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噻唑烷二酮类药物在皮肤科的应用

Thiazolidinediones in dermatology.

作者信息

Boyd Alan S

机构信息

Department of Medicine (Dermatology), Vanderbilt University, Nashville, TN, USA.

出版信息

Int J Dermatol. 2007 Jun;46(6):557-63. doi: 10.1111/j.1365-4632.2007.03273.x.

Abstract

Thiazolidinediones, also known as glitazones, represent a relatively new class of medication used for glycemic control in patients with type II diabetes mellitus. These drugs interact with the peroxisome proliferator-activated receptor gamma, a member of the nuclear receptor superfamily, which in turn heterodimerizes with retinoid X receptors to stimulate gene transcription. At a physiologic level, glitazones stimulate adipocyte differentiation, enhance insulin-sensitive glucose uptake by muscle and fat cells, suppress angiogenesis, inhibit tumor cell growth, and normalize keratinocyte differentiation. They have also demonstrated the capacity to diminish inflammatory cytokine production, most notably, that of tumor necrosis factor alpha. Patients with such disparate conditions as psoriasis, hirsutism, melanoma, angiosarcoma, lipodystrophy, and necrobiosis lipoidica have benefited from the administration of thiazolidinediones. Clinicians should become familiar with glitazones as they are experiencing a burgeoning use among patients with non-insulin-dependent diabetes mellitus and have demonstrated clinical efficacy in treating certain skin conditions.

摘要

噻唑烷二酮类药物,也被称为格列酮类药物,是用于控制II型糖尿病患者血糖的一类相对较新的药物。这些药物与过氧化物酶体增殖物激活受体γ相互作用,过氧化物酶体增殖物激活受体γ是核受体超家族的一员,它会与视黄醇X受体形成异源二聚体以刺激基因转录。在生理层面,格列酮类药物可刺激脂肪细胞分化,增强肌肉和脂肪细胞对胰岛素敏感的葡萄糖摄取,抑制血管生成,抑制肿瘤细胞生长,并使角质形成细胞分化正常化。它们还显示出减少炎性细胞因子产生的能力,最显著的是肿瘤坏死因子α。患有诸如银屑病、多毛症、黑色素瘤、血管肉瘤、脂肪营养不良和类脂质渐进性坏死等不同病症的患者已从噻唑烷二酮类药物的给药中获益。临床医生应熟悉格列酮类药物,因为它们在非胰岛素依赖型糖尿病患者中使用日益增多,并且已证明在治疗某些皮肤疾病方面具有临床疗效。

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