

无数据
Scan QR Code
1.Zhejiang Provincial Key Laboratory of Pancreatic Disease of The First Affiliated Hospital, Institute of Translational Medicine, Zhejiang University School of Medicine, Hangzhou 310029, China
2.Cancer Center, Zhejiang University, Hangzhou 310029, China
3.Institute of Fundamental and Transdisciplinary Research, Zhejiang University, Hangzhou 310029, China
收稿:2025-03-05,
修回:2025-05-13,
网络出版:2025-09-22,
纸质出版:2025-10-20
杭冰清,王宇浩.肠道微生物群与肠道脂质代谢间的相互作用:机制和影响[J].浙江大学学报(英文版)(B辑:生物医学和生物技术),2025,26(10):961-971.
Bingqing HANG, Yuhao WANG. Interplay between gut microbiota and intestinal lipid metabolism:mechanisms and implications[J]. Journal of zhejiang university-science b, 2025, 26(10): 961-971.
杭冰清,王宇浩.肠道微生物群与肠道脂质代谢间的相互作用:机制和影响[J].浙江大学学报(英文版)(B辑:生物医学和生物技术),2025,26(10):961-971. DOI: 10.1631/jzus.B2500102.
Bingqing HANG, Yuhao WANG. Interplay between gut microbiota and intestinal lipid metabolism:mechanisms and implications[J]. Journal of zhejiang university-science b, 2025, 26(10): 961-971. DOI: 10.1631/jzus.B2500102.
肠道微生物群作为人体中不可或缺的共生体系,是宿主脂质代谢稳态的关键调节因子,因此成为现代代谢性疾病病理生理机制研究的焦点。该微生物群落通过多维度机制协调宿主脂质动态平衡(吸收、代谢和储存),包括参与膳食多糖的酶促加工、肠上皮细胞长链脂肪酸摄取促进以及脂肪组织功能双向调节。越来越多研究表明,肠道微生物群衍生的代谢产物不仅能直接调控典型脂质代谢通路,而且通过与宿主免疫通路、表观遗传调控机制和生物钟系统的交互作用进而构建协调全身代谢的精密调控网络。肠道微生物群紊乱(生态失调)可破坏宿主脂质稳态,是肥胖、高脂血症和非酒精性脂肪肝等代谢性疾病的致病因素。本综述系统研究了肠道微生物群调控肠道脂质代谢的新机制,并阐明了其对理解代谢性疾病发病机制和开发靶向治疗的转化医学价值。
The gut microbiota is an indispensable symbiotic entity within the human holobiont
serving as a critical regulator of host lipid metabolism homeostasis. Therefore
it has emerged as a central subject of research in the pathophysiology of metabolic disorders. This microbial consortium orchestrates key aspects of host lipid dynamics—including absorption
metabolism
and storage—through multifaceted mechanisms such as the enzymatic processing of dietary polysaccharides
the facilitation of long-chain fatty acid uptake by intestinal epithelial cells (IECs)
and the bidirectional modulation of adipose tissue functionality. Mounting evidence underscores that gut microbiota-derived metabolites not only directly mediate canonical lipid metabolic pathways but also interface with host immune pathways
epigenetic machinery
and circadian regulatory systems
thereby establishing an intricate crosstalk that coordinates systemic metabolic outputs. Perturbations in microbial composition (dysbiosis) drive pathological disruptions to lipid homeostasis
serving as a pathogenic driver for conditions such as obesity
hyperlipidemia
and non-alcoholic fatty liver disease (NAFLD). This review systematically examines the emerging mechanistic insights into the gut microbiota-mediated regulation of intestinal lipid metabolism
while it elucidates its translational implications for understanding metabolic disease pathogenesis and developing targeted therapies.
Abumrad NA , Cabodevilla AG , Samovski D , et al. , 2021 . Endothelial cell receptors in tissue lipid uptake and metabolism . Circ Res , 128 ( 3 ): 433 - 450 . https://doi.org/10.1161/circresaha.120.318003 https://doi.org/10.1161/circresaha.120.318003
Agus A , Clément K , Sokol H , 2021 . Gut microbiota-derived metabolites as central regulators in metabolic disorders . Gut , 70 ( 6 ): 1174 - 1182 . https://doi.org/10.1136/gutjnl-2020-323071 https://doi.org/10.1136/gutjnl-2020-323071
Ahmed H , Leyrolle Q , Koistinen V , et al. , 2022 . Microbiota-derived metabolites as drivers of gut‒brain communication . Gut Microbes , 14 ( 1 ): 2102878 . https://doi.org/10.1080/19490976.2022.2102878 https://doi.org/10.1080/19490976.2022.2102878
Arnoriaga-Rodríguez M , Mayneris-Perxachs J , Burokas A , et al. , 2020 . Obesity impairs short-term and working memory through gut microbial metabolism of aromatic amino acids . Cell Metab , 32 ( 4 ): 548 - 560.e7 . https://doi.org/10.1016/j.cmet.2020.09.002 https://doi.org/10.1016/j.cmet.2020.09.002
Aronsson L , Huang Y , Parini P , et al. , 2010 . Decreased fat storage by Lactobacillus paracasei is associated with increased levels of angiopoietin-like 4 protein (ANGPTL4) . PLoS ONE , 5 ( 9 ): e13087 . https://doi.org/10.1371/journal.pone.0013087 https://doi.org/10.1371/journal.pone.0013087
Arpaia N , Campbell C , Fan XY , et al. , 2013 . Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation . Nature , 504 ( 7480 ): 451 - 455 . https://doi.org/10.1038/nature12726 https://doi.org/10.1038/nature12726
Bäckhed F , Ding H , Wang T , et al. , 2004 . The gut microbiota as an environmental factor that regulates fat storage . Proc Natl Acad Sci USA , 101 ( 44 ): 15718 - 15723 . https://doi.org/10.1073/pnas.0407076101 https://doi.org/10.1073/pnas.0407076101
Bäckhed F , Crawford PA , O'Donnell D , et al. , 2007a . Postnatal lymphatic partitioning from the blood vasculature in the small intestine requires fasting-induced adipose factor . Proc Natl Acad Sci USA , 104 ( 2 ): 606 - 611 . https://doi.org/10.1073/pnas.0605957104 https://doi.org/10.1073/pnas.0605957104
Bäckhed F , Manchester JK , Semenkovich CF , et al. , 2007b . Mechanisms underlying the resistance to diet-induced obesity in germ-free mice . Proc Natl Acad Sci USA , 104 ( 3 ): 979 - 984 . https://doi.org/10.1073/pnas.0605374104 https://doi.org/10.1073/pnas.0605374104
Brown EM , Clardy J , Xavier RJ , 2023 . Gut microbiome lipid metabolism and its impact on host physiology . Cell Host Microbe , 31 ( 2 ): 173 - 186 . https://doi.org/10.1016/j.chom.2023.01.009 https://doi.org/10.1016/j.chom.2023.01.009
Carey RA , Montag D , 2021 . Exploring the relationship between gut microbiota and exercise: short-chain fatty acids and their role in metabolism . BMJ Open Sport Exerc Med , 7 ( 2 ): e000930 . https://doi.org/10.1136/bmjsem-2020-000930 https://doi.org/10.1136/bmjsem-2020-000930
Chambers ES , Preston T , Frost G , et al. , 2018 . Role of gut microbiota-generated short-chain fatty acids in metabolic and cardiovascular health . Curr Nutr Rep , 7 ( 4 ): 198 - 206 . https://doi.org/10.1007/s13668-018-0248-8 https://doi.org/10.1007/s13668-018-0248-8
Dávalos-Salas M , Montgomery MK , Reehorst CM , et al. , 2019 . Deletion of intestinal Hdac3 remodels the lipidome of enterocytes and protects mice from diet-induced obesity . Nat Commun , 10 : 5291 . https://doi.org/10.1038/s41467-019-13180-8 https://doi.org/10.1038/s41467-019-13180-8
Deehan EC , Mocanu V , Madsen KL , 2024 . Effects of dietary fibre on metabolic health and obesity . Nat Rev Gastroenterol Hepatol , 21 ( 5 ): 301 - 318 . https://doi.org/10.1038/s41575-023-00891-z https://doi.org/10.1038/s41575-023-00891-z
Depommier C , Everard A , Druart C , et al. , 2021 . Serum metabolite profiling yields insights into health promoting effect of A . muciniphila in human volunteers with a metabolic syndrome . Gut Microbes , 13 ( 1 ): 1994270 . https://doi.org/10.1080/19490976.2021.1994270 https://doi.org/10.1080/19490976.2021.1994270
Dodd D , Spitzer MH , van Treuren W , et al. , 2017 . A gut bacterial pathway metabolizes aromatic amino acids into nine circulating metabolites . Nature , 551 ( 7682 ): 648 - 652 . https://doi.org/10.1038/nature24661 https://doi.org/10.1038/nature24661
Duan CH , Wu JH , Wang Z , et al. , 2023 . Fucose promotes intestinal stem cell-mediated intestinal epithelial development through promoting Akkermansia -related propanoate metabolism . Gut Microbes , 15 ( 1 ): 2233149 . https://doi.org/10.1080/19490976.2023.2233149 https://doi.org/10.1080/19490976.2023.2233149
Duscha A , Gisevius B , Hirschberg S , et al. , 2020 . Propionic acid shapes the multiple sclerosis disease course by an immunomodulatory mechanism . Cell , 180 ( 6 ): 1067 - 1080.e16 . https://doi.org/10.1016/j.cell.2020.02.035 https://doi.org/10.1016/j.cell.2020.02.035
Eshleman EM , Rice T , Potter C , et al. , 2024 . Microbiota-derived butyrate restricts tuft cell differentiation via histone deacetylase 3 to modulate intestinal type 2 immunity . Immunity , 57 ( 2 ): 319 - 332.e6 . https://doi.org/10.1016/j.immuni.2024.01.002 https://doi.org/10.1016/j.immuni.2024.01.002
Everard A , Belzer C , Geurts L , et al. , 2013 . Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity . Proc Natl Acad Sci USA , 110 ( 22 ): 9066 - 9071 . https://doi.org/10.1073/pnas.1219451110 https://doi.org/10.1073/pnas.1219451110
Fan Y , Pedersen O , 2021 . Gut microbiota in human metabolic health and disease . Nat Rev Microbiol , 19 : 55 - 71 . https://doi.org/10.1038/s41579-020-0433-9 https://doi.org/10.1038/s41579-020-0433-9
Frampton J , Murphy KG , Frost G , et al. , 2020 . Short-chain fatty acids as potential regulators of skeletal muscle metabolism and function . Nat Metab , 2 ( 9 ): 840 - 848 . https://doi.org/10.1038/s42255-020-0188-7 https://doi.org/10.1038/s42255-020-0188-7
Frazier K , Manzoor S , Carroll K , et al. , 2023 . Gut microbes and the liver circadian clock partition glucose and lipid metabolism . J Clin Invest , 133 ( 18 ): e162515 . https://doi.org/10.1172/jci162515 https://doi.org/10.1172/jci162515
Fuchs CD , Simbrunner B , Baumgartner M , et al. , 2025 . Bile acid metabolism and signalling in liver disease . J Hepatol , 82 ( 1 ): 134 - 153 . https://doi.org/10.1016/j.jhep.2024.09.032 https://doi.org/10.1016/j.jhep.2024.09.032
Gilijamse PW , Hartstra AV , Levin E , et al. , 2020 . Treatment with Anaerobutyricum soehngenii : a pilot study of safety and dose-response effects on glucose metabolism in human subjects with metabolic syndrome . npj Biofilms Microbiomes , 6 : 16 . https://doi.org/10.1038/s41522-020-0127-0 https://doi.org/10.1038/s41522-020-0127-0
Gray SM , Moss AD , Herzog JW , et al. , 2024 . Mouse adaptation of human inflammatory bowel diseases microbiota enhances colonization efficiency and alters microbiome aggressiveness depending on the recipient colonic inflammatory environment . Microbiome , 12 : 147 . https://doi.org/10.1186/s40168-024-01857-2 https://doi.org/10.1186/s40168-024-01857-2
Guo X , Li JH , Xu J , et al. , 2025 . Gut microbiota and epigenetic inheritance: implications for the development of IBD . Gut Microbes , 17 ( 1 ): 2490207 . https://doi.org/10.1080/19490976.2025.2490207 https://doi.org/10.1080/19490976.2025.2490207
He ZG , Liu YB , Li Z , et al. , 2023 . Gut microbiota regulates circadian oscillation in hepatic ischemia-reperfusion injury-induced cognitive impairment by interfering with hippocampal lipid metabolism in mice . Hepatol Int , 17 ( 6 ): 1645 - 1658 . https://doi.org/10.1007/s12072-023-10509-w https://doi.org/10.1007/s12072-023-10509-w
Honda A , Miyazaki T , Iwamoto J , et al. , 2020 . Regulation of bile acid metabolism in mouse models with hydrophobic bile acid composition . J Lipid Res , 61 ( 1 ): 54 - 69 . https://doi.org/10.1194/jlr.RA119000395 https://doi.org/10.1194/jlr.RA119000395
Hooper LV , Gordon JI , 2001 . Commensal host-bacterial relationships in the gut . Science , 292 ( 5519 ): 1115 - 1118 . https://doi.org/10.1126/science.1058709 https://doi.org/10.1126/science.1058709
Hooper LV , Midtvedt T , Gordon JI , 2002 . How host-microbial interactions shape the nutrient environment of the mammalian intestine . Annu Rev Nutr , 22 : 283 - 307 . https://doi.org/10.1146/annurev.nutr.22.011602.092259 https://doi.org/10.1146/annurev.nutr.22.011602.092259
Hooper LV , Littman DR , Macpherson AJ , 2012 . Interactions between the microbiota and the immune system . Science , 336 ( 6086 ): 1268 - 1273 . https://doi.org/10.1126/science.1223490 https://doi.org/10.1126/science.1223490
Huang FJ , Zheng XJ , Ma XH , et al. , 2019 . Theabrownin from Pu-erh tea attenuates hypercholesterolemia via modulation of gut microbiota and bile acid metabolism . Nat Commun , 10 : 4971 . https://doi.org/10.1038/s41467-019-12896-x https://doi.org/10.1038/s41467-019-12896-x
Jang JW , Capaldi E , Smith T , et al. , 2024 . Trimethylamine N -oxide: a meta-organismal axis linking the gut and fibrosis . Mol Med , 30 : 128 . https://doi.org/10.1186/s10020-024-00895-8 https://doi.org/10.1186/s10020-024-00895-8
Jia L , Jiang YY , Wu LL , et al. , 2024 . Porphyromonas gingivalis aggravates colitis via a gut microbiota-linoleic acid metabolism-Th17/Treg cell balance axis . Nat Commun , 15 : 1617 . https://doi.org/10.1038/s41467-024-45473-y https://doi.org/10.1038/s41467-024-45473-y
Jia W , Wei ML , Rajani C , et al. , 2021 . Targeting the alternative bile acid synthetic pathway for metabolic diseases . Protein Cell , 12 ( 5 ): 411 - 425 . https://doi.org/10.1007/s13238-020-00804-9 https://doi.org/10.1007/s13238-020-00804-9
Jin J , Huangfu BX , Xing FG , et al. , 2023 . Combined exposure to deoxynivalenol facilitates lipid metabolism disorder in high-fat-diet-induced obesity mice . Environ Int , 182 : 108345 . https://doi.org/10.1016/j.envint.2023.108345 https://doi.org/10.1016/j.envint.2023.108345
Kawano Y , Edwards M , Huang YM , et al. , 2022 . Microbiota imbalance induced by dietary sugar disrupts immune-mediated protection from metabolic syndrome . Cell , 185 ( 19 ): 3501 - 3519.e20 . https://doi.org/10.1016/j.cell.2022.08.005 https://doi.org/10.1016/j.cell.2022.08.005
Korbelius M , Kuentzel KB , Bradić I , et al. , 2023 . Recent insights into lysosomal acid lipase deficiency . Trends Mol Med , 29 ( 6 ): 425 - 438 . https://doi.org/10.1016/j.molmed.2023.03.001 https://doi.org/10.1016/j.molmed.2023.03.001
Korem T , Zeevi D , Suez J , et al. , 2015 . Growth dynamics of gut microbiota in health and disease inferred from single metagenomic samples . Science , 349 ( 6252 ): 1101 - 1106 . https://doi.org/10.1126/science.aac4812 https://doi.org/10.1126/science.aac4812
Kuang Z , Wang YH , Li Y , et al. , 2019 . The intestinal microbiota programs diurnal rhythms in host metabolism through histone deacetylase 3 . Science , 365 ( 6460 ): 1428 - 1434 . https://doi.org/10.1126/science.aaw3134 https://doi.org/10.1126/science.aaw3134
Li NH , Li J , Wang H , et al. , 2023 . Aromatic amino acids and their interactions with gut microbiota-related metabolites for risk of gestational diabetes: a prospective nested case-control study in a Chinese cohort . Ann Nutr Metab , 79 ( 3 ): 291 - 300 . https://doi.org/10.1159/000531481 https://doi.org/10.1159/000531481
Li SJ , Zhuge AX , Chen H , et al. , 2025 . Sedanolide alleviates DSS-induced colitis by modulating the intestinal FXR-SMPD3 pathway in mice . J Adv Res , 69 : 413 - 426 . https://doi.org/10.1016/j.jare.2024.03.026 https://doi.org/10.1016/j.jare.2024.03.026
Li XL , Yang YY , Zhang B , et al. , 2022 . Lactate metabolism in human health and disease . Signal Transduct Target Ther , 7 : 305 . https://doi.org/10.1038/s41392-022-01151-3 https://doi.org/10.1038/s41392-022-01151-3
Li XX , Lau HCH , Yu J , 2020 . Microbiota-mediated phytate metabolism activates HDAC3 to contribute intestinal homeostasis . Signal Transduct Target Ther , 5 : 211 . https://doi.org/10.1038/s41392-020-00321-5 https://doi.org/10.1038/s41392-020-00321-5
Li YY , Ma J , Yao K , et al. , 2020 . Circadian rhythms and obesity: timekeeping governs lipid metabolism . J Pineal Res , 69 ( 3 ): e12682 . https://doi.org/10.1111/jpi.12682 https://doi.org/10.1111/jpi.12682
Liu YL , Hou YL , Wang GJ , et al. , 2020 . Gut microbial metabolites of aromatic amino acids as signals in host-microbe interplay . Trends Endocrinol Metab , 31 ( 11 ): 818 - 834 . https://doi.org/10.1016/j.tem.2020.02.012 https://doi.org/10.1016/j.tem.2020.02.012
Lu YJ , Yang WL , Qi ZY , et al. , 2023 . Gut microbe-derived metabolite indole-3-carboxaldehyde alleviates atherosclerosis . Signal Transduct Target Ther , 8 : 378 . https://doi.org/10.1038/s41392-023-01613-2 https://doi.org/10.1038/s41392-023-01613-2
Maiuolo J , Carresi C , Gliozzi M , et al. , 2022 . The contribution of gut microbiota and endothelial dysfunction in the development of arterial hypertension in animal models and in humans . Int J Mol Sci , 23 ( 7 ): 3698 . https://doi.org/10.3390/ijms23073698 https://doi.org/10.3390/ijms23073698
Makki K , Deehan EC , Walter J , et al. , 2018 . The impact of dietary fiber on gut microbiota in host health and disease . Cell Host Microbe , 23 ( 6 ): 705 - 715 . https://doi.org/10.1016/j.chom.2018.05.012 https://doi.org/10.1016/j.chom.2018.05.012
Min BH , Devi S , Kwon GH , et al. , 2024 . Gut microbiota-derived indole compounds attenuate metabolic dysfunction-associated steatotic liver disease by improving fat metabolism and inflammation . Gut Microbes , 16 ( 1 ): 2307568 . https://doi.org/10.1080/19490976.2024.2307568 https://doi.org/10.1080/19490976.2024.2307568
Ng I , Luk IY , Nightingale R , et al. , 2023 . Intestinal-specific Hdac3 deletion increases susceptibility to colitis and small intestinal tumor development in mice fed a high-fat diet . Am J Physiol Gastrointest Liver Physiol , 325 ( 6 ): G508 - G517 . https://doi.org/10.1152/ajpgi.00160.2023 https://doi.org/10.1152/ajpgi.00160.2023
Nogal A , Valdes AM , Menni C , 2021 . The role of short-chain fatty acids in the interplay between gut microbiota and diet in cardio-metabolic health . Gut Microbes , 13 ( 1 ): 1897212 . https://doi.org/10.1080/19490976.2021.1897212 https://doi.org/10.1080/19490976.2021.1897212
Plovier H , Everard A , Druart C , et al. , 2017 . A purified membrane protein from Akkermansia muciniphila or the pasteurized bacterium improves metabolism in obese and diabetic mice . Nat Med , 23 : 107 - 113 . https://doi.org/10.1038/nm.4236 https://doi.org/10.1038/nm.4236
Qin N , Yang FL , Li A , et al. , 2014 . Alterations of the human gut microbiome in liver cirrhosis . Nature , 513 ( 7516 ): 59 - 64 . https://doi.org/10.1038/nature13568 https://doi.org/10.1038/nature13568
Rothschild D , Weissbrod O , Barkan E , et al. , 2018 . Environment dominates over host genetics in shaping human gut microbiota . Nature , 555 ( 7695 ): 210 - 215 . https://doi.org/10.1038/nature25973 https://doi.org/10.1038/nature25973
Schoeler M , Caesar R , 2019 . Dietary lipids, gut microbiota and lipid metabolism . Rev Endocr Metab Disord , 20 ( 4 ): 461 - 472 . https://doi.org/10.1007/s11154-019-09512-0 https://doi.org/10.1007/s11154-019-09512-0
Stähli BE , Scharl M , Matter CM , 2023 . A roadmap for gut microbiome-derived aromatic amino acids for improved cardiovascular risk stratification . Eur Heart J , 44 ( 32 ): 3097 - 3099 . https://doi.org/10.1093/eurheartj/ehad367 https://doi.org/10.1093/eurheartj/ehad367
Su XM , Gao YH , Yang RC , 2022 . Gut microbiota-derived tryptophan metabolites maintain gut and systemic homeostasis . Cells , 11 ( 15 ): 2296 . https://doi.org/10.3390/cells11152296 https://doi.org/10.3390/cells11152296
Thingholm LB , Rühlemann MC , Koch M , et al. , 2019 . Obese individuals with and without type 2 diabetes show different gut microbial functional capacity and composition . Cell Host Microbe , 26 ( 2 ): 252 - 264.e10 . https://doi.org/10.1016/j.chom.2019.07.004 https://doi.org/10.1016/j.chom.2019.07.004
Turnbaugh PJ , Ley RE , Mahowald MA , et al. , 2006 . An obesity-associated gut microbiome with increased capacity for energy harvest . Nature , 444 ( 7122 ): 1027 - 1031 . https://doi.org/10.1038/nature05414 https://doi.org/10.1038/nature05414
Vieujean S , Jairath V , Peyrin-Biroulet L , et al. , 2025 . Understanding the therapeutic toolkit for inflammatory bowel disease . Nat Rev Gastroenterol Hepatol , 22 ( 6 ): 371 - 394 . https://doi.org/10.1038/s41575-024-01035-7 https://doi.org/10.1038/s41575-024-01035-7
Wagner A , Wang C , Fessler J , et al. , 2021 . Metabolic modeling of single Th17 cells reveals regulators of autoimmunity . Cell , 184 ( 16 ): 4168 - 4185.e21 . https://doi.org/10.1016/j.cell.2021.05.045 https://doi.org/10.1016/j.cell.2021.05.045
Wang JJ , Zhu NN , Su XM , et al. , 2023 . Gut-microbiota-derived metabolites maintain gut and systemic immune homeostasis . Cells , 12 ( 5 ): 793 . https://doi.org/10.3390/cells12050793 https://doi.org/10.3390/cells12050793
Wang YH , Hooper LV , 2019 . Immune control of the microbiota prevents obesity . Science , 365 ( 6451 ): 316 - 317 . https://doi.org/10.1126/science.aay2057 https://doi.org/10.1126/science.aay2057
Wang YH , Kuang Z , Yu XF , et al. , 2017 . The intestinal microbiota regulates body composition through NFIL3 and the circadian clock . Science , 357 ( 6354 ): 912 - 916 . https://doi.org/10.1126/science.aan0677 https://doi.org/10.1126/science.aan0677
Wang YH , Wang M , Chen JX , et al. , 2023 . The gut microbiota reprograms intestinal lipid metabolism through long noncoding RNA Snhg9 . Science , 381 ( 6660 ): 851 - 857 . https://doi.org/10.1126/science.ade0522 https://doi.org/10.1126/science.ade0522
Wang ZN , Sun Y , Han YW , et al. , 2023 . Eucommia bark/leaf extract improves HFD-induced lipid metabolism disorders via targeting gut microbiota to activate the Fiaf-LPL gut-liver axis and SCFAs-GPR43 gut-fat axis . Phytomedicine , 110 : 154652 . https://doi.org/10.1016/j.phymed.2023.154652 https://doi.org/10.1016/j.phymed.2023.154652
Wen ST , He L , Zhong ZT , et al. , 2021 . Stigmasterol restores the balance of Treg/Th17 cells by activating the butyrate-PPARγ axis in colitis . Front Immunol , 12 : 741934 . https://doi.org/10.3389/fimmu.2021.741934 https://doi.org/10.3389/fimmu.2021.741934
Wu HQ , Mu CL , Li X , et al. , 2024a . Breed-driven microbiome heterogeneity regulates intestinal stem cell proliferation via Lactobacillus -lactate-GPR81 signaling . Adv Sci , 11 ( 33 ): 2400058 . https://doi.org/10.1002/advs.202400058 https://doi.org/10.1002/advs.202400058
Wu HQ , Mu CL , Xu LP , et al. , 2024b . Host-microbiota interaction in intestinal stem cell homeostasis . Gut Microbes , 16 ( 1 ): 2353399 . https://doi.org/10.1080/19490976.2024.2353399 https://doi.org/10.1080/19490976.2024.2353399
Wu SE , Hashimoto-Hill S , Woo V , et al. , 2020 . Microbiota-derived metabolite promotes HDAC3 activity in the gut . Nature , 586 ( 7827 ): 108 - 112 . https://doi.org/10.1038/s41586-020-2604-2 https://doi.org/10.1038/s41586-020-2604-2
Wu WR , Lv LX , Shi D , et al. , 2017 . Protective effect of Akkermansia muciniphila against immune-mediated liver injury in a mouse model . Front Microbiol , 8 : 1804 . https://doi.org/10.3389/fmicb.2017.01804 https://doi.org/10.3389/fmicb.2017.01804
Xu HT , Fang F , Wu KZ , et al. , 2023 . Gut microbiota-bile acid crosstalk regulates murine lipid metabolism via the intestinal FXR-FGF19 axis in diet-induced humanized dyslipidemia . Microbiome , 11 : 262 . https://doi.org/10.1186/s40168-023-01709-5 https://doi.org/10.1186/s40168-023-01709-5
Yadav J , Liang T , Qin TR , et al. , 2023 . Gut microbiome modified by bariatric surgery improves insulin sensitivity and correlates with increased brown fat activity and energy expenditure . Cell Rep Med , 4 ( 5 ): 101051 . https://doi.org/10.1016/j.xcrm.2023.101051 https://doi.org/10.1016/j.xcrm.2023.101051
Yin YH , Sichler A , Ecker J , et al. , 2023 . Gut microbiota promote liver regeneration through hepatic membrane phospholipid biosynthesis . J Hepatol , 78 ( 4 ): 820 - 835 . https://doi.org/10.1016/j.jhep.2022.12.028 https://doi.org/10.1016/j.jhep.2022.12.028
Younossi ZM , Koenig AB , Abdelatif D , et al. , 2016 . Global epidemiology of nonalcoholic fatty liver disease‒meta-analytic assessment of prevalence, incidence, and outcomes . Hepatology , 64 ( 1 ): 73 - 84 . https://doi.org/10.1002/hep.28431 https://doi.org/10.1002/hep.28431
Zhang D , Jian YP , Zhang YN , et al. , 2023 . Short-chain fatty acids in diseases . Cell Commun Signal , 21 : 212 . https://doi.org/10.1186/s12964-023-01219-9 https://doi.org/10.1186/s12964-023-01219-9
Zhang SW , Gang XK , Yang S , et al. , 2021 . The alterations in and the role of the Th17/Treg balance in metabolic diseases . Front Immunol , 12 : 678355 . https://doi.org/10.3389/fimmu.2021.678355 https://doi.org/10.3389/fimmu.2021.678355
Zhao LP , Zhang F , Ding XY , et al. , 2018 . Gut bacteria selectively promoted by dietary fibers alleviate type 2 diabetes . Science , 359 ( 6380 ): 1151 - 1156 . https://doi.org/10.1126/science.aao5774 https://doi.org/10.1126/science.aao5774
Zhao RQ , Ji Y , Chen X , et al. , 2023 . Flammulina velutipes polysaccharides regulate lipid metabolism disorders in HFD-fed mice via bile acids metabolism . Int J Biol Macromol , 253 : 127308 . https://doi.org/10.1016/j.ijbiomac.2023.127308 https://doi.org/10.1016/j.ijbiomac.2023.127308
Zhu BL , Wang X , Li LJ , 2010 . Human gut microbiome: the second genome of human body . Protein Cell , 1 ( 8 ): 718 - 725 . https://doi.org/10.1007/s13238-010-0093-z https://doi.org/10.1007/s13238-010-0093-z
0
浏览量
0
Downloads
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010802024621