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关于乙酰胆碱在交感神经节中释放多余乙酰胆碱的机制的研究。

Studies upon the mechanism by which acetylcholine releases surplus acetylcholine in a sympathetic ganglion.

作者信息

Collier B, Katz H S

出版信息

Br J Pharmacol. 1975 Oct;55(2):189-97. doi: 10.1111/j.1476-5381.1975.tb07628.x.

Abstract
  1. Acetylcholine (ACh) releases surplus ACh from the superior cervical ganglion of the cat and the experiments described in this paper tested whether this results from exchange of endogenous ACh with exogenous ACh; the experiments also attempted to characterize pharmacologically the mechanism of this action of ACh. 2. The surplus ACh in the ganglion was radioactively labelled by perfusion of the ganglion with [3H]-choline-Krebs solution containing diisopropylphosphofluoridate, and the release of surplus [3H]-ACh by [14C]-ACh injected close arterially to the ganglion measured. The amount of [3H]-ACh released by [14C]-ACh was 33 +/- 5 times greater than was the amount of [14C]-ACh accumulated by ganglia. The amount of exogenous ACh accumulated by ganglia that had first formed surplus ACh was not different from exogenous ACh accumulation by ganglia that had not formed surplus ACh. Thus, it is concluded that surplus ACh release by ACh is not the result of ACh exchange. 3. In other experiments, surplus [3H]-ACh was accumulated in ganglia exposed to physostigmine. Nicotine, pilocarpine or ACh released surplus ACh; the effect of both nicotine and ACh was blocked by hexamethonium; atropine blocked the effect of ACh but not that of nicotine. It is concluded that both nicotinic and muscarinic receptors can be involved in the release of surplus ACh by cholinomimetic agonists.
摘要
  1. 乙酰胆碱(ACh)从猫的颈上神经节释放多余的ACh,本文所述实验检测了这是否源于内源性ACh与外源性ACh的交换;实验还试图从药理学角度描述ACh这一作用的机制。2. 通过用含二异丙基氟磷酸酯的[3H] - 胆碱 - 克雷布斯溶液灌注神经节,使神经节中的多余ACh被放射性标记,然后测量经动脉向神经节附近注射的[14C] - ACh所释放的多余[3H] - ACh量。[14C] - ACh释放的[3H] - ACh量比神经节积累的[14C] - ACh量多33±5倍。首先形成多余ACh的神经节积累的外源性ACh量与未形成多余ACh的神经节积累的外源性ACh量没有差异。因此,得出结论:ACh释放多余ACh不是ACh交换的结果。3. 在其他实验中,多余的[3H] - ACh在暴露于毒扁豆碱的神经节中积累。尼古丁、毛果芸香碱或ACh释放多余的ACh;尼古丁和ACh的作用均被六甲铵阻断;阿托品阻断了ACh的作用,但未阻断尼古丁的作用。得出结论:拟胆碱激动剂释放多余ACh的过程中,烟碱型和毒蕈碱型受体都可能参与。

相似文献

本文引用的文献

1
The acetyloholine metabolism of a sympathetic ganglion.交感神经节的乙酰胆碱代谢
J Physiol. 1936 Dec 11;88(3):265-83. doi: 10.1113/jphysiol.1936.sp003439.
2
The chemical transmitter at synapses in a sympathetic ganglion.交感神经节突触处的化学递质。
J Physiol. 1934 Jun 9;81(3):305-19. doi: 10.1113/jphysiol.1934.sp003137.
5
The metabolism of choline by a sympathetic ganglion.交感神经节对胆碱的代谢。
Can J Physiol Pharmacol. 1969 Feb;47(2):119-26. doi: 10.1139/y69-022.

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