糖皮质激素的作用和选择性糖皮质激素受体配体的发展。

Timothy J Cole
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引用次数: 56

摘要

糖皮质激素是广泛的生理系统的重要内分泌调节剂,从呼吸发育,免疫功能到应激反应。细胞中的糖皮质激素激活细胞质糖皮质激素受体(GR),该受体二聚体,易位到细胞核,并作为配体依赖性转录调节剂发挥作用。合成糖皮质激素,如地塞米松和强的松龙,几十年来一直是炎症性疾病(如风湿性关节炎和哮喘)以及一些淋巴细胞癌临床治疗的基石,但长期使用会产生不良副作用,如肥胖、糖尿病、免疫抑制和骨质疏松症。对GR作用机制的详细了解导致了新型选择性糖皮质激素受体调节剂(SGRMs)的发展,这种调节剂有望对疾病的特定治疗有效,但副作用更少。SGRMs促进转录共调节因子的特异性募集,从而引发特异性基因反应,并在治疗炎症性疾病和2型糖尿病方面显示出更大的功效和特异性。
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Glucocorticoid action and the development of selective glucocorticoid receptor ligands.

Glucocorticoids are important endocrine regulators of a wide range of physiological systems ranging from respiratory development, immune function to responses to stress. Glucocorticoids in cells activate the cytoplasmic glucocorticoid receptor (GR) that dimerizes, translocates to the nucleus and functions as a ligand-dependent transcriptional regulator. Synthetic glucocorticoids such as dexamethasone and prednisolone have for decades been the cornerstone for the clinical treatment of inflammatory diseases, such as rheumatoid arthritis and asthma, and in some lymphoid cancers, yet its prolonged use has undesirable side effects such as obesity, diabetes, immune suppression and osteoporosis. Detailed knowledge on the mechanism of GR action has led to the development of novel selective glucocorticoid receptor modulators (SGRMs) that show promise of being efficacious for specific treatments of disease but with fewer side effects. SGRMs promote specific recruitment of transcriptional co-regulators that elicit specific gene responses and show promise of greater efficacy and specificity in treatment of inflammatory diseases and type-2 diabetes.

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