Quinn C E, Hamilton P K, Lockhart C J, McVeigh G E
Department of Therapeutics and Pharmacology, Queen's University Belfast, Belfast, UK.
Br J Pharmacol. 2008 Feb;153(4):636-45. doi: 10.1038/sj.bjp.0707452. Epub 2007 Oct 1.
Thiazolidinediones (TZDs) have been used for the treatment of hyperglycaemia in type 2 diabetes for the past 10 years. They may delay the development of type 2 diabetes in individuals at high risk of developing the condition, and have been shown to have potentially beneficial effects on cardiovascular risk factors. TZDs act as agonists of peroxisome proliferator-activated receptor-gamma (PPAR-gamma) primarily in adipose tissue. PPAR-gamma receptor activation by TZDs improves insulin sensitivity by promoting fatty acid uptake into adipose tissue, increasing production of adiponectin and reducing levels of inflammatory mediators such as tumour necrosis factor-alpha (TNF-alpha), plasminogen activator inhibitor-1(PAI-1) and interleukin-6 (IL-6). Clinically, TZDs have been shown to reduce measures of atherosclerosis such as carotid intima-media thickness (CIMT). However, in spite of beneficial effects on markers of cardiovascular risk, TZDs have not been definitively shown to reduce cardiovascular events in patients, and the safety of rosiglitazone in this respect has recently been called into question. Dual PPAR-alpha/gamma agonists may offer superior treatment of insulin resistance and cardioprotection, but their safety has not yet been assured.
在过去十年中,噻唑烷二酮类药物(TZDs)一直用于治疗2型糖尿病的高血糖症。它们可能会延缓有患2型糖尿病高风险个体的病情发展,并且已被证明对心血管危险因素具有潜在的有益作用。TZDs主要在脂肪组织中作为过氧化物酶体增殖物激活受体γ(PPAR-γ)的激动剂发挥作用。TZDs激活PPAR-γ受体可通过促进脂肪酸摄取到脂肪组织中、增加脂联素的产生以及降低炎症介质如肿瘤坏死因子-α(TNF-α)、纤溶酶原激活物抑制剂-1(PAI-1)和白细胞介素-6(IL-6)的水平来提高胰岛素敏感性。临床上,TZDs已被证明可降低动脉粥样硬化的指标,如颈动脉内膜中层厚度(CIMT)。然而,尽管对心血管风险标志物有有益作用,但TZDs尚未被明确证明可减少患者的心血管事件,并且罗格列酮在这方面的安全性最近受到了质疑。双重PPAR-α/γ激动剂可能对胰岛素抵抗和心脏保护提供更好的治疗,但它们的安全性尚未得到保证。