11β-HSD1 Inhibitors for the Treatment of Type 2 Diabetes and Cardiovascular Disease

被引:76
作者
Anderson, Anna [1 ]
Walker, Brian R. [1 ]
机构
[1] Univ Edinburgh, Queens Med Res Inst, Univ BHF Ctr Cardiovasc Sci, Edinburgh EH16 4TJ, Midlothian, Scotland
关键词
11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-1; SPLANCHNIC CORTISOL PRODUCTION; HEPATIC INSULIN SENSITIVITY; IMPROVES COGNITIVE FUNCTION; METABOLIC SYNDROME; ADIPOSE-TISSUE; HUMAN OBESITY; GLUCOCORTICOID ACTION; SELECTIVE-INHIBITION; HYPERGLYCEMIC MICE;
D O I
10.1007/s40265-013-0112-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Inhibition of the enzyme 11 beta-hydroxysteroid dehydrogenase type 1 (11 beta-HSD1) has been proposed as a novel therapeutic target for the treatment of type 2 diabetes mellitus. Over 170 new compounds targeting 11 beta-HSD1 have been developed. This article reviews the current published literature on compounds that have reached phase II clinical trials in patients with type 2 diabetes, and summarises the preclinical evidence that such agents may be useful for associated conditions, including peripheral vascular disease, coronary artery disease and cognitive decline. In clinical trials, 11 beta-HSD1 inhibitors have been well tolerated and have improved glycaemic control, lipid profile and blood pressure, and induced modest weight loss. The magnitude of the effects are small relative to other agents, so that further development of 11 beta-HSD1 inhibitors for the primary therapeutic indication of type 2 diabetes has stalled. Ongoing programmes are focused on additional benefits for cognitive function and other cardiovascular risk factors.
引用
收藏
页码:1385 / 1393
页数:9
相关论文
共 65 条
[1]   Selective inhibition of 11β-hydroxysteroid dehydrogenase type 1 improves hepatic insulin sensitivity in hyperglycemic mice strains [J].
Alberts, P ;
Nilsson, C ;
Selén, G ;
Engblom, LOM ;
Edling, NHM ;
Norling, S ;
Klingström, G ;
Larsson, C ;
Forsgren, M ;
Ashkzari, M ;
Nilsson, CE ;
Fiedler, M ;
Bergqvist, E ;
Öhman, B ;
Björkstrand, E ;
Abrahmsén, LB .
ENDOCRINOLOGY, 2003, 144 (11) :4755-4762
[2]   Selective inhibition of 11β-hydroxysteroid dehydrogenase type 1 decreases blood glucose concentrations in hyperglycaemic mice [J].
Alberts, P ;
Engblom, L ;
Edling, N ;
Forsgren, M ;
Klingström, G ;
Larsson, C ;
Rönquist-Nii, Y ;
Öhman, B ;
Abrahmsén, L .
DIABETOLOGIA, 2002, 45 (11) :1528-1532
[3]   Distinguishing the activities of 11β-hydroxysteroid dehydrogenases in vivo using isotopically labeled cortisol [J].
Andrew, R ;
Smith, K ;
Jones, GC ;
Walker, BR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (01) :277-285
[4]   The contribution of visceral adipose tissue to splanchnic cortisol production in healthy humans [J].
Andrew, R ;
Westerbacka, J ;
Wahren, J ;
Yki-Järvinen, H ;
Walker, BR .
DIABETES, 2005, 54 (05) :1364-1370
[5]   Effects of the 11β-hydroxysteroid dehydrogrenase inhibitor carbenoxolone on insulin sensitivity in men with type 2 diabetes [J].
Andrews, RC ;
Rooyackers, O ;
Walker, BR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (01) :285-291
[6]   11β-hydroxysteroid dehydrogenase type 1 gene expression is increased in ascending aorta tissue of metabolic syndrome patients with coronary artery disease [J].
Atalar, F. ;
Vural, B. ;
Ciftci, C. ;
Demirkan, A. ;
Akan, G. ;
Susleyici-Duman, B. ;
Gunay, D. ;
Akpinar, B. ;
Sagbas, E. ;
Ozbek, U. ;
Buyukdevrim, A. S. .
GENETICS AND MOLECULAR RESEARCH, 2012, 11 (03) :3122-3132
[7]   Splanchnic cortisol production occurs in humans -: Evidence for conversion of cortisone to cortisol via the 11-β hydroxysteroid dehydrogenase (11β-HSD) type 1 pathway [J].
Basu, R ;
Singh, RJ ;
Basu, A ;
Chittilapilly, EG ;
Johnson, CM ;
Toffolo, G ;
Cobelli, C ;
Rizza, RA .
DIABETES, 2004, 53 (08) :2051-2059
[8]   Liver Is the Site of Splanchnic Cortisol Production in Obese Nondiabetic Humans [J].
Basu, Rita ;
Basu, Ananda ;
Grudzien, Meagan ;
Jung, Paul ;
Jacobson, Peer ;
Johnson, Michael ;
Singh, Ravinder ;
Sarr, Michael ;
Rizza, Robert A. .
DIABETES, 2009, 58 (01) :39-45
[9]   11β-HSD1 inhibition improves triglyceridemia through reduced liver VLDL secretion and partitions lipids toward oxidative tissues [J].
Berthiaume, Magalie ;
Laplante, Mathieu ;
Festuccia, William T. ;
Cianflone, Katherine ;
Turcotte, Lorraine P. ;
Joanisse, Denis R. ;
Olivecrona, Gunilla ;
Thieringer, Rolf ;
Deshaies, Yves .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2007, 293 (04) :E1045-E1052
[10]   Muscle oxidative capacity is a better predictor of insulin sensitivity than lipid status [J].
Bruce, CR ;
Anderson, MJ ;
Carey, AL ;
Newman, DG ;
Bonen, A ;
Kriketos, AD ;
Cooney, GJ ;
Hawley, JA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (11) :5444-5451