The involvement of CGRP in acetylcholine-induced vascular relaxation.

Artery Pub Date : 1994-01-01
T M Scott, L Chafe
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引用次数: 0

Abstract

Earlier work on peptidergic fibres suggested some involvement of CGRP perivascular nerve fibres in acetylcholine-induced endothelium-dependent vascular relaxation. We have investigated the effect of blocking CGRP receptors and CGRP replacement on acetylcholine-induced endothelium-dependent vascular relaxation in the isolated perfused mesenteric arterial bed in normal Sprague-Dawley rats and in rats seven days following freeze-denervation of the superior mesenteric artery. Freeze-denervation was carried out under pentobarbital anesthesia (40 mg/Kg). It was found that the ability of acetylcholine to cause relaxation was reduced by CGRP receptor blocking with CGRP8-37 in vessels from control rats, but returned to pre-blocking levels after washout of the antagonist. Treatment with CGRP increased the relaxation due to acetylcholine in denervated vessel beds, but not in control tissues. The CGRP receptor appears to be involved in the acetylcholine-induced relaxation of blood vessels. The mechanism of action is not known, although both acetylcholine and CGRP, act through activation of K+ channels, and CGRP may facilitate the activation of K+ channels by acetylcholine.

CGRP参与乙酰胆碱诱导的血管舒张。
早期关于肽能纤维的研究表明,CGRP血管周围神经纤维参与了乙酰胆碱诱导的内皮依赖性血管松弛。我们研究了阻断CGRP受体和CGRP替代对正常Sprague-Dawley大鼠离体灌注肠系膜动脉床中乙酰胆碱诱导的内皮依赖性血管舒张的影响,以及在肠系膜上动脉冷冻去神经后7天的大鼠。在戊巴比妥(40 mg/Kg)麻醉下进行冷冻去神经。结果发现,在对照大鼠血管中,用CGRP8-37阻断CGRP受体后,乙酰胆碱引起松弛的能力降低,但在拮抗剂洗脱后恢复到阻断前的水平。CGRP治疗增加了去神经血管床因乙酰胆碱引起的松弛,但在对照组织中没有。CGRP受体似乎参与了乙酰胆碱诱导的血管松弛。其作用机制尚不清楚,尽管乙酰胆碱和CGRP都通过激活K+通道起作用,CGRP可能促进乙酰胆碱激活K+通道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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