Miki Takashi, Seino Susumu
Division of Cellular and Molecular Medicine, Kobe University Graduate School of Medicine, Chuo-ku, Japan.
J Mol Cell Cardiol. 2005 Jun;38(6):917-25. doi: 10.1016/j.yjmcc.2004.11.019. Epub 2005 Feb 5.
Physiological and pathophysiological roles of K(ATP) channels have been clarified recently in genetically engineered mice. The Kir6.2-containing K(ATP) channels in pancreatic ss-cells and the hypothalamus are essential in the regulation of glucose-induced insulin secretion and hypoglycemia-induced glucagon secretion, respectively, and are involved in glucose uptake in skeletal muscles, thus playing a key role in the maintenance of glucose homeostasis. Disruption of Kir6.1-containing K(ATP) channels in mice leads to spontaneous vascular spasm mimicking vasospastic (Prinzmetal) angina in humans, indicating that the Kir6.1-containing K(ATP) channels in vascular smooth muscles participate in the regulation of vascular tonus, especially in coronary arteries. Together with protective roles of K(ATP) channels against cardiac ischemia and hypoxia-induced seizure propagation, it is now clear that K(ATP) channels, as metabolic sensors, are critical in the maintenance of homeostasis against acute metabolic changes.
近年来,通过基因工程小鼠已阐明了K(ATP)通道的生理和病理生理作用。胰腺β细胞和下丘脑中含Kir6.2的K(ATP)通道分别在调节葡萄糖诱导的胰岛素分泌和低血糖诱导的胰高血糖素分泌中起重要作用,并参与骨骼肌中的葡萄糖摄取,从而在维持葡萄糖稳态中发挥关键作用。小鼠中含Kir6.1的K(ATP)通道的破坏会导致自发性血管痉挛,类似于人类的血管痉挛性(变异型)心绞痛,这表明血管平滑肌中含Kir6.1的K(ATP)通道参与血管张力的调节,尤其是在冠状动脉中。再加上K(ATP)通道对心脏缺血和缺氧诱导的癫痫传播的保护作用,现在很清楚,K(ATP)通道作为代谢传感器,在维持对急性代谢变化的稳态中至关重要。