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关于雪貂气管中神经源性黏液分泌的毒蕈碱控制

On muscarinic control of neurogenic mucus secretion in ferret trachea.

作者信息

Ramnarine S I, Haddad E B, Khawaja A M, Mak J C, Rogers D F

机构信息

National Heart & Lung Institute (Imperial College), London, UK.

出版信息

J Physiol. 1996 Jul 15;494 ( Pt 2)(Pt 2):577-86. doi: 10.1113/jphysiol.1996.sp021515.

Abstract
  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.
摘要
  1. 利用35SO4作为分泌黏液的标记物,在体外和体内对介导雪貂气管神经源性黏液分泌的毒蕈碱受体亚型进行了表征,使用M1受体亚型的毒蕈碱受体拮抗剂替仑西平、M2亚型的甲溴东莨菪碱和M3受体的4-二苯乙酰氧基-N-甲基哌啶甲基溴(4-DAMP)。我们还进行了受体结合和定位研究。2. 每种毒蕈碱拮抗剂均以高亲和力结合常数(KH)值分别为1.9、2.7和5.0 nM的方式取代了[甲基-3H]东莨菪碱与替仑西平、甲溴东莨菪碱和4-DAMP的结合。毒蕈碱M1和M3受体定位于黏膜下腺,而M2受体则不然。3. 在体外,电刺激(50 V,10 Hz,0.5 ms,持续5分钟)使35SO4输出增加了160%。替仑西平在其KH值两倍或二十倍的浓度下并未抑制神经源性分泌反应,也未抑制乙酰胆碱(ACh)诱导的分泌。4-DAMP在其KH值两倍和二十倍的浓度下分别抑制神经源性分泌80%和95%,并抑制ACh诱导的分泌。甲溴东莨菪碱以剂量相关(5.4 - 100 nM)的方式增强了在2.5 Hz(50 V,0.5 ms,持续5分钟)诱导的神经源性分泌,比电刺激值增加了33 - 451%。甲溴东莨菪碱在10 Hz时并未增强分泌,对ACh诱导的分泌也没有任何影响。4. 在体内,迷走神经刺激(10 V,10 Hz,2 ms,持续8分钟)使35SO4输出增加了约120%。替仑西平对神经源性分泌没有显著影响。甲溴东莨菪碱使刺激反应增加了约一倍,而4-DAMP则消除了刺激分泌反应。5. 我们得出结论,在雪貂气管中,胆碱能神经刺激通过黏膜下腺上的毒蕈碱M3受体增加黏液分泌。分泌反应的幅度由神经元M2毒蕈碱受体调节。定位于黏膜下腺的毒蕈碱M1受体似乎与黏液分泌无关。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d0/1160657/889435f71c49/jphysiol00397-0264-a.jpg

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