乙酰胆碱诱导大鼠肠系膜上动脉床松弛的l -name抗性成分是神经依赖性的。

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

摘要

使用L-NAME和钾通道阻滞剂apamin,我们研究了当肠系膜动脉床失神经时乙酰胆碱引起的血管松弛丧失的成分。我们已经证实,在α激动剂甲氧苄胺和唑啉存在时,血管去神经支配使乙酰胆碱引起松弛的能力降低高达35%。在对照血管制剂中,单次暴露于L-NAME 30分钟可使乙酰胆碱弛豫率降低44%,在去神经制剂中降低85%。在对照制剂中,长时间暴露于L-NAME可使乙酰胆碱弛豫率降低66%,在存在维生素a时降低77%。在去神经制剂中,长时间暴露于L-NAME使乙酰胆碱弛豫降低96%。长时间暴露于L-NAME去神经制剂后,乙酰胆碱诱导的松弛几乎完全丧失(甲氧苄胺96.6%,唑啉93.9%),这表明神经支配参与了大鼠肠系膜上动脉床对乙酰胆碱的L-NAME抗性松弛的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The L-name-resistant component of acetylcholine-induced relaxation of the rat superior mesenteric arterial bed is innervation-dependent.

Using L-NAME and the potassium channel blocker apamin we have investigated the component of acetylcholine-induced vascular relaxation lost when the mesenteric arterial bed is denervated. We have confirmed that vascular denervation produces a reduction of up to 35% in the ability of ACh to cause relaxation in the presence of the alpha agonists methoxamine and cirazoline. A single 30 minute exposure to L-NAME reduced the relaxation to ACh by up to 44% in control vascular preparations and by 85% in denervated preparations. In control preparations, prolonged exposure to L-NAME reduced the relaxation to ACh by up to 66% and by 77% in the presence of apamin. In denervated preparations prolonged exposure to L-NAME reduced the relaxation to ACh by 96%. The almost complete loss of acetylcholine-induced relaxation following prolonged exposure to L-NAME (96.6% in methoxamine and 93.9% in cirazoline) in denervated preparations suggests that innervation is involved in the expression of the L-NAME-resistant relaxation to acetylcholine in the superior mesenteric arterial bed of the rat.

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