef]
  21. Wyatt, R.D.; Tung, H.T.; Donaldson, W.E.; Hamilton, P.B. A New Description of Riboflavin Deficiency Syndrome in Chickens. Poult. Sci. 1973, 52, 237–244. [Google Scholar] [CrossRef]
  22. Serafin, J. Studies on the Riboflavin, Niacin, Pantothenic Acid and Choline Requirements of Young Bobwhite Quail. Poult. Sci. 1974, 53, 1522–1532. [Google Scholar] [CrossRef]
  23. Lee, D.J.W. Growth, erythrogyte glutathione redugtase and liver flavin as indicators of riboflavin status in Turkey poults. Br. Poult. Sci. 1982, 23, 263–272. [Google Scholar] [CrossRef] [PubMed]
  24. Roth-Maier, D.A.; Kirchgessner, M. Investigations on riboflavin requirement of fattening chickens. Arch. Geflügelkunde 1997, 61, 14–16. [Google Scholar]
  25. Olkowski, A.; Classen, H.L. The study of riboflavin requirement in broiler chickens. Int. J. Vitam. Nutr. Res. 1998, 68, 316–327. [Google Scholar] [PubMed]
  26. Cogburn, L.A.; Smarsh, D.N.; Wang, X.; Trakooljul, N.; Carré, W.; White, H.B. Transcriptional profiling of liver in riboflavin-deficient chicken embryos explains impaired lipid utilization, energy depletion, massive hemorrhaging, and delayed feathering. BMC Genom. 2018, 19, 177. [Google Scholar] [CrossRef]
  27. Gržinić, G.; Piotrowicz-Cieślak, A.; Klimkowicz-Pawlas, A.; Górny, R.L.; Ławniczek-Wałczyk, A.; Piechowicz, L.; Olkowska, E.; Potrykus, M.; Tankiewicz, M.; Krupka, M.; et al. Intensive poultry farming: A review of the impact on the environment and human health. Sci. Total Environ. 2023, 858 Pt 3, 160014. [Google Scholar] [CrossRef]
  28. Balasubramaniam, S.; Yaplito-Lee, J. Riboflavin metabolism: Role in mitochondrial function. J. Transl. Genet. Genom. 2020, 4, 285–306. [Google Scholar] [CrossRef]
  29. Poudel, S.; Tabler, G.T.; Lin, J.; Zhai, W.; Zhang, L. Riboflavin and Bacillus subtilis effects on growth performance and woody-breast of Ross 708 broilers with or without Eimeria spp. challenge. J. Anim. Sci. Technol. 2022, 64, 443–461. [Google Scholar] [CrossRef]
  30. Ashoori, M.; Saedisomeolia, A. Riboflavin (vitamin B2) and oxidative stress: A review. Br. J. Nutr. 2014, 111, 1985–1991. [Google Scholar] [CrossRef]
  31. Olfat, N.; Ashoori, M.; Saedisomeolia, A. Riboflavin is an antioxidant: A review update. Br. J. Nutr. 2022, 128, 1887–1895. [Google Scholar] [CrossRef]
  32. Alagawany, M.; Elnesr, S.S.; Farag, M.R.; Tiwari, R.; Yatoo, M.I.; Karthik, K.; Michalak, I.; Dhama, K. Nutritional significance of amino acids, vitamins and minerals as nutraceuticals in poultry production and health—A comprehensive review. Vet. Q. 2020, 41, 1–29. [Google Scholar] [CrossRef]
  33. Cai, Z.; Blumbergs, P.C.; Finnie, J.W.; Manavis, J.; Thompson, P.D. Selective vulnerability of peripheral nerves in avian riboflavin deficiency demyelinating polyneuropathy. Vet. Pathol. 2009, 46, 88–96. [Google Scholar] [CrossRef] [PubMed]
  34. Fischer, M.; Bacher, A. Biosynthesis of vitamin B2 in plants. Physiol. Plant. 2006, 126, 304–331. [Google Scholar] [CrossRef]
  35. Kleyn, R.; Chrystal, P. Vitamins. In Broiler Nutrition: Masterclass; Context Products Ltd.: Leicestershire, UK, 2020; pp. 129–142. [Google Scholar]
  36. Witten, S. Characterisation of Organic Cereals and Grain Legumes as Feedstuffs for Monogastric Animals: Effects of Variety and Environmental Conditions on the Contents of Crude Nutrients, Amino Acids, Thiamine, Riboflavin, and In Vitro Digestibility of Crude Protein and Amino Acids. Ph.D. Thesis, Georg-August-Universität Göttingen, Göttingen, Germany, 2018. [Google Scholar]
  37. Szczuko, M.; Ziętek, M.; Kulpa, D.; Seidler, T. Riboflavin-properties, occurrence and its use in medicine. Pteridines 2019, 30, 33–47. [Google Scholar] [CrossRef]
  38. Liu, S.; Hu, W.; Wang, Z.; Chen, T. Production of riboflavin and related cofactors by biotechnological processes. Microb. Cell Factories 2020, 19, 31. [Google Scholar] [CrossRef] [PubMed]
  39. Rivero, M.; Boneta, S.; Novo, N.; Velázquez-Campoy, A.; Polo, V.; Medina, M. Riboflavin kinase and pyridoxine 5′-phosphate oxidase complex formation envisages transient interactions for FMN cofactor delivery. Front. Mol. Biosci. 2023, 10, 1167348. [Google Scholar] [CrossRef] [PubMed]
  40. Huerta, C.; Borek, D.; Machius, M.; Grishin, N.V.; Zhang, H. Structure and Mechanism of a Eukaryotic FMN Adenylyltransferase. J. Mol. Biol. 2009, 389, 388–400. [Google Scholar] [CrossRef]
  41. Friedmann, H.C. Flavin Mononucleotide. In Methods of Enzymatic Analysis, 2nd ed.; Bergmeyer, H.U., Ed.; Academic Press: Cambridge, MA, USA, 1974; pp. 2179–2181. [Google Scholar] [CrossRef]
  42. Pinto, J.T.; Zempleni, J. Riboflavin. Adv. Nutr. Int. Rev. J. 2016, 7, 973–975. [Google Scholar] [CrossRef]
  43. Oprian, D.D.; Coon, M.J. Oxidation-reduction states of FMN and FAD in NADPH-cytochrome P-450 reductase during reduction by NADPH. J. Biol. Chem. 1982, 257, 8935–8944. [Google Scholar] [CrossRef]
  44. Mansoorabadi, S.O.; Thibodeaux, C.J.; Liu, H.-W. The Diverse Roles of Flavin Coenzymes—Nature’s Most Versatile Thespians. J. Org. Chem. 2007, 72, 6329–6342. [Google Scholar] [CrossRef]
  45. Toyomizu, M.; Kikusato, M.; Kawabata, Y.; Azad, A.K.; Inui, E.; Amo, T. Meat-type chickens have a higher efficiency of mitochondrial oxidative phosphorylation than laying-type chickens. Comp. Biochem. Physiol. Part A Mol. Integr. Physiol. 2011, 159, 75–81. [Google Scholar] [CrossRef]
  46. Hubert, S.; Athrey, G. Transcriptomic signals of mitochondrial dysfunction and OXPHOS dynamics in fast-growth chicken. PeerJ 2022, 10, e13364. [Google Scholar] [CrossRef] [PubMed]
  47. Scott, M.L.; Nesheim, M.C.; Young, R.S. Riboflavin. In Nutrition of the Chicken; Scott, M.L., Ed.; Associate Publishing: Ithaca, NY, USA, 1982; pp. 196–204. [Google Scholar]
  48. Jastroch, M.; Divakaruni, A.S.; Mookerjee, S.; Treberg, J.R.; Brand, M.D. Mitochondrial proton and electron leaks. Essays Biochem. 2010, 47, 53–67. [Google Scholar] [CrossRef] [PubMed]
  49. Friedman, J.; Mourokh, L.; Vittadello, M. Mechanism of Proton Pumping in Complex I of the Mitochondrial Respiratory Chain. Quantum Rep. 2021, 3, 425–434. [Google Scholar] [CrossRef]
  50. Teixeira, F.K.; Sanchez, C.G.; Hurd, T.R.; Seifert, J.R.K.; Czech, B.; Preall, J.B.; Hannon, G.J.; Lehmann, R. ATP synthase promotes germ cell differentiation independent of oxidative phosphorylation. Nature 2015, 17, 689–696. [Google Scholar] [CrossRef]
  51. Qin, Y.; Zhou, J.; Xiong, X.; Huang, J.; Li, J.; Wang, Q.; Yang, H.; Yin, Y. Effect of riboflavin on intestinal development and intestinal epithelial cell function of weaned piglets. J. Anim. Physiol. Anim. Nutr. 2022, 107, 518–528. [Google Scholar] [CrossRef] [PubMed]
  52. Russell, A.P.; Schrauwen, P.; Somm, E.; Gastaldi, G.; Hesselink, M.K.C.; Schaart, G.; Kornips, E.; Lo, S.K.; Bufano, D.; Giacobino, J.-P.; et al. Decreased Fatty Acid β-Oxidation in Riboflavin-Responsive, Multiple Acylcoenzyme A Dehydrogenase-Deficient Patients Is Associated with an Increase in Uncoupling Protein-3. J. Clin. Endocrinol. Metab. 2003, 88, 5921–5926. [Google Scholar] [CrossRef]
  53. Parsons, H.G.; Dias, V.C. Intramitochondrial fatty acid metabolism: Riboflavin deficiency and energy production. Biochem. Cell Biol. 1991, 69, 490–497. [Google Scholar] [CrossRef]
  54. Ruiz, N.; Harms, R.H. Conversion of Tryptophan into Niacin in the Turkey (Meleagris gallipavos). Poult. Sci. 1990, 69, 446–450. [Google Scholar] [CrossRef]
  55. FNB (Food and Nutrition Board, Institute of Medicine, National Academy of Sciences). Dietary Reference Intakes: Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline; National Academy Press: Washington, DC, USA, 1998. [Google Scholar]
  56. Naber, E.C.; Squires, M.W. Research Note: Early Detection of the Absence of a Vitamin Premix in Layer Diets by Egg Albumen Riboflavin Analysis. Poult. Sci. 1993, 72, 1989–1993. [Google Scholar] [CrossRef]
  57. Wang, Z.; Brannick, E.; Abasht, B. Integrative transcriptomic and metabolomic analysis reveals alterations in energy metabolism and mitochondrial functionality in broiler chickens with wooden breast. Sci. Rep. 2023, 13, 4747. [Google Scholar] [CrossRef]
  58. Shastak, Y.; Gordillo, A.; Pelletier, W. The relationship between vitamin A status and oxidative stress in animal production. J. Appl. Anim. Res. 2023, 51, 546–553. [Google Scholar] [CrossRef]
  59. Cordona, N.; Payne, I. Absorption of Riboflavin in Chickens. Poult. Sci. 1967, 46, 1176–1179. [Google Scholar] [CrossRef]
  60. Ruiz, N.; Harms, R. Riboflavin Requirement of Broiler Chicks Fed a Corn-Soybean Diet. Poult. Sci. 1988, 67, 794–799. [Google Scholar] [CrossRef] [PubMed]
  61. Ruiz, N.; Harms, R. Riboflavin Requirement of Turkey Poults Fed a Corn-Soybean Meal Diet from 1 to 21 Days of Age. Poult. Sci. 1989, 68, 715–718. [Google Scholar] [CrossRef]
  62. Banaszkiewicz, T. Nutritional Value of Soybean Meal. In Soybean and Nutrition; El-Shemy, H., Ed.; IntechOpen: Rijeka, Croatia, 2011; pp. 1–20. Available online: https://www.intechopen.com/books/soybean-and-nutrition/nutritional-value-of-soybeanmeal (accessed on 26 August 2023).
  63. Merrill, A.H.; Lambeth, J.D.; Edmondson, D.E.; McCormick, D.B. Formation and mode of action of flavoproteins. Annu. Rev. Nutr. 1981, 1, 281–317. [Google Scholar] [CrossRef]
  64. Chung, T.K.; Baker, D.H. Riboflavin Requirement of Chicks Fed Purified Amino Acid and Conventional Corn-Soybean Meal Diets. Poult. Sci. 1990, 69, 1357–1363. [Google Scholar] [CrossRef]
  65. Dove, R.; Cook, D.A. Water-Soluble Vitamins in Swine Nutrition. In Swine Nutrition; Lewis, A.J., Southern, L.L., Eds.; CRC Press: New York, NY, USA, 2000; pp. 315–356. [Google Scholar]
  66. Sheraz, M.A.; Kazi, S.H.; Ahmed, S.; Anwar, Z.; Ahmad, I. Photo, thermal and chemical degradation of riboflavin. Beilstein J. Org. Chem. 2014, 10, 1999–2012. [Google Scholar] [CrossRef]
  67. Hynd, P.I. Digestion in the mono-gastric animal. In Animal Nutrition: From Theory to Practice; Hynd, P.I., Ed.; CSIRO Publishing: Clayton, Australia, 2019; pp. 42–63. [Google Scholar]
  68. White, H.B., III; Merrill, A.H., Jr. Riboflavin-Binding Proteins. Annu. Rev. Nutr. 1988, 8, 279–299. [Google Scholar] [CrossRef]
  69. M’Clelland, D.A. The Refolding of Riboflavin Binding Protein. Ph.D. Thesis, Department of Biological and Molecular Sciences, University of Stirling, Stirling, UK, 1996. [Google Scholar]
  70. EFSA (the European Food Safety Authority). Tolerable Upper Intake Levels for Vitamins and Minerals. Scientific Committee on Food, Scientific Panel on Dietetic Products, Nutrition and Allergies. 2006. Available online: https://www.efsa.europa.eu/sites/default/files/efsa_rep/blobserver_assets/ndatolerableuil.pdf (accessed on 28 August 2023).
  71. Shastak, Y.; Pelletier, W. Delving into vitamin A supplementation in poultry nutrition: Current knowledge, functional effects, and practical implications. World’s Poult. Sci. J. 2023, 1–23. [Google Scholar] [CrossRef]
  72. McCormick, D.B. Riboflavin. In Present Knowledge in Nutrition, 10th ed.; Erdman, J.W., Macdonald, I.A., Zeisel, S.H., Eds.; Wiley-Blackwell: Washington, DC, USA, 2012; pp. 280–292. [Google Scholar]
  73. Zheng, D.B.; Lim, H.M.; Pène, J.J.; White, H.B., 3rd. Chicken riboflavin-binding protein. cDNA sequence and homology with milk folate-binding protein. J. Biol. Chem. 1988, 263, 11126–11129. [Google Scholar] [CrossRef]
  74. Monaco, H.L. Crystal structure of chicken riboflavin-binding protein. EMBO J. 1997, 16, 1475–1483. [Google Scholar] [CrossRef] [PubMed]
  75. Miller, M.S.; Benore-Parsons, M.; White, H.B. Dephosphorylation of chicken riboflavin-binding protein and phosvitin decreases their uptake by oocytes. J. Biol. Chem. 1982, 257, 6818–6824. [Google Scholar] [CrossRef] [PubMed]
  76. Mac Lachlan, I.; Nimpf, J.; Schneider, W. Avian riboflavin binding protein binds to lipoprotein receptors in association with vitellogenin. J. Biol. Chem. 1994, 269, 24127–24132. [Google Scholar] [CrossRef] [PubMed]
  77. Loch, J.I.; Lipowska, J.; Lewinski, K. Crystal Structure of Chicken Riboflavin Binding Protein in “Apo” Form at 2.5 A Resolution; Protein Data Bank, Brookhaven National Laboratory: New York, NY, USA, 2018. [Google Scholar] [CrossRef]
  78. Combs, G.F.; McClung, J.P. Riboflavin. In The Vitamins; Combs, G.F., McClung, J.P., Eds.; Academic Press: London, UK, 2017; pp. 110–159, 315–329. [Google Scholar]
  79. Norioka, N.; Okada, T.; Hamazume, Y.; Mega, T.; Ikenaka, T. Comparison of the Amino Acid Sequences of Hen Plasma-, Yolk-, and White-Riboflavin Binding Proteins. J. Biochem. 1985, 97, 19–28. [Google Scholar] [CrossRef]
  80. Hamazume, Y.; Mega, T.; Ikenaka, T. Characterization of Hen Egg White- and Yolk-Riboflavin Binding Proteins and Amino Acid Sequence of Egg White-Riboflavin Binding Protein. J. Biochem. 1984, 95, 1633–1644. [Google Scholar] [CrossRef]
  81. Hamazume, Y.; Mega, T.; Ikenaka, T. Positions of disulfide bonds in riboflavin-binding protein of hen egg white. J. Biochem. 1987, 101, 217–223. [Google Scholar] [CrossRef]
  82. Kirchhausen, T.; Owen, D.; Harrison, S.C. Molecular Structure, Function, and Dynamics of Clathrin-Mediated Membrane Traffic. Cold Spring Harb. Perspect. Biol. 2014, 6, a016725. [Google Scholar] [CrossRef]
  83. Carlsson, E.V.; Sherman, H.C. Riboflavin and a Further Growth Essential in the Tissues: Quantitative Distribution and the Influence of the Food, Two Figures. J. Nutr. 1938, 15, 57–65. [Google Scholar] [CrossRef]
  84. Hodson, A.Z. The Influence of Dietary Riboflavin on the Content of This Vitamin in Chicken Tissue. J. Nutr. 1940, 20, 377–382. [Google Scholar] [CrossRef]
  85. Leonhardt, M.; Wenk, C. Animal species and muscle related differences in thiamine and riboflavin contents of Swiss meat. Food Chem. 1997, 59, 449–452. [Google Scholar] [CrossRef]
  86. Rivlin, R.S. Hormonal Regulation of Riboflavin Metabolism. In Riboflavin; Rivlin, R.S., Ed.; Springer: Boston, MA, USA, 1975. [Google Scholar] [CrossRef]
  87. McCormick, D.B. Riboflavin. In Encyclopedia of Toxicology, 3rd ed.; Wexler, P., Ed.; Academic Press: Cambridge, MA, USA, 2014; pp. 128–129. [Google Scholar] [CrossRef]
  88. Fischer, M.; Bacher, A. Riboflavin Biosynthesis. In Comprehensive Natural Products II; Liu, H.-W., Mander, L., Eds.; Elsevier: Singapore, 2010; pp. 3–36. [Google Scholar] [CrossRef]
  89. Karthikeyan, S.; Zhou, Q.; Mseeh, F.; Grishin, N.V.; Osterman, A.L.; Zhang, H. Crystal Structure of Human Riboflavin Kinase Reveals a β Barrel Fold and a Novel Active Site Arch. Structure 2003, 11, 265–273. [Google Scholar] [CrossRef] [PubMed]
  90. Norris, L.; Heuser, C.G.F.; Wilgus, H.S. Is the chief value of milk for feeding poultry due to the presence of a new vitamin? Poult. Sci. 1930, 9, 133–140. [Google Scholar] [CrossRef]
  91. Lepkovsky, S.; Jukes, T.H. The Response of Rats, Chicks and Turkey Poults to Crystalline Vitamin G (Flavin). J. Nutr. 1936, 12, 515–526. [Google Scholar] [CrossRef]
  92. Norris, L.; Wilgus, C.H.S.; Ringrose, A.T.; Heiman, V.; Heuser, G.F. The vitamin G requirements of poultry. Cornell Agr. Exp. Stn. Bull. 1936, 600, 1. [Google Scholar]
  93. Bethke, R.M.; Record, P.R.; Wilder, O.H.M. Further studies on vitamin G in chick nutrition with special reference to flavins. Poult. Sci. 1937, 16, 175–182. [Google Scholar] [CrossRef]
  94. Heuser, G.; Wilgus, H.; Norris, L. The Quantitative Vitamin-G Requirement of Chicks. Poult. Sci. 1938, 17, 105–108. [Google Scholar] [CrossRef]
  95. Bethke, R.; Record, P. The Relation of Riboflavin to Growth and Curled-toe Paralysis in Chicks. Poult. Sci. 1942, 21, 147–154. [Google Scholar] [CrossRef]
  96. Biagi, E.; Mengucci, C.; Barone, M.; Picone, G.; Lucchi, A.; Celi, P.; Litta, G.; Candela, M.; Manfreda, G.; Brigidi, P.; et al. Effects of Vitamin B2 Supplementation in Broilers Microbiota and Metabolome. Microorganisms 2020, 8, 1134. [Google Scholar] [CrossRef]
  97. Northrop-Clewes, C.A.; Thurnham, D.I. The Discovery and Characterization of Riboflavin. Ann. Nutr. Metab. 2012, 61, 224–230. [Google Scholar] [CrossRef]
  98. Chou, S.T.; Sell, J.L.; Kondra, P.A. Interrelationships between riboflavin and dietary energy and protein utilisation in growing chicks. Br. J. Nutr. 1971, 26, 323–333. [Google Scholar] [CrossRef]
  99. De Oliveira, J.E.; Uni, Z.; Ferket, P.R. Important metabolic pathways in poultry embryos prior to hatch. World’s Poult. Sci. J. 2008, 64, 488–499. [Google Scholar] [CrossRef]
  100. Van Every, H.A.; Schmidt, C.J. Transcriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chicken. BMC Genom. 2021, 22, 380. [Google Scholar] [CrossRef] [PubMed]
  101. Tu, B.P.; Ho-Schleyer, S.C.; Travers, K.J.; Weissman, J.S. Biochemical Basis of Oxidative Protein Folding in the Endoplasmic Reticulum. Science 2000, 290, 1571–1574. [Google Scholar] [CrossRef] [PubMed]
  102. Zhang, B.; Cao, J.-T.; Wu, Y.-B.; Gao, K.-X.; Xie, M.; Zhou, Z.-K.; Tang, J.; Hou, S.-S. Riboflavin (Vitamin B2) Deficiency Induces Apoptosis Mediated by Endoplasmic Reticulum Stress and the CHOP Pathway in HepG2 Cells. Nutrients 2022, 14, 3356. [Google Scholar] [CrossRef] [PubMed]
  103. Taniguchi, M.; Nakamura, M. Effects of riboflavin deficiency on the lipids of rat liver. J. Nutr. Sci. Vitaminol. 1976, 22, 135–146. [Google Scholar] [CrossRef]
  104. Manthey, K.C.; Chew, Y.C.; Zempleni, J. Riboflavin Deficiency Impairs Oxidative Folding and Secretion of Apolipoprotein B-100 in HepG2 Cells, Triggering Stress Response Systems. J. Nutr. 2005, 135, 978–982. [Google Scholar] [CrossRef]
  105. Xin, Z.; Pu, L.; Gao, W.; Wang, Y.; Wei, J.; Shi, T.; Yao, Z.; Guo, C. Riboflavin deficiency induces a significant change in proteomic profiles in HepG2 cells. Sci. Rep. 2017, 7, srep45861. [Google Scholar] [CrossRef]
  106. Lambertz, C.; Leopold, J.; Ammer, S.; Leiber, F.; Thesing, B.; Wild, C.; Damme, K. Demand-oriented riboflavin supply of organic broiler using a feed material from fermentation of Ashbya gossypii. Animal 2021, 15, 100003. [Google Scholar] [CrossRef]
  107. Patrick, H.; Darrow, M.; Morgan, C. The Role of Riboflavin in Turkey Poult Nutrition. Poult. Sci. 1944, 23, 146–148. [Google Scholar] [CrossRef]
  108. Thesing, B.; Göppel, S.; Weindl, P.; Lambertz, C.; Damme, K.; Bellof, G. Efficiency of an Organic Farming Compatible Yeast Product to Ensure the Riboflavin-Supply of Organically raised B.U.T. 6 Turkey Poults–Effects on Animal Performance and Health; Verlag Eugen Ulmer: Stuttgart, Germany, 2021. [Google Scholar]
  109. Lepkovsky, S.; Taylor, L.W.; Jukes, T.H.; Almquist, H.J. The effect of riboflavin and the filtrate factor on egg production and hatchability. Hilgardia 1938, 11, 559–591. [Google Scholar] [CrossRef]
  110. Jukes, T.H.; Stokstad, E.L.R.; Belt, M. Deficiencies of Certain Vitamins as Studied with Turkey Poults on a Purified Diet: I. Pteroylglutamic Acid, Riboflavin, Niacin and Inositol: Six Figures. J. Nutr. 1947, 33, 1–12. [Google Scholar] [CrossRef] [PubMed]
  111. Coles, R.; Cumber, F. Observations on the relationship between riboflavin, hatchability and clubbed down. J. Agric. Sci. 1955, 46, 191–198. [Google Scholar] [CrossRef]
  112. Haves, R.O.; Buss, E.G. The use of the ribollavinless gene (rd) in determining the cause of clubbed down. Poultry Sci. 1965, 44, 773–778. [Google Scholar]
  113. Brean, S.E. Dietary Riboflavin and the Production of Clubbed Down in Chick Embryo. Master’s Thesis, Oregon State University, Department of Poultry Science, Corvallis, OR, USA, 1989. [Google Scholar]
  114. Alibardi, L.; Toni, M. Cytochemical and molecular characteristics of the process of cornification during feather morphogenesis. Prog. Histochem. Cytochem. 2008, 43, 1–69. [Google Scholar] [CrossRef]
  115. Kleiber, M.; Jukes, T.H. Metabolism and Food Utilization of Riboflavin-Deficient Chicks. Proc. Soc. Exp. Biol. Med. 1942, 49, 34–37. [Google Scholar] [CrossRef]
  116. Tang, J.; Hegeman, M.A.; Hu, J.; Xie, M.; Shi, W.; Jiang, Y.; de Boer, V.; Guo, Y.; Hou, S.; Keijer, J. Severe riboflavin deficiency induces alterations in the hepatic proteome of starter Pekin ducks. Br. J. Nutr. 2017, 118, 641–650. [Google Scholar] [CrossRef]
  117. Summers, J.D.; Shen, H.; Leeson, S.; Julian, R.J. Influence of Vitamin Deficiency and Level of Dietary Protein on the Incidence of Leg Problems in Broiler Chicks. Poult. Sci. 1984, 63, 1115–1121. [Google Scholar] [CrossRef]
  118. Squires, M.W.; Naber, E.C. Vitamin Profiles of Eggs as Indicators of Nutritional Status in the Laying Hen: Riboflavin Study. Poult. Sci. 1993, 72, 483–494. [Google Scholar] [CrossRef]
  119. Forrester, S.J.; Kikuchi, D.S.; Hernandes, M.S.; Xu, Q.; Griendling, K.K. Reactive Oxygen Species in Metabolic and Inflammatory Signaling. Circ. Res. 2018, 122, 877–902. [Google Scholar] [CrossRef]
  120. Donaldson, W. Interaction of lead toxicity and riboflavin status in chicks (Gallus domesticus). Comp. Biochem. Physiol. Part C Comp. Pharmacol. 1986, 85, 1–3. [Google Scholar] [CrossRef]
  121. Deyhim, F.; Belay, T.; Teeter, R.G. An evaluation of dietary riboflavin supplementation on growth rate, feed efficiency, ration metabolizable energy content, and glutathione reductase activity of broilers. Nutr. Res. 1992, 12, 1123–1130. [Google Scholar] [CrossRef]
  122. Stepuro, I.I.; Adamchuk, R.I.; Stepuro, A.I. Interaction of riboflavin and hemoproteins with organic free radicals and superoxide anions generated in the ultrasound field. Biofizika 2002, 47, 977–988. [Google Scholar] [PubMed]
  123. Mishra, B.; Jha, R. Oxidative Stress in the Poultry Gut: Potential Challenges and Interventions. Front. Vet. Sci. 2019, 6, 60. [Google Scholar] [CrossRef] [PubMed]
  124. Surai, P.F.; Kochish, I.I.; Fisinin, V.I.; Kidd, M.T. Antioxidant Defence Systems and Oxidative Stress in Poultry Biology: An Update. Antioxidants 2019, 8, 235. [Google Scholar] [CrossRef]
  125. Shastak, Y.; Obermueller-Jevic, U.; Pelletier, W. A Century of Vitamin E: Early Milestones and Future Directions in Animal Nutrition. Agriculture 2023, 13, 1526. [Google Scholar] [CrossRef]
  126. Alamin, B.M.; Ibrahim, Y.; Salih, N.K.M. Effect of some vitamins and electrolytes on chickens infected with Infectious Bursal Disease. World Appl. Sci. J. 2009, 7, 366–370. [Google Scholar]
  127. King’ori, A.M. Review of the factors that influence egg fertility and hatchability in poultry. Int. J. Poult. Sci. 2011, 10, 483–484. [Google Scholar] [CrossRef]
  128. Davis, H.J.; Norris, L.C.; Heuser, G.F. The Rôle of Vitamin G in Reproduction in Poultry. Poult. Sci. 1938, 17, 81–86. [Google Scholar] [CrossRef]
  129. Schumacher, A.; Heuser, G. The Importance of Riboflavin in Reproduction in Poultry. Poult. Sci. 1939, 18, 369–374. [Google Scholar] [CrossRef]
  130. Abrams, V.A.; Han, C.-C.; White, H.B. Riboflavin-deficient chicken embryos: Hypoglycemia without dicarboxylic aciduria. Comp. Biochem. Physiol. Part B Biochem. Mol. Biol. 1995, 111, 233–241. [Google Scholar] [CrossRef]
  131. Benore-Parsons, M. The Transport of Riboflavin-Binding Protein to the Hen Oocyte. Ph.D. Thesis, University of Delaware, Newark, DE, USA, 1986. [Google Scholar]
  132. Engel, R.; Phillips, P.; Halpin, J.G. The Effect of a Riboflavin Deficiency in the Hen upon Embryonic Development of the Chick. Poult. Sci. 1940, 19, 135–142. [Google Scholar] [CrossRef]
  133. Tuite, P.; Austic, R. Studies on a Possible Interaction between Riboflavin and Vitamin B12 as it Affects Hatchability of the Hen’s Egg. Poult. Sci. 1974, 53, 2125–2136. [Google Scholar] [CrossRef] [PubMed]
  134. Juriloff, D.; Roberts, C. Genetics of Cleft Palate in Chickens and the Relationship Between the Occurrence of the Trait and Maternal Riboflavin Deficiency. Poult. Sci. 1975, 54, 334–346. [Google Scholar] [CrossRef] [PubMed]
  135. Anisha, M.; Karnani, S. Choudhary and Manju. Nutritional Factors: Affecting Egg Quality and Hatchability in Poultry. Pashu Sandesh. Available online: https://pashusandesh.com/Nutritional-Factors-Affecting-Egg-Quality- (accessed on 28 August 2023).
  136. Wilson, H.R. Effects of maternal nutrition on hatchability. Poult. Sci. 1997, 76, 134–143. [Google Scholar] [CrossRef]
  137. Folmes, C.D.L.; Terzic, A. Metabolic determinants of embryonic development and stem cell fate. Reprod. Fertil. Dev. 2015, 27, 82–88. [Google Scholar] [CrossRef]
  138. Givisiez, P.E.N.; Moreira Filho, A.L.B.; Santos, M.R.B.; Oliveira, H.B.; Ferket, P.R.; Oliveira, C.J.B.; Malheiros, R.D. Chicken embryo development: Metabolic and morphological basis for in ovo feeding technology. Poult. Sci. 2020, 99, 6774–6782. [Google Scholar] [CrossRef]
  139. Scanes, C.G.; Christensen, K.D. Fundamentals in Poultry Nutrition. In Poultry Science; Waveland Press, Inc.: Long Grove, IL, USA, 2020; pp. 109–131. [Google Scholar]
  140. Loetscher, Y.; Hospenthal, A.R.; Kreuzer, M.; Messikommer, R.E. Do antioxidants induce feed selection behavior in laying hens? Preference for, and palatability of, different antioxidant sources. Eur. Poult. Sci. 2014, 78, 1–11. [Google Scholar] [CrossRef]
  141. Yigit, A.; Panda, A.; Cherian, G. The avian embryo and its antioxidant defence system. World’s Poult. Sci. J. 2014, 70, 563–574. [Google Scholar] [CrossRef]
  142. Vieira, S. Chicken embryo utilization of egg micronutrients. Braz. J. Poult. Sci. 2007, 9, 1–8. [Google Scholar] [CrossRef]
  143. McDowell, L.R. Riboflavin. In Vitamins in Animal and Human Nutrition; McDowell, L.R., Ed.; Iowa State University Press: Ames, IA, USA, 2000; pp. 331–346. [Google Scholar]
  144. Anonymous. Riboflavin No. 1170; Hoffmann-La Roche: Basel, Switzerland, 1969. [Google Scholar]
  145. Zhang, B.; Tang, J.; Wu, Y.; Cao, J.; Xing, G.; Sun, P.; Huang, W.; Xie, M.; Hou, S. Effects of riboflavin deficiency on the lipid metabolism of duck breeders and duck embryos. Poult. Sci. 2021, 100, 101342. [Google Scholar] [CrossRef]
  146. Onwudike, O.; Adegbola, A. Riboflavin requirement of laying hens for egg production and reproduction in the humid tropics. Trop. Agric. 1984, 61, 205–2007. [Google Scholar]
  147. Leeson, S.; Reinhart, B.S.; Summers, J.D. Response of white leghorn and rhode island red breeder hens to dietary deficiencies of synthetic vitamins. 2. embryo mortality and abnormalities. Can. J. Anim. Sci. 1979, 59, 569–575. [Google Scholar] [CrossRef]
  148. Ribeiro, M.; Bittencourt, L.; Hermes, R.; Rönnau, M.; Rorig, A.; Lima, F.; Fernandes, J. Mineral Source and Vitamin Level in Broiler Diets: Effects on Performance, Yield, and Meat Quality. Braz. J. Poult. Sci. 2020, 22, 1–14. [Google Scholar] [CrossRef]
  149. NASEM (National Academies of Sciences, Engineering, and Medicine). Nutrient Requirements of Poultry, 9th ed.; National Academy Press: Washington, DC, USA, 1994. [Google Scholar]
  150. GfE (Gesellschaft für Ernährungsphysiologie). Empfehlungen zur Energie- und Nährstoffversorgung von Legehennen und Masthühnern (Broiler); Gesellschaft für Ernährungsphysiologie, DLG-Verlag: Frankfurt, Germany, 1999. [Google Scholar]
  151. Rostagno, H.S. (Ed.) Brazilian Tables for Poultry and Swine. In Composition of Feedstuffs and Nutritional Requirements, 3rd ed.; Universidade Federal de Viçosa—Departamento de Zootecnia: Viçosa, Brazil, 2011. [Google Scholar]
  152. FEDNA (Fundacion Espanola Deserrollo Nutricion Animal). Necesidades Nutricionales para Avicultura, 2nd ed.; Normas FEDNA; Santoma, G., Mateos, G.G., Eds.; Fundacion Espanola para el Desarrollo Nutricion Animal: Madrid, Spain, 2018. [Google Scholar]
  153. Cobb 500 Broiler Performance & Nutrition Supplement. 2022. Available online: https://www.cobb-vantress.com/assets/Cobb-Files/product-guides/5502e86566/2022-Cobb500-Broiler-Performance-Nutrition-Supplement.pdf (accessed on 28 July 2023).
  154. ROSS Broiler: Nutrition Specifications. 2022. Available online: https://aviagen.com/eu/brands/ross/products/ross-308 (accessed on 28 July 2023).
  155. Nicholas and, B.U.T. Heavy Lines Feeding Guidelines. 2015. Available online: https://www.aviagenturkeys.com/uploads/2015/11/20/NU06%20Feeding%20Guidelines%20for%20Nicholas%20&%20BUT%20Heavy%20Lines%20EN.pdf (accessed on 28 July 2023).
  156. Hubbard Management Guide. 2006. Available online: https://www.hubbardbreeders.com/media/manual_broiler_management_en___013796700_1441_27062016.pdf (accessed on 28 July 2023).
  157. Hybrid Turkeys Vitamin and Trace Mineral Supplementation. 2016. Available online: https://www.hybridturkeys.com/en/resources/commercial-management/feed-and-water/vitamin-and-trace-mineral-supplementation/ (accessed on 28 July 2023).
  158. Lohmann LSL-Lite Management Guide. 2014. Available online: https://lohmann-breeders.com/media/strains/cage/management/LOHMANN-LSL-Lite-Cage-1.pdf (accessed on 25 August 2016).
  159. Hy-Line W-36 Commercial Layers. 2020. Available online: https://www.hyline.com/filesimages/Hy-Line-Products/Hy-Line-Product-PDFs/W-36/36%20COM%20ENG.pdf (accessed on 25 July 2023).
  160. H&N Management Guide. 2016. Available online: https://www.hngb.co.uk/uploadedresources/1652881742-use_this_one_-_brown_management_guide_feb_22__version_6.pdf (accessed on 23 February 2018).
  161. ISA Nutrition Management Guide. 2018. Available online: https://www.isa-poultry.com/en/product/isa-brown/ (accessed on 22 February 2018).
  162. Dekalb Nutrition Management Guide. 2017. Available online: https://www.dekalb-poultry.com/ (accessed on 22 February 2018).
  163. Babcock Nutrition Management Guide. 2017. Available online: https://www.babcock-poultry.com/en/news/laying-hens-management-guide-alternative-systems/ (accessed on 22 February 2018).
  164. Hisex Nutrition Management Guide. 2017. Available online: https://www.hisex.com/en/news/laying-hens-management-guide-alternative-systems/ (accessed on 22 February 2018).
  165. Poudel, S.; Zhang, L.; Tabler, G.T.; Lin, J.; Zhai, W. Effects of riboflavin and Bacillus subtilis on internal organ development and intestinal health of Ross 708 male broilers with or without coccidial challenge. Poult. Sci. 2020, 100, 100973. [Google Scholar] [CrossRef]
  166. Leeson, S.; Summers, J.D. Commercial Poultry Nutrition. In Scott’s Nutrition of the Chicken, 3rd ed.; Leeson, S., Ed.; Nottingham University Press: Nottingham, UK, 2001; p. 398. [Google Scholar]
  167. Motyl, K.J.; Guntur, A.R.; Carvalho, A.L.; Rosen, C.J. Energy Metabolism of Bone. Toxicol. Pathol. 2017, 45, 887–893. [Google Scholar] [CrossRef]
  168. Costello, L.C.; Franklin, R.B.; Reynolds, M.A.; Chellaiah, M. The Important Role of Osteoblasts and Citrate Production in Bone Formation: “Osteoblast Citration” as a New Concept for an Old Relationship. Open Bone J. 2012, 4, 27–34. [Google Scholar] [CrossRef]
  169. Witten, S.; Aulrich, K. Exemplary calculations of native thiamine (vitamin B1) and riboflavin (vitamin B2) contents in common cereal-based diets for monogastric animals. Org. Agric. 2018, 9, 155–164. [Google Scholar] [CrossRef]
  170. Burgos, S.; Bohorquez, D.V.; Burgos, S.A. Vitamin Deficiency-Induced Neurological Diseases of Poultry. Int. J. Poult. Sci. 2006, 5, 804–807. [Google Scholar]
  171. Van Limbergen, T.; Ronsmans, S.; Maes, D.; Van Erum, J.; Van Ginderachter, J.; Verlinden, M.; Boel, F.; Garmyn, A.; Dewulf, J.; Ducatelle, R. A case of clubbed down syndrome in broilers. Avian Pathol. 2020, 50, 112–123. [Google Scholar] [CrossRef] [PubMed]
  172. Hanna, M.; Jaqua, E.; Nguyen, V.; Clay, J. B Vitamins: Functions and Uses in Medicine. Perm. J. 2022, 26, 89–97. [Google Scholar] [CrossRef]
  173. Pedrolli, D.B.; Jankowitsch, F.; Schwarz, J.; Langer, S.; Nakanishi, S.; Frei, E.; Mack, M. Riboflavin Analogs as Antiinfectives: Occurrence, Mode of Action, Metabolism and Resistance. Curr. Pharm. Des. 2013, 19, 2552–2560. [Google Scholar] [CrossRef] [PubMed]
  174. Hemasa, A.L.; Mack, M.; Saliba, K.J. Roseoflavin, a Natural Riboflavin Analogue, Possesses In Vitro and In Vivo Antiplasmodial Activity. Antimicrob. Agents Chemother. 2022, 66, e0054022. [Google Scholar] [CrossRef] [PubMed]
  175. Graham, D.W.; Brown, J.E.; Ashton, W.T.; Brown, R.D.; Rogers, E.F. Anticoccidial riboflavine antagonists. Cell. Mol. Life Sci. 1977, 33, 1274–1276. [Google Scholar] [CrossRef]
  176. Mansjö, M.; Johansson, J. The Riboflavin analog Roseoflavin targets an FMN-riboswitch and blocks Listeria monocytogenes growth, but also stimulates virulence gene-expression and infection. RNA Biol. 2011, 8, 674–680. [Google Scholar] [CrossRef] [PubMed]
  177. Farah, N.; Chin, V.K.; Chong, P.P.; Lim, W.F.; Lim, C.W.; Basir, R.; Chang, S.K.; Lee, T.Y. Riboflavin as a promising antimicrobial agent? A multi-perspective review. Curr. Res. Microb. Sci. 2022, 3, 100111. [Google Scholar] [CrossRef]
  178. Moss, A.F.; Chrystal, P.V.; Cadogan, D.J.; Wilkinson, S.J.; Crowley, T.M.; Choct, M. Precision feeding and precision nutrition: A paradigm shift in broiler feed formulation? Anim. Biosci. 2021, 34, 354–362. [Google Scholar] [CrossRef]
  179. Patel, H.; Sana, A. Role of Computer Science (Artificial Intelligence) In Poultry Management. Devot. J. Res. Community Serv. 2022, 3, 2068–2088. [Google Scholar] [CrossRef]
  180. Mohamadi, M.A.; Farshi, P.; Ahmadi, P.; Ahmadi, A.; Yousefi, M.; Ghorbani, M.; Hosseini, S.M. Encapsulation of Vitamins Using Nanoliposome: Recent Advances and Perspectives. Adv. Pharm. Bull. 2023, 13, 48–68. [Google Scholar] [CrossRef]
  181. Date, A.A.; Hanes, J.; Ensign, L.M. Nanoparticles for oral delivery: Design, evaluation and state-of-the-art. J. Control. Release 2016, 240, 504–526. [Google Scholar] [CrossRef]
  182. Hirakawa, R.; Nurjanah, S.; Furukawa, K.; Murai, A.; Kikusato, M.; Nochi, T.; Toyomizu, M. Heat Stress Causes Immune Abnormalities via Massive Damage to Effect Proliferation and Differentiation of Lymphocytes in Broiler Chickens. Front. Vet. Sci. 2020, 7, 46. [Google Scholar] [CrossRef]
  183. Akinyemi, F.; Adewole, D. Environmental Stress in Chickens and the Potential Effectiveness of Dietary Vitamin Supplementation. Front. Anim. Sci. 2021, 2, 1–21. [Google Scholar] [CrossRef]
  184. Mosegaard, S.; Dipace, G.; Bross, P.; Carlsen, J.; Gregersen, N.; Olsen, R.K.J. Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism. Int. J. Mol. Sci. 2020, 21, 3847. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Chemical structure and nomenclature of flavins (Liu et al. [38]). RF = riboflavin; FMN = flavin mononucleotide; FAD = adenine dinucleotide; AMP = adenosine monophosphate.
Figure 1. Chemical structure and nomenclature of flavins (Liu et al. [38]). RF = riboflavin; FMN = flavin mononucleotide; FAD = adenine dinucleotide; AMP = adenosine monophosphate.
Animals 13 03554 g001
Figure 2. Schematic diagram of flavocoenzymes in mitochondrial energy metabolism (Balasubramaniam et al. [28]). “The OXPHOS system is a 5-enzyme complex which encompasses the mitochondrial respiratory chain (Complexes I-IV), Complex V, and two mobile electron shuttles (coenzyme Q10 and cytochrome c). Electrons derived from oxidation of pyruvate mediated by pyruvate dehydrogenase (PDH) and fatty acid oxidation are transferred via NADH to Complex I (FMN-dependent NADH-ubiquinone oxidoreductase), while electrons from succinate in the Krebs cycle, amino acid metabolism, and fatty acid oxidation are transferred to Complex II (FAD-dependent succinate-ubiquinone oxidoreductase) via FADH2. Electrons are subsequently transferred to ubiquinone (Coenzyme Q10) and then to Complex III (reduced CoQ-cytochrome c reductase), and via cytochrome c to cytochrome c oxidase (COX) (Complex IV), the terminal oxidase of the RC before finally reducing molecular oxygen to water. The free energy liberated during this sequential electron transfer is used to generate an electrochemical gradient of protons, which is finally used by Complex V (ATP synthase or F1F0 ATPase) to drive ATP synthesis from ADP and inorganic phosphate. RF: Riboflavin; RF kinase: riboflavin kinase; Q: Coenzyme Q10; CytC: cytochrome c oxidase; FMN: flavin mononucleotide; FAD: flavin adenine dinucleotide”.
Figure 2. Schematic diagram of flavocoenzymes in mitochondrial energy metabolism (Balasubramaniam et al. [28]). “The OXPHOS system is a 5-enzyme complex which encompasses the mitochondrial respiratory chain (Complexes I-IV), Complex V, and two mobile electron shuttles (coenzyme Q10 and cytochrome c). Electrons derived from oxidation of pyruvate mediated by pyruvate dehydrogenase (PDH) and fatty acid oxidation are transferred via NADH to Complex I (FMN-dependent NADH-ubiquinone oxidoreductase), while electrons from succinate in the Krebs cycle, amino acid metabolism, and fatty acid oxidation are transferred to Complex II (FAD-dependent succinate-ubiquinone oxidoreductase) via FADH2. Electrons are subsequently transferred to ubiquinone (Coenzyme Q10) and then to Complex III (reduced CoQ-cytochrome c reductase), and via cytochrome c to cytochrome c oxidase (COX) (Complex IV), the terminal oxidase of the RC before finally reducing molecular oxygen to water. The free energy liberated during this sequential electron transfer is used to generate an electrochemical gradient of protons, which is finally used by Complex V (ATP synthase or F1F0 ATPase) to drive ATP synthesis from ADP and inorganic phosphate. RF: Riboflavin; RF kinase: riboflavin kinase; Q: Coenzyme Q10; CytC: cytochrome c oxidase; FMN: flavin mononucleotide; FAD: flavin adenine dinucleotide”.
Animals 13 03554 g002
Figure 3. Crystal structure of chicken riboflavin-binding protein in “Apo” form at 2.5 A resolution (Loch et al. [77]).
Figure 3. Crystal structure of chicken riboflavin-binding protein in “Apo” form at 2.5 A resolution (Loch et al. [77]).
Animals 13 03554 g003
Figure 4. Conversion of oxidized glutathione (GSSG) to the reduced form (GSH) by glutathione reductase requires riboflavin in the flavin adenine dinucleotide (FAD) coenzyme form for its activity (Suwannasom et al. [10]). G-6P-D = glucose-6-phosphate dehydrogenase.
Figure 4. Conversion of oxidized glutathione (GSSG) to the reduced form (GSH) by glutathione reductase requires riboflavin in the flavin adenine dinucleotide (FAD) coenzyme form for its activity (Suwannasom et al. [10]). G-6P-D = glucose-6-phosphate dehydrogenase.
Animals 13 03554 g004
Figure 5. Riboflavin is converted by riboflavin kinase into flavin monophosphate (FMN) and flavin adenine dinucleotide (FAD), which are essential cofactors of the phagocytic NADPH oxidase 2 (Nox2) to generate reactive oxygen species (ROS). Riboflavin deficiency renders the phagocyte Nox2 incapable of producing ROS, a process crucial for deactivating phagocytosed microbes and regulating the inflammatory response in innate immune cells (Suwannasom et al. [10]). TNF = tumor necrosis factor; TNFR1 = tumor necrosis factor receptor 1.
Figure 5. Riboflavin is converted by riboflavin kinase into flavin monophosphate (FMN) and flavin adenine dinucleotide (FAD), which are essential cofactors of the phagocytic NADPH oxidase 2 (Nox2) to generate reactive oxygen species (ROS). Riboflavin deficiency renders the phagocyte Nox2 incapable of producing ROS, a process crucial for deactivating phagocytosed microbes and regulating the inflammatory response in innate immune cells (Suwannasom et al. [10]). TNF = tumor necrosis factor; TNFR1 = tumor necrosis factor receptor 1.
Animals 13 03554 g005
Table 1. Functions of riboflavin.
Table 1. Functions of riboflavin.
FunctionDescriptionReference
Redox reactions and energy productionRiboflavin is essential for producing energy via two key coenzymes, flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD).[28,29]
Antioxidant capacity Riboflavin possesses indirect antioxidant properties, aiding in the neutralization of harmful free radicals within the body.[11,30,31]
Metabolism of fats, drugs, and steroidsRiboflavin participates in the enzymatic reactions associated with the metabolism of lipids, xenobiotic substances, and steroid compounds.[32]
Cellular function, growth, and developmentRiboflavin plays a fundamental role in the regulation of cellular functions, growth, and developmental processes.[26]
Reproductive functionsRiboflavin is essential for the reproductive performance of poultry. It affects fertility, embryonic development, and hatchability.[11,26]
Nerve functionRiboflavin deficiency has been associated with peripheral nerve demyelination in poultry, resulting in symptoms such as leg weakness and curled toe paralysis.[5,33]
Table 2. Impact of riboflavin supplementation on the performance and leg abnormalities of poultry.
Table 2. Impact of riboflavin supplementation on the performance and leg abnormalities of poultry.
Poultry SpeciesDietary
Supplemental Riboflavin
Levels in Feed
Effects of Riboflavin
Supplementation on Performance and Leg Abnormalities
Reference
Broiler chicken0.0, 0.9, 2.0, 2.8, 3.6, 4.4 mg/kgImproved body weight, feed intake, FCR, and reduced occurrence of leg paralysis[60]
Broiler chicken2.75, 2.78, 3.05, 3.40, 3.71 mg/kgImproved body weight, feed intake, FCR, and reduced occurrence of curled-toe
paralysis
[98]
Turkey poults0.0, 0.6, 1.1, 1.7, 3.1, 4.4 mg/kgImproved body weight, feed intake, FCR, and reduced occurrence of leg paralysis[61]
Broiler chicken1.7, 3.7, 11.7 mg/kgBilateral leg weakness and rotation of the metatarsus with flexion of the digits and hock lesions in “the 1.7 mg/kg group” as well as leg weakness in “the 3.7 mg/kg group” compared to the “11.7 mg/kg group”.[5]
Broiler chicken1.0–5.0 mg/kgImproved body weight and FCR[25]
Broiler chicken4.0-10.4 mg/kgImproved daily weight gain, FCR, and European broiler index 1[106]
Pekin ducks0.0 and 10.0 mg/kgLower mortality, improved average daily gain, feed intake, and gain/feed ratio[116]
Broiler chicken0.0, 1.0, 2.0, 3.0, 4.0, 8.0 mg/kgLower mortality, improved body weight, feed intake, FCR, and reduced occurrence of leg paralysis[24]
Broiler chicken0.0, 0.2, 0.5, 0.9, 4.5 mg/kgLower mortality, improved body weight, and reduced occurrence of leg paralysis[21]
Broiler chicken0.0, 9.0 mg/kgImproved weight gain and FCR and reduced occurrence of leg paralysis[117]
Bobwhite quail0.0, 0.8, 1.5, 2.5, 3.5, 5.0 mg/kgLower mortality, improved body weight and FCR[22]
Ringnecked pheasants0.0, 0.4, 0.9, 1.3, 1.8, 2.4 mg/kgImproved weight gain and reduced occurrence of leg abnormalities[20]
Broiler chicken0.8, 6.6, 20.0 mg/kgImproved FCR[29]
Laying hen0.0 and 2.9 mg/kgImproved egg weight[56]
Broiler breeders2.5 and 4.0 mg/kgNo effect[7]
Broiler chicken2.5 and 4.0 mg/kgImproved growth rate and feed consumption [7]
Turkey poults0.0, 2.0, 4.0 or 8.0 mg/kgHigher body weight[23]
Laying hen1.55, 2.20, 4.40, and 8.80 mg/kgImproved egg production and egg weight[118]
1 European broiler index = daily weight gain (g) × survival rate (%)/feed conversion (kg feed/kg body weight gain) × 10.
Table 3. Impact of riboflavin supplementation on poultry reproductive performance and hatchability.
Table 3. Impact of riboflavin supplementation on poultry reproductive performance and hatchability.
Poultry SpeciesDietary
Supplemental Riboflavin
Levels in Feed
Effects of Riboflavin
Supplementation on Reproductive Performance and Hatchability
Reference
Laying hen0.0 and 2.9 mg/kgImproved hatchability[56]
Laying hen1.55, 2.20, 4.40, and 8.80 mg/kgImproved egg production, egg weight, hatchability, and hen weight as well as reduced incidence of hemorrhagic embryos and clubbed down[118]
Duck breeder0.0 and 10.0 mg/kgImproved hatchability[12]
Duck breeder0.0 and 16.5 mg/kgImproved hatchability and embryo weight[145]
Broiler breeders2.5 and 4.0 mg/kgNo effect[7]
Duck breeder0, 2.5, 5, 10, and 15 mg/kgImproved hatchability[11]
Laying hen0.9–8.1 mg/kgImproved egg production and hatchability[146]
White leghorn and Rhode island red breeder hens1.0 and 2.5 mg/kgReduced embryo mortality and number of malpositioned embryos[147]
Table 4. Vitamin B2 guidelines for poultry: requirement estimates (NASEM), allowances (GfE), and recommendations (remaining sources).
Table 4. Vitamin B2 guidelines for poultry: requirement estimates (NASEM), allowances (GfE), and recommendations (remaining sources).
SourceVitamin A Requirement, mg/kg Feed
BroilersLaying HensBroiler BreedersTurkeys
NASEM [149]3.62.1 4n/a2.5–4.0
GfE [150]2.92.52.5n/a
Brazilian tables [151]4.7–9.14.8 48.0n/a
FEDNA [152]3.1–6.54.07.05.5–10.0
Cobb [153]6.0–9.0n/a13.0n/a
Aviagen [154,155] 17.0–9.0n/a10.0–16.04.0–10.0
Hubbard [156]6.0–8.0n/a12n/a
Hendrix (Hybrid turkeys) [157]n/an/an/a8.0–15.0
EW Group (laying hens) 2 [158,159,160]n/a4.0–6.6n/an/a
Hendrix (laying hens) 3 [161,162,163,164]n/a5.0n/an/a
1 Valid for Ross, Arbor Acres, and Indian River broiler breeds as well as Nicholas and B.U.T. medium and heavy turkey lines; 2 valid for Lohmann, Hy-Line, and H&N Nick layer breeds; 3 valid for ISA, Dekalb, Shaver, Bovans, Babcock, and Hisex layer breeds. 4 At 100 g of feed per hen daily. n/a = not applicable.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Shastak, Y.; Pelletier, W. From Metabolism to Vitality: Uncovering Riboflavin’s Importance in Poultry Nutrition. Animals 2023, 13, 3554. https://doi.org/10.3390/ani13223554

AMA Style

Shastak Y, Pelletier W. From Metabolism to Vitality: Uncovering Riboflavin’s Importance in Poultry Nutrition. Animals. 2023; 13(22):3554. https://doi.org/10.3390/ani13223554

Chicago/Turabian Style

Shastak, Yauheni, and Wolf Pelletier. 2023. "From Metabolism to Vitality: Uncovering Riboflavin’s Importance in Poultry Nutrition" Animals 13, no. 22: 3554. https://doi.org/10.3390/ani13223554

APA Style

Shastak, Y., & Pelletier, W. (2023). From Metabolism to Vitality: Uncovering Riboflavin’s Importance in Poultry Nutrition. Animals, 13(22), 3554. https://doi.org/10.3390/ani13223554

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