Tsunetoshi T, Otsuka A, Mikami H, Katahira K, Moriguchi A, Ogihara T
Department of Geriatric Medicine, Osaka University Medical School, Japan.
Basic Res Cardiol. 1991 Jan-Feb;86(1):49-55. doi: 10.1007/BF02193871.
We evaluated whether cromakalim (BRL 34915), a vasorelaxant agent which acts by opening potassium channels, could affect the systemic effects of endothelin, a newly discovered vasoconstrictive peptide. Intravenous administration of endothelin alone (400 pmol/kg) to anesthetized dogs produced blood pressure elevation, which was associated with an increase in cardiac output in the early phase, and was associated with an increase in total peripheral resistance in the late phase. Electrocardiogram showed significant ST-elevation in II, III, and aVF, and ST-depression in aVR and aVL. The same dose of endothelin given to dogs pretreated with cromakalim did not induce these hemodynamic and electrocardiographic changes. Thus, cromakalim, a potassium activator, inhibited the hemodynamic and electrocardiographic actions of endothelin, suggesting that hyperpolarization due to potassium channel activation inhibited the voltage-dependent calcium channel, which is thought to be a major mechanism for the pressor action of endothelin.
我们评估了可通过开放钾通道发挥作用的血管舒张剂克罗卡林(BRL 34915)是否会影响内皮素(一种新发现的血管收缩肽)的全身效应。单独向麻醉犬静脉注射内皮素(400 pmol/kg)会导致血压升高,早期与心输出量增加相关,后期与总外周阻力增加相关。心电图显示II、III和aVF导联有明显的ST段抬高,aVR和aVL导联有ST段压低。给预先用克罗卡林处理过的犬注射相同剂量的内皮素并未引起这些血流动力学和心电图变化。因此,钾通道激活剂克罗卡林抑制了内皮素的血流动力学和心电图作用,这表明钾通道激活引起的超极化抑制了电压依赖性钙通道,而电压依赖性钙通道被认为是内皮素升压作用的主要机制。