• 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

胆汁酸在白色脂肪组织中的新作用。

The emerging role of bile acids in white adipose tissue.

作者信息

Schmid Andreas, Karrasch Thomas, Schäffler Andreas

机构信息

Basic Research Laboratory for Molecular Endocrinology, Adipocyte Biology, and Biochemistry, University of Giessen, D 35392 Giessen, Germany.

Department of Internal Medicine III - Endocrinology, Diabetology, and Metabolism, University of Giessen, D 35392 Giessen, Germany.

出版信息

Trends Endocrinol Metab. 2023 Nov;34(11):718-734. doi: 10.1016/j.tem.2023.08.002. Epub 2023 Aug 29.

DOI:10.1016/j.tem.2023.08.002
PMID:37648561
Abstract

The effects of bile acids (BAs) on liver, enteroendocrine function, small intestine, and brown adipose tissue have been described extensively. Outside the liver, BAs in the peripheral circulation system represent a specific but underappreciated physiological compartment. We discuss how systemic BAs can be regarded as specific steroidal hormones that act on white adipocytes, and suggest the name 'bilokines' ('bile hormones') for the specific FXR/TGR5 receptor interaction in adipocytes. Some BAs and their agonists regulate adipocyte differentiation, lipid accumulation, hypoxia, autophagy, adipokine and cytokine secretion, insulin signaling, and glucose uptake. BA signaling could provide a new therapeutic avenue for adipoflammation and metaflammation in visceral obesity, the causal mechanisms underlying insulin resistance and type 2 diabetes mellitus (T2D).

摘要

胆汁酸(BAs)对肝脏、肠内分泌功能、小肠和棕色脂肪组织的影响已被广泛描述。在肝脏之外,外周循环系统中的胆汁酸代表了一个特定但未得到充分认识的生理区室。我们讨论了全身胆汁酸如何被视为作用于白色脂肪细胞的特定甾体激素,并建议将脂肪细胞中特定的法尼醇X受体(FXR)/G蛋白偶联胆汁酸受体5(TGR5)受体相互作用命名为“胆汁因子”(“胆汁激素”)。一些胆汁酸及其激动剂可调节脂肪细胞分化、脂质积累、缺氧、自噬、脂肪因子和细胞因子分泌、胰岛素信号传导以及葡萄糖摄取。胆汁酸信号传导可能为内脏肥胖中的脂肪炎症和代谢炎症、胰岛素抵抗和2型糖尿病(T2D)的潜在因果机制提供一条新的治疗途径。

相似文献

1
The emerging role of bile acids in white adipose tissue.胆汁酸在白色脂肪组织中的新作用。
Trends Endocrinol Metab. 2023 Nov;34(11):718-734. doi: 10.1016/j.tem.2023.08.002. Epub 2023 Aug 29.
2
Hepatic Bile Acid Reuptake in the Rat Depends on Bile Acid Conjugation but Not on Agonistic Properties towards FXR and TGR5.在大鼠中,肝脏胆汁酸再摄取依赖于胆汁酸的结合,但不依赖于 FXR 和 TGR5 的激动特性。
Molecules. 2020 May 20;25(10):2371. doi: 10.3390/molecules25102371.
3
Bile acids contribute to the development of non-alcoholic steatohepatitis in mice.胆汁酸会促使小鼠发生非酒精性脂肪性肝炎。
JHEP Rep. 2021 Oct 13;4(1):100387. doi: 10.1016/j.jhepr.2021.100387. eCollection 2022 Jan.
4
Red ginseng extracts ameliorate high-fat diet-induced obesity and insulin resistance by activating the intestinal TGR5-mediated bile acids signaling pathway.红参提取物通过激活肠道 TGR5 介导的胆汁酸信号通路改善高脂饮食诱导的肥胖和胰岛素抵抗。
Phytomedicine. 2023 Oct;119:154982. doi: 10.1016/j.phymed.2023.154982. Epub 2023 Jul 22.
5
Evidence of functional bile acid signaling pathways in adipocytes.脂肪细胞中功能性胆汁酸信号通路的证据。
Mol Cell Endocrinol. 2019 Mar 1;483:1-10. doi: 10.1016/j.mce.2018.12.006. Epub 2018 Dec 11.
6
Bile acids induce energy expenditure by promoting intracellular thyroid hormone activation.胆汁酸通过促进细胞内甲状腺激素激活来诱导能量消耗。
Nature. 2006 Jan 26;439(7075):484-9. doi: 10.1038/nature04330. Epub 2006 Jan 8.
7
Bile acids as regulators of hepatic lipid and glucose metabolism.胆汁酸作为肝脏脂质和糖代谢的调节剂。
Dig Dis. 2010;28(1):220-4. doi: 10.1159/000282091. Epub 2010 May 7.
8
Functional changes of the gastric bypass microbiota reactivate thermogenic adipose tissue and systemic glucose control via intestinal FXR-TGR5 crosstalk in diet-induced obesity.饮食诱导肥胖中,胃旁路手术微生物群的功能变化通过肠道 FXR-TGR5 串扰重新激活产热脂肪组织和全身葡萄糖控制。
Microbiome. 2022 Jun 24;10(1):96. doi: 10.1186/s40168-022-01264-5.
9
Adipocyte-specific ablation of the Ca pump SERCA2 impairs whole-body metabolic function and reveals the diverse metabolic flexibility of white and brown adipose tissue.脂肪细胞特异性敲除 Ca 泵 SERCA2 会损害全身代谢功能,并揭示白色和棕色脂肪组织不同的代谢灵活性。
Mol Metab. 2022 Sep;63:101535. doi: 10.1016/j.molmet.2022.101535. Epub 2022 Jun 24.
10
[Role of metaflammation as a systemic manifestation of metabolic diseases].[代谢性炎症作为代谢性疾病的一种全身表现的作用]
Inn Med (Heidelb). 2023 Apr;64(4):313-322. doi: 10.1007/s00108-022-01416-7. Epub 2022 Nov 8.

引用本文的文献

1
Anti-Obesity Mechanisms of Plant and Fungal Polysaccharides: The Impact of Structural Diversity.植物和真菌多糖的抗肥胖机制:结构多样性的影响
Biomolecules. 2025 Aug 7;15(8):1140. doi: 10.3390/biom15081140.
2
Unraveling the complexities of diet induced obesity and glucolipid dysfunction in metabolic syndrome.解析代谢综合征中饮食诱导的肥胖和糖脂功能障碍的复杂性。
Diabetol Metab Syndr. 2025 Jul 22;17(1):292. doi: 10.1186/s13098-025-01837-y.
3
Crosstalk Between Bile Acids and Intestinal Epithelium: Multidimensional Roles of Farnesoid X Receptor and Takeda G Protein Receptor 5.
胆汁酸与肠上皮细胞之间的相互作用:法尼酯X受体和武田G蛋白偶联受体5的多维作用
Int J Mol Sci. 2025 Apr 29;26(9):4240. doi: 10.3390/ijms26094240.
4
Dynamics of the human bile acid metabolome during weight loss.人类胆汁酸代谢组在减肥过程中的动态变化。
Sci Rep. 2024 Oct 28;14(1):25743. doi: 10.1038/s41598-024-75831-1.
5
Bile Acids as Emerging Players at the Intersection of Steatotic Liver Disease and Cardiovascular Diseases.胆汁酸作为脂肪性肝病与心血管疾病交汇点的新兴参与者。
Biomolecules. 2024 Jul 12;14(7):841. doi: 10.3390/biom14070841.
6
The Potential Mechanism of Remission in Type 2 Diabetes Mellitus After Vertical Sleeve Gastrectomy.胃袖状切除术治疗 2 型糖尿病缓解的潜在机制
Obes Surg. 2024 Aug;34(8):3071-3083. doi: 10.1007/s11695-024-07378-z. Epub 2024 Jul 1.
7
Unveiling the Potential of Natural Compounds: A Comprehensive Review on Adipose Thermogenesis Modulation.揭示天然化合物的潜力:脂肪细胞产热调控的综合综述。
Int J Mol Sci. 2024 Apr 30;25(9):4915. doi: 10.3390/ijms25094915.
8
Hepatic interoception in health and disease.肝脏内脏感知在健康和疾病中的作用。
Auton Neurosci. 2024 Jun;253:103174. doi: 10.1016/j.autneu.2024.103174. Epub 2024 Mar 29.