11β-Hydroxysteroid Dehydrogenase 1: Translational and Therapeutic Aspects

被引:154
作者
Gathercole, Laura L. [1 ]
Lavery, Gareth G. [1 ]
Morgan, Stuart A. [1 ]
Cooper, Mark S. [1 ]
Sinclair, Alexandra J. [1 ]
Tomlinson, Jeremy W. [1 ]
Stewart, Paul M. [1 ]
机构
[1] Univ Birmingham, Sch Clin & Expt Med, Ctr Endocrinol Diabet & Metab, Birmingham B15 2TT, W Midlands, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会; 欧洲研究理事会;
关键词
POLYCYSTIC-OVARY-SYNDROME; BETA-HYDROXYSTEROID DEHYDROGENASE; PITUITARY-ADRENAL AXIS; CORTISONE-REDUCTASE DEFICIENCY; BODY-FAT DISTRIBUTION; HUMAN ADIPOSE-TISSUE; HEALTHY ELDERLY-MEN; SELECTIVE; 11-BETA-HSD1; INHIBITOR; NONALCOHOLIC HEPATIC STEATOSIS; INSULIN-RECEPTOR SUBSTRATE-1;
D O I
10.1210/er.2012-1050
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
11 beta-Hydroxysteroid dehydrogenase type 1 (11 beta-HSD1) interconverts the inactive glucocorticoid cortisone and its active form cortisol. It is widely expressed and, although bidirectional, in vivo it functions predominantly as an oxoreductase, generating active glucocorticoid. This allows glucocorticoid receptor activation to be regulated at a prereceptor level in a tissue-specific manner. In this review, we will discuss the enzymology and molecular biology of 11 beta-HSD1 and the molecular basis of cortisone reductase deficiencies. We will also address how altered 11 beta-HSD1 activity has been implicated in a number of disease states, and we will explore its role in the physiology and pathologies of different tissues. Finally, we will address the current status of selective 11 beta-HSD1 inhibitors that are in development and being tested in phase II trials for patients with the metabolic syndrome. Although the data are preliminary, therapeutic inhibition of 11 beta-HSD1 is also an exciting prospect for the treatment of a variety of other disorders such as osteoporosis, glaucoma, intracranial hypertension, and cognitive decline.
引用
收藏
页码:525 / 555
页数:31
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