Suppr超能文献

α2肾上腺素能受体介导的豚鼠气管支气管树兴奋性非肾上腺素能、非胆碱能神经传递的抑制作用。

Inhibition of the excitatory non-adrenergic, non-cholinergic neurotransmission in the guinea pig tracheo-bronchial tree mediated by alpha 2-adrenoceptors.

作者信息

Grundström N, Andersson R G, Wikberg J E

出版信息

Acta Pharmacol Toxicol (Copenh). 1984 Jan;54(1):8-14. doi: 10.1111/j.1600-0773.1984.tb01889.x.

Abstract

Guinea pig main bronchi were studied in vitro for the presence of motor innervation. Field stimulation of the main bronchi revealed that besides the excitatory cholinergic component a slow and atropine resistant contraction similar to that previously found in the hilus bronchi (Grundström et al. 1981a) was present also at this level of the airways. This slow contraction was blocked by tetrodotoxin whereas it was left unaffected by a number of conventional antagonists (i.e. atropine, guanethidine, propranolol, yohimbine and prazosin) suggesting that it was due to activation of non-adrenergic, non-cholinergic neurones. In the presence of a beta-adrenoceptor blocking drug, noradrenaline inhibited the slow contractions induced by field stimulation in both the main and hilus bronchi. By contrast, contractions elicited by histamine were left unaffected by noradrenaline. In order to characterize the receptor for noradrenaline the effects of alpha1-and alpha2-adrenoceptor blockers were evaluated. The results indicate that in the guinea pig bronchi noradrenaline inhibits non-adrenergic, non-cholinergic neurotransmission by acting on prejunctional alpha 2-adrenoceptors.

摘要

对豚鼠的主支气管进行体外研究,以确定其是否存在运动神经支配。对主支气管进行场刺激发现,除了兴奋性胆碱能成分外,在此气道水平还存在一种缓慢且对阿托品耐药的收缩,类似于先前在肺门支气管中发现的收缩(Grundström等人,1981a)。这种缓慢收缩被河豚毒素阻断,而不受多种传统拮抗剂(即阿托品、胍乙啶、普萘洛尔、育亨宾和哌唑嗪)的影响,这表明它是由非肾上腺素能、非胆碱能神经元的激活引起的。在存在β-肾上腺素能受体阻断药物的情况下,去甲肾上腺素抑制了主支气管和肺门支气管中场刺激诱导的缓慢收缩。相比之下,组胺引起的收缩不受去甲肾上腺素的影响。为了表征去甲肾上腺素的受体,评估了α1和α2肾上腺素能受体阻断剂的作用。结果表明,在豚鼠支气管中,去甲肾上腺素通过作用于突触前α2肾上腺素能受体来抑制非肾上腺素能、非胆碱能神经传递。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验