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International Journal of Membranes Review Article

Nutrition Induced Remodeling Dynamics of Cell Membranes: Implications for Performance, Health, and Welfare Issues in Food Animals

  1. Md. Emran Hossain Department of Animal Science and Nutrition, Chattogram Veterinary and Animal Sciences University, Khulshi

Abstract

Cell membranes represent dynamic structural and functional platforms that integrate nutritional signals with cellular metabolism, immune competence, and physiological adaptation in food animals. Beyond their classical role as selective barriers, membranes actively regulate nutrient transport, signal transduction, and bioenergetics through highly responsive lipid and protein networks. Dietary components, particularly fatty acids, vitamins, minerals, amino acids, and bioactive compounds, critically influence membrane composition, fluidity, and stability, thereby shaping cellular function and systemic performance. Nutrition induced membrane remodeling operates through coordinated mechanisms involving lipid turnover, oxidative balance, and microbiota mediated metabolic interactions, which collectively determine membrane resilience under physiological and environmental stress. These remodeling processes exert profound effects on mitochondrial efficiency, gut barrier integrity, immune responsiveness, and neurocellular plasticity, linking membrane biology directly to growth efficiency, feed conversion, thermoregulation, health outcomes, and animal welfare. Emerging evidence highlights that targeted nutritional strategies can mitigate oxidative membrane damage, enhance disease resistance, and improve behavioral and stress related responses, particularly in intensive production systems. Advanced methodological approaches including lipidomics, biophysical imaging, and biomarker profiling now enable deeper characterization of membrane dynamics and their nutritional modulation. Despite significant progress, critical knowledge gaps remain regarding tissue specific remodeling patterns, long term functional consequences, and translational applicability under commercial farm conditions. This review synthesizes current mechanistic and applied insights into nutrition driven membrane remodeling in food animals, emphasizes its relevance for sustainable and welfare-oriented production, and outlines future directions including integrative multiomics and precision nutrition approaches aimed at optimizing membrane function for improved productivity and health.

Keywords

References (94)

  1. Lopreiato V, Mezzetti M, Cattaneo L, Ferronato G, Minuti A, Trevisi E. Role of nutraceuticals during the transition period of dairy cows: a review. J Anim Sci Biotechnol. 2020 Aug 27;11(1):96.
  2. Plaizier JC, Mesgaran MD, Derakhshani H, Golder H, Khafipour E, Kleen JL, et al. Enhancing gastrointestinal health in dairy cows. 2018 Dec;12(S2):S399–418.
  3. Abdisa T. Review on the reproductive health problem of dairy cattle. Dairy Vet Sci J. 2018 Feb 5;5(1):555655.
  4. Herich R, Szabóová R, Karaffová V, et al. A narrative review on the impact of probiotic supplementation on muscle development, metabolic regulation, and fiber traits related to meat quality. 2025. Available from: https://pmc.ncbi.nlm.nih.gov/articles/PMC12029878/.
  5. Soliman SM, El-Saadony MT, Saad A, Mosa WF, Khalil Ameen FM, Ezzat Ahmed A, et al. The impacts of thermal stress on dairy cattle physiology, metabolism, health, and performance–a comprehensive review. Ann Anim Sci. 2026 Jan 30;26(1):27–50.
  6. Yan R, Zeng X, Shen J, Wu Z, Guo Y, Du Q, et al. New clues for postbiotics to improve host health: A review from the perspective of function and mechanisms. J Sci Food Agric. 2024 Aug 30;104(11):6376–87.
  7. Clemente-Suárez VJ, Rubio-Zarapuz A, Belinchón-deMiguel P, Beltrán-Velasco AI, Martín-Rodríguez A, Tornero-Aguilera JF. Impact of physical activity on cellular metabolism across both neurodegenerative and general neurological conditions: A narrative review. 2024 Nov 22;13(23):1940.
  8. Jamwal S, Jena MK, Tyagi N, Kancharla S, Kolli P, Mandadapu G, et al. Proteomic approaches to unravel the molecular dynamics of early pregnancy in farm animals: An in-depth review. J Dev Biol. 2023 Dec 30;12(1):2.
  9. Holwerda AM, van Loon LJC. The impact of collagen protein ingestion on musculoskeletal connective tissue remodeling: A narrative review. Nutr Rev. 2022 Jun 1;80(6):1497–514.
  10. Wei X, Tsai T, Howe S, Zhao J. Weaning induced gut dysfunction and nutritional interventions in nursery pigs: A partial review. Animals (Basel). 2021 Apr 29;11(5):1279.
  11. Latino F, Cataldi S, Carvutto R, De Candia M, D’Elia F, Patti A, et al. The importance of lipidomic approach for mapping and exploring the molecular networks underlying physical exercise: A systematic review. Int J Mol Sci. 2021 Aug 13;22(16):8734.
  12. Ribeiro ES. Symposium review: Lipids as regulators of conceptus development: Implications for metabolic regulation of reproduction in dairy cattle. J Dairy Sci. 2018 Apr 1;101(4):3630–41.
  13. Wysoczański T, Sokoła-Wysoczańska E, Pękala J, Lochyński S, Czyż K, Bodkowski R, et al. Omega-3 Fatty Acids and their Role in Central Nervous System - A Review. Current Medicinal Chemistry. 2016;23(8):816-831. doi:10.2174/0929867323666160122114439
  14. Gefen A, Weihs D. Mechanical cytoprotection: A review of cytoskeleton-protection approaches for cells. J Biomech. 2016;49(9):1321–9. Available from https://www.sciencedirect.com/ science/article/pii/S0021929015005783.
  15. Amawi A, AlKasasbeh W, Jaradat M, Almasri A, Alobaidi S, Hammad AA, et al. Athletes’ nutritional demands: a narrative review of nutritional requirements. Frontiers in Nutrition. 2024;10. doi:10.3389/fnut.2023.1331854
  16. Yüksel E, Kort R, Voragen AGJ. Structure and degradation dynamics of dietary pectin. Critical Reviews in Food Science and Nutrition. 2024;65(29):6249-6268. doi:10.1080/10408398.2024.2437573
  17. Mahajan R, Lau DH, Brooks AG, Shipp NJ, Manavis J, Wood JPM, et al. Electrophysiological, Electroanatomical, and Structural Remodeling of the Atria as Consequences of Sustained Obesity. Journal of the American College of Cardiology. 2015;66(1):1-11. doi:10.1016/j.jacc.2015.04.058
  18. Geay Y, Bauchart D, Hocquette JF, et al. Effect of nutritional factors on biochemical, structural and metabolic characteristics of muscles in ruminants: Consequences on dietetic value and sensory qualities of meat. Reprod Nutr Dev. 2001;41(1):1–26. Available from: https://rnd.edpsciences.org/articles/rnd/abs/2001/01/r1101/r1101.html.
  19. Jeong JH, Han JS, Jung Y, Lee SM, Park SH, et al. A new AMPK isoform mediates glucose-restriction-induced longevity non-cell autonomously by promoting membrane fluidity. Nat Commun. 2023;14:35952. Available from: https://www.nature.com/articles/s41467-023-35952-z.
  20. Li Y, et al. Ruminal fluid transplantation accelerates rumen microbial remodeling and improves feed efficiency in yaks. 2023;11(8):1964. Available from: https://www.mdpi.com/2076-2607/11/8/1964.
  21. Patra AK, Kar I. Heat stress effects on microbiota composition, gut barrier integrity, nutrient transport, and production performance in farm animals and strategies for amelioration. Animals (Basel). 2021;11(4):1007. Available from: https://pmc.ncbi.nlm.nih.gov/articles/PMC8071753/.
  22. Reis A, Perez-Gregorio R, Mateus N, de Freitas V. Interactions of dietary polyphenols with epithelial lipids: advances from membrane and cell models in the study of polyphenol absorption, transport and delivery to the epithelium. Critical Reviews in Food Science and Nutrition. 2020;61(18):3007-3030. doi:10.1080/10408398.2020.1791794
  23. Stringer DM, Zahradka P, Taylor CG. Glucose transporters: Cellular links to hyperglycemia in insulin resistance and diabetes. Nutr Rev. 2015;73(3):140–54. Available from: https://academic.oup.com/nutritionreviews/article-abstract/73/3/140/1837371.
  24. Stringer DM, Zahradka P, Taylor CG. Glucose transporters: Cellular links to hyperglycemia in insulin resistance and diabetes. Nutr Rev. 2015;73(3):140–54. Available from: https://academic.oup.com/nutritionreviews/article-abstract/73/3/140/1837371.
  25. Li L, et al. Dietary supplementation with naringin improves systemic metabolic status and alleviates oxidative stress in transition cows via modulation of adipose tissue metabolism. Antioxidants (Basel). 2024;13(6):638. Available from: https://www.mdpi.com/2076–3921/13/6/638.
  26. Machado SA, Pasquarelli-do-Nascimento G, da Silva DS, Farias GR, de Oliveira Santos I, Baptista LB, et al. Browning of the white adipose tissue regulation: new insights into nutritional and metabolic relevance in health and diseases. Nutrition & Metabolism. 2022;19(1). doi:10.1186/s12986-022-00694-0
  27. Winn NC, Cottam MA, Wasserman DH, Hasty AH. Exercise and Adipose Tissue Immunity: Outrunning Inflammation. Obesity. 2021;29(5):790-801. doi:10.1002/oby.23147
  28. Daemen S, van Polanen N, et al. The effect of diet and exercise on lipid droplet dynamics in human muscle tissue. J Exp Biol. 2018;221(Suppl 1):jeb167015. Available from: https://journals.biologists.com/jeb/article-abstract/221/Suppl_1/jeb167015/34002.
  29. Daemen S, van Polanen N, et al. The effect of diet and exercise on lipid droplet dynamics in human muscle tissue. J Exp Biol. 2018;221(Suppl 1):jeb167015. Available from: https://journals.biologists.com/jeb/article-abstract/221/Suppl_1/jeb167015/34002.
  30. Boengler K, Kosiol M, Mayr M, Schulz R, Rohrbach S. Mitochondria and ageing: role in heart, skeletal muscle and adipose tissue. Journal of Cachexia, Sarcopenia and Muscle. 2017;8(3):349-369. doi:10.1002/jcsm.12178
  31. Penke B, Paragi G, Gera J, Berkecz R, et al. The role of lipids and membranes in the pathogenesis of Alzheimer’s disease: A comprehensive view. Curr Alzheimer Res. 2018;15(13):1191-212. Available from: https://www.ingentaconnect.com/content/ben/car/2018/00000015/00000013 /art00002.
  32. Reis A, de Freitas V. When polyphenols meet lipids: challenges in membrane biophysics and opportunities in epithelial lipidomics. Food Chem. 2020;321:126702. Available from: https://www.sciencedirect.com/science/article/pii/S0308814620313716.
  33. Mavrommatis A, Tsiplakou E, Zerva A, Pantiora PD, Georgakis ND, Tsintzou GP, et al. Microalgae as a Sustainable Source of Antioxidants in Animal Nutrition, Health and Livestock Development. Antioxidants. 2023;12(10):1882. doi:10.3390/antiox12101882
  34. Pinilla-González V, Rojas-Solé C, Gómez-Hevia F, et al. Tapping into nature’s arsenal: Harnessing the potential of natural antioxidants for human health and disease prevention. 2024;13(13):1999. Available from: https://www.mdpi.com/2304-8158/13/13/1999.
  35. Vignaud J, Loiseau C, Hérault J, Mayer C, Côme M, et al. Microalgae produce antioxidant molecules with potential preventive effects on mitochondrial functions and skeletal muscular oxidative stress. Antioxidants (Basel). 2023;12(5):1050. Available from: https://www.mdpi.com/ 2076-3921/12/5/1050.
  36. Ferramosca A, Zara V. Diet and male fertility: The impact of nutrients and antioxidants on sperm energetic metabolism. Int J Mol Sci. 2022;23(5):2542. Available from: https://www.mdpi.com/ 1422–0067/23/5/2542.
  37. Pang BPS, Chan WS, Chan CB. Mitochondria homeostasis and oxidant/antioxidant balance in skeletal muscle—do myokines play a role? Antioxidants (Basel). 2021;10(2):179. Available from: https://www.mdpi.com/2076-3921/10/2/179.
  38. Skaperda Z, Veskoukis AS, et al. Farm animal welfare, productivity and meat quality: Interrelation with redox status regulation and antioxidant supplementation as a nutritional intervention. World Acad Sci J. 2019;1(4):177–90. Available from: https://www.spandidos-publications.com/wasj/ 1/4/177.
  39. Surai PF, Kochish II, Fisinin VI, Kidd MT. Antioxidant defence systems and oxidative stress in poultry biology: An update. Antioxidants (Basel). 2019;8(7):235. Available from: https://www.mdpi.com/2076–3921/8/7/235.
  40. Brancaccio M, Mennitti C, Cesaro A, Fimiani F, et al. The biological role of vitamins in athletes’ muscle, heart and microbiota. Int J Environ Res Public Health. 2022;19(3):1249. Available from: https://www.mdpi.com/1660–4601/19/3/1249.
  41. Crescioli C. Vitamin D restores skeletal muscle cell remodeling and myogenic program: Potential impact on human health. Int J Mol Sci. 2021;22(4):1760. Available from: https://www.mdpi.com/ 1422-0067/22/4/1760.
  42. Vieira-Neto A, Lean IJ, Santos JEP. Periparturient mineral metabolism: Implications for health and productivity. Animals (Basel). 2024;14(8):1232. Available from: https://www.mdpi.com/2076–2615/14/8/1232.
  43. Wu G, Bazer FW, Dai Z, Li D, Wang J, Wu Z. Amino acid nutrition in animals: protein synthesis and beyond. Annu Rev Anim Biosci. 2014;2:387–417. doi:10.1146/annurev-animal-022513–114113.
  44. Corsetti G, Pasini E, Scarabelli TM, Romano C, Singh A, et al. Importance of energy, dietary protein sources, and amino acid composition in the regulation of metabolism: An indissoluble dynamic combination for life. 2024;16(15):2417. Available from: https://www. mdpi.com/2072-6643/16/15/2417.
  45. Xie X, et al. Lipid metabolism in germinated tree peony (Paeonia suffruticosa) seeds: From energy mobilization to nutrient accumulation. Food Chem. 2025;451:138936. Available from: https://www.sciencedirect.com/science/article/pii/S0308814625027050.
  46. Nicolson GL, de Mattos GF, Ash M, Settineri R, et al. Fundamentals of membrane lipid replacement: A natural medicine approach to repairing cellular membranes and reducing fatigue, pain, and other symptoms. Membranes (Basel). 2021;11(12):944. Available from: https://www.mdpi.com/2077–0375/11/12/944.
  47. De la Fuente FP, Quezada L, Sepúlveda C, et al. Exercise regulates lipid droplet dynamics in normal and fatty liver. Biochim Biophys Acta Mol Cell Biol Lipids. 2019;1864(12):158519. Available from: https://www.sciencedirect.com/science/article/pii/S1388198119301593.
  48. Hao Y, Xing M, Gu X. Research progress on oxidative stress and its nutritional regulation strategies in pigs. Animals (Basel). 2021;11(5):1384. Available from: https://www.mdpi.com/2076–2615/11/5/1384.
  49. Vargas-Mendoza N, Angeles-Valencia M, et al. Oxidative stress, mitochondrial function and adaptation to exercise: New perspectives in nutrition. Life (Basel). 2021;11(11):1269. Available from: https://www.mdpi.com/2075–1729/11/11/1269.
  50. Iddir M, Brito A, Dingeo G, Del Campo SSF, et al. Strengthening the immune system and reducing inflammation and oxidative stress through diet and nutrition: Considerations during the COVID-19 crisis. 2020;12(6):1562. Available from: https://www.mdpi.com/2072–6643/12/6/1562.
  51. Celi P, Gabai G. Oxidant/Antioxidant Balance in Animal Nutrition and Health: The Role of Protein Oxidation. Frontiers in Veterinary Science. 2015;2. doi:10.3389/fvets.2015.00048
  52. Perin M, Chinigò G, Genova T, Mussano F, Munaron L. The Impact of Plasma Membrane Ion Channels on Bone Remodeling in Response to Mechanical Stress, Oxidative Imbalance, and Acidosis. Antioxidants. 2023;12(3):689. doi:10.3390/antiox12030689
  53. Kumar KMK, Nagesh R, Kumar MN, et al. Oxidative stress in modulation of immune function in livestock. In: Recent Issues in Climate Smart Livestock Production. Elsevier; 2022. Available from: https://www.sciencedirect.com/science/article/pii/B9780128222652000089.
  54. Ciancarelli I, Morone G, Iosa M, Cerasa A, Calabrò RS, Iolascon G, et al. Influence of Oxidative Stress and Inflammation on Nutritional Status and Neural Plasticity: New Perspectives on Post-Stroke Neurorehabilitative Outcome. Nutrients. 2022;15(1):108. doi:10.3390/nu15010108
  55. Santhiravel S, Bekhit AEDA, Mendis E, Jacobs JL, Dunshea FR, Rajapakse N, et al. The Impact of Plant Phytochemicals on the Gut Microbiota of Humans for a Balanced Life. International Journal of Molecular Sciences. 2022;23(15):8124. doi:10.3390/ijms23158124
  56. Garrido-Romero M, Díez-Municio M, Moreno FJ. Exploring the impact of olive-derived bioactive components on gut microbiota: Implications for digestive health. 2025;14(14):2413. Available from: https://www.mdpi.com/2304–8158/14/14/2413.
  57. Schneider E, O’Riordan KJ, Clarke G, Cryan JF. Feeding gut microbes to nourish the brain: Unravelling the diet–microbiota–gut–brain axis. Nat Metab. Available from: https://www.nature.com/articles/s42255-024-01108-6.
  58. Wang X, Qi Y, Zheng H. Dietary Polyphenol, Gut Microbiota, and Health Benefits. Antioxidants. 2022;11(6):1212. doi:10.3390/antiox11061212
  59. González Olmo BM, Butler MJ, Barrientos RM. Evolution of the Human Diet and Its Impact on Gut Microbiota, Immune Responses, and Brain Health. Nutrients. 2021;13(1):196. doi:10.3390/nu13010196
  60. Esposito G, Irons PC, Webb EC, Chapwanya A. Interactions between negative energy balance, metabolic diseases, uterine health and immune response in transition dairy cows. Animal Reproduction Science. 2014;144(3-4):60-71. doi:10.1016/j.anireprosci.2013.11.007
  61. Hassan FU, Nadeem A, Li Z, Javed M, Liu Q, Azhar J, et al. Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Energy Homeostasis of Dairy Animals: Exploiting Their Modulation through Nutrigenomic Interventions. International Journal of Molecular Sciences. 2021;22(22):12463. doi:10.3390/ijms222212463
  62. Jiang S, Yan FF, Hu JY, Mohammed A, Cheng HW. Bacillus subtilis-Based Probiotic Improves Skeletal Health and Immunity in Broiler Chickens Exposed to Heat Stress. Animals. 2021;11(6):1494. doi:10.3390/ani11061494
  63. Osorio JS. Gut health, stress, and immunity in neonatal dairy calves: the host side of host-pathogen interactions. Journal of Animal Science and Biotechnology. 2020;11(1). doi:10.1186/s40104-020-00509-3
  64. Barathan M, Ng SL, Lokanathan Y, Ng MH, Law JX. The Profound Influence of Gut Microbiome and Extracellular Vesicles on Animal Health and Disease. International Journal of Molecular Sciences. 2024;25(7):4024. doi:10.3390/ijms25074024
  65. Shehata AA, Yalçın S, Latorre JD, Basiouni S, Attia YA, Abd El-Wahab A, et al. Probiotics, Prebiotics, and Phytogenic Substances for Optimizing Gut Health in Poultry. Microorganisms. 2022;10(2):395. doi:10.3390/microorganisms10020395
  66. Mattson MP, Leak RK. The hormesis principle of neuroplasticity and neuroprotection. Cell Metab. Available from: https://www.cell.com/cell-metabolism/fulltext/S1550–4131(23)00473–4.
  67. Palmano K, Rowan A, Guillermo R, Guan J, McJarrow P. The Role of Gangliosides in Neurodevelopment. Nutrients. 2015;7(5):3891-3913. doi:10.3390/nu7053891
  68. Clemente-Suárez VJ, Martín-Rodríguez A, et al. Neuro-nutrition and exercise synergy: Exploring the bioengineering of cognitive enhancement and mental health optimization. Bioengineering (Basel). 2025;12(2):208. Available from: https://www.mdpi.com/2306-5354/12/2/208.
  69. Stefanello C, Rosa DP, Dalmoro YK, Segatto AL, Vieira MS, Moraes ML, et al. Protected Blend of Organic Acids and Essential Oils Improves Growth Performance, Nutrient Digestibility, and Intestinal Health of Broiler Chickens Undergoing an Intestinal Challenge. Frontiers in Veterinary Science. 2020;6. doi:10.3389/fvets.2019.00491
  70. Jize Z, Zhuoga D, Xiaoqing Z, Na T, Jiacuo G, Cuicheng L, et al. Different feeding strategies can affect growth performance and rumen functions in Gangba sheep as revealed by integrated transcriptome and microbiome analyses. Frontiers in Microbiology. 2022;13. doi:10.3389/fmicb.2022.908326
  71. Millward DJ. Interactions between Growth of Muscle and Stature: Mechanisms Involved and Their Nutritional Sensitivity to Dietary Protein: The Protein-Stat Revisited. Nutrients. 2021;13(3):729. doi:10.3390/nu13030729
  72. Zhao JX, Li Q, Zhang RX, Liu WZ, Ren YS, et al. Effect of dietary grape pomace on growth performance, meat quality and antioxidant activity in ram lambs. Anim Feed Sci Technol. 2018;236:76–85. Available from: https://www.sciencedirect.com/science/article/pii/S0377840 117312555.
  73. Koletzko B, Aggett PJ, Bindels JG, Bung P, et al. Growth, development and differentiation: A functional food science approach. Br J Nutr. 1998;80(Suppl 1):S5–S45. Available from: https://www.cambridge.org/core/journals/british-journal-of-nutrition/article/growth-development-and-differentiation-a-functional-food-science-approach/3D543771FDD804529A80B473FF6BC65D.
  74. Abdelli N, Solà-Oriol D, Pérez JF. Phytogenic Feed Additives in Poultry: Achievements, Prospective and Challenges. Animals. 2021;11(12):3471. doi:10.3390/ani11123471
  75. Jackman JA, Boyd RD, Elrod CC. Medium-chain fatty acids and monoglycerides as feed additives for pig production: towards gut health improvement and feed pathogen mitigation. Journal of Animal Science and Biotechnology. 2020;11(1). doi:10.1186/s40104-020-00446-1
  76. De Lange CFM, Pluske J, Gong J, Nyachoti CM. Strategic use of feed ingredients and feed additives to stimulate gut health and development in young pigs. Livest Sci. 2010;134(1–3):124–34. Available from: https://www.sciencedirect.com/science/article/pii/S187114131000329X.
  77. Baumgard LH, Rhoads RP, Rhoads ML, Gabler NK, Ross JW, Keating AF, et al. Impact of Climate Change on Livestock Production. Environmental Stress and Amelioration in Livestock Production. 2012:413-468. doi:10.1007/978-3-642-29205-7_15
  78. Kirgiafini D, Kyrgiafini MA, Gournaris T, Mamuris Z. Understanding Circular RNAs in Health, Welfare, and Productive Traits of Cattle, Goats, and Sheep. Animals. 2024;14(5):733. doi:10.3390/ani14050733
  79. Vlasova AN, Saif LJ. Bovine Immunology: Implications for Dairy Cattle. Frontiers in Immunology. 2021;12. doi:10.3389/fimmu.2021.643206
  80. Qiao K, Jiang R, Contreras GA, Xie L, Pascottini OB, Opsomer G, et al. The Complex Interplay of Insulin Resistance and Metabolic Inflammation in Transition Dairy Cows. Animals. 2024;14(6):832. doi:10.3390/ani14060832
  81. Sato T, Sato S. Circadian regulation of metabolism: Commitment to health and diseases. 2023;164(7):bqad086. Available from: https://academic.oup.com/endo/article-abstract/164/7/bqad086/7186648.
  82. Li X, et al. Understanding the causes of keel bone damage and its effects on the welfare of laying hens. Animals (Basel). 2024;14(24):3655. Available from: https://www.mdpi.com/2076–2615/14/24/3655.
  83. Bertoni G, Trevisi E, Houdijk J, Calamari L, Athanasiadou S. Welfare Is Affected by Nutrition Through Health, Especially Immune Function and Inflammation. Animal Welfare. 2016:85-113. doi:10.1007/978-3-319-27356-3_5
  84. Nutrition and the Welfare of Farm Animals. Animal Welfare. 2016. doi:10.1007/978-3-319-27356-3
  85. Dauncey MJ. Nutrition, environment and gene expression: impact on health, welfare and production. In: Nutrition, Environment and Gene Expression. Wallingford: CABI Publishing; 2014. Available from: https://www.researchgate.net.
  86. Ayaz A, Zaman W, Radák Z, Gu Y. Green strength: the role of micronutrients in plant-based diets for athletic performance enhancement. 2024;10:e8834. Available from: https://www.cell.com/heliyon/fulltext/S2405–8440(24)08834–0.
  87. Watson RR, Preedy VR, Zibadi S, editors. Polyphenols in Human Health and Disease. Amsterdam: Academic Press; 2013.
  88. Cheeke PR, Dierenfeld ES. Comparative Animal Nutrition and Metabolism. Wallingford: CABI Publishing; 2010.
  89. Case LP, Daristotle L, Hayek MG, Raasch MF. Canine and feline nutrition: A resource for companion animal professionals. Elsevier Health Sciences; 2010 May 19. Huang C, Li Y, Wang K, Xi J, Xu Y, Si X, Pei D, Lyu S, Xia G, Wang J, Li P. Analysis of lipidomics profile of Carya cathayensis nuts and lipid dynamic changes during embryonic development. Food Chem. 2022 Feb 15;370:130975.
  90. Hyötyläinen T, Bondia-Pons I, Orešič M. Lipidomics in nutrition and food research. Mol Nutr Food Res. 2013 Aug;57(8):1306–18.
  91. Markus I, Constantini K, Hoffman JR, Bartolomei S, Gepner Y. Exercise-induced muscle damage: Mechanism, assessment and nutritional factors to accelerate recovery. Eur J Appl Physiol. 2021 Apr;121(4):969–92.
  92. Pande S, Raisuddin S. Molecular and cellular regulatory roles of sirtuin protein. Crit Rev Food Sci Nutr. 2023 Nov 17;63(29):9895–913.
  93. Lee S, Kelleher SL. Biological underpinnings of breastfeeding challenges: The role of genetics, diet, and environment on lactation physiology. Am J Physiol Endocrinol Metab. 2016 Aug 1;311(2):E405–22.
  94. Lee S, Kelleher SL. Biological underpinnings of breastfeeding challenges: The role of genetics, diet, and environment on lactation physiology. Am J Physiol Endocrinol Metab. 2016 Aug 1;311(2):E405–22.