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大鼠肛门尾骨肌中非肾上腺素能非胆碱能传递的接头前抑制

Prejunctional inhibition of non-adrenergic non-cholinergic transmission in the rat anococcygeus muscle.

作者信息

Li C G, Rand M J

机构信息

Department of Pharmacology, University of Melbourne, Victoria, Australia.

出版信息

Eur J Pharmacol. 1989 Sep 1;168(1):107-10. doi: 10.1016/0014-2999(89)90640-7.

Abstract

The muscarinic agonist McN-A-343 did not affect the tone or nitroprusside-induced relaxations of the rat anococcygeus, but inhibited non-adrenergic non-cholinergic (NANC) relaxations. Atropine, pirenzepine and gallamine blocked the McN-A-343 inhibition of NANC relaxations. Agonists of alpha 1-(methoxamine) or alpha 2-adrenoceptors (clonidine, rilmenidine) increased tone and reduced NANC relaxations. Carbachol also increased tone but produced a greater reduction of NANC relaxations. The findings suggest that activation of prejunctional muscarinic receptors on NANC terminals inhibits transmitter release, but there is no evidence for prejunctional alpha-adrenoceptors.

摘要

毒蕈碱激动剂 McN - A - 343 不影响大鼠肛门尾骨肌的张力或硝普钠诱导的舒张,但可抑制非肾上腺素能非胆碱能(NANC)舒张。阿托品、哌仑西平和加拉明可阻断 McN - A - 343 对 NANC 舒张的抑制作用。α1 - 肾上腺素受体激动剂(甲氧明)或α2 - 肾上腺素受体激动剂(可乐定、利美尼定)可增加张力并减少 NANC 舒张。卡巴胆碱也可增加张力,但对 NANC 舒张的减少作用更大。这些发现表明,NANC 神经末梢上的节前毒蕈碱受体激活可抑制递质释放,但没有证据表明存在节前α - 肾上腺素受体。

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