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尼古丁对血管肾上腺素能神经效应器传递的作用机制。

The mechanism of action of nicotine on vascular adrenergic neuroeffector transmission.

作者信息

Nedergaard O A, Schrold J

出版信息

Eur J Pharmacol. 1977 Apr 21;42(4):315-29. doi: 10.1016/0014-2999(77)90165-0.

Abstract

The aim of this study was to determine the site and mechanism of action of nicotine on sympathetic neuroeffector transmission in the isolated pulmonary artery of the rabbit. Nicotine and cocaine potentiated the constrictor response elicited by electrical-field stimulation of postganglionic adrenergic neurones. The potentiation was reversible and in the case of nicotine, no tachyphylaxis developed. The nicotine-induced potentiation was characterized by a rapid onset and an initial, transitory peak, while the enhancement caused by cocaine progressed more slowly and was monophasic. Hexamethonium and (+)-tubocurarine prevented the potentiation caused by nicotine. Nicotine did not prevent the adrenergic neurone blocking effect of bretylium on the response to field stimulation. Nicotine increased the stimulation-induced outflow of tritium from pulmonary artery preloaded with 3H-(--)-noradrenaline. Contractions of the artery elicited by tyramine were enhanced by pargyline, unaltered by nicotine and blocked by cocaine. Nicotine did not alter the concentration--response curve of exogenous (--)-noradrenaline while cocaine moved it to the left. The accumulation of 3H-(--)-noradrenaline by rabbit isolated aorta was not altered by nicotine, hexamethonium and (+)-tubocurarine. The accumulation of 3H-nicotine by the aorta was much lower than that seen with 3H-(--)-noradrenaline. The disposition of the 3H-nicotine accumulation into adventitia and media was concentration-independent. These results suggest (1) that nicotine potentiates the neurogenic vasoconstriction response in part by increasing the stimulation-induced release of transmitter from adrenergic neurone terminals; (2) that the site of the nicotinic receptors mediating this action is located on the outer surface of the neurones; and (3) that the potentiation is not due to blockade of noradrenaline re-uptake.

摘要

本研究的目的是确定尼古丁对兔离体肺动脉交感神经效应器传递的作用部位和作用机制。尼古丁和可卡因增强了节后肾上腺素能神经元电场刺激所引发的收缩反应。这种增强是可逆的,就尼古丁而言,未出现快速耐受性。尼古丁诱导的增强表现为起效迅速且有一个初始的短暂峰值,而可卡因引起的增强进展较为缓慢且呈单相性。六甲铵和(+) - 筒箭毒碱可阻止尼古丁引起的增强作用。尼古丁不能阻止溴苄铵对电场刺激反应的肾上腺素能神经元阻断作用。尼古丁增加了预先用3H - ( - ) - 去甲肾上腺素加载的肺动脉中刺激诱导的氚流出。帕吉林增强了酪胺引起的动脉收缩,尼古丁对其无影响,而可卡因则阻断了该作用。尼古丁未改变外源性( - ) - 去甲肾上腺素的浓度 - 反应曲线,而可卡因使其左移。尼古丁、六甲铵和(+) - 筒箭毒碱未改变兔离体主动脉对3H - ( - ) - 去甲肾上腺素的摄取。主动脉对3H - 尼古丁的摄取远低于对3H - ( - ) - 去甲肾上腺素的摄取。3H - 尼古丁在主动脉外膜和中膜中的摄取分布与浓度无关。这些结果表明:(1)尼古丁部分通过增加刺激诱导的肾上腺素能神经元末梢递质释放来增强神经源性血管收缩反应;(2)介导此作用的烟碱受体部位位于神经元外表面;(3)这种增强不是由于去甲肾上腺素再摄取的阻断所致。

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