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血管平滑肌中ATP敏感性钾通道的功能作用

Functional roles of KATP channels in vascular smooth muscle.

作者信息

Brayden Joseph E

机构信息

Department of Pharmacology, The University of Vermont, College of Medicine, Burlington, Vermont 05405, USA.

出版信息

Clin Exp Pharmacol Physiol. 2002 Apr;29(4):312-6. doi: 10.1046/j.1440-1681.2002.03650.x.

Abstract
  1. ATP-sensitive potassium channels (K(ATP)) are present in vascular smooth muscle cells and play important roles in the vascular responses to a variety of pharmacological and endogenous vasodilators. 2. The K(ATP) channels are composed of four inwardly rectifying K+ channel subunits and four regulatory sulphonylurea receptors. The K(ATP) channels are inhibited by intracellular ATP and by sulphonylurea agents. 3. Pharmacological vasodilators such as cromakalim, pinacidil and diazoxide directly activate K(ATP) channels. The associated membrane hyperpolarization closes voltage-dependent Ca2+ channels, which leads to a reduction in intracellular Ca2+ and vasodilation. 4. Endogenous vasodilators such as calcitonin gene-related peptide, vasoactive intestinal polypeptide, prostacylin and adenosine activate K(ATP) by stimulating the formation of cAMP and increasing the activity of protein kinase A. Part of the mechanism of contraction of endogenous vasoconstrictors is due to inhibition of K(ATP) channels. 5. The K(ATP) channels appear to be tonically active in some vascular beds and contribute to the physiological regulation of vascular tone and blood flow. These channels also are activated under pathophysiological conditions, such as hypoxia, ischaemia, acidosis and septic shock, and, in these disease states, may play an important role in the regulation of tissue perfusion.
摘要
  1. ATP敏感性钾通道(K(ATP))存在于血管平滑肌细胞中,在血管对多种药理和内源性血管舒张剂的反应中发挥重要作用。2. K(ATP)通道由四个内向整流钾通道亚基和四个调节性磺脲类受体组成。K(ATP)通道受细胞内ATP和磺脲类药物抑制。3. 药理血管舒张剂如克罗卡林、匹那地尔和二氮嗪直接激活K(ATP)通道。相关的膜超极化关闭电压依赖性钙通道,导致细胞内钙减少和血管舒张。4. 内源性血管舒张剂如降钙素基因相关肽、血管活性肠肽、前列环素和腺苷通过刺激cAMP形成和增加蛋白激酶A的活性来激活K(ATP)。内源性血管收缩剂的部分收缩机制是由于抑制K(ATP)通道。5. K(ATP)通道似乎在某些血管床中具有紧张性活性,有助于血管张力和血流的生理调节。这些通道在病理生理条件下如缺氧、缺血、酸中毒和脓毒性休克时也被激活,并且在这些疾病状态下可能在组织灌注调节中起重要作用。

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