The role of botanical triterpenoids and steroids in bile acid metabolism, transport, and signaling: Pharmacological and toxicological implications

IF 14.7 1区 医学 Q1 PHARMACOLOGY & PHARMACY Acta Pharmaceutica Sinica. B Pub Date : 2024-08-01 DOI:10.1016/j.apsb.2024.04.027
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Abstract

Bile acids (BAs) are synthesized by the host liver from cholesterol and are delivered to the intestine, where they undergo further metabolism by gut microbes and circulate between the liver and intestines through various transporters. They serve to emulsify dietary lipids and act as signaling molecules, regulating the host's metabolism and immune homeostasis through specific receptors. Therefore, disruptions in BA metabolism, transport, and signaling are closely associated with cholestasis, metabolic disorders, autoimmune diseases, and others. Botanical triterpenoids and steroids share structural similarities with BAs, and they have been found to modulate BA metabolism, transport, and signaling, potentially exerting pharmacological or toxicological effects. Here, we have updated the research progress on BA, with a particular emphasis on new-found microbial BAs. Additionally, the latest advancements in targeting BA metabolism and signaling for disease treatment are highlighted. Subsequently, the roles of botanical triterpenoids in BA metabolism, transport, and signaling are examined, analyzing their potential pharmacological, toxicological, or drug interaction effects through these mechanisms. Finally, a research paradigm is proposed that utilizes the gut microbiota as a link to interpret the role of these important natural products in BA signaling.

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植物三萜类和类固醇在胆汁酸代谢、转运和信号传递中的作用:药理学和毒理学意义
胆汁酸(BA)由宿主肝脏从胆固醇中合成并释放出来,然后输送到肠道,在肠道微生物的作用下进一步代谢,并通过各种转运体在肝脏和肠道之间循环。它们的作用是乳化食物中的脂质,并作为信号分子,通过特定受体调节宿主的新陈代谢和免疫平衡。因此,BA 代谢、运输和信号传递的紊乱与胆汁淤积症、代谢紊乱、自身免疫性疾病等密切相关。植物三萜类化合物和类固醇在结构上与胆碱酯酶有相似之处,它们可调节胆碱酯酶的代谢、转运和信号传导,从而产生潜在的药理或毒理作用。在此,我们更新了有关生物碱的研究进展,特别强调了新发现的微生物生物碱。此外,我们还重点介绍了针对 BA 代谢和信号转导进行疾病治疗的最新进展。随后,研究了植物三萜类化合物在 BA 代谢、转运和信号转导中的作用,分析了它们通过这些机制可能产生的药理、毒理或药物相互作用效应。最后,提出了一种研究范式,利用肠道微生物群作为纽带,解释这些重要天然产品在 BA 信号转导中的作用。
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来源期刊
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica. B Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
22.40
自引率
5.50%
发文量
1051
审稿时长
19 weeks
期刊介绍: The Journal of the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association oversees the peer review process for Acta Pharmaceutica Sinica. B (APSB). Published monthly in English, APSB is dedicated to disseminating significant original research articles, rapid communications, and high-quality reviews that highlight recent advances across various pharmaceutical sciences domains. These encompass pharmacology, pharmaceutics, medicinal chemistry, natural products, pharmacognosy, pharmaceutical analysis, and pharmacokinetics. A part of the Acta Pharmaceutica Sinica series, established in 1953 and indexed in prominent databases like Chemical Abstracts, Index Medicus, SciFinder Scholar, Biological Abstracts, International Pharmaceutical Abstracts, Cambridge Scientific Abstracts, and Current Bibliography on Science and Technology, APSB is sponsored by the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association. Its production and hosting are facilitated by Elsevier B.V. This collaborative effort ensures APSB's commitment to delivering valuable contributions to the pharmaceutical sciences community.
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