Institute of Clinical Physiology, National Research Council, Pisa, Italy.
Curr Pharm Des. 2013;19(13):2420-31. doi: 10.2174/1381612811319130010.
Cardiometabolic risk comprises a cluster of traditional and emerging factors that are good indicators of a patient's overall risk for type 2 diabetes and cardiovascular disease. The insulin resistance, a key feature common to obesity and type 2 diabetes, is associated with impaired vascular response and contributes to increased cardiovascular risk. Abnormal vascular insulin signalling induces endothelial dysfunction, the initial step of atherosclerotic process, characterized by attenuated nitric oxide-mediated vasodilatation and atherogenic response. Insulin resistance and endothelial dysfunction are two pathological conditions that can co-exist, even if their cause-effect relationship is not yet clarified. Multiple signaling pathways shared by insulin resistance and endothelial dysfunction include hyperinsulinemia, glucotoxicity, lipotoxicity, and inflammation. These mechanisms selectively impair PI3K-dependent insulin in vascular endothelium harming endothelial balance and strengthening the evidence of the close association between metabolic and cardiovascular disease. The present review analyzes the close relationship between endothelial dysfunction and insulin resistance and explores the common mechanisms, with clinical considerations and pharmacological strategies.
心血管代谢风险包含了一组传统和新兴的因素,这些因素是预测 2 型糖尿病和心血管疾病整体风险的良好指标。胰岛素抵抗是肥胖和 2 型糖尿病的共同特征,与血管反应受损有关,并导致心血管风险增加。异常的血管胰岛素信号会导致内皮功能障碍,这是动脉粥样硬化过程的初始步骤,其特征是一氧化氮介导的血管舒张和动脉粥样硬化反应减弱。胰岛素抵抗和内皮功能障碍是两种可能同时存在的病理状况,尽管它们之间的因果关系尚不清楚。胰岛素抵抗和内皮功能障碍共同的多个信号通路包括高胰岛素血症、糖毒性、脂毒性和炎症。这些机制选择性地损害了血管内皮细胞中依赖 PI3K 的胰岛素,损害了内皮平衡,并加强了代谢和心血管疾病之间密切关联的证据。本综述分析了内皮功能障碍和胰岛素抵抗之间的密切关系,并探讨了共同的机制,同时考虑了临床和药理学策略。