Nakamura M, Funakoshi T, Yoshida H, Arakawa N, Suzuki T, Hiramori K
Department of Internal Medicine II, Iwate Medical University, Japan.
J Cardiovasc Pharmacol. 1992 Dec;20(6):949-54. doi: 10.1097/00005344-199212000-00015.
We have examined the effects of local intra-arterial infusion of enalaprilat (an angiotensin converting enzyme inhibitor) on responses initiated by concomitantly infused acetylcholine (an endothelium-dependent vasodilator) and sodium nitroprusside (a direct dilator of smooth muscle) in the forearm arterial beds of healthy volunteers. Although the angiotensin converting enzyme inhibitor alone did not affect basal forearm blood flow or vascular resistance, it significantly augmented the increase in blood flow and reduction in vascular resistance induced by acetylcholine (both p < 0.05). Coinfusion of enalaprilat did not enhance sodium nitroprusside-induced vasodilation. Pretreatment with NG-monomethyl-L-arginine blocked the augmentation of blood flow induced by the angiotensin converting enzyme inhibitor. The effect of enalaprilat was still observed after the administration of acetylsalicylic acid (p < 0.05). These results suggest that angiotensin converting enzyme inhibitors potentiate nonprostanoid endothelium-derived relaxing factor in normal human forearm vasculature.
我们研究了在健康志愿者的前臂动脉床中,局部动脉内输注依那普利拉(一种血管紧张素转换酶抑制剂)对同时输注的乙酰胆碱(一种内皮依赖性血管扩张剂)和硝普钠(一种平滑肌直接扩张剂)引发的反应的影响。尽管单独使用血管紧张素转换酶抑制剂并不影响基础前臂血流量或血管阻力,但它显著增强了乙酰胆碱诱导的血流量增加和血管阻力降低(两者p均<0.05)。联合输注依那普利拉并未增强硝普钠诱导的血管舒张作用。用N-单甲基-L-精氨酸预处理可阻断血管紧张素转换酶抑制剂诱导的血流量增加。在给予乙酰水杨酸后,依那普利拉的作用仍然存在(p<0.05)。这些结果表明,血管紧张素转换酶抑制剂可增强正常人前臂血管系统中非前列腺素类内皮源性舒张因子的作用。