首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Evidence for inhibition of sympathetic neurotransmission by endogenously released acetylcholine in the guinea-pig trachea.
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Evidence for inhibition of sympathetic neurotransmission by endogenously released acetylcholine in the guinea-pig trachea.

机译:豚鼠气管中内源性释放的乙酰胆碱抑制交感神经传递的证据。

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摘要

1. Interactions between pulmonary cholinergic and noradrenergic nerves were studied in the innervated tracheal tube preparation isolated from guinea-pigs anaesthetized with urethane. Relaxations of the trachealis smooth muscle in response to postganglionic stimulation of the sympathetic nerve were recorded as decreases in the intraluminal pressure of the tracheal tube after the pressure had been raised with the stable thromboxane-mimetic, U46619. In contrast, contractions following preganglionic stimulation of the vagal nerve trunk were recorded as increases in intraluminal pressure. 2. In approximately half of the preparations studied, concurrent stimulation of of the vagal nerve trunk the vagal nerve trunk inhibited relaxation responses elicited by stimulation of the sympathetic nerves. The vagi were stimulated at parameters which caused no change in intraluminal pressure, excluding the involvement of postjunctional mechanisms. 3. The effect of simultaneous stimulation of the sympathetic nerve trunk was studied on contractile responses evoked by preganglionic stimulation of the vagus nerve. In 80% of the preparations tested the vagal responses were inhibited. This inhibitory effect of sympathetic nerve stimulation was antagonized by propranolol. 4. The potassium channel agonist, cromakalim, endothelins 1 and 3 and the neuropeptides, vasoactive intestinal peptide, neurokinin A and substance P, did not significantly modulate sympathetic nerve-induced relaxations. 5. The anticholinesterase drug, physostigmine, induced a concentration-dependent increase in the intraluminal pressure of the tracheal tube and potentiated the postjunctional action of exogenously applied acetylcholine to contract the guinea-pig trachealis muscle. In the presence of higher concentrations of physostigmine both vagally-induced contractions and sympathetic nerve-induced relaxations were reduced.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在从经尿烷麻醉的豚鼠中分离出的气管导管中,研究了肺胆碱能神经和去甲肾上腺素能神经之间的相互作用。记录到交感神经节后刺激引起的气管平滑肌松弛是由于稳定的血栓烷模拟物U46619升高了气管管腔内压力后的结果。相反,神经节前刺激迷走神经干后的收缩被记录为腔内压升高。 2.在研究的大约一半制剂中,迷走神经干的同时刺激,迷走神经干抑制了交感神经刺激引起的松弛反应。迷走神经以不引起管腔内压力变化的参数刺激,不包括结后机制的参与。 3.研究了同时刺激交感神经干对迷走神经节前刺激引起的收缩反应的影响。在80%的测试制剂中,迷走神经反应得到抑制。普萘洛尔拮抗了交感神经刺激的这种抑制作用。 4.钾通道激动剂克罗卡林,内皮素1和3和神经肽,血管活性肠肽,神经激肽A和P物质均未显着调节交感神经诱发的松弛。 5.抗胆碱酯酶药物毒扁豆碱诱导气管管腔内压力的浓度依赖性增加,并增强外源性乙酰胆碱收缩豚鼠气管肌肉的结后作用。在较高浓度的毒扁豆碱存在下,阴道引起的收缩和交感神经引起的松弛均减少。(摘要截短为250字)

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