• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肠道微生物群对胆汁酸代谢塑造的性别特异性影响。

Sex-specific effects of gut microbiome on shaping bile acid metabolism.

作者信息

Yang Yifei, Chi Liang, Hsiao Yun-Chung, Lu Kun

机构信息

Department of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, NC, 27599, United States.

出版信息

bioRxiv. 2024 Jun 27:2024.06.27.601003. doi: 10.1101/2024.06.27.601003.

DOI:10.1101/2024.06.27.601003
PMID:38979196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11230406/
Abstract

Gut microbiome is a group of microorganisms that plays important roles in contributing to health and diseases. These bacterial compositions have been demonstrated to impact bile acids (BAs) profiles, either by directly metabolizing primary BAs to secondary BAs or indirect ways through host metabolism by influencing BAs synthesis, transportation and conjugation in liver. It has been observed sexually dimorphic gut microbiome and bile acids composition, with variations in expression levels of bile acid metabolizing genes in the liver. However, associations between sex-specific differences in gut microbiome and BAs profiles are not well understood. This study aimed to investigate whether gut microbiome could influence BAs profiles in host in a sexspecific manner. We transplanted cecum feces of male and female C57BL/6 mice to male mice and measured BAs concentrations in feces, serum and liver samples 7 days after fecal transplantation. We found different BAs profiles between mice with male and female gut microbiome, including altering levels and proportions of secondary BAs. We also observed varied expression levels of genes related to bile acid metabolism in the liver and distal ileum. Our results highlight sex-specific effects of gut microbiome on shaping bile acid metabolism through gut bacteria and regulation of host genes.

摘要

肠道微生物群是一组在促进健康和引发疾病方面发挥重要作用的微生物。这些细菌组成已被证明会影响胆汁酸(BAs)谱,其方式要么是将初级胆汁酸直接代谢为次级胆汁酸,要么是通过影响肝脏中胆汁酸的合成、运输和结合,以间接方式通过宿主代谢来实现。已经观察到肠道微生物群和胆汁酸组成存在性别差异,肝脏中胆汁酸代谢基因的表达水平也有所不同。然而,肠道微生物群的性别特异性差异与胆汁酸谱之间的关联尚未得到充分理解。本研究旨在调查肠道微生物群是否能够以性别特异性方式影响宿主中的胆汁酸谱。我们将雄性和雌性C57BL/6小鼠的盲肠粪便移植到雄性小鼠体内,并在粪便移植7天后测量粪便、血清和肝脏样本中的胆汁酸浓度。我们发现具有雄性和雌性肠道微生物群的小鼠之间存在不同的胆汁酸谱,包括次级胆汁酸水平和比例的改变。我们还观察到肝脏和回肠末端中与胆汁酸代谢相关基因的表达水平有所不同。我们的结果突出了肠道微生物群通过肠道细菌和宿主基因调控对塑造胆汁酸代谢的性别特异性影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/87dffc622ab7/nihpp-2024.06.27.601003v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/0b26427964eb/nihpp-2024.06.27.601003v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/8dcb87adeb35/nihpp-2024.06.27.601003v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/96206a2f607e/nihpp-2024.06.27.601003v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/0f7e1e38ec9c/nihpp-2024.06.27.601003v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/b537b8d6953a/nihpp-2024.06.27.601003v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/87dffc622ab7/nihpp-2024.06.27.601003v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/0b26427964eb/nihpp-2024.06.27.601003v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/8dcb87adeb35/nihpp-2024.06.27.601003v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/96206a2f607e/nihpp-2024.06.27.601003v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/0f7e1e38ec9c/nihpp-2024.06.27.601003v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/b537b8d6953a/nihpp-2024.06.27.601003v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bae/11230406/87dffc622ab7/nihpp-2024.06.27.601003v1-f0006.jpg

相似文献

1
Sex-specific effects of gut microbiome on shaping bile acid metabolism.肠道微生物群对胆汁酸代谢塑造的性别特异性影响。
bioRxiv. 2024 Jun 27:2024.06.27.601003. doi: 10.1101/2024.06.27.601003.
2
ameliorates cholestatic liver injury through inhibiting bile acid synthesis and promoting bile acid excretion.通过抑制胆汁酸合成和促进胆汁酸排泄来改善胆汁淤积性肝损伤。
Gut Microbes. 2024 Jan-Dec;16(1):2390176. doi: 10.1080/19490976.2024.2390176. Epub 2024 Aug 29.
3
Growth performance, bile acid profile, fecal microbiome and serum metabolomics of growing-finishing pigs fed diets with bile acids supplementation.生长性能、胆汁酸谱、粪便微生物组和胆汁酸添加饲粮对生长育肥猪的血清代谢组学。
J Anim Sci. 2023 Jan 3;101. doi: 10.1093/jas/skad393.
4
Comprehensive Analysis of Serum and Fecal Bile Acid Profiles and Interaction with Gut Microbiota in Primary Biliary Cholangitis.原发性胆汁性胆管炎血清和粪便胆汁酸谱的综合分析及其与肠道微生物群的相互作用。
Clin Rev Allergy Immunol. 2020 Feb;58(1):25-38. doi: 10.1007/s12016-019-08731-2.
5
The Relationship Between Gut Microbiome and Bile Acids in Primates With Diverse Diets.不同饮食的灵长类动物肠道微生物群与胆汁酸之间的关系
Front Microbiol. 2022 May 11;13:899102. doi: 10.3389/fmicb.2022.899102. eCollection 2022.
6
Genetic hypogonadal mouse model reveals niche-specific influence of reproductive axis and sex on intestinal microbial communities.遗传型性腺功能减退症小鼠模型揭示了生殖轴和性别对肠道微生物群落的特定小生境影响。
Biol Sex Differ. 2023 Nov 6;14(1):79. doi: 10.1186/s13293-023-00564-1.
7
Altered gut microbiome, bile acid composition and metabolome in sarcopenia in liver cirrhosis.肝硬化性肌少症中肠道微生物组、胆汁酸组成和代谢组的改变。
J Cachexia Sarcopenia Muscle. 2023 Dec;14(6):2676-2691. doi: 10.1002/jcsm.13342. Epub 2023 Sep 28.
8
Gut Microbiota Dysbiosis Is Associated with Altered Bile Acid Metabolism in Infantile Cholestasis.肠道微生物群失调与婴儿胆汁淤积症中胆汁酸代谢改变有关。
mSystems. 2019 Dec 17;4(6):e00463-19. doi: 10.1128/mSystems.00463-19.
9
Bile acid is a significant host factor shaping the gut microbiome of diet-induced obese mice.胆汁酸是一个重要的宿主因素,可塑造饮食诱导肥胖小鼠的肠道微生物组。
BMC Biol. 2017 Dec 14;15(1):120. doi: 10.1186/s12915-017-0462-7.
10
Antarctic krill oil ameliorates liver injury in rats exposed to alcohol by regulating bile acids metabolism and gut microbiota.南极磷虾油通过调节胆汁酸代谢和肠道微生物群改善酒精暴露大鼠的肝损伤。
J Nutr Biochem. 2022 Sep;107:109061. doi: 10.1016/j.jnutbio.2022.109061. Epub 2022 May 22.

本文引用的文献

1
The Effect of Lithocholic Acid on the Gut-Liver Axis.石胆酸对肠-肝轴的影响。
Front Pharmacol. 2022 Jul 7;13:910493. doi: 10.3389/fphar.2022.910493. eCollection 2022.
2
Protective effects of taurocholic acid on excessive hepatic lipid accumulation regulation of bile acid metabolism in grouper.牛磺胆酸对过度肝脂质积累的保护作用 调节石斑鱼胆汁酸代谢。
Food Funct. 2022 Mar 7;13(5):3050-3062. doi: 10.1039/d1fo04085e.
3
Up to date on cholesterol 7 alpha-hydroxylase (CYP7A1) in bile acid synthesis.胆汁酸合成中胆固醇7α-羟化酶(CYP7A1)的最新进展。
Liver Res. 2020 Jun;4(2):47-63. doi: 10.1016/j.livres.2020.05.001. Epub 2020 Jun 3.
4
Bile Acid Profile and its Changes in Response to Cefoperazone Treatment in MR1 Deficient Mice.MR1缺陷小鼠中胆汁酸谱及其对头孢哌酮治疗的反应变化
Metabolites. 2020 Mar 26;10(4):127. doi: 10.3390/metabo10040127.
5
Gut microbiota-derived metabolites as key actors in inflammatory bowel disease.肠道微生物衍生代谢物作为炎症性肠病的关键因素。
Nat Rev Gastroenterol Hepatol. 2020 Apr;17(4):223-237. doi: 10.1038/s41575-019-0258-z. Epub 2020 Feb 19.
6
Lipid and Cholesterol Homeostasis after Arsenic Exposure and Antibiotic Treatment in Mice: Potential Role of the Microbiota.砷暴露和抗生素治疗后小鼠的脂质和胆固醇稳态:微生物组的潜在作用。
Environ Health Perspect. 2019 Sep;127(9):97002. doi: 10.1289/EHP4415. Epub 2019 Sep 18.
7
Macronutrient metabolism by the human gut microbiome: major fermentation by-products and their impact on host health.人体肠道微生物组的宏量营养素代谢:主要发酵副产物及其对宿主健康的影响。
Microbiome. 2019 Jun 13;7(1):91. doi: 10.1186/s40168-019-0704-8.
8
Sex, gut microbiome, and cardiovascular disease risk.性别、肠道微生物组与心血管疾病风险。
Biol Sex Differ. 2019 Jun 10;10(1):29. doi: 10.1186/s13293-019-0240-z.
9
The gut microbiome: Relationships with disease and opportunities for therapy.肠道微生物组:与疾病的关系及治疗机会。
J Exp Med. 2019 Jan 7;216(1):20-40. doi: 10.1084/jem.20180448. Epub 2018 Oct 15.
10
Taurocholic acid is an active promoting factor, not just a biomarker of progression of liver cirrhosis: evidence from a human metabolomic study and in vitro experiments.牛磺胆酸是一种活性促进因子,而非仅仅是肝硬化进展的生物标志物:来自一项人体代谢组学研究和体外实验的证据。
BMC Gastroenterol. 2018 Jul 11;18(1):112. doi: 10.1186/s12876-018-0842-7.