类固醇
可药性
多囊卵巢
激素
胆汁酸
生物化学
生物
类固醇激素
生物转化
化学
受体
新陈代谢
胆固醇
肠道菌群
酶
内分泌学
基因
胰岛素抵抗
胰岛素
作者
Heidi L. Doden,Jason M. Ridlon
出处
期刊:Microorganisms
[Multidisciplinary Digital Publishing Institute]
日期:2021-02-24
卷期号:9 (3): 469-469
被引量:83
标识
DOI:10.3390/microorganisms9030469
摘要
Bile acids (BAs) and glucocorticoids are steroid hormones derived from cholesterol that are important signaling molecules in humans and other vertebrates. Hydroxysteroid dehydrogenases (HSDHs) are encoded both by the host and by their resident gut microbiota, and they reversibly convert steroid hydroxyl groups to keto groups. Pairs of HSDHs can reversibly epimerize steroids from α-hydroxy conformations to β-hydroxy, or β-hydroxy to ω-hydroxy in the case of ω-muricholic acid. These reactions often result in products with drastically different physicochemical properties than their precursors, which can result in steroids being activators or inhibitors of host receptors, can affect solubility in fecal water, and can modulate toxicity. Microbial HSDHs modulate sterols associated with diseases such as colorectal cancer, liver cancer, prostate cancer, and polycystic ovary syndrome. Although the role of microbial HSDHs is not yet fully elucidated, they may have therapeutic potential as steroid pool modulators or druggable targets in the future. In this review, we explore metabolism of BAs and glucocorticoids with a focus on biotransformation by microbial HSDHs.
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