Next Article in Journal
Essential Oil Nanoemulsions—A New Strategy to Extend the Shelf Life of Smoothies
Next Article in Special Issue
Bixin, a New Atheroprotective Carotenoid Candidate, Prevents oxLDL-Induced Cytotoxicity and Mitochondrial Dysfunction in Macrophages: Involvement of the Nrf2 and NF-κB Pathways
Previous Article in Journal
Screening Probiotics for Anti-Helicobacter pylori and Investigating the Effect of Probiotics on Patients with Helicobacter pylori Infection
Previous Article in Special Issue
The Potential of Chicken–Herb Essence to Improve Milk Production and Infant Health in the Sprague Dawley Animal Model
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Effect of Bioactive Peptides on Gut Microbiota and Their Relations to Human Health

by
Tharuka Wijesekara
1,
Edirisinghe Dewage Nalaka Sandun Abeyrathne
2,* and
Dong Uk Ahn
3,*
1
Department of Food Science and Agricultural Chemistry, Faculty of Agricultural and Environmental Sciences, McGill University, Sainte-Anne-de-Bellevue, QC H9X 3V9, Canada
2
Department of Animal Science, Uva Wellassa University, Badulla 90000, Sri Lanka
3
Department of Animal Science, Iowa State University, Ames, IA 50011, USA
*
Authors to whom correspondence should be addressed.
Foods 2024, 13(12), 1853; https://doi.org/10.3390/foods13121853
Submission received: 19 April 2024 / Revised: 4 June 2024 / Accepted: 6 June 2024 / Published: 13 June 2024
(This article belongs to the Special Issue Advances in Bioactive Compounds from Food on Human Health)

Abstract

:
Bioactive peptides derived from both exogenous and endogenous origins have been studied extensively to use their beneficial effects in humans and animals. Bioactive peptides exhibit beneficial bodily functions and contribute to a healthy gastrointestinal system by influencing barrier functions, immune responses, and gut microbiota. Gut microbiota is a diverse microbial community that significantly influences the overall well-being and homeostasis of the body. Factors such as diet, age, lifestyle, medication, and environmental circumstances can affect the composition and diversity of the gut microbiota. The disturbances or imbalances in the gut microbiota have been associated with various health problems. The interplays between bioactive peptides and gut microbiota are not fully understood, but bioactive peptides hold promise as modulators of the gut microbiota to promote gut health. Almost all the bioactive research on human health, including the development of therapeutics and nutritional interventions, uses cell culture, even though their direct biofunctional activities can only occur when absorbed in the intestine and into the blood system. This review focuses on the current understanding of bioactive peptides in gut microbiota and their impact and mechanisms on gut and human health. The novelty of this review lies in its comprehensive analysis of the multifaceted interactions between bioactive peptides and gut microbiota, integrating knowledge from diverse disciplines between microbiology and nutrition. By elucidating the underlying mechanisms and identifying current research gaps, this review offers an outlook on the potential of bioactive peptides in promoting gut health and shaping future therapeutic and nutritional interventions.

Graphical Abstract

1. Introduction

Gut microbiota harbors in the gastrointestinal tract of living organisms [1]. Although bacteria are the main group of this gut microbiota family, other microbes such as fungi, viruses, archaea, and protozoans also coexist within the alimentary tract [2]. Gut microbiota significantly influences the host’s physiological functions, especially in maintaining homeostasis and promoting overall well-being [3]. Gut microbiota exerts multifaceted roles, including nutrient metabolism, biosynthesis of vital molecules, modulation of the immune system, and defense against pathogens and xenobiotics, and its dysregulation may contribute to the pathogenesis of hosts under diverse conditions, including obesity, diabetes, inflammatory bowel disease, and mental disorders. Various factors, including diet, age, genetic makeup, lifestyle, medication, and environmental circumstances, can impact the composition and heterogeneity of gut microbiota [2,4].
Various bioactive peptides are recommended for their applications in the food, pharmaceutical, and cosmeceutical industries [4,5]. These bioactive peptides are derived from plants, animals, insects, fungi, and microbes [6,7]. They are reported to prevent chronic ailments, regulate physiological functions, impact gut microbiota, promote beneficial bacteria, and regulate immune function [8,9]. The interplays between bioactive peptides and gut microbiota are complex [9] and still not extensively studied [10]. Certain peptides influence the gut microbiota by enhancing beneficial bacteria and modulating immune responses [7]. They have diverse health-promoting effects and potential applications in therapeutics and nutritional interventions, particularly through the gut microbiota [11]. Endogenous bioactive peptides benefit health and are categorized into three types: produced through biosynthesis, directly encoded, and derived from cryptic proteins [12]. There is an increasing interest in exploring the development of food additives and functional products and the development of new therapeutics using these bioactive peptides [13]. This review investigates the effects of bioactive peptides on the gut microbiota and their potential applications in developing new therapeutics and nutritional interventions.
This review presents a comprehensive examination of the interactions between bioactive peptides and gut microbiota, highlighting their potential applications in promoting gut health and overall well-being. It uniquely integrates knowledge of how bioactive peptides influence gut microbiota and human health. By delving into the underlying mechanisms of peptide–microbiota interactions, the review provides deeper insights into their functional roles and identifies current research gaps, paving the way for future studies. The implications of these findings are significant, suggesting that bioactive peptides could be harnessed to develop new therapeutic and nutritional interventions aimed at preventing and managing chronic diseases linked to gut microbiota dysregulation.

2. Bioactive Peptides

2.1. Animal-Derived Bioactive Peptides

Animal-derived bioactive peptides are mostly derived from milk, meat, eggs, and fish [14]. However, not all peptides released from the original protein sources have bioactive properties. The animal breeds, the specific cut, and the cooking technique significantly affect the levels of all bioactive compounds [15].
Peptides derived from milk have various functions, including antimicrobial, immune-modulatory, antioxidant, enzyme-inhibitory, antithrombotic, and antagonistic effects against harmful agents [16]. Many phosphopeptides released from casein (CPPs) have been widely applied as mineral supplements and functional foods enriched with calcium or iron. Especially complexing CPPs with amorphous calcium phosphate (ACP) stabilized calcium and phosphate [17]. This CPP-ACP complex helped to re-mineralize enamel, reduced the streptococci mutan colonization and biofilm formation, and improved teeth health [18]. The phosphopeptides produced from egg yolk phosvitin are also expected to have similar functions and bioactivity to CPPs because they share common structural characteristics [19]. Requena et al. [20] found that consuming 750 mg/kg of egg white hydrolysate (EWH) for 12 weeks increases the amount of Lactobacillus/Enterococcus and Clostridium leptum bacteria in the gut and modifies the production of gut microbiota metabolites, notably elevating total short-chain fatty acids in feces. Fish protein hydrolysates and specific peptides derived from other hydrolysates have a wide range of biological activities [21]. Fish is a rich source of antimicrobial peptides, including defensins, cathelicidins, hepcidins, and peptides derived from histones [22]. Fishbone and other body parts such as gills and mucous layers are also identified as possible peptide sources [23].
An expanding body of research demonstrates the discovery of an ever-increasing number of insect-derived biopeptides. Recent studies involving in vitro and in vivo screening, utilizing surrogate model hosts like C. elegans, have highlighted the promising antimicrobial activity of insect-derived AMPs against human pathogens [24]. Mylonakis et al. [24] found that the insect cricket produces a peptide called Defensin-1, which exhibits antimicrobial properties. Another investigation focused on the silkworm and identified three peptides, namely SPKFCW, DQDPFRP, and PDPSKF, which also possess antimicrobial activity. These findings highlight the potential of insects as a source of bioactive peptides with antimicrobial properties, suggesting their possible applications in various fields such as medicine and biotechnology [25]. Table 1 shows the bioactivity of animal-derived peptides from various animal sources.

2.2. Plant-Derived Bioactive Peptides

Plant peptides can be produced from leaves, seeds, and fruits, with seeds being the most cost-effective protein source [36]. Soy proteins are a significant source of plant-derived bioactive peptides, with glycinin and beta-conglycinin accounting for more than 85% of soy proteins [37]. Plant-derived peptides have antimicrobial properties that inhibit the growth of Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, and Salmonella enterica. They also act as antioxidants by scavenging ABTS+ and DPPH radicals and inhibiting β-carotene oxidation and possess anticancer properties by inhibiting the growth of human colon, lung, and liver cancer cells [38,39]. Wheat gluten hydrolysates show antioxidant, antihypertensive, and immunomodulatory effects [40]. The chickpea and pumpkin seed protein hydrolysates showed antioxidant, hypocholesterolemic, Angiotensin Converting Enzyme (ACE)-inhibitory properties, metal-chelating ability, antihyperlipidemic, antitumor, and antiproliferative effects [41,42]. Therefore, plant-derived peptides have enormous potential as ingredients in developing healthcare and functional products. In Table 1 and Table 2, many specific peptides with specific bioactivities are listed, but they should not be considered the only ones with the activities.

2.3. Microbial Bioactive Peptides

Microbial fermentation is an alternative approach to produce bioactive peptides using bacterial enzymes. Many bacteria are used as starter cultures in industrial settings to produce strong proteolytic enzymes [49]. Thus, both primer and non-primer bacteria used in fermented foods have the potential to produce bioactive peptides. Lactobacillales, a diverse group of beneficial bacteria found in nature and the human gastrointestinal tract, are used to produce bioactive peptides. In addition to their physiological effects, these microorganisms contribute to fermented products’ texture and flavor with technological significance [5].
Numerous starter cultures utilized in the dairy industry possess a remarkable ability to degrade proteins. As a result, both starter and non-starter bacteria engaged in the fermentation process of dairy products can generate bioactive peptides. Lactococcus lactis, L. helveticus, and L. delbrueckii ssp. bulgaricus have been thoroughly investigated for their proficiency in protein hydrolysis [50]. However, all the bioactive functions mentioned in Table 1 and Table 2 are obtained by chemical analyses or a combination of chemical and in vitro biological analyses, and none of them are analyzed using animal models. In vitro studies may overlook issues like poor absorption and degradation of peptides into individual amino acids, making animal studies and human clinical trials essential. However, animal trials require significant investment and standardization of protocols to overcome challenges and should obtain health claims for functional food products in countries with regulations [51].

3. Bioactive Peptides in the Viability and Diversity of Gut Microbiota and Their Consequences to Human Health

Naturally occurring or food protein-derived peptides with bioactivities have multiple functions in various biological processes, especially for promoting the health and function of the gut [11]. Previous literature reported that some bioactive peptides are nonspecific and might show multiple properties. However, only the major functions of peptides were studied without studying the influence of other peptides [52]. Also, it is very important to point out that peptides, including bioactive peptides, can hardly be absorbed in the gut and moved into the circulatory system because they should be hydrolyzed into mono-amino acids before penetrating into the circulatory system. Even if the microvilli can absorb some bioactive peptides, their amount would be small, and it is difficult to reach the critical levels to exert their positive functions [53]. Therefore, the dietary bioactive peptides could have functional effects on human health through their indirect effects on gut microbiota, such as maintaining a healthy gastrointestinal system by influencing barrier function, immune responses within the gastrointestinal system, and gut microbiota composition. The liberation of bioactive peptides from food proteins and gut microbes can impede the proliferation of external bacteria and viruses, thereby upholding the equilibrium and steadiness of the gut microbiota [53]. The mechanism through which bioactive peptides exert their effects on external bacteria and viruses is demonstrated in Figure 1.

3.1. Prebiotics and Probiotics

Prebiotics are food ingredients that the host cannot digest but selectively stimulate the growth of beneficial microbes in the host, thereby promoting the proliferation of probiotics. Probiotics are living microorganisms that offer health benefits to the host when consumed in various ways, such as supplements, fermented foods, probiotic-enriched beverages, and dairy products, with the required amount crucial for achieving the desired positive effects on health [54]. The effectiveness of probiotics is dose dependent, and the most frequently utilized probiotic genera are Lactobacillus and Bifidobacterium [55]. Probiotics help maintain a healthy balance of intestinal microorganisms and have a variety of beneficial bioactivities [56]. The primary source of nutrients for the growth of intestinal microorganisms is derived from undigested food components that reach the colon. These components include oligosaccharides, dietary fibers, undigested proteins, and endogenous sources. Any food that enters the colon, such as nondigestible carbohydrates, certain peptides, proteins, and some lipids, has the potential to act as a prebiotic. Oligosaccharides, such as lactulose, galactooligosaccharides, oligofructose, and maltooligosaccharides, are the most effective prebiotics studied thus far [57]. However, the methods for producing oligosaccharides are low in yield and expensive and only produce a single type of prebiotic [58,59,60]. Thus, identifying new types of prebiotics is of great interest to researchers. Recent research has demonstrated that proteins, protein hydrolysates, and peptides can stimulate the proliferation of probiotics [61].
Although some peptides have been identified as prebiotics, the interaction mechanisms between peptides and gut microbiota are poorly understood. Some scientists believe peptides in the gut act as a nitrogesn source and promote bacterial growth, while others believe they can improve polypeptide transport to precise locations in cells by acting as carriers or facilitators [61,62]. Raveschot et al. [63] reported that the growth of Lactobacillus lactis is heavily reliant on oligopeptides as a nitrogen source, and oligopeptides have been identified as the primary nitrogen source for lactic acid bacteria (LAB).
The activity of proteolytic enzymes influences the efficiency of protein utilization by bacteria [64]. Probiotics display varying abilities of using proteins in different conditions and do not require additional proteins when sufficient nutrients are available [65]. Prebiotics can substitute or supplement for probiotics. However, different types of prebiotics can stimulate the growth of specific types of gut bacteria [57]. Prebiotics have significant potential for altering the gut microbiota, but the changes are specific to individual strains and species and are difficult to predict in advance.
Conversely, probiotic bacteria can generate organic acids through the process of fermentation. When the organic acid concentrations reach a certain threshold, the bacteria may undergo autolysis, resulting in a decline in viable bacteria. Protein hydrolysates could be utilized to counteract and enhance the survival of the probiotic bacteria and preserve their numbers even in acidic environments [61].

3.2. Anti-Inflammatory Effects

Inflammation is a natural bodily response to infections, irritations, and injuries, resulting in the emergence of persistent illnesses such as cancer, obesity, asthma, and diabetes [66]. During inflammation, pro-inflammatory molecules, like tumor necrosis factor-α (TNF-α), interleukin (IL)-1, IL-6, IL-8, and interferon-g (INF-γ), are produced to protect the body. However, excessive production of pro-inflammatory molecules can cause damage to the tissues and impair immune functions [67]. The inflammatory response can be acute or chronic, and chronic inflammation has been linked to type 2 diabetes, inflammatory bowel disease (IBD), arthritis, atherosclerosis, and other cardiovascular diseases. Different cell types can interact with pro-inflammatory molecules, producing an amplified inflammatory response [68].
Peptides derived from various sources are capable of counteracting the effects of inflammation in cell culture studies. Dipeptides derived from yeast extracts and edible beans have anti-inflammatory activity in Caco-2 cells and specifically inhibit the secretion of pro-inflammatory cytokines IL-8, IL-6, and IL-1b while increasing the expression of anti-inflammatory cytokine IL-10 in the TNF-α-induced cells [69]. Tripeptides such as IPP (Ile-Pro-Pro) and VPP (Val-Pro-Pro) derived from the casein in milk exhibit anti-inflammatory characteristics [70]. Oligopeptides and polypeptides from various sources with anti-inflammatory properties inhibit the activity of pro-inflammatory cytokines and enzymes, thereby reducing inflammation [71,72]. However, these bioactivities have been examined using cell cultures and in vitro methods, and their health effects are not proven in in vivo systems. Therefore, studies using animal models and human subjects are needed to further explore the potential use of these bioactive peptides.

3.3. Antimicrobial Effects

Antimicrobial peptides (AMPs) regulate the interactions between commensal microbes and host tissues. Antimicrobial peptides exhibit antimicrobial effects via various mechanisms, including sequestering essential growth nutrients and disrupting bacterial membranes [61]. These peptides, also known as host defense peptides, act as an important barrier against pathogenic bacterial invasion of the body [73]. Antimicrobial peptides are classified into four categories based on their origin: microbial, animal, plant, and others, and their antibacterial effects vary depending on their sources [74]. Antimicrobial peptide functions are in three stages: the initial attraction to the bacterial cell wall, subsequent binding to the cell membrane, and eventual insertion of peptides into the host cell membrane, causing membrane permeabilization. Antimicrobial peptides can use various antimicrobial strategies, including membrane destabilization, bacterial cell filamentation by peptide insertion, inhibiting DNA replication, and hindering the membrane proteins involved in septum formation. Antimicrobial peptides also have lectin-like properties and anti-toxin activities [75].
Milk is a good source of nutrients and has a variety of biological functions that are primarily attributed to its peptides and proteins. Milk’s antimicrobial properties come mainly from lactoferrin, lactoperoxidase, and lysozyme. Milk also contains antibacterial peptides, crucial parts of innate immunity, and helps protect animals against possible harmful microorganisms [76]. Milk proteins nourish and protect newborns and produce bioactive peptides that can protect against infectious agents. The peptides that can be obtained from lactoferrin, caseins (αS1, αS2, β, and κ-casein), α-lactalbumin, β-lactoglobulin, protease-peptone-3, and lysozyme can serve as antibacterial agents in the fields of therapy, functional foods, and infant formulas [77]. Microorganisms such as bacteria and fungi are a source of antimicrobial peptides. Nisin and gramicidin are commonly recognized peptides derived from Lactococcus lactis, Bacillus subtilis, and Bacillus brevis [78]. Epithelial cells can also produce antimicrobial peptides which help protect the animal body from harmful microorganisms. The primary sources of antimicrobial peptides in the gastrointestinal tract are Paneth cells and enterocytes, although immune cells in the tissue can also produce these molecules [79]. Defensins, cathelicidins, and regenerating Gene III alpha/beta/gamma are the three primary types of antimicrobial peptides in the gut. These peptides have dual roles: preventing pathogen infection and influencing the microbiome composition. Their antimicrobial activity is broad spectrum and can interfere with microbial growth and metabolism [80]. They can also affect immune responses and cell signaling that impact innate and adaptive immunity. Antimicrobial peptides could be a therapeutic approach to treat diseases associated with microbiome imbalances, especially in light of the growing problem of antibiotic-resistant pathogens [81].

3.4. Anti-Obesity Effects

Previous research suggested that gut microorganisms could help people lose weight by regulating their energy balance and food consumption. Furthermore, they can reduce inflammation caused by obesity by modifying the expression of inflammation-related transcription factors. Protein hydrolysates and peptides can inhibit the growth of gut bacteria that cause obesity. These compounds promote the growth of beneficial gut bacteria while improving their resistance to extreme pH conditions. Hence, protein hydrolysates/peptides can be considered promising therapeutic agents for obesity and the associated complications, enabling the development of innovative strategies to combat obesity [82].
The gut’s microbial makeup can vary depending on acidity and oxygen levels. Firmicutes, Lactobacilli, and Proteobacteria mostly populate the area closer to the beginning of the digestive tract, while the region further down is mainly inhabited by Bacteroidetes, Firmicutes, and Akkermansia muciniphila [83]. Recent research [84] indicated a noticeable shift in the makeup and structure of the gut microbiota in individuals who are obese. Specifically, obese individuals tend to have a higher prevalence of Firmicutes clusters, while those with lean body mass tend to have more Bacteroidetes. The consensus among studies is that this gut microbiota imbalance can disrupt the host’s capacity to extract energy from food efficiently and consequently influence energy storage and utilization in adipose tissues, ultimately contributing to changes in body weight [82].
Obesity is commonly linked to dietary habits as they can influence the makeup of the gut microbiota. Consequently, recent attempts to address obesity have centered around the role of gut microbiota in weight gain. Certain types of gut microbiota can increase the likelihood of obesity by affecting the body’s physiological pathways involved in weight gain [85]. Requena et al. reported changes in gut microbiota composition when egg white hydrolysate peptides were fed to obese rats [20]. Han et al. showed that pepsin-hydrolyzed peptides from soybean 7S globulin lowered body weight and influenced gut microbiota composition in obese individuals [86]. In rats, feeding with hydrolyzed α-lactalbumin derived from cows increased the proportion of Bacteroidetes/Firmicutes and a greater relative abundance of Lachnospiraceae and Blautia in the gut microbiota [87]. Collagen peptides derived from the skin of walleye pollock reduced obesity by influencing the gut microbiota in mice fed a high-fat diet. The mice that were given collagen peptides had an increased number of beneficial bacteria, such as Lactobacillus, Akkermansia muciniphila, Parabacteroides, and Odoribacter spp., and fewer bacteria, such as Erysipelatoclostridium and Alistipes, that cause inflammation in the gut [88,89]. The pH balance of the gut environment fluctuates between acidic and alkaline states, and fermentation by gut bacteria produces organic acids, which can alter the pH balance. Some bacteria are sensitive to pH changes, and exposure to highly acidic conditions can cause autolysis, decreasing the number of viable colonies in the gut [61]. The findings confirm that consuming hydrolysates/peptides can help sustain a healthier balance of gut microbiota and decrease obesity-associated effects on the host, which implies that hydrolysates/peptides can act as prebiotic agents for managing inflammation and oxidative stress triggered by obesity-induced dysbiosis in the gut microbiota of obese people.

3.5. Modulating Gut–Brain Axis and Enhancing Gut Immunity

The communication between the gastrointestinal tract (GIT) and the brain is a multifaceted and reciprocal process that occurs through the circulation of blood and the cranial nerves. Enteroendocrine cells (EECs) release hormones that stimulate the brain through chemical signals in the bloodstream or neural pathways [90]. The enteric nervous system (ENS) is sometimes referred to as the “second brain” because it contains millions of neurons capable of controlling many aspects of gut function, such as regulating digestive enzyme secretion, controlling blood flow to the gut, and coordinating smooth muscle contraction in the digestive tract [91]. The enteric nervous system (ENS) interacts with the central nervous system (CNS) through various channels, including the vagus nerve, the primary conduit for transmitting sensory and motor signals between the gut and the brain. The vagus nerve connects the brainstem to the ENS and innervates many organs in the body, including the heart, lungs, liver, pancreas, and gut [92]. Numerous scientific investigations have proposed that modifying one’s everyday diet may benefit the microbiota–gut–brain axis, potentially preventing neurodegenerative diseases. Maintaining a healthy gut and a balanced gut microbiota composition is closely linked to diet composition and dietary practices. An imbalance in the gut microbiota, also known as dysbiosis, can disrupt the communication between the gut and the brain in both directions [93].
Peptides derived from dietary protein digestion or consumed as supplements play a crucial role in regulating gut microbiota and maintaining the balance of reactive oxygen species (ROS) in the gut, which is important for overall gut and host health [94]. Furthermore, certain peptides have therapeutic benefits for neurodegenerative illnesses. The gut–brain axis plays a significant role in the onset and advancement of various neurological conditions, such as Alzheimer’s disease (AD), Parkinson’s disease (PD), and autism [95].
The peptides derived from fermented dairy products show neuroprotective effects and alleviated symptoms associated with Alzheimer’s disease and other neurodegenerative conditions [96]. Also, those peptides ameliorate cognitive impairment by suppressing the activity of monoamine oxidase-B, an enzyme responsible for breaking down neurotransmitters such as dopamine. Inhibiting monoamine oxidase-B increases dopamine levels in brain tissue, improves cognitive function, and slows neurodegenerative disease progression [97]. These peptides reduce inflammation and oxidative stress and promote nerve cell survival in the brain. The Maillard reaction products of soybean peptides reduce oxidative stress and systemic inflammation that directly contributes to cognitive decline and aging [61]. The digestion products of whey and casein proteins stimulate the secretion of cholecystokinin (CCK) and glucagon-like peptide-1 (GLP-1) hormones, which are associated with satiety and food control [98]. These bioactive peptides improve gut microbiota and intestinal mucosa immunity, suggesting potential interventions to impact the gut–microbiome–immune axis positively. Bao and Wu [11] reported that dietary peptides are involved in various aspects of intestinal mucosal functions, including cell proliferation, microbial diversity, mucin production, tight junction protein expression, and antioxidant and immune cell activities, and are crucial in regulating gastrointestinal barrier functions that protect against pathogens and inflammation and promote overall gut health.

4. Assessing the Safety and Potential Risks of Peptides in Gut Microbiota

Bioactive peptides can exhibit diverse biological functions and involve numerous physiological processes that benefit human health. However, the safety of bioactive peptides is also an important consideration for their use in clinical studies and food applications. Thus, it is critical to ensure the safety of peptides despite the common misconception that bioactive peptides are safe because they are derived from food proteins using food-grade proteases. It is critical to acknowledge the existence of many naturally occurring toxic proteins and peptides [99]. Consuming peptides from food or concentrated forms is believed to have no adverse physiological effects [4]. The potential acute and repeated oral toxicity of casein hydrolysate that contains antihypertensive peptides RYLGY and AYFYPEL showed that a maximum oral dose in the 4-week repeated dose had non-observable toxic effects. Furthermore, no toxicity was observed after a single oral-limit dose, indicating a low potential for oral toxicity [100].
However, many naturally occurring peptides and enzymes in plants, animal by-products, and dried food products can potentially be toxic to unicellular and multicellular organisms [101,102]. Peptide toxicity is the underlying cause of celiac disease. Phallotoxins and amatoxins are two toxic peptides present in mushrooms, and those two cause severe damage to the liver by blocking RNA polymerase II activity, leading to impaired protein synthesis, cellular death, acute liver failure, and ultimately mortality [103]. Auestad and Layman [104] identified specific milk peptides that can cause allergies. These peptides are derived from casein and whey and serve various functions, including ACE inhibition.

5. The Implications of Research on Bioactive Peptides and Gut Microbiota

5.1. Development of New Therapeutics Using Bioactive Peptides

Exploration of bioactive peptides has emerged as a pivotal avenue for advancing novel therapeutic strategies due to their distinct biological activities [105]. Researchers aim to create innovative treatments that address various medical challenges by harnessing the inherent properties of biopeptides. The ACE-inhibitory properties of bioactive peptides in living organisms were studied through systematic blood pressure measurements in spontaneously hypertensive rats (SHRs) within in vivo settings. The assessments used diverse administration routes, including intravenous, intraperitoneal injections, and oral gavage, to determine the impact of these peptides on blood pressure levels. Bioactive peptides from food sources were suggested to offer a natural approach to controlling blood pressure without some side effects associated with traditional ACE inhibitors. These bioactive peptides work by inhibiting the enzyme that causes blood vessels to constrict, resulting in reduced blood pressure [106]. Chen et al. [107] reported that peptides could be passed through the intestinal membrane by active transport, passive transcellular diffusion, transcytosis, and tight junctions. However, absorbing the intact lactotripeptide in biologically functional amounts through the intestinal membrane and penetration into the bloodstream would be marginal. It is well accepted that single amino acids and di- and tripeptides can pass through the brush border membrane, but almost all the di- and tripeptides are digested into single amino acids by various digestive enzymes before penetrating into the bloodstream [108]. Even if some small peptides pass through the brush border and into the bloodstream, their amount should be very low. Therefore, it is almost impossible for the functional peptides to move to the target organs and generate their expected functions [109,110].
Bioactive peptides with antimicrobial properties offer a remarkable breadth of activity, capable of eliminating bacteria, fungi, viruses, and even cancer cells. Their potency is underpinned by a unique mode of action that challenges bacteria to develop resistance [111]. The significance of these peptides extends further as they possess the exceptional ability to hinder the formation of biofilms—an intricate alliance of microorganisms that cling to surfaces and evade immune responses and conventional antibiotics. These biofilms contribute to persistent infections linked to medical devices and pose formidable challenges to eradication. Remarkably, some antimicrobial peptides exhibit the power to impede biofilm formation or dismantle established biofilm fields [112]. In addition to their formidable antimicrobial prowess, antimicrobial peptides exhibit a virtue of paramount importance: their minimal toxicity towards mammalian cells. This trait positions them as a prospective therapeutic arsenal against infections, capable of effectively combating pathogens while protecting the host from substantial harm. However, employing antimicrobial peptides as clinical antimicrobial agents is still nascent, and addressing challenges between their present promise and integration into established clinical practices is important [113].
Notably, casein and phosvitin phosphopeptides possess multifaceted benefits. Their mineral-binding attributes are crucial in facilitating the absorption of vital minerals like calcium, iron, and magnesium [114,115]. As convergence of science and health, the potential of casein and phosvitin phosphopeptides to enhance therapeutic strategies emerges as a remarkable avenue of exploration. Many studies proposed their anticancer potential attributed to shielding cells against the pernicious onslaught of reactive oxygen species (ROS), including hydrogen peroxide, superoxide anion, and hydroxyl radicals. While such shielding proves effective in cell culture, its translation to animal models remains challenging [116]. The journey of formulating novel therapies hinging on these revelations holds tantalizing prospects in the combat against cancer and the refinement of cancer-related interventions in the days ahead.
Similarly, some peptides harbor the ability to forestall damages orchestrated by reactive nitrogen species (RNS), encompassing peroxynitrite and nitric oxide, the latter recognized as the most potent oxidant [117]. It is imperative to note that ROS/RNS have garnered infamy as culprits behind a gamut of chronic ailments, spanning diabetes, renal impairment, Parkinson’s disease, cardiovascular events, and an array of inflammatory disorders, skin aging, cancers, cardiovascular maladies, osteoporosis, and gastrointestinal afflictions [118,119]. The vista that unfolds before us beckons toward the horizon of bioactive peptides as therapeutic forerunners. However, to fully harness their potential, the roadmaps of ongoing research necessitate robust expeditions of intense pre-clinical evaluations, and clinical trials will etch their safety and efficacy onto the annals of specific medical interventions. As the curtain lifts on the future of medicine, bioactive peptides stand poised to play a transformational role, offer solutions to a diverse array of ailments, and elevate human health to new heights.

5.2. The Use of Bioactive Peptides in Food Processing

Bioactive peptides have gained significant attention as functional food ingredients due to their potential health benefits. Bioactive peptides can be incorporated into food products and improve food quality by influencing physical and chemical properties [4]. Furthermore, bioactive peptides can help change the viscosity of food, affecting its mouthfeel and texture [120]. Bioactive peptides derived from food by-products, such as collagen, whey, and soy, have emulsifying properties due to their amphiphilic nature. Plant-derived peptides, such as those from potatoes [121] and soybeans [122], have been identified as potential emulsifiers. These peptides are extracted from food by-products or produced via enzymatic hydrolysis and used as natural emulsifying agents in food and cosmetic products [123].
Antioxidant peptides can be used in food products to prevent lipid oxidation and extend shelf life. They also provide health benefits by protecting against oxidative stress and lowering the risk of chronic diseases. Farvin et al. [124] discovered fish protein hydrolysates containing antioxidant peptides that prevent lipid oxidation in fish oil emulsions. Antimicrobial peptides can be used in food products as natural preservatives to inhibit the growth of spoilage and pathogenic microorganisms. Pan et al. [125] reported that whey protein hydrolysates containing antimicrobial peptides inhibit the growth of common foodborne pathogens. However, emphasizing specific peptides as antioxidant or antimicrobial agents in food processing should be avoided because it is not practical to differentiate them according to their specific function. These peptides have gained attention in the food industry due to their potential health benefits and functional properties.

6. Future Research on the Bioactive Peptides and Gut Microbiota and Their Applications

Human gut microbiota comprises various microorganisms, including bacteria, fungi, and archaea. Bacteroidetes and Firmicutes phyla are the most prevalent among bacterial species, while the rest of the population belongs to Actinobacteria, Proteobacteria, Fusobacteria, Spirochaetes, Verrucomicrobia, and Lentisphaerae. These microorganisms significantly outnumber human cells and genes in the gut, and they play essential roles in various health functions of an individual. The gut microbiota is associated with maintaining homeostasis, regulating energy balance, modulating allergies, controlling appetite, and contributing to various diseases such as cardiovascular diseases, immunity, obesity, and diabetes. The microorganisms present in the colon play a crucial role in facilitating the digestion and absorption of nutrients, breaking down indigestible dietary components, and supplying micronutrients to the host. Some groups of colonic bacteria, such as Lactobacilli and Bifidobacteria, possess immunomodulatory properties, produce digestive enzymes, and help restore the gut microbiome’s equilibrium following antibiotic treatment. The complex interactions within the gut microbiota highlight the importance of studying gut microorganisms for maintaining human health. Several factors can affect the composition of gut microbiota, with diet being the most significant. Bioactive peptides can have a prebiotic effect by selectively promoting the growth of beneficial bacteria in the gut. They can also have an antimicrobial effect by inhibiting the growth of harmful bacteria.
Moreover, bioactive peptides possess anti-inflammatory characteristics, which may assist in diminishing gut inflammation and promoting healthy gut microbiota. Overall, bioactive peptides have the potential to modulate the gut microbiota and promote gut health. Therefore, bioactive peptides can be considered gut microbiota modulators. While di- and tripeptides are known to be absorbed by the intestine, only limited information on the absorption of higher-molecular-weight bioactive peptides is available [109]. After absorption, these bioactive peptides are carried by the bloodstream and interact with specific receptors, or the concentrations reaching the target cells or receptors are measurable for sustained responses [126]. The study of bioactive peptides is complex, and more research is required to understand their fate in the human body fully. Specific factors such as the nature of the peptide and its chain length influence absorption. Also, the extent of absorption might vary for each bioactive peptide [127].

7. Conclusions

Bioactive peptides have positive effects on gut microbiota. Bioactive peptides help maintain a balanced microbial environment, counteract obesity, and enhance gut–brain communication and immunity. Bioactive peptides play a significant role in modulating the immune response, particularly inflammation and related diseases. These peptides possess immunomodulatory properties, interacting with immune cells and signaling pathways and producing specific immune mediators. Some bioactive peptides have direct and indirect anti-inflammatory effects and reduce pro-inflammatory cytokines, thus helping manage chronic inflammatory conditions. Moreover, bioactive peptides influence gut health and gut microbiota, impacting the immune system indirectly. A balanced gut microbiota supports a well-regulated immune response, and the strengthened gut immunity offers protection against infections, which reduces inflammation and supports overall gut health. These peptides, with their diverse functionalities, encompass prebiotic and probiotic effects. By selectively stimulating the growth of beneficial bacteria and inhibiting pathogens, they contribute to gut health and immune function.
Consequently, bioactive peptides are crucial in maintaining a well-functioning gastrointestinal system. They promote a balanced gut microbiota and reinforce gut immunity, which makes them valuable in managing inflammation and associated diseases. Further research in this field on the mechanisms of how dietary bioactive peptides can influence hosts should be elucidated. This knowledge will help optimize the design of functional foods and dietary interventions to target specific health benefits related to gut health and beyond. While there is promising evidence for the potential health benefits of bioactive peptides, research to establish their bioavailability, absorption, interaction with gut microbiota, and efficacy in human subjects is needed. Understanding these factors is essential for harnessing the full potential of bioactive peptides and incorporating them into functional foods, therapeutics, and nutraceuticals that can effectively promote human health.

Author Contributions

Conceptualization, E.D.N.S.A. and D.U.A.; investigation, T.W., E.D.N.S.A. and D.U.A.; resources, T.W.; data curation, T.W.; writing—original draft preparation, T.W.; writing—review and editing, E.D.N.S.A. and D.U.A.; supervision, E.D.N.S.A. and D.U.A.; project administration, E.D.N.S.A. and D.U.A.; funding acquisition, E.D.N.S.A. 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.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Acknowledgments

This study was funded by a research grant from Uva Wellassa University (UWU/RG/2022/11) and the Iowa Agriculture and Home Economics Experiment Station, Ames, Iowa.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Ashaolu, T.J. Soy Bioactive Peptides and the Gut Microbiota Modulation. Appl. Microbiol. Biotechnol. 2020, 104, 9009–9017. [Google Scholar] [CrossRef] [PubMed]
  2. Jandhyala, S.M.; Talukdar, R.; Subramanyam, C.; Vuyyuru, H.; Sasikala, M.; Reddy, D.N. Role of the Normal Gut Microbiota. World J. Gastroenterol. 2015, 21, 8836–8847. [Google Scholar] [CrossRef] [PubMed]
  3. Thursby, E.; Juge, N. Introduction to the Human Gut Microbiota. Biochem. J. 2017, 474, 1823–1836. [Google Scholar] [CrossRef] [PubMed]
  4. Zaky, A.A.; Simal-Gandara, J.; Eun, J.B.; Shim, J.H.; Abd El-Aty, A.M. Bioactivities, Applications, Safety, and Health Benefits of Bioactive Peptides from Food and By-Products: A Review. Front. Nutr. 2022, 8, 815640. [Google Scholar] [CrossRef] [PubMed]
  5. Akbarian, M.; Khani, A.; Eghbalpour, S.; Uversky, V.N. Bioactive Peptides: Synthesis, Sources, Applications, and Proposed Mechanisms of Action. Int. J. Mol. Sci. 2022, 23, 1445. [Google Scholar] [CrossRef] [PubMed]
  6. Daliri, E.B.M.; Oh, D.H.; Lee, B.H. Bioactive Peptides. Foods 2017, 6, 32. [Google Scholar] [CrossRef] [PubMed]
  7. Wang, J.; Wu, Y.; Chen, Z.; Chen, Y.; Lin, Q.; Liang, Y. Exogenous Bioactive Peptides Have a Potential Therapeutic Role in Delaying Aging in Rodent Models. Int. J. Mol. Sci. 2022, 23, 1421. [Google Scholar] [CrossRef] [PubMed]
  8. Peighambardoust, S.H.; Karami, Z.; Pateiro, M.; Lorenzo, J.M. A Review on Health-promoting, Biological, and Functional Aspects of Bioactive Peptides in Food Applications. Biomolecules 2021, 11, 631. [Google Scholar] [CrossRef] [PubMed]
  9. Wu, S.; Bhat, Z.F.; Gounder, R.S.; Ahmed, I.A.M.; Al-Juhaimi, F.Y.; Ding, Y.; Bekhit, A.E.D.A. Effect of Dietary Protein and Processing on Gut Microbiota—A Systematic Review. Nutrients 2022, 14, 453. [Google Scholar] [CrossRef]
  10. Chakrabarti, S.; Guha, S.; Majumder, K. Food-Derived Bioactive Peptides in Human Health: Challenges and Opportunities. Nutrients 2018, 10, 1738. [Google Scholar] [CrossRef]
  11. Bao, X.; Wu, J. Impact of Food-Derived Bioactive Peptides on Gut Function and Health. Food Res. Int. 2021, 147, 110485. [Google Scholar] [CrossRef]
  12. Dave, L.A.; Hayes, M.; Montoya, C.A.; Rutherfurd, S.M.; Moughan, P.J. Human Gut Endogenous Proteins as a Potential Source of Angiotensin-I-Converting Enzyme (ACE-I), Renin Inhibitory and Antioxidant Peptides. Peptides 2016, 76, 30–44. [Google Scholar] [CrossRef]
  13. Mahgoub, S.; Alagawany, M.; Nader, M.; Omar, S.M.; El-hack, M.E.A.; Swelum, A.; Elnesr, S.S.; Asmaa, F.; Taha, A.E.; Farag, M.R.; et al. Recent Development in Bioactive Peptides from Plant and Animal Products and Their Impact on the Human Health. Food Rev. Int. 2021, 37, 511–536. [Google Scholar] [CrossRef]
  14. Bhat, Z.F.; Kumar, S.; Bhat, H.F. Bioactive Peptides of Animal Origin: A Review. J. Food Sci. Technol. 2015, 52, 5377–5392. [Google Scholar] [CrossRef]
  15. Jayasena, D.D.; Jung, S.; Bae, Y.S.; Park, H.B.; Lee, J.H.; Jo, C. Comparison of the Amounts of Endogenous Bioactive Compounds in Raw and Cooked Meats from Commercial Broilers and Indigenous Chickens. J. Food Compos. Anal. 2015, 37, 20–24. [Google Scholar] [CrossRef]
  16. Nielsena, S.D.; Beverlya, R.L.; Qua, Y.; Dallas, D.C. Milk Bioactive Peptide Database: A Comprehensive Database of Milk Protein-Derived Bioactive Peptides and Novel Visualization Søren. Physiol. Behav. 2018, 176, 139–148. [Google Scholar] [CrossRef]
  17. Alawadhi, N.B.; Lippert, F.; Gregory, R.L. Effects of Casein Phosphopeptide-Amorphous Calcium Phosphate Crème on Nicotine-Induced Streptococcus Mutans Biofilm In Vitro. Clin. Oral Investig. 2020, 24, 3513–3518. [Google Scholar] [CrossRef] [PubMed]
  18. Dashper, S.G.; Catmull, D.V.; Liu, S.W.; Myroforidis, H.; Zalizniak, I.; Palamara, J.E.A.; Huq, N.L.; Reynolds, E.C. Casein Phosphopeptide-Amorphous Calcium Phosphate Reduces Streptococcus Mutans Biofilm Development on Glass Ionomer Cement and Disrupts Established Biofilms. PLoS ONE 2016, 11, e0162322. [Google Scholar] [CrossRef] [PubMed]
  19. Huang, X.; Moon, S.H.; Lee, J.; Paik, H.; Lee, E.J.; Min, B.; Ahn, D.U. Effective Preparation Method of Phosphopeptides from Phosvitin and the Analysis of Peptide Profiles Using Tandem Mass Spectrometry. J. Agric. Food Chem. 2019, 67, 14086–14101. [Google Scholar] [CrossRef]
  20. Requena, T.; Miguel, M.; Garcés-Rimón, M.; Martínez-Cuesta, M.C.; López-Fandiño, R.; Peláez, C. Pepsin Egg White Hydrolysate Modulates Gut Microbiota in Zucker Obese Rats. Food Funct. 2017, 8, 437–443. [Google Scholar] [CrossRef]
  21. Heffernan, S.; Giblin, L.; O’Brien, N. Assessment of the Biological Activity of Fish Muscle Protein Hydrolysates Using In Vitro Model Systems. Food Chem. 2021, 359, 129852. [Google Scholar] [CrossRef] [PubMed]
  22. Valero, Y.; Saraiva-Fraga, M.; Costas, B.; Guardiola, F.A. Antimicrobial Peptides from Fish: Beyond the Fight against Pathogens. Rev. Aquac. 2020, 12, 224–253. [Google Scholar] [CrossRef]
  23. Senevirathne, M.; Kim, S.K. Development of Bioactive Peptides from Fish Proteins and Their Health Promoting Ability. In Advances in Food and Nutrition Research; Elsevier Inc.: Amsterdam, The Netherlands, 2012; Volume 65, pp. 235–248. [Google Scholar]
  24. Mylonakis, E.; Podsiadlowski, L.; Muhammed, M.; Vilcinskas, A. Diversity, Evolution and Medical Applications of Insect Antimicrobial Peptides. Philos. Trans. R. Soc. B Biol. Sci. 2016, 371, 20150290. [Google Scholar] [CrossRef]
  25. Altomare, A.A.; Baron, G.; Aldini, G.; Carini, M.; D’Amato, A. Silkworm Pupae as Source of High-Value Edible Proteins and of Bioactive Peptides. Food Sci. Nutr. 2020, 8, 2652–2661. [Google Scholar] [CrossRef]
  26. Marcone, S.; Belton, O.; Fitzgerald, D.J. Milk-Derived Bioactive Peptides and Their Health Promoting Effects: A Potential Role in Atherosclerosis. Br. J. Clin. Pharmacol. 2017, 83, 152–162. [Google Scholar] [CrossRef] [PubMed]
  27. Moreno-Montoro, M.; Olalla-Herrera, M.; Rufián-Henares, J.Á.; Martínez, R.G.; Miralles, B.; Bergillos, T.; Navarro-Alarcón, M.; Jauregi, P. Antioxidant, ACE-Inhibitory and Antimicrobial Activity of Fermented Goat Milk: Activity and Physicochemical Property Relationship of the Peptide Components. Food Funct. 2017, 8, 2783–2791. [Google Scholar] [CrossRef]
  28. Mann, B.; Athira, S.; Sharma, R.; Kumar, R.; Sarkar, P. Bioactive Peptides from Whey Proteins. In Whey Proteins: From Milk to Medicine; Elsevier Inc.: Amsterdam, The Netherlands, 2018; pp. 519–547. ISBN 9780128121245. [Google Scholar]
  29. Cai, W.W.; Hu, X.M.; Wang, Y.M.; Chi, C.F.; Wang, B. Bioactive Peptides from Skipjack Tuna Cardiac Arterial Bulbs: Preparation, Identification, Antioxidant Activity, and Stability against Thermal, PH, and Simulated Gastrointestinal Digestion Treatments. Mar. Drugs 2022, 20, 626. [Google Scholar] [CrossRef] [PubMed]
  30. Kong, J.; Hu, X.M.; Cai, W.W.; Wang, Y.M.; Chi, C.F.; Wang, B. Bioactive Peptides from Skipjack Tuna Cardiac Arterial Bulbs (II): Protective Function on UVB-Irradiated HaCaT Cells through Antioxidant and Anti-Apoptotic Mechanisms. Mar. Drugs 2023, 21, 105. [Google Scholar] [CrossRef] [PubMed]
  31. Gomez, H.L.R.; Peralta, J.P.; Tejano, L.A.; Chang, Y.W. In Silico and In Vitro Assessment of Portuguese Oyster (Crassostrea angulata) Proteins as Precursor of Bioactive Peptides. Int. J. Mol. Sci. 2019, 20, 5191. [Google Scholar] [CrossRef]
  32. Ambigaipalan, P.; Shahidi, F. Bioactive Peptides from Shrimp Shell Processing Discards: Antioxidant and Biological Activities. J. Funct. Foods 2017, 34, 7–17. [Google Scholar] [CrossRef]
  33. Stadnik, J.; Keska, P. Meat and Fermented Meat Products as a Source of Bioactive Peptides. Acta Sci. Pol. Technol. Aliment. 2015, 14, 181–190. [Google Scholar] [CrossRef] [PubMed]
  34. Rezaharsamto, B.; Subroto, E. A Review on Bioactive Peptides Derived from Various Sources of Meat and Meat By-Products. Int. J. Sci. Technol. Res. 2019, 8, 3151–3156. [Google Scholar]
  35. Liu, D.; Chen, X.; Huang, J.; Huang, M.; Zhou, G. Generation of Bioactive Peptides from Duck Meat during Post-Mortem Aging. Food Chem. 2017, 237, 408–415. [Google Scholar] [CrossRef]
  36. Patil, S.P.; Goswami, A.; Kalia, K.; Kate, A.S. Plant-Derived Bioactive Peptides: A Treatment to Cure Diabetes. Int. J. Pept. Res. Ther. 2020, 26, 955–968. [Google Scholar] [CrossRef] [PubMed]
  37. Qin, P.; Wang, T.; Luo, Y. A Review on Plant-Based Proteins from Soybean: Health Benefits and Soy Product Development. J. Agric. Food Res. 2022, 7, 100265. [Google Scholar] [CrossRef]
  38. Agyei, D. Bioactive Proteins and Peptides from Soybeans. Recent Pat. Food. Nutr. Agric. 2015, 7, 100–107. [Google Scholar] [CrossRef] [PubMed]
  39. Sultana, A.; Luo, H.; Ramakrishna, S. Antimicrobial Peptides and Their Applications in Biomedical Sector. Antibiotics 2021, 10, 1094. [Google Scholar] [CrossRef] [PubMed]
  40. Cruz-Chamorro, I.; Álvarez-Sánchez, N.; Santos-Sánchez, G.; Pedroche, J.; Fernández-Pachón, M.S.; Millán, F.; Millán-Linares, M.C.; Lardone, P.J.; Bejarano, I.; Guerrero, J.M.; et al. Immunomodulatory and Antioxidant Properties of Wheat Gluten Protein Hydrolysates in Human Peripheral Blood Mononuclear Cells. Nutrients 2020, 12, 1673. [Google Scholar] [CrossRef]
  41. Matemu, A.; Nakamura, S.; Katayama, S. Health Benefits of Antioxidative Peptides Derived from Legume Proteins with a High Amino Acid Score. Antioxidants 2021, 10, 316. [Google Scholar] [CrossRef]
  42. Mazloomi, S.N.; Sadeghi-Mahoonak, A.; Ranjbar-Nedamani, E.; Nourmohammadi, E. Production of Antioxidant Peptides through Hydrolysis of Paper Skin Pumpkin Seed Protein Using Pepsin Enzyme and the Evaluation of Their Functional and Nutritional Properties. ARYA Atheroscler. 2019, 15, 218–227. [Google Scholar]
  43. Chatterjee, C.; Gleddie, S.; Xiao, C.W. Soybean Bioactive Peptides and Their Functional Properties. Nutrients 2018, 10, 1211. [Google Scholar] [CrossRef]
  44. Maggioni, M.; Stuknytė, M.; De Luca, P.; Cattaneo, S.; Fiorilli, A.; De Noni, I.; Ferraretto, A. Transport of Wheat Gluten Exorphins A5 and C5 through an in Vitro Model of Intestinal Epithelium. Food Res. Int. 2016, 88, 319–326. [Google Scholar] [CrossRef]
  45. Chanput, W.; Lawyer, R. The Potential of Fractionated Rice Bran Protein Hydrolysates as Antioxidative and Anti-Inflammatory Agents. J. Nutr. Sci. Vitaminol. 2020, 66, S349–S355. [Google Scholar] [CrossRef]
  46. Jakubczyk, A.; Karaś, M.; Baraniak, B.; Pietrzak, M. The Impact of Fermentation and in Vitro Digestion on Formation Angiotensin Converting Enzyme (ACE) Inhibitory Peptides from Pea Proteins. Food Chem. 2013, 141, 3774–3780. [Google Scholar] [CrossRef] [PubMed]
  47. Tawalbeh, D.; Al-U’datt, M.H.; Wan Ahmad, W.A.N.; Ahmad, F.; Sarbon, N.M. Recent Advances in In Vitro and In Vivo Studies of Antioxidant, ACE-Inhibitory and Anti-Inflammatory Peptides from Legume Protein Hydrolysates. Molecules 2023, 28, 2423. [Google Scholar] [CrossRef]
  48. Cruz-Chamorro, I.; Santos-Sánchez, G.; Bollati, C.; Bartolomei, M.; Li, J.; Arnoldi, A.; Lammi, C. Hempseed (Cannabis sativa) Peptides WVSPLAGRT and IGFLIIWV Exert Anti-Inflammatory Activity in the LPS-Stimulated Human Hepatic Cell Line. J. Agric. Food Chem. 2022, 70, 577–583. [Google Scholar] [CrossRef] [PubMed]
  49. Cruz-Casas, D.E.; Aguilar, C.N.; Ascacio-Valdés, J.A.; Rodríguez-Herrera, R.; Chávez-González, M.L.; Flores-Gallegos, A.C. Enzymatic Hydrolysis and Microbial Fermentation: The Most Favorable Biotechnological Methods for the Release of Bioactive Peptides. Food Chem. Mol. Sci. 2021, 3, 100047. [Google Scholar] [CrossRef]
  50. Korhonen, H.; Pihlanto, A. Bioactive Peptides: Production and Functionality. Int. Dairy J. 2006, 16, 945–960. [Google Scholar] [CrossRef]
  51. Turpeinen, A.M.; Järvenpää, S.; Kautiainen, H.; Korpela, R.; Vapaatalo, H. Antihypertensive Effects of Bioactive Tripeptides—A Random Effects Meta-Analysis. Ann. Med. 2013, 45, 51–56. [Google Scholar] [CrossRef]
  52. Zhou, J.; Chen, M.; Wu, S.; Liao, X.; Wang, J.; Wu, Q.; Zhuang, M.; Ding, Y. A Review on Mushroom-Derived Bioactive Peptides: Preparation and Biological Activities. Food Res. Int. 2020, 134, 109230. [Google Scholar] [CrossRef]
  53. Guo, Z.; Yi, D.; Hu, B.; Shi, Y.; Xin, Y.; Gu, Z.; Liu, H.; Zhang, L. The Alteration of Gut Microbiota by Bioactive Peptides: A Review. Syst. Microbiol. Biomanufact. 2021, 1, 363–377. [Google Scholar] [CrossRef]
  54. Hill, C.; Guarner, F.; Reid, G.; Gibson, G.R.; Merenstein, D.J.; Pot, B.; Morelli, L.; Canani, R.B.; Flint, H.J.; Salminen, S.; et al. The International Scientific Association for Probiotics and Prebiotics Consensus Statement on the Scope and Appropriate Use of the Term Probiotic. Nat. Rev. Gastroenterol. Hepatol. 2014, 11, 506–514. [Google Scholar] [CrossRef] [PubMed]
  55. Sanders, M.E.; Merenstein, D.; Merrifield, C.A.; Hutkins, R. Probiotics for Human Use. Nutr. Bull. 2018, 43, 212–225. [Google Scholar] [CrossRef]
  56. Sharifi-Rad, J.; Rodrigues, C.F.; Stojanović-Radić, Z.; Dimitrijević, M.; Aleksić, A.; Neffe-Skocińska, K.; Zielińska, D.; Kołożyn-Krajewska, D.; Salehi, B.; Prabu, S.M.; et al. Probiotics: Versatile Bioactive Components in Promoting Human Health. Medicina 2020, 56, 433. [Google Scholar] [CrossRef]
  57. Markowiak, P.; Ślizewska, K. Effects of Probiotics, Prebiotics, and Synbiotics on Human Health. Nutrients 2017, 9, 1021. [Google Scholar] [CrossRef]
  58. Dong, C.; Tsai, M.; Nargotra, P.; Kour, B.; Chen, C.; Sun, P.; Sharma, V. Heliyon Bioprocess Development for the Production of Xylooligosaccharide Prebiotics from Agro-Industrial Lignocellulosic Waste. Heliyon 2023, 9, e18316. [Google Scholar] [CrossRef] [PubMed]
  59. Rinninella, E.; Costantini, L. Polyunsaturated Fatty Acids as Prebiotics: Innovation or Confirmation? Foods 2022, 11, 146. [Google Scholar] [CrossRef]
  60. Plamada, D.; Vodnar, D.C. Polyphenols—Gut Microbiota Interrelationship: A Transition to a New Generation of Prebiotics. Nutrients 2022, 14, 137. [Google Scholar] [CrossRef]
  61. Zhang, C.; Zhang, Y.; Li, H.; Liu, X. The Potential of Proteins, Hydrolysates and Peptides as Growth Factors for: Lactobacillus and Bifidobacterium: Current Research and Future Perspectives. Food Funct. 2020, 11, 1946–1957. [Google Scholar] [CrossRef]
  62. Terada, T.; Inui, K.I. Recent Advances in Structural Biology of Peptide Transporters. In Current Topics in Membranes; Elsevier: Amsterdam, The Netherlands, 2012; Volume 70, pp. 257–274. [Google Scholar]
  63. Raveschot, C.; Cudennec, B.; Coutte, F.; Flahaut, C.; Fremont, M.; Drider, D.; Dhulster, P. Production of Bioactive Peptides by Lactobacillus Species: From Gene to Application. Front. Microbiol. 2018, 9, 2354. [Google Scholar] [CrossRef]
  64. Zhao, H.; Bai, F.; Zhou, F.; Walczak, P.; Jiang, X.; Zhang, B. Characterization of Soybean Protein Hydrolysates Able to Promote the Proliferation of Streptococcus Thermophilus ST. J. Food Sci. 2013, 78, 575–581. [Google Scholar]
  65. Światecka, D.; Światecki, A.; Kostyra, H.; Marciniak-Darmochwa, F.K.; Kostyra, E. The Impact of Pea Protein Hydrolysates on Bacterial Physiological Activity-An In Vitro Study. Int. J. Food Microbiol. 2010, 140, 263–270. [Google Scholar] [CrossRef]
  66. Altmann, K.; Wutkowski, A.; Klempt, M.; Clawin-Rädecker, I.; Meisel, H.; Lorenzen, P.C. Generation and Identification of Anti-Inflammatory Peptides from Bovine β-Casein Using Enzyme Preparations from Cod and Hog. J. Sci. Food Agric. 2016, 96, 868–877. [Google Scholar] [CrossRef]
  67. Schuerwegh, A.J.; Dombrecht, E.J.; Stevens, W.J.; Van Offel, J.F.; Bridts, C.H.; De Clerck, L.S. Influence of Pro-Inflammatory (IL-1α, IL-6, TNF-α, IFN-γ) and Anti-Inflammatory (IL-4) Cytokines on Chondrocyte Function. Osteoarthr. Cartil. 2003, 11, 681–687. [Google Scholar] [CrossRef]
  68. Guha, S.; Majumder, K. Structural-Features of Food-Derived Bioactive Peptides with Anti-Inflammatory Activity: A Brief Review. J. Food Biochem. 2019, 43, 12531. [Google Scholar] [CrossRef]
  69. Zhang, H.; Kovacs-Nolan, J.; Kodera, T.; Eto, Y.; Mine, Y. γ-Glutamyl Cysteine and γ-Glutamyl Valine Inhibit TNF-α Signaling in Intestinal Epithelial Cells and Reduce Inflammation in a Mouse Model of Colitis via Allosteric Activation of the Calcium-Sensing Receptor. Biochim. Biophys. Acta Mol. Basis Dis. 2015, 1852, 792–804. [Google Scholar] [CrossRef]
  70. Chakrabarti, S.; Wu, J. Milk-Derived Tripeptides IPP (Ile-Pro-Pro) and VPP (Val-Pro- Pro) Promote Adipocyte Differentiation and Inhibit Inflammation in 3T3-F442A Cells. PLoS ONE 2015, 10, e0117492. [Google Scholar] [CrossRef]
  71. Zhou, J.; Ma, L.; Xu, H.; Gao, Y.; Jin, Y.; Zhao, L.; Li, D.X.A.; Zhan, D.; Zhang, S. Immunomodulating Effects of Casein-Derived Peptides QEPVL and QEPV on Lymphocytes In Vitro and In Vivo. Food Funct. 2014, 5, 2061–2069. [Google Scholar]
  72. González-Montoya, M.; Hernández-Ledesma, B.; Silván, J.M.; Mora-Escobedo, R.; Martínez-Villaluenga, C. Peptides Derived from in Vitro Gastrointestinal Digestion of Germinated Soybean Proteins Inhibit Human Colon Cancer Cells Proliferation and Inflammation. Food Chem. 2018, 242, 75–82. [Google Scholar] [CrossRef]
  73. Diamond, G.; Beckloff, N.; Weinberg, A.; Kisich, K. The Roles of Antimicrobial Peptides in Innate Host Defense. Curr. Pharm. Des. 2009, 15, 2377–2392. [Google Scholar] [CrossRef]
  74. Gong, T.; Fu, J.; Shi, L.; Chen, X.; Zong, X. Antimicrobial Peptides in Gut Health: A Review. Front. Nutr. 2021, 8, 751010. [Google Scholar] [CrossRef]
  75. López-garcía, G.; Dublan-garcía, O.; Arizmendi-cotero, D.; Oliván, L.M.G. Antioxidant and Antimicrobial Peptides Derived from Food Proteins. Molecules 2022, 27, 1343. [Google Scholar] [CrossRef]
  76. Khan, M.U.; Pirzadeh, M.; Förster, C.Y.; Shityakov, S.; Shariati, M.A. Role of Milk-Derived Antibacterial Peptides in Modern Food Biotechnology: Their Synthesis, Applications and Future Perspectives. Biomolecules 2018, 8, 110. [Google Scholar] [CrossRef]
  77. Jabbari, S.; Hasani, R.; Kafilzadeh, F.; Janfeshan, S. Antimicrobial Peptides from Milk Proteins: A Prospectus. Ann. Biol. Res. 2012, 3, 5313–5318. [Google Scholar]
  78. Huan, Y.; Kong, Q.; Mou, H.; Yi, H. Antimicrobial Peptides: Classification, Design, Application and Research Progress in Multiple Fields. Front. Microbiol. 2020, 11, 582779. [Google Scholar] [CrossRef]
  79. Gubatan, J.; Rogalla, S.; Holman, D.R.; Puntasecca, C.J.; Polevoi, D.; Rubin, S.J.S. Antimicrobial Peptides and the Gut Microbiome in Inflammatory Bowel Disease. World J. Gastroenterol. 2021, 27, 7402–7422. [Google Scholar] [CrossRef]
  80. Muniz, L.R.; Knosp, C.; Yeretssian, G. Intestinal Antimicrobial Peptides during Homeostasis, Infection, and Disease. Front. Immunol. 2012, 3, 310. [Google Scholar] [CrossRef]
  81. Zong, X.; Fu, J.; Xu, B.; Wang, Y.; Jin, M. Interplay between Gut Microbiota and Antimicrobial Peptides. Anim. Nutr. 2020, 6, 389–396. [Google Scholar] [CrossRef]
  82. Aloo, S.O.; Oh, D.H. The Functional Interplay between Gut Microbiota, Protein Hydrolysates/Bioactive Peptides, and Obesity: A Critical Review on the Study Advances. Antioxidants 2022, 11, 333. [Google Scholar] [CrossRef]
  83. Bouter, K.E.; van Raalte, D.H.; Groen, A.K.; Nieuwdorp, M. Role of the Gut Microbiome in the Pathogenesis of Obesity and Obesity-Related Metabolic Dysfunction. Gastroenterology 2017, 152, 1671–1678. [Google Scholar] [CrossRef]
  84. Zsálig, D.; Berta, A.; Tóth, V.; Szabó, Z.; Simon, K.; Figler, M.; Pusztafalvi, H.; Polyák, É. A Review of the Relationship between Gut Microbiome and Obesity. Appl. Sci. 2023, 13, 610. [Google Scholar] [CrossRef]
  85. Cindy, D.D. The Gut Microbiome and Its Role in Obesity. Nutr. Today 2016, 51, 167–174. [Google Scholar]
  86. Han, K.; Luo, D.; Zou, Y.; Dong, S.; Wan, Z.; Yang, X. Modulation of Gut Microbiota by Soybean 7S Globulin Peptide That Involved Lipopolysaccharide-Peptide Interaction. J. Agric. Food Chem. 2019, 67, 2201–2211. [Google Scholar] [CrossRef]
  87. Li, T.; Gao, J.; Du, M.; Mao, X. Bovine α-Lactalbumin Hydrolysates Ameliorate Obesity-Associated Endotoxemia and Inflammation in High-Fat Diet-Fed Mice through Modulation of Gut Microbiota. Food Funct. 2019, 10, 3368–3378. [Google Scholar] [CrossRef]
  88. Wang, S.; Lv, Z.; Zhao, W.; Wang, L.; He, N. Collagen Peptide from Walleye Pollock Skin Attenuated Obesity and Modulated Gut Microbiota in High-Fat Diet-Fed Mice. J. Funct. Foods 2020, 74, 104194. [Google Scholar] [CrossRef]
  89. Hu, J.; Zhao, H.; Wang, Y.; Yin, Z.; Kang, Y. The Bacterial Community Structures in Response to the Gut Passage of Earthworm (Eisenia fetida) Feeding on Cow Dung and Domestic Sludge: Illumina High-Throughput Sequencing-Based Data Analysis. Ecotoxicol. Environ. Saf. 2020, 190, 110149. [Google Scholar] [CrossRef]
  90. Pizarroso, N.A.; Fuciños, P.; Gonçalves, C.; Pastrana, L.; Amado, I.R. A Review on the Role of Food-Derived Bioactive Molecules and the Microbiota–Gut–Brain Axis in Satiety Regulation. Nutrients 2021, 13, 632. [Google Scholar] [CrossRef]
  91. Cryan, J.F.; O’riordan, K.J.; Cowan, C.S.M.; Sandhu, K.V.; Bastiaanssen, T.F.S.; Boehme, M.; Codagnone, M.G.; Cussotto, S.; Fulling, C.; Golubeva, A.V.; et al. The Microbiota-Gut-Brain Axis. Physiol. Rev. 2019, 99, 1877–2013. [Google Scholar] [CrossRef]
  92. Chalazonitis, A.; Rao, M. Enteric Nervous System Manifestations of Neurodegenerative Disease. Brain Res. 2018, 1693, 207–213. [Google Scholar] [CrossRef]
  93. Wang, S.; Harvey, L.; Martin, R.; van der Beek, E.M.; Knol, J.; Cryan, J.F.; Renes, I.B. Targeting the Gut Microbiota to Influence Brain Development and Function in Early Life. Neurosci. Biobehav. Rev. 2018, 95, 191–201. [Google Scholar] [CrossRef]
  94. Wu, S.; Bekhit, A.E.D.A.; Wu, Q.; Chen, M.; Liao, X.; Wang, J.; Ding, Y. Bioactive Peptides and Gut Microbiota: Candidates for a Novel Strategy for Reduction and Control of Neurodegenerative Diseases. Trends Food Sci. Technol. 2021, 108, 164–176. [Google Scholar] [CrossRef]
  95. Wei, P.; Keller, C.; Li, L. Neuropeptides in Gut-Brain Axis and Their Influence on Host Immunity and Stress. Comput. Struct. Biotechnol. J. 2020, 18, 843–851. [Google Scholar] [CrossRef]
  96. Ano, Y.; Nakayama, H. Preventive Effects of Dairy Products on Dementia and the Underlying Mechanisms. Int. J. Mol. Sci. 2018, 19, 1927. [Google Scholar] [CrossRef]
  97. Ano, Y.; Ayabe, T.; Kutsukake, T.; Ohya, R.; Takaichi, Y.; Uchida, S.; Yamada, K.; Uchida, K.; Takashima, A.; Nakayama, H. Novel Lactopeptides in Fermented Dairy Products Improve Memory Function and Cognitive Decline. Neurobiol. Aging 2018, 72, 23–31. [Google Scholar] [CrossRef]
  98. Luhovyy, B.L.; Akhavan, T.; Anderson, G.H. Whey Proteins in the Regulation of Food Intake and Satiety. J. Am. Coll. Nutr. 2007, 26, 704S–712S. [Google Scholar] [CrossRef]
  99. Lafarga, T.; Hayes, M. Bioactive Protein Hydrolysates in the Functional Food Ingredient Industry: Overcoming Current Challenges. Food Rev. Int. 2017, 33, 217–246. [Google Scholar] [CrossRef]
  100. Anadón, A.; Martínez, M.A.; Ares, I.; Ramos, E.; Martínez-Larrañaga, M.R.; Contreras, M.M.; Ramos, M.; Recio, I. Acute and Repeated Dose (4 Weeks) Oral Toxicity Studies of Two Antihypertensive Peptides, RYLGY and AYFYPEL, That Correspond to Fragments (90–94) and (143–149) from αs1-Casein. Food Chem. Toxicol. 2010, 48, 1836–1845. [Google Scholar] [CrossRef]
  101. Doorten, A.Y.P.S.; Vd Wiel, J.A.G.; Jonker, D. Safety Evaluation of an IPP Tripeptide-Containing Milk Protein Hydrolysate. Food Chem. Toxicol. 2009, 47, 55–61. [Google Scholar] [CrossRef]
  102. Khan, F.; Niaz, K.; Abdollahi, M. Toxicity of Biologically Active Peptides and Future Safety Aspects: An Update. Curr. Drug Discov. Technol. 2018, 15, 236–242. [Google Scholar] [CrossRef]
  103. Santi, L.; Maggioli, C.; Mastroroberto, M.; Tufoni, M.; Napoli, L.; Caraceni, P. Acute Liver Failure Caused by Amanita Phalloides Poisoning. Int. J. Hepatol. 2012, 2012, 487480. [Google Scholar] [CrossRef]
  104. Auestad, N.; Layman, D.K. Dairy Bioactive Proteins and Peptides: A Narrative Review. Nutr. Rev. 2021, 79, 36–47. [Google Scholar] [CrossRef]
  105. Aguilar-Toalá, J.E.; Santiago-López, L.; Peres, C.M.; Peres, C.; Garcia, H.S.; Vallejo-Cordoba, B.; González-Córdova, A.F.; Hernández-Mendoza, A. Assessment of Multifunctional Activity of Bioactive Peptides Derived from Fermented Milk by Specific Lactobacillus Plantarum Strains. J. Dairy Sci. 2017, 100, 65–75. [Google Scholar] [CrossRef]
  106. Korhonen, H. Milk-Derived Bioactive Peptides: From Science to Applications. J. Funct. Foods 2009, 1, 177–187. [Google Scholar] [CrossRef]
  107. Chen, G.; Kang, W.; Li, W.; Chen, S.; Gao, Y. Oral delivery of protein and peptide drugs: From non-specific formulation approaches to intestinal cell targeting strategies. Theranostics 2022, 12, 1419–1439. [Google Scholar] [CrossRef]
  108. Fernández-Tomé, S.; Hernández-Ledesma, B. Gastrointestinal Digestion of Food Proteins under the Effects of Released Bioactive Peptides on Digestive Health. Mol. Nutr. Food Res. 2020, 64, 2000401. [Google Scholar] [CrossRef]
  109. Rutherfurd-Markwick, K.J. Food Proteins as a Source of Bioactive Peptides with Diverse Functions. Br. J. Nutr. 2012, 108, 149–157. [Google Scholar] [CrossRef]
  110. Shen, W.; Matsui, T. Current Knowledge of Intestinal Absorption of Bioactive Peptides. Food Funct. 2017, 8, 4306–4314. [Google Scholar] [CrossRef]
  111. Gilmore, K.; Chen, P.; Leung, K.P.; Gilmore, K.; Chen, P.; Peptides, K.P.L.A. Anti-Microbial Peptides for Plaque Control and Beyond. J. Calif. Dent. Assoc. 2023, 37, 779–788. [Google Scholar] [CrossRef]
  112. Galdiero, E.; Lombardi, L.; Falanga, A.; Libralato, G.; Guida, M.; Carotenuto, R. Biofilms: Novel Strategies Based on Antimicrobial Peptides. Pharmaceutics 2019, 11, 322. [Google Scholar] [CrossRef]
  113. Kharidia, R.; Tu, Z.; Chen, L. Activity and Selectivity of Histidine-Containing Lytic Peptides to Antibiotic-Resistant Bacteria. Arch. Microbiol. 2012, 194, 769–778. [Google Scholar] [CrossRef]
  114. Jauhiainen, T.; Korpela, R. Milk Peptides and Blood Pressure. J. Nutr. 2007, 137, 825–829. [Google Scholar] [CrossRef]
  115. Liu, W.; Lin, J.; Zhang, C.; Yang, Z.; Shan, H.; Jiang, J.; Wan, X.; Wang, Z. Effect of Dietary Casein Phosphopeptide Addition on the Egg Production Performance, Egg Quality, and Eggshell Ultrastructure of Late Laying Hens. Foods 2023, 12, 1712. [Google Scholar] [CrossRef]
  116. Zhang, Y.; Wang, C.; Zhang, W.; Li, X. Bioactive Peptides for Anticancer Therapies. Biomater. Transl. 2023, 4, 5–17. [Google Scholar] [PubMed]
  117. Lobo, V.; Patil, A.; Phatak, A.; Chandra, N. Free Radicals, Antioxidants and Functional Foods: Impact on Human Health. Pharmacogn. Rev. 2010, 4, 118–126. [Google Scholar] [CrossRef]
  118. Lee, J.E.; An, B.J.; Jo, C.; Min, B.; Paik, H.D.; Ahn, D.U. The Elastase and Melanogenesis Inhibitory and Anti-Inflammatory Activities of Phosvitin Phosphopeptides Produced Using High-Temperature and Mild-Pressure (HTMP) Pretreatment and Enzyme Hydrolysis Combinations. Poult. Sci. 2023, 102, 102680. [Google Scholar] [CrossRef] [PubMed]
  119. Lee, J.E.; Lee, J.H.; Min, B.; Kim, K.T.; Ahn, D.U.; Paik, H.D. Immunostimulatory Effect of Egg Yolk Phosvitin Phosphopeptides Produced by High-Temperature and Mild-Pressure Pretreatment and Enzyme Combinations in RAW 264.7 Cells via TLR2/MAPK Signaling Pathway. J. Funct. Foods 2022, 98, 105264. [Google Scholar] [CrossRef]
  120. Faustino, M.; Veiga, M.; Sousa, P.; Costa, E.M.; Silva, S.; Pintado, M. Agro-Food Byproducts as a New Source of Natural Food Additives. Molecules 2019, 24, 1056. [Google Scholar] [CrossRef] [PubMed]
  121. García-Moreno, P.J.; Gregersen, S.; Nedamani, E.R.; Olsen, T.H.; Marcatili, P.; Overgaard, M.T.; Andersen, M.L.; Hansen, E.B.; Jacobsen, C. Identification of Emulsifier Potato Peptides by Bioinformatics: Application to Omega-3 Delivery Emulsions and Release from Potato Industry Side Streams. Sci. Rep. 2020, 10, 690. [Google Scholar] [CrossRef]
  122. Tsumura, K.; Kugimiya, W.; Inouye, K. Emulsifying Properties of a Peptide from Peptic Hydrolysates of Soy Glycinin. Food Sci. Technol. Res. 2005, 11, 46–51. [Google Scholar] [CrossRef]
  123. Lam, R.S.H.; Nickerson, M.T. Food Proteins: A Review on Their Emulsifying Properties Using a Structure-Function Approach. Food Chem. 2013, 141, 975–984. [Google Scholar] [CrossRef]
  124. Farvin, K.H.S.; Lystbæk, L.; Hauch, H.; Jacobsen, C.; Jakobsen, G.; Johansson, I.; Jessen, F. Antioxidant Activity of Cod (Gadus morhua) Protein Hydrolysates: In Vitro Assays and Evaluation in 5 % Fish Oil-in-Water Emulsion. Food Chem. 2014, 149, 326–334. [Google Scholar] [CrossRef] [PubMed]
  125. Pan, M.; Liu, K.; Yang, J.; Liu, S.; Wang, S.; Wang, S. Advances on Food-Derived Peptidic Antioxidants—A Review. Antioxidants 2020, 9, 799. [Google Scholar] [CrossRef] [PubMed]
  126. Chabance, B.; Marteau, P.; Rambaud, J.C.; Migliore-Samour, D.; Boynard, M.; Perrotin, P.; Guillet, R.; Jollès, P.; Fiat, A.M. Casein Peptide Release and Passage to the Blood in Humans during Digestion of Milk or Yogurt. Biochimie 1998, 80, 155–165. [Google Scholar] [CrossRef] [PubMed]
  127. Amigo, L.; Hernández-Ledesma, B. Current Evidence on the Bioavailability of Food. Molecules 2020, 25, 4479. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The mechanism of bioactive peptides on external bacteria and viruses. The release of bioactive peptides from intestinal cells and gut microbes inhibits the growth of external bacteria and viruses, maintaining the gut microbiota’s balance and stability. The gut microbiota is crucial for inducing the expression of antimicrobial peptides that defend against pathogens. These peptides are vital components of innate immunity, controlling pathogen growth within the intestine. Paneth cells can directly sense gut microbiota through MyD88-dependent TLR activation, leading to the expression of α-defensins and C-type lectins. β-defensin interacts with intestinal epithelial cells via CCR6, promoting epithelial resistance.
Figure 1. The mechanism of bioactive peptides on external bacteria and viruses. The release of bioactive peptides from intestinal cells and gut microbes inhibits the growth of external bacteria and viruses, maintaining the gut microbiota’s balance and stability. The gut microbiota is crucial for inducing the expression of antimicrobial peptides that defend against pathogens. These peptides are vital components of innate immunity, controlling pathogen growth within the intestine. Paneth cells can directly sense gut microbiota through MyD88-dependent TLR activation, leading to the expression of α-defensins and C-type lectins. β-defensin interacts with intestinal epithelial cells via CCR6, promoting epithelial resistance.
Foods 13 01853 g001
Table 1. Animal-derived bioactive peptides.
Table 1. Animal-derived bioactive peptides.
Animal SourceMain ProteinType of Peptides DerivedBioactivityAnalysis MethodReference
MilkCaseinCasomorphinsACE-inhibitory, antimicrobialBiochemical, Microbial[26,27]
Whey proteinα-LactorphinACE-inhibitory, antioxidantChemical[28]
FishTunaQGD, GEQSN, PKK, GPQ, GEEGD AntioxidantChemical[29,30]
ShellfishOysterOyster peptide hydrolysateAntioxidant, anti-inflammatoryChemical[31]
ShrimpVal-Gly-Pro, Isoleu-Pro-ProACE-inhibitory, antimicrobialEnzymatic[32]
MeatBeefGFHI, DFHING, FHG, GLSDGEWQAntioxidant, anti-obesityChemical, Enzymatic[33]
PorkThe titin-derived pentapeptides KAPVA, PTPVPACE-inhibitory, anti-inflammatoryChemical, Enzymatic[34]
ChickenLKA, LKP, LAP, IKW, FQKPKR, FKGRYYP, IVGRPRHQGACE-inhibitoryEnzymatic[35]
DuckTrp-Tyr-Pro-Ala-ProACE-inhibitory, antioxidantChemical, Enzymatic[36]
InsectsCricketDefensin-1antimicrobialMicrobial[24]
SilkwormSPKFCW, DQDPFRP, PDPSKFAntimicrobialMicrobial[25]
Table 2. Plant-derived bioactive peptides.
Table 2. Plant-derived bioactive peptides.
Plant SourcePeptide Producing CompoundType of PeptidesHealth BenefitsReference
SoybeansLunasinSKWQHQQDSCRKQKQ, GVNLTPCEKHIMEKIQ, GRGDDDDDDDDDAnti-inflammatory, anticancer, cholesterol-lowering activity[43]
WheatGluten exorphinsGE A5, GE C5Opioid-like activity[44]
RiceRice bran peptidesTrypsin-hydrolyzed rice branAntioxidant, anti-inflammatory, immune-modulating activity[45]
PeasACE-inhibitory peptidesKEDDEEEEQGEEEBlood pressure regulation, cardiovascular health activity[46]
ChickpeasACE-inhibitory and antioxidant peptidesLeu-Thr-Glu-IIe-IIe-ProBlood pressure regulation, cardiovascular health, cellular protection, oxidative stress reduction[47]
Hemp seedsAntioxidant and anti-inflammatory peptidesWVSPLAGRT (H2), IGFLIIWV (H3)Cellular protection, oxidative stress reduction, inflammation reduction[48]
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

Wijesekara, T.; Abeyrathne, E.D.N.S.; Ahn, D.U. Effect of Bioactive Peptides on Gut Microbiota and Their Relations to Human Health. Foods 2024, 13, 1853. https://doi.org/10.3390/foods13121853

AMA Style

Wijesekara T, Abeyrathne EDNS, Ahn DU. Effect of Bioactive Peptides on Gut Microbiota and Their Relations to Human Health. Foods. 2024; 13(12):1853. https://doi.org/10.3390/foods13121853

Chicago/Turabian Style

Wijesekara, Tharuka, Edirisinghe Dewage Nalaka Sandun Abeyrathne, and Dong Uk Ahn. 2024. "Effect of Bioactive Peptides on Gut Microbiota and Their Relations to Human Health" Foods 13, no. 12: 1853. https://doi.org/10.3390/foods13121853

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