类固醇生成酶 - 维基百科,自由的百科全书
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![](http://upload.wikimedia.org/wikipedia/commons/thumb/f/f5/Steroidogenesis_%28zh-tw%29.svg/600px-Steroidogenesis_%28zh-tw%29.svg.png)
类固醇生成酶类(英語:Steroidogenic enzymes)是指一大类涉及甾体激素生物合成与代谢的酶类[2][3][4][5]。这些酶参与合成的甾体激素包括性激素类(雄激素、雌激素、孕激素)和肾上腺皮质激素类(糖皮质激素和盐皮质激素,以及由胆固醇生成的神经甾体[3][4][5]。类固醇生成酶在涉及类固醇生成的组织,如睾丸、卵巢、肾上腺皮质里有很高的表达,但也存在于身体的其他组织[3][4][5]。
类固醇生成酶类列表
[编辑]- 甾体碳链裂解酶类
- Steroid hydroxylases
- 11β-Hydroxylase – corticosteroid synthesis
- 17α-羟化酶 – 雄激素与糖皮质激素生成
- 18-Hydroxylase (aldosterone synthase) – mineralocorticoid synthesis
- 21-Hydroxylase – corticosteroid synthesis
- 其它细胞色素P450氧化酶(如CYP1、2、3)– 雌激素代谢
- 羟基类固醇脱氢酶类(也即酮类固醇还原酶类)
- 3α-Hydroxysteroid dehydrogenase – androgen, progestogen, and neurosteroid synthesis and metabolism
- 3β-Hydroxysteroid dehydrogenase/Δ5-4-isomerase (1, 2) – androgen, progestogen, and neurosteroid synthesis
- 11β-羟基类固醇脱氢酶(1、2)– 肾上腺皮质激素合成与代谢
- 17β-羟基类固醇脱氢酶(1–15)– 三种性激素的合成与代谢
- 20α-Hydroxysteroid dehydrogenase – progestogen synthesis and metabolism
- 20β-羟基类固醇脱氢酶 – 孕激素的合成与代谢
![](http://upload.wikimedia.org/wikipedia/commons/thumb/d/df/Trimethyl_steroid-nomenclature.png/400px-Trimethyl_steroid-nomenclature.png)
- 甾体还原酶类
- Conjugation (and deconjugation)
- Glucuronosyltransferase (UGT2Bs) – steroid metabolism[6]
- Glucuronidase (β-glucuronidase) – steroid synthesis[7]
- Steroid sulfotransferase (SULT1A1, 1E1, 2A1, 2B1a, 2B1b) – steroid metabolism, neurosteroid synthesis[8]
- Steroid sulfatase – steroid synthesis, neurosteroid metabolism[8]
- 其它
- 芳香化酶(雌激素合成酶,CYP19A1)合成雌激素
另见
[编辑]参考文献
[编辑]- ^ Häggström, Mikael; Richfield, David. Diagram of the pathways of human steroidogenesis. WikiJournal of Medicine. [2019-06-28]. doi:10.15347/wjm/2014.005. (原始内容存档于2021-02-28) (英语).
- ^ Hanukoglu I. Steroidogenic enzymes: structure, function, and role in regulation of steroid hormone biosynthesis. The Journal of Steroid Biochemistry and Molecular Biology. Dec 1992, 43 (8): 779–804. PMID 22217824. doi:10.1016/0960-0760(92)90307-5.
- ^ 3.0 3.1 3.2 Payne AH, Hales DB. Overview of steroidogenic enzymes in the pathway from cholesterol to active steroid hormones. Endocr. Rev. 2004, 25 (6): 947–70. PMID 15583024. doi:10.1210/er.2003-0030.
- ^ 4.0 4.1 4.2 Luu-The V, Labrie F. The intracrine sex steroid synthesis pathways. Prog. Brain Res. 2010, 181: 177–92. PMID 20478438. doi:10.1016/S0079-6123(08)81010-2.
- ^ 5.0 5.1 5.2 Honour JW. Diagnosis of diseases of steroid hormone production, metabolism and action. J Clin Res Pediatr Endocrinol. 2009, 1 (5): 209–26. PMC 3005746
. PMID 21274298. doi:10.4274/jcrpe.v1i5.209.
- ^ Guillemette C, Lévesque E, Harvey M, Bellemare J, Menard V. UGT genomic diversity: beyond gene duplication. Drug Metab. Rev. 2010, 42 (1): 24–44. PMID 19857043. doi:10.3109/03602530903210682.
- ^ William Fishman. Metabolic Conjugation and Metabolic Hydrolysis, Volume II. Elsevier. 2 December 2012: 1–. ISBN 978-0-323-14308-0.
- ^ 8.0 8.1 Mueller JW, Gilligan LC, Idkowiak J, Arlt W, Foster PA. The Regulation of Steroid Action by Sulfation and Desulfation. Endocr. Rev. 2015, 36 (5): 526–63. PMC 4591525
. PMID 26213785. doi:10.1210/er.2015-1036.