Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Campus Mitte, Berlin, Germany.
Mol Cell Endocrinol. 2013 Nov 5;380(1-2):32-40. doi: 10.1016/j.mce.2013.01.026. Epub 2013 Feb 8.
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 genomic 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.
糖皮质激素(GCs)广泛用于治疗各种风湿性疾病和其他炎症性疾病。它们主要通过细胞溶质糖皮质激素受体(cGR)介导的所谓基因组机制发挥其强大的抗炎和免疫抑制作用。这种 GC 作用机制可分为反式激活和反式抑制过程。然而,GC 还存在快速作用,这是由特定和非特异性非基因组机制介导的。这种 GC 作用方式的临床相关性假定为通过膜结合糖皮质激素受体介导的作用,但对潜在机制的详细了解仍然缺乏。过去,人们做出了巨大努力来减少 GC 引起的不良反应,从而提高药物的获益/风险比。除了改善临床医生目前可用的常规 GC 治疗的方法外,还正在开发新型创新 GC 或 GC 受体配体。