Optimized glucocorticoid therapy: Teaching old drugs new tricks

被引:70
|
作者
Strehl, Cindy [1 ]
Buttgereit, Frank [1 ]
机构
[1] Charite, Dept Rheumatol & Clin Immunol, D-10117 Berlin, Germany
关键词
Glucocorticoids; Genomic and nongenomic mechanisms of action; Membrane-bound glucocorticoid receptors; Clinical effects; STEROID-HORMONE RECEPTORS; ANTIGEN-INDUCED ARTHRITIS; LIGAND-SPECIFIC DYNAMICS; BLOOD MONONUCLEAR-CELLS; BONE-MINERAL DENSITY; NF-KAPPA-B; RHEUMATOID-ARTHRITIS; TRANSCRIPTIONAL ACTIVATION; TRANSACTIVATION DOMAIN; NUCLEAR RECEPTORS;
D O I
10.1016/j.mce.2013.01.026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glucocorticoids (GCs) are commonly used in the treatment of a wide range of rheumatic and other inflammatory diseases. They exert their potent anti-inflammatory and immunosuppressive effects primarily via so called genomie mechanisms, mediated by the cytosolic glucocorticoid receptor (cGR). This mechanism of GC action can be divided into the transactivation and the transrepression processes. However, also rapid effects of GCs exist which are mediated by specific and unspecific non-genomic mechanisms. A clinical relevance of this mode of GC action is assumed for effects mediated by membrane-bound glucocorticoid receptors, but detailed knowledge on the underlying mechanisms is still missing. Great efforts have been made in the past to diminish GC-induced adverse effects, thus improving the benefit/risk ratio of the drugs. Besides approaches to improve the treatment with conventional glucocorticoids currently available to clinicians, new innovative GCs or GC receptor ligands are also being developed. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
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页码:32 / 40
页数:9
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