Kemme M J, Bruning T A, Chang P C, Van Zwieten P A
Department of Nephrology, University Hospital Leiden, The Netherlands.
Blood Press. 1995 Sep;4(5):293-9. doi: 10.3109/08037059509077610.
In arterioles, acetylcholine (ACh) is a well known vasodilator. However, in veins a wide variation in responses to ACh has been reported. In the present study the effects of the cholinergic agonists acetylcholine and methacholine (MCh) were determined simultaneously both in arterial and venous vasculature in the forearm vascular bed of healthy volunteers by means of venous occlusion plethysmography. The vasodilator sodium nitroprusside (SNP) served as an endothelium-independent control agent. The vascular beds were preconstricted by the selective alpha 1-adrenoceptor agonist methoxamine. Atropine, a non-selective muscarinic receptor antagonist, was used to antagonize the dilator effect of MCh. Overall we observed a weaker relaxant effect of ACh, MCh and SNP in the veins compared with their dilator responses in the arteries. ACh, which is highly sensitive to the hydrolytic inactivation by choline esterases, failed to induce a significant vasodilation in the venous vascular bed. Atropine blocked the dilator effects of MCh, indicating the involvement of muscarinic receptors. In arteries, MCh did not induce a significantly stronger vasodilatation than SNP on a molar basis. However, in veins, MCh had a weaker relaxant effect (p < 0.05).
在小动脉中,乙酰胆碱(ACh)是一种众所周知的血管扩张剂。然而,据报道静脉对ACh的反应存在很大差异。在本研究中,通过静脉阻塞体积描记法,同时测定了健康志愿者前臂血管床中动脉和静脉血管系统对胆碱能激动剂乙酰胆碱和醋甲胆碱(MCh)的作用。血管扩张剂硝普钠(SNP)用作不依赖内皮的对照剂。血管床用选择性α1-肾上腺素能受体激动剂甲氧明预先收缩。阿托品是一种非选择性毒蕈碱受体拮抗剂,用于拮抗MCh的扩张作用。总体而言,我们观察到与动脉中的扩张反应相比,静脉中ACh、MCh和SNP的舒张作用较弱。ACh对胆碱酯酶的水解失活高度敏感,未能在静脉血管床中诱导出显著的血管舒张。阿托品阻断了MCh的扩张作用,表明毒蕈碱受体参与其中。在动脉中,按摩尔计算,MCh诱导的血管舒张作用并不比SNP显著更强。然而,在静脉中,MCh的舒张作用较弱(p < 0.05)。