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噻唑烷二酮类药物——近期进展

Thiazolidinediones -- some recent developments.

作者信息

Stumvoll Michael

机构信息

Medizinische Klinik, Abteilung für Endokrinologie, Stoffwechsel und Pathobiochemie, Eberhard-karls-Universität, Tübingen, Germany.

出版信息

Expert Opin Investig Drugs. 2003 Jul;12(7):1179-87. doi: 10.1517/13543784.12.7.1179.

Abstract

The role of thiazolidinediones (currently rosiglitazone and pioglitazone) in the treatment of Type 2 diabetes is firmly established. The mechanism of action involves binding to the peroxisome proliferator-activated receptor-gamma, a transcription factor that regulates the expression of specific genes especially in fat cells but also other cell types such as endothelial cells, macrophages and monocytes, vascular smooth muscle cells and colonic epithelium. Thiazolidinediones have been shown to interfere with expression and release of mediators of insulin resistance originating in adipose tissue (e.g., increased free fatty acids, decreased adiponectin) in a way that results in net improvement of insulin sensitivity (i.e., in muscle and liver). A direct or indirect effect on AMP-dependent protein kinase may also be involved. Prevention of lipid accumulation in tissues critical to glycaemia such as visceral adipocytes, liver, muscle and beta-cells at the expense of lipids accumulating at the less harmful subcutaneous site may be central to their net metabolic effect. The sustained beneficial effect of troglitazone on beta-cell function in women with previous gestational diabetes in addition to the insulin-sensitising properties point to an important role of this class of drugs in the prevention of Type 2 diabetes. Original safety concerns based on animal and in vitro studies (e.g., fatty bone marrow transformation, colonic cancer, adipogenic transdifferentiation of blood cells) remain theoretical issues but become less pressing practically with prolonged uneventful clinical use. Hepatotoxicity for troglitazone and fluid retention, which can aggravate pre-existing heart failure, are the most important side effects. In summary, with the thiazolidinediones, a novel concept for the treatment of insulin resistance and possibly preservation of beta-cell function is available that could become effective in the prevention of Type 2 diabetes. Moreover, their anti-inflammatory properties also make them interesting in the prevention and treatment of atherosclerosis and possibly other inflammatory conditions (e.g., inflammatory bowel disease). Long-term data will be necessary for a final risk-benefit assessment of these substances.

摘要

噻唑烷二酮类药物(目前包括罗格列酮和吡格列酮)在2型糖尿病治疗中的作用已得到明确确立。其作用机制包括与过氧化物酶体增殖物激活受体γ结合,该受体是一种转录因子,可调节特定基因的表达,特别是在脂肪细胞中,但也存在于其他细胞类型中,如内皮细胞、巨噬细胞和单核细胞、血管平滑肌细胞及结肠上皮细胞。噻唑烷二酮类药物已被证明可干扰源自脂肪组织的胰岛素抵抗介质的表达和释放(如游离脂肪酸增加、脂联素减少),从而使胰岛素敏感性(即肌肉和肝脏中的胰岛素敏感性)得到净改善。这可能还涉及对AMP依赖性蛋白激酶的直接或间接作用。以减少有害的皮下部位脂质蓄积为代价,防止脂质在对血糖至关重要的组织(如内脏脂肪细胞、肝脏、肌肉和β细胞)中蓄积,可能是其净代谢效应的核心。曲格列酮对既往有妊娠糖尿病的女性β细胞功能具有持续有益作用,除了其胰岛素增敏特性外,这表明这类药物在预防2型糖尿病中具有重要作用。基于动物和体外研究的最初安全性担忧(如脂肪性骨髓转化、结肠癌、血细胞的脂肪生成转分化)仍然只是理论问题,但随着长期平稳的临床应用,这些问题在实际中变得不那么紧迫。曲格列酮的肝毒性以及可加重已有的心力衰竭的液体潴留是最重要的副作用。总之,噻唑烷二酮类药物提供了一种治疗胰岛素抵抗以及可能保护β细胞功能的新观念,这可能对预防2型糖尿病有效。此外,它们的抗炎特性也使其在预防和治疗动脉粥样硬化以及可能的其他炎症性疾病(如炎症性肠病)方面具有吸引力。对于这些药物进行最终的风险效益评估需要长期数据。

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