Yue Tian-Li
Department of Investigative and Cardiac Biology, GlaxoSmithKline Pharmaceuticals, King of Prussia, PA 19406, USA.
Drugs Today (Barc). 2003 Dec;39(12):949-60. doi: 10.1358/dot.2003.39.12.799413.
Greater myocardial injury in response to ischemia/ reperfusion (I/R) and increased incidence of congestive heart failure and death in noninsulin-dependent diabetes mellitus, or type 2 diabetes, patients has been clearly identified. Thiazolidinediones (TZDs), peroxisome proliferator-activated receptor-gamma (PPAR-gamma) agonists, act as insulin sensitizers and are a novel class of oral antidiabetic drugs. An emerging body of evidence, mainly from preclinical studies, suggest that TZDs protect the heart from acute I/R injury and also might attenuate cardiac remodeling and heart failure. The mechanisms involved in this cardioprotection by TZDs are multi-factorial and not completely understood. These novel activities of TZDs could benefit type 2 diabetes patients and offer benefits beyond glycemic control. This new knowledge about the cardioprotective effects of TZDs is still limited, and more investigations, especially clinical studies, are required.
在非胰岛素依赖型糖尿病(即2型糖尿病)患者中,对缺血/再灌注(I/R)的心肌损伤加剧,以及充血性心力衰竭和死亡的发生率增加,这一点已得到明确证实。噻唑烷二酮类药物(TZDs),即过氧化物酶体增殖物激活受体γ(PPAR-γ)激动剂,作为胰岛素增敏剂,是一类新型的口服抗糖尿病药物。主要来自临床前研究的越来越多的证据表明,TZDs可保护心脏免受急性I/R损伤,还可能减轻心脏重塑和心力衰竭。TZDs这种心脏保护作用的机制是多因素的,尚未完全明确。TZDs的这些新活性可能使2型糖尿病患者受益,并提供血糖控制以外的益处。关于TZDs心脏保护作用的这一新知识仍然有限,需要更多的研究,尤其是临床研究。