Role of PPAR- gamma agonist thiazolidinediones in treatment of pre-diabetic and diabetic individuals: a cardiovascular perspective.

Rupal Dumasia, Kim A Eagle, Eva Kline-Rogers, Niquole May, Leslie Cho, Debabrata Mukherjee
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引用次数: 59

Abstract

The peroxisome proliferator-activated receptors (PPARs) are nuclear fatty acid receptors, which contain a type II zinc finger DNA binding motif and a hydrophobic ligand binding pocket. These receptors are thought to play an important role in metabolic diseases such as obesity, insulin resistance, and coronary artery disease. Three subtypes of PPAR receptors have been described: PPARalpha, PPARdelta/beta, and PPARgamma. PPARalpha is found in the liver, muscle, kidney, and heart. In the liver, its role is to up-regulate genes involved in fatty acid uptake (beta-oxidation and omega-oxidation). PPARdelta/beta is involved in fatty acid oxidation in muscle. PPARgamma has high expression in fat, low expression in the liver, and very low expression in the muscle. The thiazolidinediones (TZD) are synthetic ligands of PPARgamma. By activating a number of genes in tissues, PPARgamma increases glucose and lipid uptake, increases glucose oxidation, decreases free fatty acid concentration, and decreases insulin resistance. There is a sound rationale for the use of TZDs in patients with type 2 diabetes mellitus and promising preliminary data in patients with patients with pre-diabetes. In patients with type 2 diabetes, thiazolidinediones had been shown to decrease mean HbA(1c)by 1.5% and lower HbA(1c) to less than 7% in 30% of patients. Decreased muscle insulin resistance primarily mediates the glucose lowering effect. In addition, there are several nonhypoglycemic effects of TZDs which may be beneficial to both diabetics and patients with pre-diabetes. These include effects on lipid metabolism, blood pressure, endothelial function, atherosclerotic plaque, coagulation, and albuminuria. In a pilot study, we recently demonstrated that insulin sensitizers such as thiazolidinediones appear to be associated with better clinical outcomes compared to insulin providers in diabetic patients presenting with acute coronary syndromes. In another study, we showed that the prediabetic state is a marker for worse prognosis in patients with acute coronary syndromes. In this article, we review the existing literature on the effectiveness of PPAR-gamma agonists in patients with either overt diabetes or a prediabetic state.

PPAR- γ激动剂噻唑烷二酮在治疗糖尿病前期和糖尿病患者中的作用:心血管的观点。
过氧化物酶体增殖体激活受体(ppar)是一种核脂肪酸受体,它包含一个II型锌指DNA结合基序和一个疏水配体结合袋。这些受体被认为在代谢性疾病如肥胖、胰岛素抵抗和冠状动脉疾病中起重要作用。PPAR受体有三种亚型:PPAR α、PPAR δ / β和PPAR γ。ppar存在于肝脏、肌肉、肾脏和心脏中。在肝脏中,它的作用是上调参与脂肪酸摄取(β -氧化和ω -氧化)的基因。ppar δ / β参与肌肉中的脂肪酸氧化。PPARgamma在脂肪中高表达,在肝脏中低表达,在肌肉中极低表达。噻唑烷二酮(TZD)是PPARgamma的合成配体。通过激活组织中的许多基因,PPARgamma增加葡萄糖和脂质摄取,增加葡萄糖氧化,降低游离脂肪酸浓度,并降低胰岛素抵抗。在2型糖尿病患者中使用TZDs有充分的理由,在糖尿病前期患者中使用TZDs的初步数据也很有希望。在2型糖尿病患者中,噻唑烷二酮类药物已被证明可使平均HbA(1c)降低1.5%,30%的患者的HbA(1c)降低至7%以下。肌肉胰岛素抵抗降低主要介导降血糖作用。此外,TZDs还有一些非降糖作用,可能对糖尿病患者和糖尿病前期患者都有益。这些包括对脂质代谢、血压、内皮功能、动脉粥样硬化斑块、凝血和蛋白尿的影响。在一项初步研究中,我们最近证明,在急性冠状动脉综合征的糖尿病患者中,与胰岛素提供者相比,胰岛素增敏剂如噻唑烷二酮类药物似乎与更好的临床结果相关。在另一项研究中,我们发现糖尿病前期状态是急性冠状动脉综合征患者预后较差的标志。在这篇文章中,我们回顾了ppar - γ激动剂对显性糖尿病或糖尿病前期患者有效性的现有文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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