11β-hydroxysteroid dehydrogenase Type 1 as a novel therapeutic target in metabolic and neurodegenerative disease

被引:38
作者
Walker, BR [1 ]
Seckl, JR [1 ]
机构
[1] Univ Edinburgh, Western Gen Hosp, Endocrinol Unit, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
11 beta-hydroxysteroid dehydrogenase Type I (11HSD1); cognitive impairment no dementia; glucocordcoids; hypertension; metabolic syndrome;
D O I
10.1517/eott.7.6.771.22573
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
11beta-Hydroxysteroid dehydrogenase Type 1 (11HSD1) catalyses regeneration of active 11-hydroxy glucocorticoids from inactive 11-keto metabolites within target tissues. Inhibition of 11HSD1 has been proposed as a novel strategy to lower intracellular glucocorticoid concentrations, without affecting circulating glucocorticoid levels and their responsiveness to stress. Increased 11HSD1 activity may be pathogenic, for example, in adipose tissue in obesity. Experiments in transgenic mice and using prototype inhibitors in humans show benefits of 11HSD1 inhibition in liver, adipose and brain tissue in treating features of the metabolic syndrome and cognitive dysfunction with ageing. The clinical development of potent selective 11HSD1 inhibitors is now a high priority.
引用
收藏
页码:771 / 783
页数:13
相关论文
共 136 条
[1]  
AGARWAL AK, 1994, J BIOL CHEM, V269, P25959
[2]  
AGARWAL AK, 1989, J BIOL CHEM, V264, P18939
[3]   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
[4]   CLONING AND TISSUE DISTRIBUTION OF THE HUMAN 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-2 ENZYME [J].
ALBISTON, AL ;
OBEYESEKERE, VR ;
SMITH, RE ;
KROZOWSKI, ZS .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1994, 105 (02) :R11-R17
[5]   Obesity and gender influence cortisol secretion and metabolism in man [J].
Andrew, R ;
Phillips, DIW ;
Walker, BR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (05) :1806-1809
[6]   Abnormal cortisol metabolism and tissue sensitivity to cortisol in patients with glucose intolerance [J].
Andrews, RC ;
Herlihy, O ;
Livingstone, DEW ;
Andrew, R ;
Walker, BR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (12) :5587-5593
[7]   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
[8]   Arylsulfonamidothiazoles as a new class of potential antidiabetic drugs.: Discovery of potent and selective inhibitors of the 11β-hydroxysteroid dehydrogenase type 1 [J].
Barf, T ;
Vallgårda, J ;
Emond, R ;
Häggström, C ;
Kurz, G ;
Nygren, A ;
Larwood, V ;
Mosialou, E ;
Axelsson, K ;
Olsson, R ;
Engblom, L ;
Edling, N ;
Rönquist-Nii, Y ;
Öhman, B ;
Alberts, P ;
Abrahmsén, L .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (18) :3813-3815
[9]   Hypothalamic arousal, insulin resistance and Type 2 diabetes mellitus [J].
Björntorp, P ;
Holm, G ;
Rosmond, R .
DIABETIC MEDICINE, 1999, 16 (05) :373-383
[10]   11 beta OH-progesterone affects vascular glucocorticoid metabolism and contractile response [J].
Brem, AS ;
Bina, RB ;
King, T ;
Morris, DJ .
HYPERTENSION, 1997, 30 (03) :449-454