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The effects of plant extracts on lipid metabolism of chickens — A review

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The fat deposition is an important factor affecting chicken meat quality, which is closely related to lipid metabolism of chickens. Therefore, it is important to regulate the lipid metabolism of chickens to improve the chicken meat quality. Plant extracts have special regulatory effects on animal’s growth and health and have been widely used in chicken breeding. Some plant extracts have been reported to have functions of changing the fatty acid composition, reducing abdominal fat percentage, and enhancing the intramuscular fat content of chickens by improving the antioxidant capacity, regulating the expression of genes, enzymes, and signaling pathways related to lipid metabolism, modulating intestinal microbiota, affecting hormones level, and regulating DNA methylation. This paper reviewed the application and mechanism of plant extracts on regulating lipid metabolism of chickens to provide a reference for the further application of plant extracts in chicken breeding.

Abstract

The fat deposition is an important factor affecting chicken meat quality, which is closely related to lipid metabolism of chickens. Therefore, it is important to regulate the lipid metabolism of chickens to improve the chicken meat quality. Plant extracts have special regulatory effects on animal’s growth and health and have been widely used in chicken breeding. Some plant extracts have been reported to have functions of changing the fatty acid composition, reducing abdominal fat percentage, and enhancing the intramuscular fat content of chickens by improving the antioxidant capacity, regulating the expression of genes, enzymes, and signaling pathways related to lipid metabolism, modulating intestinal microbiota, affecting hormones level, and regulating DNA methylation. This paper reviewed the application and mechanism of plant extracts on regulating lipid metabolism of chickens to provide a reference for the further application of plant extracts in chicken breeding.

참고문헌 (96)

  1. Ordaz-Trinidad N, "Patents on phytochemicals : methodologies of extraction, application in food and pharmaceutical industry", Recent Pat Biotechnol, 9, pp.158~167 (2015)[DOI]
  2. Righi F, "Plant feed additives as natural alternatives to the use of synthetic antioxidant vitamins on poultry performances, health, and oxidative status : a review of the literature in the last 20 years", Antioxidants, 10, pp.659~ (2021)[DOI]
  3. Bosco AD, "Effect of slaughtering age in different commercial chicken genotypes reared according to the organic system : 1. Welfare, carcass and meat traits", Ital J Anim Sci, 13, pp.3308~ (2014)[DOI]
  4. Mahiza MIN, "Fatty acid profile in the breast and thigh muscles of the slow-and fast-growing birds under the same management system", Trop Anim Health Prod, 53, pp.409~ (2021)[DOI]
  5. Devatkal SK, "Quality, composition, and consumer evaluation of meat from slow-growing broilers relative to commercial broilers", Poult Sci, 98, pp.6177~6186 (2019)[DOI]
  6. Increasing efficiency of lean tissue deposition in broiler chickens, "Choct M", Rural Industries Research and Development Corporation, ~, pp.RIRDC Publication No 98 (2000), 123
  7. Demeure O, "Genome-wide interval mapping using SNPs identifies new QTL for growth, body composition and several physiological variables in an F2intercross between fat and lean chicken lines", Genet Sel Evol, 45, pp.36~ (2013)[DOI]
  8. Sohaib M, "Lipid stability, antioxidant potential and fatty acid composition of broilers breast meat as influenced by quercetin in combination with α-tocopherol enriched diets", Lipids Health Dis, 14, pp.61~ (2015)[DOI]
  9. Hager-Theodorides AL, "Hesperidin and naringin improve broiler meat fatty acid profile and modulate the expression of genes involved in fatty acid β-oxidation and antioxidant defense in a dose dependent manner", Foods, 10, pp.739~ (2021)[DOI]
  10. Wan Xiaoli, "Effects of lycopene on abdominal fat deposition, serum lipids levels and hepatic lipid metabolism-related enzymes in broiler chickens", Animal Bioscience, 34(3), pp.385~392 (2021), 아세아·태평양축산학회[DOI]
  11. Xie Z, "Curcumin supplementation regulates lipid metabolism in broiler chickens", Poult Sci, 98, pp.422~429 (2019)[DOI]
  12. Uwineza PA, "Recent advances in supercritical fluid extraction of natural bioactive compounds from natural plant materials", Molecules, 25, pp.3847~ (2020)[DOI]
  13. Lefebvre T, "Selective extraction of bioactive compounds from plants using recent extraction techniques : a review", J Chromatogr A, 1635, pp.461770~ (2021)[DOI]
  14. Lv Z, "Dietary genistein alleviates lipid metabolism disorder and inflammatory response in laying hens with fatty liver syndrome", Front Physiol, 9, pp.1493~ (2018)[DOI]
  15. Anna Stochmal, "Alfalfa (Medicago sativa L.) flavonoids. 2. tricin and chrysoeriol glycosides from aerial parts", Journal of Agricultural and Food Chemistry, 49(11), pp.5310~5314 (2001), American Chemical Society (ACS)[DOI]
  16. Ouyang K, "Effects of alfalfa flavonoids on broiler performance, meat quality, and gene expression", Can J Anim Sci, 96, pp.332~341 (2016)[DOI]
  17. Graham HN, "Green tea composition, consumption, and polyphenol chemistry", Prev Med, 21, pp.334~350 (1992)[DOI]
  18. Huang J, "Green tea polyphenols alleviate obesity in broiler chickens through the regulation of lipidmetabolism-related genes and transcription factor expression", J Agric Food Chem, 61, pp.8565~8572 (2013)[DOI]
  19. John Shi, "Polyphenolics in Grape Seeds―Biochemistry and Functionality", Journal of Medicinal Food, 6(4), pp.291~299 (2003), 한국식품영양과학회
  20. Farahat MH, "Effect of dietary supplementation of grape seed extract on the growth performance, lipid profile, antioxidant status and immune response of broiler chickens", Animal, 11, pp.771~777 (2017)[DOI]
  21. Gil MI, "Antioxidant activity of pomegranate juice and its relationship with phenolic composition and processing", J Agric Food Chem, 48, pp.4581~4589 (2000)[DOI]
  22. Shen M, "Effect of bamboo leaf extract on antioxidant status and cholesterol metabolism in broiler chickens", Animals, 9, pp.699~ (2019)[DOI]
  23. Shen MM, "Effects of bamboo leaf extract on growth performance, meat quality, and meat oxidative stability in broiler chickens", Poult Sci, 98, pp.6787~6796 (2019)[DOI]
  24. Shehzad A, "Curcumin in cancer chemoprevention : molecular targets, pharmacokinetics, bioavailability, and clinical trials", Arch Pharm, 343, pp.489~499 (2010)[DOI]
  25. Jia-li L, "Analyses of the contents of total flavonoids and hesperidin in citrus peel", Hunan Agric Sci, 11, pp.58~62 (2020)[DOI]
  26. Zuorro A, "Enzyme-assisted lycopene extraction from tomato processing waste", Enzyme Microb Technol, 49, pp.567~573 (2011)[DOI]
  27. Yusong Z, "Exploitation of sea bucthorn resource and extraction of flavone", Food Res Dev, 3, pp.46~47 (2005)[DOI]
  28. Ma JS, "Effects of flavones of sea buckthorn fruits on growth performance, carcass quality, fat deposition and lipometabolism for broilers", Poult Sci, 94, pp.2641~2649 (2015)[DOI]
  29. Fernández C, "Effect of source of betaine on growth performance and carcass traits in lambs", Anim Feed Sci Technol, 86, pp.71~82 (2000)[DOI]
  30. Leng Z, "Increased fatty acid β-oxidation as a possible mechanism for fat-reducing effect of betaine in broilers", Anim Sci J, 87, pp.1005~1010 (2016)[DOI]
  31. Ruiqi F, "Research on body fat distribution and deposition pattern of beijing-you chickens", Chinese J Anim Nutr, 25, pp.1465~1472 (2013)[DOI]
  32. Ghasemi HA, "Effect of synbiotic supplementation and dietary fat sources on broiler performance, serum lipids, muscle fatty acid profile and meat quality", Br Poult Sci, 57, pp.71~76 (2016)[DOI]
  33. Zhao GP, "Comparison of breast muscle meat quality in 2 broiler breeds", Poult Sci, 90, pp.2355~2359 (2011)[DOI]
  34. Wiktorowska-Owczarek A, "PUFAs : structures, metabolism and functions", Adv Clin Exp Med, 24, pp.931~941 (2015)[DOI]
  35. Ahmadipour B, "Evaluation of hepatic lipogenesis and antioxidant status of broiler chickens fed mountain celery", BMC Vet Res, 14, pp.234~ (2018)[DOI]
  36. Jiang ZY, "Effects of soybean isoflavone on growth performance, meat quality, and antioxidation in male broilers", Poult Sci, 86, pp.1356~1362 (2007)[DOI]
  37. Kamboh AA, "Individual and combined effects of genistein and hesperidin supplementation on meat quality in meat-type broiler chickens", J Sci Food Agric, 93, pp.3362~3367 (2013)[DOI]
  38. Zhao JS, "Effects of chlorogenic acid-enriched extract from Eucommia ulmoides leaf on performance, meat quality, oxidative stability, and fatty acid profile of meat in heat-stressed broilers", Poult Sci, 98, pp.3040~3049 (2019)[DOI]
  39. Lv Z, "Supplementing genistein for breeder hens alters the fatty acid metabolism and growth performance of offsprings by epigenetic modification", Oxid Med Cell Longev, 2019, pp.9214209~ (2019)[DOI]
  40. Oskoueian E, "Manipulation of broiler meat fatty acid composition using quercetin", 59th International Congress of Meat Science and Technology (2013)
  41. Kamboh AA, "Effect of increasing levels of bioflavonoids in broiler feed on plasma anti-oxidative potential, lipid metabolites, and fatty acid composition of meat", Poult Sci, 92, pp.454~461 (2013)[DOI]
  42. Galli GM, "Combination of herbal components(curcumin, carvacrol, thymol, cinnamaldehyde)in broiler chicken feed : Impacts on response parameters, performance, fatty acid profiles, meat quality and control of coccidia and bacteria", Microb Pathog, 139, pp.103916~ (2020)[DOI]
  43. Ahmed ST, "Meat composition, fatty acid profile and oxidative stability of meat from broilers supplemented with pomegranate(Punica granatum L. )by-products", Food Chem, 188, pp.481~488 (2015)[DOI]
  44. Ahmed ST, "Improving the nutritional quality and shelf life of broiler meat by feeding diets supplemented with fermented pomegranate(Punica granatum L. )byproducts", Br Poult Sci, 58, pp.694~703 (2017)[DOI]
  45. Kersten S, "Physiological regulation of lipoprotein lipase", Biochim Biophys Acta Mol Cell Biol Lipids, 1841, pp.919~933 (2014)[DOI]
  46. Han W, "A mutation in the chicken lipoprotein lipase gene is associated with adipose traits", Anim Prod Sci, 52, pp.905~910 (2012)[DOI]
  47. Griffin HD, "Contribution of lipoprotein lipase to differences in fatness between broiler and layer-strain chickens", Br Poult Sci, 28, pp.197~206 (1987)[DOI]
  48. Sato K, "Lipoprotein hydrolysis and fat accumulation in chicken adipose tissues are reduced by chronic administration of lipoprotein lipase monoclonal antibodies", Poult Sci, 78, pp.1286~1291 (1999)[DOI]
  49. Abudilida S, "Developmental Changes of A-FABP, H-FABP and PPAR-γ genes mRNA expression and its correlation with intramuscular fat content in baicheng you chicken", China Poult, 41, pp.5~11 (2019)[DOI]
  50. Wang Y, "Association of A-FABP gene polymorphism and mRNA expression with intramuscular fat content(IMF)in Baicheng-You chicken", J Anim Physiol Anim Nutr, 103, pp.1447~1452 (2019)[DOI]
  51. Wang Y, "Correlation of the A-FABP gene polymorphism and mRNA expression with intramuscular fat content in three-yellow chicken and hetian-black chicken", Anim Biotechnol, 28, pp.37~43 (2017)[DOI]
  52. Fu RQ, "Expression profiles of key transcription factors involved in lipid metabolism in Beijing-You chickens", Gene, 537, pp.120~125 (2014)[DOI]
  53. Cui H, "Identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens", BMC Genomics, 19, pp.55~ (2018)[DOI]
  54. Hassan FAM, "Growth performance, antioxidant capacity, lipid-related transcript expression and the economics of broiler chickens fed different levels of rutin", Animals, 9, pp.7~ (2019)[DOI]
  55. Ouyang WW, "Effect of quercetin on cAMP signaling pathway in chicken adipocytes", Scientia Agricultura Sinica, 46, pp.2769~2776 (2013)[DOI]
  56. Wang M, "Effect of quercetin on lipids metabolism through modulating the gut microbial and AMPK", PPAR signaling pathway in broilers, 2021, pp.9, 616219~
  57. Wang M, "Quercetin improving lipid metabolism by regulating lipid metabolism pathway of ileum mucosa in broilers", Oxid Med Cell Longev, 2020, pp.8686248~ (2020)[DOI]
  58. Huang J, "Green tea polyphenols alter lipid metabolism in the livers of broiler chickens through increased phosphorylation of AMP-activated protein kinase", PLoS One, 12, pp.e0187061~ (2017)[DOI]
  59. Huang JB, "Effects of epigallocatechin gallate on lipid metabolism and its underlying molecular mechanism in broiler chickens", J Anim Physiol Anim Nutr, 99, pp.719~727 (2015)[DOI]
  60. Gou ZY, "Effects of dietary incorporation of linseed oil with soybean isoflavone on fatty acid profiles and lipid metabolism-related gene expression in breast muscle of chickens", Animal, 14, pp.2414~2422 (2020)[DOI]
  61. Ouyang K, "Effects of alfalfa flavones on growth performance and carcass quality of female Chongren chickens", Acta Prataculturae Sinica, 22, pp.340~345 (2013)[DOI]
  62. Cui TT, "Genetic and epigenetic regulation of PPARγ during adipogenesis", Hereditas, 39, pp.1066~1077 (2017)[DOI]
  63. Sun YN, "Epigenetic DNA methylation in the promoters of peroxisome proliferator-activated receptor γ in chicken lines divergently selected for fatness", J Anim Sci, 92, pp.48~53 (2014)[DOI]
  64. Hu Y, "Maternal betaine supplementation decreases hepatic cholesterol deposition in chicken offspring with epigenetic modulation of SREBP2 and CYP7A1 genes", Poult Sci, 99, pp.3111~3120 (2020)[DOI]
  65. Mildner AM, "Porcine fatty acid synthase : cloning of a complementary DNA, tissue distribution of its mRNA and suppression of expression by somatotropin and dietary protein", J Nutr, 121, pp.900~907 (1991)[DOI]
  66. Zou XT, "Effect of betaine on the regulation of the lipid metabolism in laying hen", Scientia Agricultura Sinica, 3, pp.325~330 (2002)[DOI]
  67. He S, "Effects of dietary betaine on growth performance, fat deposition and serum lipids in broilers subjected to chronic heat stress", Anim Sci J, 86, pp.897~903 (2015)[DOI]
  68. Xing J, "Effect of dietary betaine supplementation on lipogenesis gene expression and CpG methylation of lipoprotein lipase gene in broilers", Mol Biol Rep, 38, pp.1975~1981 (2011)[DOI]
  69. Hu Y, "In ovo injection of betaine affects hepatic cholesterol metabolism through epigenetic gene regulation in newly hatched chicks", PLoS One, 10, pp.e0122643~ (2015)[DOI]
  70. Cui X, "Follicle-stimulating hormone increases the intramuscular fat content and expression of lipid biosynthesis genes in chicken breast muscle", J Zhejiang Univ Sci B, 17, pp.303~310 (2016)[DOI]
  71. Cui X, "Decreased testosterone levels after caponization leads to abdominal fat deposition in chickens", BMC Genomics, 19, pp.344~ (2018)[DOI]
  72. Huang HY, "Brain natriuretic peptide stimulates lipid metabolism through its receptor npr1 and the glycerolipid metabolism pathway in chicken adipocytes", Biochemistry, 54, pp.6622~6630 (2015)[DOI]
  73. Kim DH, "Adipogenic and myogenic potentials of chicken embryonic fibroblasts in vitro : combination of fatty acids and insulin induces adipogenesis", Lipids, 55, pp.163~171 (2020)[DOI]
  74. Yan J, "Adiponectin-impaired adipocyte differentiation negatively regulates fat deposition in chicken", J Anim Physiol Anim Nutr, 98, pp.530~537 (2014)[DOI]
  75. Jiang Z, "Genistein activated adenosine 5′-monophosphate-activated protein kinase–sirtuin1", peroxisome proliferator-activated receptor γ coactivator-1α pathway potentially through adiponectin and estrogen receptor β signaling to suppress fat deposition in broiler chickens, 2021, pp.100, 246~255
  76. Wang M, "Effects of glucocorticoid and dietary fat level on lipid metabolism of broilers", Chinese J Anim Nutr, 30, pp.3772~3780 (2018)[DOI]
  77. Abobaker H, "Dietary betaine supplementation increases adrenal expression of steroidogenic acute regulatory protein and yolk deposition of corticosterone in laying hens", Poult Sci, 96, pp.4389~4398 (2017)[DOI]
  78. Omer NA, "Dietary betaine improves egg-laying rate in hens through hypomethylation and glucocorticoid receptor-mediated activation of hepatic lipogenesisrelated genes", Poult Sci, 99, pp.3121~3132 (2020)[DOI]
  79. Zhou Y, "Nuciferine reduced fat deposition by controlling triglyceride and cholesterol concentration in broiler chickens", Poult Sci, 99, pp.7101~7108 (2020)[DOI]
  80. Xiao Y, "Microbial community mapping in intestinal tract of broiler chicken", Poult Sci, 96, pp.1387~ (2017)[DOI]
  81. Venardou B, "Effects of dietary supplementation with a laminarin-rich extract on the growth performance and gastrointestinal health in broilers", Poult Sci, 100, pp.101179~ (2021)[DOI]
  82. Long LN, "Research Note : Effects of polysaccharide-enriched Acanthopanax senticosus extract on growth performance, immune function, antioxidation, and ileal microbial populations in broiler chickens", Poult Sci, 100, pp.101028~ (2021)[DOI]
  83. Yesilbag D, "Effects of dietary rosemary, rosemary volatile oil and vitamin E on broiler performance, meat quality and serum SOD activity", Br Poult Sci, 52, pp.472~482 (2011)[DOI]
  84. Wen C, "The gut microbiota is largely independent of host genetics in regulating fat deposition in chickens", ISME J, 13, pp.1422~1436 (2019)[DOI]
  85. Indiani C, "Childhood obesity and firmicutes", bacteroidetes ratio in the gut microbiota : a systematic review, 2018, pp.14, 501~509
  86. Zhao X, "Effects of Clostridium butyricum and Enterococcus faecium on growth performance, lipid metabolism, and cecal microbiota of broiler chickens", Appl Microbiol Biotechnol, 97, pp.6477~6488 (2013)[DOI]
  87. Zhao X, "Effects of Clostridium butyricum on breast muscle lipid metabolism of broilers", Ital J Anim Sci, 17, pp.1010~1020 (2018)[DOI]
  88. Gheorghe A, "Effects of dietary extruded linseed and Lactobacillus acidophilus on growth performance, carcass traits, plasma lipoprotein response, and caecal bacterial populations in broiler chicks", Ital J Anim Sci, 19, pp.822~832 (2020)[DOI]
  89. Zhang J, "SCFAs-Induced GLP-1 secretion links the regulation of gut microbiome on hepatic lipogenesis in chickens", Front Microbiol, 10, pp.2176~ (2019)[DOI]
  90. Lin HV, "Butyrate and propionate protect against diet-induced obesity and regulate gut hormones via free fatty acid receptor 3-independent mechanisms", PLoS One, 7, pp.e35240~ (2012)[DOI]
  91. Li H, "Propionate inhibits fat deposition via affecting feed intake and modulating gut microbiota in broilers", Poult Sci, 100, pp.235~245 (2021)[DOI]
  92. Zhao L, "Low and high concentrations of butyrate regulate fat accumulation in chicken adipocytes via different mechanisms", Adipocyte, 9, pp.120~131 (2020)[DOI]
  93. Wang J, "Assessing the effects of ginger extract on polyphenol profiles and the subsequent impact on the fecal microbiota by simulating digestion and fermentation in vitro", Nutrients, 12, pp.3194~ (2020)[DOI]
  94. Chai M, "Effects of Macleaya cordata extracts instead of antibiotics on growth performance, caecum microbes and tight junction gene expression of yellowfeathered broilers", Acta Microbiologica Sinica, 60, pp.1718~1728 (2020)[DOI]
  95. Chen X, "The growth performance, meat quality, and gut bacteria of broilers raised with or without antibiotics and green tea powder", J Appl Poult Res, 28, pp.712~721 (2019)[DOI]
  96. Li W, "In vitro and in vivo antioxidant activity of eucalyptus leaf polyphenols extract and its effect on chicken meat quality and cecum microbiota", Food Res Int, 136, pp.109302~ (2020)[DOI]

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