Vincent Michelle A, Montagnani Monica, Quon Michael J
Diabetes Unit, Laboratory of Clinical Investigation, NCCAM, National Institutes of Health, 10 Center Drive, Building 10, Room 6C-205, Bethesda, MD 20892-1632, USA.
Curr Diab Rep. 2003 Aug;3(4):279-88. doi: 10.1007/s11892-003-0018-9.
Insulin has important vascular actions that regulate blood flow, in addition to its classical actions to coordinate glucose homeostasis. Insulin-stimulated production of nitric oxide in vascular endothelium results in capillary recruitment and vasodilation that diverts and increases blood flow to skeletal muscle and consequently increases glucose disposal. Thus, vascular actions of insulin may be essential for coupling hemodynamic and metabolic homeostasis. A complete biochemical signaling pathway linking the insulin receptor to activation of endothelial nitric oxide synthase in vascular endothelium has recently been elucidated. Moreover, the time course and dose response for capillary recruitment in response to physiologic concentrations of insulin parallels that of insulin-mediated glucose uptake in vivo. Taken together, these observations suggest a molecular mechanism that may help to explain how insulin resistance contributes to cardiovascular components of the metabolic syndrome and vascular complications of diabetes.
胰岛素除了具有协调葡萄糖稳态的经典作用外,还具有调节血流的重要血管作用。胰岛素刺激血管内皮细胞产生一氧化氮,导致毛细血管增生和血管舒张,从而使血液分流并增加流向骨骼肌的血流量,进而增加葡萄糖的处置。因此,胰岛素的血管作用可能对于耦合血液动力学和代谢稳态至关重要。最近已经阐明了一条将胰岛素受体与血管内皮细胞中内皮型一氧化氮合酶激活相联系的完整生化信号通路。此外,生理浓度胰岛素引起的毛细血管增生的时间进程和剂量反应与体内胰岛素介导的葡萄糖摄取相似。综上所述,这些观察结果提示了一种分子机制,或许有助于解释胰岛素抵抗如何导致代谢综合征的心血管组分以及糖尿病的血管并发症。