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Pre- and post-synaptic actions of McN-A-343 in the neuromuscular junction: myographic and electrophysiologic studies in vitro.

作者信息

Simioni L R, Fontana M O, Prado W A, Corrado A P

出版信息

Gen Pharmacol. 1984;15(6):559-62. doi: 10.1016/0306-3623(84)90217-9.

DOI:10.1016/0306-3623(84)90217-9
PMID:6084629
Abstract

McN-A-343 (McN) concentrations up to 1.0 micrograms/ml increased the amplitude of the indirectly elicited muscular contractions of the isolated rat diaphragm. The effect was accompanied by an increase in both frequency and amplitude of miniature endplate potentials. The latter effects were abolished by tetrodotoxin, thus suggesting that McN increases the permeability of presynaptic membrane to sodium ions. Larger doses of McN block the neurotransmission probably acting at post-synaptic level.

摘要

相似文献

1
Pre- and post-synaptic actions of McN-A-343 in the neuromuscular junction: myographic and electrophysiologic studies in vitro.
Gen Pharmacol. 1984;15(6):559-62. doi: 10.1016/0306-3623(84)90217-9.
2
Effects of McN-A-343, a cholinomimetic drug, on endplate currents in the frog.拟胆碱药 McN - A - 343 对青蛙终板电流的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Jun;312(2):117-21. doi: 10.1007/BF00569719.
3
A comparative study of the effects induced by MCN-A-343 and acetylcholine on the isolated toad rectus abdominis.MCN - A - 343与乙酰胆碱对离体蟾蜍腹直肌作用的比较研究。
Gen Pharmacol. 1976 Aug;7(2-3):127-32. doi: 10.1016/0306-3623(76)90048-3.
4
Dual effect of the muscarinic agonist McN-A-343 on vascular neuroeffector transmission.
Acta Pharmacol Toxicol (Copenh). 1981 Nov;49(5):354-65. doi: 10.1111/j.1600-0773.1981.tb00917.x.
5
Functional determination of McN-A-343 affinity for M1 muscarinic receptors.McN-A-343对M1毒蕈碱受体亲和力的功能测定
J Pharmacol Exp Ther. 1990 Apr;253(1):310-4.
6
The effect of McN-A-343 on muscarinic receptors in the cerebral cortex and heart.McN-A-343对大脑皮层和心脏毒蕈碱受体的作用。
Br J Pharmacol. 1983 Feb;78(2):257-9. doi: 10.1111/j.1476-5381.1983.tb09388.x.
7
Dimethylsulfonium analogues of the muscarinic agent McN-A-343: [4-[[N-(3- or 4-halophenyl)carbamoyl]oxy]-2-butynyl] dimethylsulfonium perchlorates.毒蕈碱剂 McN-A-343 的二甲基锍类似物:高氯酸[4-[[N-(3-或 4-卤代苯基)氨基甲酰基]氧基]-2-丁炔基]二甲基锍
J Med Chem. 1989 Jul;32(7):1590-3. doi: 10.1021/jm00127a031.
8
Emesis induced by 4-(m-chlorophenylcarbamoyloxy)-2-butynyltrimethylammonium chloride (McN-A-343): evidence for a predominant central muscarinic M1 mediation.4-(间氯苯基氨甲酰氧基)-2-丁炔基三甲基氯化铵(McN-A-343)诱导的呕吐:主要由中枢毒蕈碱M1介导的证据
Neuropharmacology. 1988 Sep;27(9):949-56. doi: 10.1016/0028-3908(88)90123-2.
9
Pharmacological analysis of the muscarinic receptors involved when McN-A 343 stimulates acid secretion in the mouse isolated stomach.对 McN - A 343 刺激小鼠离体胃分泌胃酸时所涉及的毒蕈碱受体进行药理学分析。
Br J Pharmacol. 1985 Nov;86(3):609-17. doi: 10.1111/j.1476-5381.1985.tb08937.x.
10
Modulation by the muscarinic agonist McN-A-343 of noradrenaline release from vascular sympathetic neurones.毒蕈碱激动剂McN-A-343对血管交感神经元去甲肾上腺素释放的调节作用。
J Cardiovasc Pharmacol. 1980 Sep-Oct;2(5):629-43. doi: 10.1097/00005344-198009000-00012.