Pub Date : 2026-03-01Epub Date: 2026-01-21DOI: 10.1016/j.fbio.2026.108308
Yong-bo Liu, Wei Li
Panax ginseng has attracted considerable interest due to its notable pharmacological properties. Historically, research and applications have primarily focused on the roots and rhizomes, leading to the long-term neglect of the potentially valuable non-medicinal parts such as stems and leaves. Recent studies have shown that ginseng stems and leaves (GSL), which are rich in ginsenosides, amino acids, vitamins, and minerals, exhibit significant antioxidant, anti-inflammatory, and immunomodulatory activities. These properties create new opportunities for application in functional foods, dietary supplements, and cosmetics. Moreover, owing to their high ginsenoside content and cost-effectiveness, GSL have emerged as promising raw materials for extracting total ginsenosides and isolating individual ginsenosides, thereby facilitating the development of value-added products. This review provides a comprehensive evaluation of the bioactivities of GSL (including neuroprotective modulation, cardiovascular protection, antitumor activity, immune function enhancement, and anti-fatigue effects) and their potential in product development, with an emphasis on extraction, separation, ginsenoside transformation, the development of functional foods and dietary supplements. Finally, we discuss the translational implications and key challenges in translating bioactivity evidence into practical applications, thereby supporting the sustainable utilization of ginseng resources and the long-term development of the ginseng industry.
{"title":"From bioactivity to application: Utilization of non-medicinal ginseng stems and leaves","authors":"Yong-bo Liu, Wei Li","doi":"10.1016/j.fbio.2026.108308","DOIUrl":"10.1016/j.fbio.2026.108308","url":null,"abstract":"<div><div><em>Panax ginseng</em> has attracted considerable interest due to its notable pharmacological properties. Historically, research and applications have primarily focused on the roots and rhizomes, leading to the long-term neglect of the potentially valuable non-medicinal parts such as stems and leaves. Recent studies have shown that ginseng stems and leaves (GSL), which are rich in ginsenosides, amino acids, vitamins, and minerals, exhibit significant antioxidant, anti-inflammatory, and immunomodulatory activities. These properties create new opportunities for application in functional foods, dietary supplements, and cosmetics. Moreover, owing to their high ginsenoside content and cost-effectiveness, GSL have emerged as promising raw materials for extracting total ginsenosides and isolating individual ginsenosides, thereby facilitating the development of value-added products. This review provides a comprehensive evaluation of the bioactivities of GSL (including neuroprotective modulation, cardiovascular protection, antitumor activity, immune function enhancement, and anti-fatigue effects) and their potential in product development, with an emphasis on extraction, separation, ginsenoside transformation, the development of functional foods and dietary supplements. Finally, we discuss the translational implications and key challenges in translating bioactivity evidence into practical applications, thereby supporting the sustainable utilization of ginseng resources and the long-term development of the ginseng industry.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108308"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076248","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-20DOI: 10.1016/j.fbio.2026.108329
Cécile Touche, Vincenza Ferraro
Collagen peptides were investigated in-vitro as potential inhibitors of lipoxygenase, trypsin and monoamine oxidases (MAO), and proteins thermal denaturation. When overexpressed or dysregulated, those enzymes, and denatured proteins, mediate several inflammatory mechanisms, and also neurodegenerative diseases. Besides, they can compromise food and drugs storage. Several synthetic and plant compounds were investigated and applied as inhibitors; however, research on bioactive peptides is lagging behind, in particular if animal-derived. In this study, collagen was extracted from bovine bone by a French National Research Institute for Agriculture, Food and Environment (INRAE) patented process, and hydrolysed afterwards. Three endopeptidases were considered – bromelain, collagenase and papain – since they generate peptides that inhibit several oxidative species, which are linked to inflammation, cognitive decline, and loss of quality in several products. Two ratios enzyme/collagen (E/C), 1/20 and 1/50 (w/w), and two peptides sizes, ≤1000 Da and ≤3000, were considered. For the E/C 1/50, ≤1000 Da fraction, the synergy among peptides generated by the three proteases was evaluated. Significant biological activity emerged, which was mainly linked to the collagen protease specificity instead of peptides concentration. Lipoxygenase was inhibited by all the peptides, and those from collagenase showed the most important effect. Modulation of the trypsin activity was noticed; complete inhibition was obtained when the trypsin substrate was albumin. When that was casein, papain was the most effective protease, while bromelain and collagenase derived peptides increased the trypsin activity; this effect disappeared when peptides fractions were mixed. Only papain derived peptides were able to inhibit MAO. Outcome of this research can be considered encouraging for the investigated application.
{"title":"Inhibitory capacity of bovine bone collagen peptides towards inflammation mediators in-vitro - Impact of the hydrolysing protease, of peptides size and of peptides synergy","authors":"Cécile Touche, Vincenza Ferraro","doi":"10.1016/j.fbio.2026.108329","DOIUrl":"10.1016/j.fbio.2026.108329","url":null,"abstract":"<div><div>Collagen peptides were investigated <em>in-vitro</em> as potential inhibitors of lipoxygenase, trypsin and monoamine oxidases (MAO), and proteins thermal denaturation. When overexpressed or dysregulated, those enzymes, and denatured proteins, mediate several inflammatory mechanisms, and also neurodegenerative diseases. Besides, they can compromise food and drugs storage. Several synthetic and plant compounds were investigated and applied as inhibitors; however, research on bioactive peptides is lagging behind, in particular if animal-derived. In this study, collagen was extracted from bovine bone by a French National Research Institute for Agriculture, Food and Environment (INRAE) patented process, and hydrolysed afterwards. Three endopeptidases were considered – bromelain, collagenase and papain – since they generate peptides that inhibit several oxidative species, which are linked to inflammation, cognitive decline, and loss of quality in several products. Two ratios enzyme/collagen (E/C), 1/20 and 1/50 (w/w), and two peptides sizes, ≤1000 Da and ≤3000, were considered. For the E/C 1/50, ≤1000 Da fraction, the synergy among peptides generated by the three proteases was evaluated. Significant biological activity emerged, which was mainly linked to the collagen protease specificity instead of peptides concentration. Lipoxygenase was inhibited by all the peptides, and those from collagenase showed the most important effect. Modulation of the trypsin activity was noticed; complete inhibition was obtained when the trypsin substrate was albumin. When that was casein, papain was the most effective protease, while bromelain and collagenase derived peptides increased the trypsin activity; this effect disappeared when peptides fractions were mixed. Only papain derived peptides were able to inhibit MAO. Outcome of this research can be considered encouraging for the investigated application.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108329"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076301","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-16DOI: 10.1016/j.fbio.2026.108312
Yue Zhang , Xiaotong Li , Hongbo Qu , Min Zhang , Lina Sun , Ye Jin
Adipose tissue in ruminants is crucial for energy storage and lipid metabolism regulation. Understanding the metabolic characteristics of distinct fat depots and their dietary responses is essential for elucidating lipid regulatory networks and improving meat quality. The study selected 12 healthy male lambs (3 months old, 22.37 ± 2.05 kg, Dorper ewes × Suffolk rams), which were randomly assigned to a control group and a sodium butyrate (SB) group. Lipidomic and transcriptomic analyses were conducted to evaluate the tissue-specific effects of SB on subcutaneous adipose tissue (SAT) and perirenal adipose tissue (PAT). The results showed that SB reduced the saturated fatty acids (C12:0, C13:0, C16:0) in SAT and the unsaturated fatty acids (C18:1n9c, C18:2n6c, C18:3n3, C20:4n6) in PAT, altering fatty acid profiles. Lipidomics showed that SB enhanced membrane stability in SAT by increasing lysophosphatidylcholine, phosphatidylinositol, and ceramide, and promoted lipid catabolism in PAT by downregulating triglyceride, diglyceride, phosphatidic acid. Transcriptomics revealed that SB activated immunometabolic genes (Interleukin-6, mitogen-activated protein kinase kinase kinase 8) in SAT and lipolysis-related genes (methylsterol monooxygenase 1, squalene epoxidase) in PAT. Integrated analysis indicated that SB regulates lipid metabolism via distinct mechanisms, enhancing membrane lipid composition through stearoyl-CoA desaturase 5 and 3-hydroxyacyl-CoA dehydratase 1 in SAT, and promoting glycerophospholipid metabolism and lipid signaling via heme oxygenase 1 and 4-aminobutyrate aminotransferase in PAT. This study reveals the tissue-specific mechanisms of SB in lambs, highlighting its novelty in demonstrating differential depot responses and its significance for guiding fat deposition and lipid homeostasis in ruminants.
{"title":"Integrated lipidomics and transcriptomics reveal the tissue-specific regulatory mechanisms of dietary sodium butyrate on adipose tissue in lambs","authors":"Yue Zhang , Xiaotong Li , Hongbo Qu , Min Zhang , Lina Sun , Ye Jin","doi":"10.1016/j.fbio.2026.108312","DOIUrl":"10.1016/j.fbio.2026.108312","url":null,"abstract":"<div><div>Adipose tissue in ruminants is crucial for energy storage and lipid metabolism regulation. Understanding the metabolic characteristics of distinct fat depots and their dietary responses is essential for elucidating lipid regulatory networks and improving meat quality. The study selected 12 healthy male lambs (3 months old, 22.37 ± 2.05 kg, Dorper ewes × Suffolk rams), which were randomly assigned to a control group and a sodium butyrate (SB) group. Lipidomic and transcriptomic analyses were conducted to evaluate the tissue-specific effects of SB on subcutaneous adipose tissue (SAT) and perirenal adipose tissue (PAT). The results showed that SB reduced the saturated fatty acids (C12:0, C13:0, C16:0) in SAT and the unsaturated fatty acids (C18:1n9c, C18:2n6c, C18:3n3, C20:4n6) in PAT, altering fatty acid profiles. Lipidomics showed that SB enhanced membrane stability in SAT by increasing lysophosphatidylcholine, phosphatidylinositol, and ceramide, and promoted lipid catabolism in PAT by downregulating triglyceride, diglyceride, phosphatidic acid. Transcriptomics revealed that SB activated immunometabolic genes (<em>Interleukin-6, mitogen-activated protein kinase kinase kinase 8</em>) in SAT and lipolysis-related genes (<em>methylsterol monooxygenase 1, squalene epoxidase</em>) in PAT. Integrated analysis indicated that SB regulates lipid metabolism via distinct mechanisms, enhancing membrane lipid composition through <em>stearoyl-CoA desaturase 5</em> and <em>3-hydroxyacyl-CoA dehydratase 1</em> in SAT, and promoting glycerophospholipid metabolism and lipid signaling via <em>heme oxygenase 1</em> and <em>4-aminobutyrate aminotransferase</em> in PAT. This study reveals the tissue-specific mechanisms of SB in lambs, highlighting its novelty in demonstrating differential depot responses and its significance for guiding fat deposition and lipid homeostasis in ruminants.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108312"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076302","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-24DOI: 10.1016/j.fbio.2026.108363
Ge Xu , Longbin Tan , Jiewen Tan , Wenzhu Zhao , Zhipeng Yu
Tilapia skin collagen peptides possess multiple biological functions, yet their potential value remains underdeveloped and underutilized. This study investigated the efficacy and mechanisms of tilapia skin collagen peptides (TSCPs) in mitigating aging. TSCPs significantly delayed aging progression in H2O2- and glucose-induced zebrafish models. Three tyrosinase-inhibitory peptides and five antiglycation peptides were identified in TSCPs through targeted screening. Specifically, peptides Ser-Glu-Gly-Lys (SEGK) and Asp-Asp-Asp (DDD) exhibited the strongest in vitro tyrosinase-inhibitory and antiglycation activity, respectively. Molecular dynamics simulations revealed that both peptides bound more stably to anti-aging targets (tyrosinase and receptor for advanced glycation end products (RAGE)) through hydrogen bonds and electrostatic interactions. Moreover, SEGK and DDD reduced reactive oxygen species (ROS), malondialdehyde (MDA), and advanced glycation end products (AGEs) levels in zebrafish models, thereby contributing to the preferable aging mitigation effects. These findings provide in-depth insights into the mechanisms by which TSCPs mitigate aging from the perspectives of antioxidation, antiglycation, and tyrosinase inhibition, offering a theoretical basis for the development of TSCPs-based functional foods.
{"title":"Identification and molecular mechanism of tilapia skin-derived collagen peptides mitigating aging using zebrafish aging model","authors":"Ge Xu , Longbin Tan , Jiewen Tan , Wenzhu Zhao , Zhipeng Yu","doi":"10.1016/j.fbio.2026.108363","DOIUrl":"10.1016/j.fbio.2026.108363","url":null,"abstract":"<div><div>Tilapia skin collagen peptides possess multiple biological functions, yet their potential value remains underdeveloped and underutilized. This study investigated the efficacy and mechanisms of tilapia skin collagen peptides (TSCPs) in mitigating aging. TSCPs significantly delayed aging progression in H<sub><sub>2</sub></sub>O<sub>2</sub>- and glucose-induced zebrafish models. Three tyrosinase-inhibitory peptides and five antiglycation peptides were identified in TSCPs through targeted screening. Specifically, peptides Ser-Glu-Gly-Lys (SEGK) and Asp-Asp-Asp (DDD) exhibited the strongest <em>in vitro</em> tyrosinase-inhibitory and antiglycation activity, respectively. Molecular dynamics simulations revealed that both peptides bound more stably to anti-aging targets (tyrosinase and receptor for advanced glycation end products (RAGE)) through hydrogen bonds and electrostatic interactions. Moreover, SEGK and DDD reduced reactive oxygen species (ROS), malondialdehyde (MDA), and advanced glycation end products (AGEs) levels in zebrafish models, thereby contributing to the preferable aging mitigation effects. These findings provide in-depth insights into the mechanisms by which TSCPs mitigate aging from the perspectives of antioxidation, antiglycation, and tyrosinase inhibition, offering a theoretical basis for the development of TSCPs-based functional foods.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108363"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cholesterol, as a key lipid component in pork, has a role in meat quality that is still not well comprehended. This study conducts an in-depth investigation into the differential changes in metabolome and transcriptome in pork with high- and low-cholesterol content. The results identified 314 differentially accumulated metabolites (DAMs) and 766 differentially expressed genes (DEGs), respectively. DAMs involved in the glycolysis/pentose phosphate pathway, amino acid derivatives, and glycerophospholipids were significantly different between the groups. DEGs were also involved in the extracellular matrix, PI3K-AKT signaling pathway, etc. Enhanced glycolysis/pentose phosphate pathway, activation of amino acid transamination, and remodeling of glycerophospholipid metabolism collectively regulate cholesterol levels in the skeletal muscle. Additionally, cholesterol content is correlated with eye muscle area, drip loss, and pH. These findings offer new perspectives on how cholesterol influences meat quality and its accumulation in pork.
{"title":"Integrated metabolomics and transcriptomics analyses elucidate functional pathways and candidate genes linked to cholesterol content in pork","authors":"Qi Chen, Weilong Tang, Hao Jiang, Yuheng Li, Yadong Li, Jie Chen, Lifan Zhang","doi":"10.1016/j.fbio.2026.108421","DOIUrl":"10.1016/j.fbio.2026.108421","url":null,"abstract":"<div><div>Cholesterol, as a key lipid component in pork, has a role in meat quality that is still not well comprehended. This study conducts an in-depth investigation into the differential changes in metabolome and transcriptome in pork with high- and low-cholesterol content. The results identified 314 differentially accumulated metabolites (DAMs) and 766 differentially expressed genes (DEGs), respectively. DAMs involved in the glycolysis/pentose phosphate pathway, amino acid derivatives, and glycerophospholipids were significantly different between the groups. DEGs were also involved in the extracellular matrix, PI3K-AKT signaling pathway, etc. Enhanced glycolysis/pentose phosphate pathway, activation of amino acid transamination, and remodeling of glycerophospholipid metabolism collectively regulate cholesterol levels in the skeletal muscle. Additionally, cholesterol content is correlated with eye muscle area, drip loss, and pH. These findings offer new perspectives on how cholesterol influences meat quality and its accumulation in pork.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108421"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147399302","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-02-03DOI: 10.1016/j.fbio.2026.108411
Hongwei Cao , Mengting Huang , Qilong Huang , Hongdong Song , Kai Huang , Yu Zhang , Jun Lu , Xiao Guan
Microwave heating and the Maillard reaction (MR) are pivotal in modern food processing, yet critical gaps persist: insufficient clarity on dielectric property-modulated MR selectivity and the synergistic/antagonistic roles of microwave thermal vs. non-thermal effects. This review systematically synthesizes experimental and theoretical literature to evaluate how microwave parameters influence MR kinetics, formation of flavor compounds, pigments, and harmful byproducts. Key findings: microwaves alter MR pathways via dual effects, with excessive power exacerbating toxicants; dielectric properties are core regulators of MR selectivity. Practical implications: optimizing microwave parameters enables targeted enhancement of food sensory quality while minimizing undesirable MR products, offering a sustainable approach for efficient, safe food processing.
{"title":"Microwave-mediated regulation of the Maillard reaction: Mechanisms, influencing factors, and impacts on food quality","authors":"Hongwei Cao , Mengting Huang , Qilong Huang , Hongdong Song , Kai Huang , Yu Zhang , Jun Lu , Xiao Guan","doi":"10.1016/j.fbio.2026.108411","DOIUrl":"10.1016/j.fbio.2026.108411","url":null,"abstract":"<div><div>Microwave heating and the Maillard reaction (MR) are pivotal in modern food processing, yet critical gaps persist: insufficient clarity on dielectric property-modulated MR selectivity and the synergistic/antagonistic roles of microwave thermal vs. non-thermal effects. This review systematically synthesizes experimental and theoretical literature to evaluate how microwave parameters influence MR kinetics, formation of flavor compounds, pigments, and harmful byproducts. Key findings: microwaves alter MR pathways via dual effects, with excessive power exacerbating toxicants; dielectric properties are core regulators of MR selectivity. Practical implications: optimizing microwave parameters enables targeted enhancement of food sensory quality while minimizing undesirable MR products, offering a sustainable approach for efficient, safe food processing.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108411"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147399417","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-29DOI: 10.1016/j.fbio.2026.108353
Lin-Lin Ding , Haiyan Sun , Xuan-Yi Xu , Yu Zhang , Ai-Mei Liao , Yin-Chen Hou , Ji-Hong Huang , Long Pan
Environmental cold exposure compromises host immunity, necessitating effective nutritional mitigation strategies. Although bovine lactoferrin (BLF) is a potent immunomodulator, its natural scarcity limits large-scale industrial use. Herein, we evaluate the immune protective efficacy and mechanism of a scalable recombinant bovine lactoferrin (UBLF) expressed in Pichia pastoris. Guided by proteomic analysis indicating immune-regulatory potential, we employed a cold-stress murine model integrating physiological monitoring, serum immunology and 16 S rRNA sequencing to assess UBLF activity. Results showed that prophylactic oral UBLF effectively mitigated physiological deficits, preventing stress-induced weight loss (maintaining weight gain vs. −0.38 g loss in the model group) and hypothermia. Systemic inflammation was significantly attenuated by downregulating serum IL-6, IL-8, IL-1β, and TNF-α (P < 0.05), while bolstering serum immunoglobulin (IgG/IgA) levels and preserving thymic and splenic architecture. Crucially, UBLF exerted a protective effect on the lungs, significantly reducing the lung index (0.69 % vs. 1.16 % in the model group) and alleviating pulmonary pathologies, including alveolar wall thickening and inflammatory cell infiltration. Microbiome profiling demonstrated that UBLF ameliorated cold stress–induced gut dysbiosis by re-establishing normal microbial α-diversity and reducing the Firmicutes/Bacteroidetes ratio (from 1.48 to 0.98). This microbial restoration coincided with the selective enrichment of beneficial genera, notably Akkermansia. Collectively, our results suggest that the protective effects against cold stress–induced immunosuppression are linked to the concurrent restoration of gut microbial homeostasis and the mitigation of pulmonary inflammation, highlighting the potential involvement of the gut-lung axis. UBLF therefore emerges as a novel functional food ingredient with industrial scalability, designed to enhance host stress resilience via the gut-lung axis.
{"title":"Recombinant bovine lactoferrin ameliorates cold stress-induced immunosuppression by modulating the gut microbiota in mice","authors":"Lin-Lin Ding , Haiyan Sun , Xuan-Yi Xu , Yu Zhang , Ai-Mei Liao , Yin-Chen Hou , Ji-Hong Huang , Long Pan","doi":"10.1016/j.fbio.2026.108353","DOIUrl":"10.1016/j.fbio.2026.108353","url":null,"abstract":"<div><div>Environmental cold exposure compromises host immunity, necessitating effective nutritional mitigation strategies. Although bovine lactoferrin (BLF) is a potent immunomodulator, its natural scarcity limits large-scale industrial use. Herein, we evaluate the immune protective efficacy and mechanism of a scalable recombinant bovine lactoferrin (UBLF) expressed in <em>Pichia pastoris</em>. Guided by proteomic analysis indicating immune-regulatory potential, we employed a cold-stress murine model integrating physiological monitoring, serum immunology and 16 S rRNA sequencing to assess UBLF activity. Results showed that prophylactic oral UBLF effectively mitigated physiological deficits, preventing stress-induced weight loss (maintaining weight gain vs. −0.38 g loss in the model group) and hypothermia. Systemic inflammation was significantly attenuated by downregulating serum IL-6, IL-8, IL-1β, and TNF-α (P < 0.05), while bolstering serum immunoglobulin (IgG/IgA) levels and preserving thymic and splenic architecture. Crucially, UBLF exerted a protective effect on the lungs, significantly reducing the lung index (0.69 % vs. 1.16 % in the model group) and alleviating pulmonary pathologies, including alveolar wall thickening and inflammatory cell infiltration. Microbiome profiling demonstrated that UBLF ameliorated cold stress–induced gut dysbiosis by re-establishing normal microbial α-diversity and reducing the Firmicutes/Bacteroidetes ratio (from 1.48 to 0.98). This microbial restoration coincided with the selective enrichment of beneficial genera, notably <em>Akkermansia</em>. Collectively, our results suggest that the protective effects against cold stress–induced immunosuppression are linked to the concurrent restoration of gut microbial homeostasis and the mitigation of pulmonary inflammation, highlighting the potential involvement of the gut-lung axis. UBLF therefore emerges as a novel functional food ingredient with industrial scalability, designed to enhance host stress resilience via the gut-lung axis.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108353"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147399460","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-30DOI: 10.1016/j.fbio.2026.108386
Naseer Ahmad , Zhongshi Zhu , Fu Xingwei , Li Danni , Wen Qinghua , Lei Zhang , Hao Yuan , Yuxuan Song
Milk contains a rich profile of oligosaccharides, bioactive peptides and short-chain fatty acids that may beneficially modulate host–microbiome interactions, yet its mechanistic role in intestinal inflammation remains unclear. This study seeks to assess the protective benefits of sheep milk (SM) and cow milk (CM) in a dextran sodium sulfate (DSS) induced colitis model in mice, in light of the increasing interest in functional food ingredients for gut health and the management of inflammatory conditions. SM administration markedly reduced disease activity index, prevent body weight loss, preserved colon length and alleviated epithelial injury, demonstrating strong mitigation of DSS-induced pathology. These improvements were accompanied by significant suppression of pro-inflammatory cytokines (IL-1β, TNF-α, TLR4) and enhanced expression of mucosal barrier-associated genes (MUC1, MUC3, TFF3). Inflammatory and pathway analysis showed that SM down-regulated key inflammatory signaling markers (TNF-α, IL-1β, and MYD88), suggesting attenuation of TLR4–NF-κB signaling, and modulated short-chain fatty acids (SCFAs) receptor and oxidative response–related genes (Hcar2, Ffar2, Nrf2, HO1). 16 S rRNA sequencing revealed that SM selectively restored beneficial gut microbes, most notably Akkermansia, Duncaniella, and Ligilactobacillus, whereas CM produced minimal microbial recovery. SM also significantly increased fecal SCFAs including acetate, propionate and butyrate indicating reactivation of microbial fermentation pathways essential for epithelial repair. Together, these findings identify a coordinated Akkermansia-SCFAs intestinal barrier mechanism through which SM exerts superior protection compared with CM. This work highlights SM as a promising microbiome-active functional food ingredient with potential applications for supporting gut health and mitigating intestinal inflammation.
{"title":"Sheep milk protects while cow milk exacerbates DSS-induced colitis by differentially modulating the Akkermansia–short chain fatty acids–barrier axis","authors":"Naseer Ahmad , Zhongshi Zhu , Fu Xingwei , Li Danni , Wen Qinghua , Lei Zhang , Hao Yuan , Yuxuan Song","doi":"10.1016/j.fbio.2026.108386","DOIUrl":"10.1016/j.fbio.2026.108386","url":null,"abstract":"<div><div>Milk contains a rich profile of oligosaccharides, bioactive peptides and short-chain fatty acids that may beneficially modulate host–microbiome interactions, yet its mechanistic role in intestinal inflammation remains unclear. This study seeks to assess the protective benefits of sheep milk (SM) and cow milk (CM) in a dextran sodium sulfate (DSS) induced colitis model in mice, in light of the increasing interest in functional food ingredients for gut health and the management of inflammatory conditions. SM administration markedly reduced disease activity index, prevent body weight loss, preserved colon length and alleviated epithelial injury, demonstrating strong mitigation of DSS-induced pathology. These improvements were accompanied by significant suppression of pro-inflammatory cytokines (<em>IL-1β, TNF-α, TLR4</em>) and enhanced expression of mucosal barrier-associated genes (<em>MUC1, MUC3, TFF3</em>). Inflammatory and pathway analysis showed that SM down-regulated key inflammatory signaling markers (<em>TNF-α, IL-1β, and MYD88</em>), suggesting attenuation of <em>TLR4–NF-κB</em> signaling, and modulated short-chain fatty acids (SCFAs) receptor and oxidative response–related genes (<em>Hcar2, Ffar2, Nrf2, HO1</em>). 16 S rRNA sequencing revealed that SM selectively restored beneficial gut microbes, most notably <em>Akkermansia</em>, <em>Duncaniella</em>, and <em>Ligilactobacillus</em>, whereas CM produced minimal microbial recovery. SM also significantly increased fecal SCFAs including acetate, propionate and butyrate indicating reactivation of microbial fermentation pathways essential for epithelial repair. Together, these findings identify a coordinated <em>Akkermansia</em>-SCFAs intestinal barrier mechanism through which SM exerts superior protection compared with CM. This work highlights SM as a promising microbiome-active functional food ingredient with potential applications for supporting gut health and mitigating intestinal inflammation.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108386"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147399464","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-02-05DOI: 10.1016/j.fbio.2026.108427
Salinthip Thongdechsri , Chanathip Kamonnat , Tanatcha Sanguanphun , Pichnaree Kraokaew , Prapaporn Jattujan , Nakorn Niamnont , Stuart J. Smith , Scott F. Cummins , Nopporn Jongkamonwiwat , Prasert Sobhon , Krai Meemon
The black sea cucumber Holothuria leucospilota, an Asian traditional food and medicine, has been explored for health benefits, including neuroprotective effects. Although its anti-Parkinson's effects have been demonstrated, its potential anti-Alzheimer's effects remain unexplored. Therefore, this study aimed to investigate the effects and underlying mechanisms of H. leucospilota extracts on amyloid-β (Aβ) proteotoxicity in a Caenorhabditis elegans model of Alzheimer's disease (AD). All fractions of H. leucospilota extracts were proven to be non-toxic to C. elegans. Among them, the ethyl acetate fraction (HLEA) at 500 μg/mL exhibited the greatest efficacy due to its ability to delay Aβ-induced paralysis in muscular Aβ-expressing C. elegans. Moreover, HLEA at 500 μg/mL rescued the chemotaxis defects in neuronal Aβ-expressing worms. The levels of Aβ oligomers and deposits declined after HLEA treatment of AD worms. Correspondingly, HLEA alleviated Aβ toxicity by lowering ROS levels and extending the lifespan of AD worms. Furthermore, differential RNA sequencing analysis revealed that the lysosome, proteasome, and antioxidant pathways were activated in HLEA-treated AD worms. RT-qPCR assays confirmed that HLEA upregulated ubiquitin-proteasome system, autophago-lysosomal, and antioxidant genes. Moreover, HLEA treatment promoted the nuclear localization of key transcription factors, SKN-1 and DAF-16, along with upregulation of their downstream antioxidant genes, indicating activation of SKN-1 and DAF-16 signaling pathways. Lastly, mass spectrometry analysis revealed that HLEA was predominantly composed of triterpenoid saponins. In summary, HLEA at 500 μg/mL diminished Aβ proteotoxicity by activating the protein clearance mechanism and SKN-1 and DAF-16 stress resistance pathways in the C. elegans AD model.
黑海参(Holothuria leucospilota)是一种亚洲传统食品和药物,它对健康的益处,包括神经保护作用,已经得到了探索。尽管其抗帕金森病的作用已被证实,但其潜在的抗阿尔茨海默病的作用仍未被探索。因此,本研究旨在探讨白螺杆藻提取物对阿尔茨海默病(AD)秀丽隐杆线虫模型中淀粉样蛋白-β (a β)蛋白毒性的影响及其机制。结果表明,各部位提取物对秀丽隐杆线虫均无毒性。其中,500 μg/mL乙酸乙酯部位(HLEA)对a β-表达的秀丽隐杆线虫具有延缓麻痹的作用,效果最好。此外,500 μg/mL的HLEA可修复表达神经元a β的线虫的趋化性缺陷。HLEA处理AD蠕虫后,Aβ低聚物和沉积水平下降。相应地,HLEA通过降低ROS水平和延长AD蠕虫的寿命来减轻Aβ毒性。此外,差异RNA测序分析显示,在hlea处理的AD蠕虫中,溶酶体、蛋白酶体和抗氧化途径被激活。RT-qPCR检测证实,HLEA上调泛素-蛋白酶体系统、自噬溶酶体和抗氧化基因。此外,HLEA处理促进了关键转录因子SKN-1和DAF-16的核定位,并上调了其下游抗氧化基因,表明SKN-1和DAF-16信号通路被激活。质谱分析表明,HLEA主要由三萜皂苷组成。综上所述,500 μg/mL的HLEA通过激活秀丽隐杆线虫AD模型中的蛋白质清除机制和SKN-1和DAF-16抗性途径,降低了Aβ蛋白毒性。
{"title":"Triterpenoid saponin-containing Holothuria leucospilota extract mitigates amyloid-β proteotoxicity in transgenic C. elegans through activations of protein clearance and stress resistance pathways","authors":"Salinthip Thongdechsri , Chanathip Kamonnat , Tanatcha Sanguanphun , Pichnaree Kraokaew , Prapaporn Jattujan , Nakorn Niamnont , Stuart J. Smith , Scott F. Cummins , Nopporn Jongkamonwiwat , Prasert Sobhon , Krai Meemon","doi":"10.1016/j.fbio.2026.108427","DOIUrl":"10.1016/j.fbio.2026.108427","url":null,"abstract":"<div><div>The black sea cucumber <em>Holothuria leucospilota</em>, an Asian traditional food and medicine, has been explored for health benefits, including neuroprotective effects. Although its anti-Parkinson's effects have been demonstrated, its potential anti-Alzheimer's effects remain unexplored. Therefore, this study aimed to investigate the effects and underlying mechanisms of <em>H. leucospilota</em> extracts on amyloid-β (Aβ) proteotoxicity in a <em>Caenorhabditis elegans</em> model of Alzheimer's disease (AD). All fractions of <em>H. leucospilota</em> extracts were proven to be non-toxic to <em>C. elegans.</em> Among them, the ethyl acetate fraction (HLEA) at 500 μg/mL exhibited the greatest efficacy due to its ability to delay Aβ-induced paralysis in muscular Aβ-expressing <em>C. elegans</em>. Moreover, HLEA at 500 μg/mL rescued the chemotaxis defects in neuronal Aβ-expressing worms. The levels of Aβ oligomers and deposits declined after HLEA treatment of AD worms. Correspondingly, HLEA alleviated Aβ toxicity by lowering ROS levels and extending the lifespan of AD worms. Furthermore, differential RNA sequencing analysis revealed that the lysosome, proteasome, and antioxidant pathways were activated in HLEA-treated AD worms. RT-qPCR assays confirmed that HLEA upregulated ubiquitin-proteasome system, autophago-lysosomal, and antioxidant genes. Moreover, HLEA treatment promoted the nuclear localization of key transcription factors, SKN-1 and DAF-16, along with upregulation of their downstream antioxidant genes, indicating activation of SKN-1 and DAF-16 signaling pathways. Lastly, mass spectrometry analysis revealed that HLEA was predominantly composed of triterpenoid saponins. In summary, HLEA at 500 μg/mL diminished Aβ proteotoxicity by activating the protein clearance mechanism and SKN-1 and DAF-16 stress resistance pathways in the <em>C. elegans</em> AD model.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108427"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147399596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-26DOI: 10.1016/j.fbio.2026.108377
Yingying Huang , Yanchun Shao , Chenglong Yang , István Molnár
Monascus azaphilone pigments (MPs) are widely used functional food additives. However, Monascus may simultaneously produce the mycotoxin citrinin (CIT), compromising MPs safety. Here, we used comparative genome, transcriptome, and quantitative data-independent acquisition mass spectrometry (DIA-MS) proteome analyses to compare three representative Monascus purpureus strains: M3 with high MPs and high CIT titers, M34 with high MPs and low CIT titers, and M69 with low titers of both products. Comparative genomic analysis confirmed high similarity among these strains. Differentially expressed genes (DEGs) and differentially abundant proteins (DAPs) were identified by pairwise comparisons among the strains during peak metabolite production, and selected DEGs and DAPs were verified by reverse transcription quantitative polymerase chain reaction and parallel reaction monitoring. An integrated analysis revealed DEG/DAPs correlating with altered MPs and CIT production, providing insights for strain breeding to engineer safer and more efficient MPs production processes in the food, cosmetics and pharmaceutical industries.
{"title":"Integrated transcriptome and data-independent acquisition proteome analysis of the biosynthesis of Monascus azaphilone pigments and citrinin","authors":"Yingying Huang , Yanchun Shao , Chenglong Yang , István Molnár","doi":"10.1016/j.fbio.2026.108377","DOIUrl":"10.1016/j.fbio.2026.108377","url":null,"abstract":"<div><div><em>Monascus</em> azaphilone pigments (MPs) are widely used functional food additives. However, <em>Monascus</em> may simultaneously produce the mycotoxin citrinin (CIT), compromising MPs safety. Here, we used comparative genome, transcriptome, and quantitative data-independent acquisition mass spectrometry (DIA-MS) proteome analyses to compare three representative <em>Monascus purpureus</em> strains: M3 with high MPs and high CIT titers, M34 with high MPs and low CIT titers, and M69 with low titers of both products. Comparative genomic analysis confirmed high similarity among these strains. Differentially expressed genes (DEGs) and differentially abundant proteins (DAPs) were identified by pairwise comparisons among the strains during peak metabolite production, and selected DEGs and DAPs were verified by reverse transcription quantitative polymerase chain reaction and parallel reaction monitoring. An integrated analysis revealed DEG/DAPs correlating with altered MPs and CIT production, providing insights for strain breeding to engineer safer and more efficient MPs production processes in the food, cosmetics and pharmaceutical industries.</div></div>","PeriodicalId":12409,"journal":{"name":"Food Bioscience","volume":"77 ","pages":"Article 108377"},"PeriodicalIF":5.9,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076304","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}