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On muscarinic control of neurogenic mucus secretion in ferret trachea.

机译:关于毒蕈碱控制雪貂气管中神经源性粘液的分泌。

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摘要

1. Muscarinic receptor subtypes mediating neurogenic mucus secretion in ferret trachea were characterized in vitro and in vivo using 35SO4 as a label for secreted mucus, and the muscarinic receptor antagonists telenzepine for the M1 receptor subtype, methoctramine for the M2 subtype and 4-diphenylacetoxy-N-methylpiperidine methobromide (4-DAMP) for the M3 receptor. We also performed receptor binding and mapping studies. 2. Each muscarinic antagonist displaced [N-methyl-3H]scopolamine binding with high-affinity binding constant (KH) values of 1.9, 2.7 and 5.0 nM for telenzepine, methoctramine and 4-DAMP, respectively. Muscarinic M1 and M3 receptors localized to submucosal glands, whereas M2 receptors did not. 3. In vitro, electrical stimulation (50 V, 10 Hz, 0.5 ms for 5 min) increased 35SO4 output by 160%. Telenzepine did not inhibit the neurogenic secretory response at concentrations two-or twentyfold its KH value, nor did it inhibit secretion induced by acetylcholine (ACh). 4-DAMP inhibited neurogenic secretion by 80 and 95%, respectively, at concentrations two-and twentyfold its KH value, and also inhibited ACh-induced secretion. Methoctramine potentiated neurogenic secretion induced at 2.5 Hz (50 V, 0.5 ms for 5 min) in a dose-related (5.4-100 nM) manner with increases of 33-451% above electrically stimulated values. Methoctramine did not potentiate secretion induced at 10 Hz and did not have any effect on ACh-induced secretion. 4. In vivo, vagal stimulation (10 V, 10 Hz, 2 ms for 8 min) increased output of 35SO4 by approximately 120%. Telenzepine had no significant effect on neurogenic secretion. Methoctramine approximately doubled the stimulated response, whereas 4-DAMP abolished the stimulated secretory response. 5. We conclude that in ferret trachea, cholinergic nerve stimulation increases mucus secretion via muscarinic M3 receptors on the submucosal glands. The magnitude of the secretory response is regulated by neuronal M2 muscarinic receptors. The muscarinic M1 receptors localized to the submucosal glands do not appear to be involved with mucus secretion.
机译:1.利用35SO4作为分泌性粘液的标记,对雪貂气管中神经源性粘液分泌的毒蕈碱受体亚型进行了体外和体内表征,M1受体亚型的毒蕈碱受体拮抗剂Telenzepine,M2亚型的甲辛达明和4-二苯基乙酰氧基- N-甲基哌啶甲基溴化物(4-DAMP)用于M3受体。我们还进行了受体结合和作图研究。 2.每种毒蕈碱拮抗剂置换的[N-甲基-3H]东pol碱结合剂对替硝西平,甲基辛特拉明和4-DAMP的高亲和力结合常数(KH)值分别为1.9、2.7和5.0 nM。毒蕈碱型M1和M3受体位于粘膜下腺,而M2受体则不。 3.在体外,电刺激(50 V,10 Hz,0.5 ms持续5分钟)使35SO4的产量增加了160%。 Telenzepine在其KH值的2到20倍的浓度下不会抑制神经源性分泌反应,也不会抑制乙酰胆碱(ACh)诱导的分泌。 4-DAMP在其KH值的两倍和二十倍的浓度下分别抑制神经源性分泌80%和95%,还抑制ACh诱导的分泌。在2.5 Hz(50 V,0.5 ms,5分钟)以剂量相关(5.4-100 nM)的方式诱导甲氧辛胺增强的神经源性分泌,比电刺激值增加33-451%。甲硫拉明不能增强10 Hz诱导的分泌,并且对ACh诱导的分泌没有任何影响。 4.在体内,迷走神经刺激(10 V,10 Hz,2 ms,持续8分钟)将35SO4的输出增加了约120%。 Telenzepine对神经源性分泌没有明显影响。甲硫拉明大约使刺激的反应加倍,而4-DAMP消除了刺激的分泌反应。 5.我们得出结论,在雪貂气管中,胆碱能神经刺激通过粘膜下腺上的毒蕈碱M3受体增加粘液分泌。分泌反应的强度由神经元M2毒蕈碱受体调节。定位于粘膜下腺的毒蕈碱M1受体似乎与粘液分泌无关。

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