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Evidence for the release of two atropine-resistant spasmogens from Auerbachs plexus

机译:从奥尔巴赫神经丛中释放出两种对阿托品具有抗性的痉挛的证据

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摘要

1. Two atropine-resistant response-components of nervous origin have been detected in plexus-containing preparations of the longitudinal muscle from the guinea-pig ileum, by alternate field stimulation with equal numbers of pulses at 50 Hz (response A) and at 5 Hz (response B). With trains of ten or more pulses, response A is always larger than B; the ratio of A/B (1·2-21·3) is subject to animal variation.2. Both responses are abolished by tetrodotoxin and are absent from plexus-free preparations.3. Neither response is reduced by ganglion-block with (+)-tubocurarine, dimethyltubocurarine or hexamethonium, or by ganglion-paralysing doses of nicotine; the contribution of excited preganglionic endings to these responses is therefore negligible.4. Neither response is due to a release of histamine, 5-hydroxytryptamine (5-HT) or prostaglandins, since both A and B persist in the presence of mepyramine, methysergide and the prostaglandin-antagonist SC-19220 (1-acetyl-2(8-chloro-10,11-dihydrodibenz [b,f] [1,4]oxazepine-10-carbonyl) hydrazine).5. The two response-components are affected differentially by a number of drugs.6. Histamine, 0·1 μg/ml., reduces response A to the level of B; this selective inhibition of the histamine-sensitive component in A is specifically antagonized by nicotine, 1-2·5 × 10-5 g/ml.7. 5-HT, 0·1 μg/ml., and strychnine, 20-40 μg/ml., also reduce response A to the level of B, but these selective inhibitions are not antagonized by nicotine.8. Diphenhydramine, 10 μg/ml., produces equality of the two responses by depressing A and potentiating B.9. The inhibitory effects of the foregoing drugs are not due to catecholamine release, since they persist after α + β adrenoceptor blockade with phentolamine and pronethalol, and after previous reserpinization of the guinea-pigs.10. In atropinized plexus-containing preparations of the longitudinal muscle from the guinea-pig descending colon, the responses elicited at 50 Hz and at 5 Hz are virtually equal and both appear to be of Type B since they are not inhibited by histamine, 5-HT or strychnine; diphenhydramine produces strong contractions.
机译:1.通过交替场刺激以50 Hz(响应A)和5 Hz相等的脉冲频率,在豚鼠回肠的含丛神经的纵向肌肉制剂中检测到了两种神经源的抗阿托品抗性反应成分Hz(响应B)。对于十个或更多脉冲序列,响应A始终大于B;响应B始终大于B。 A / B(1·2-21·3)的比例容易受到动物的影响; 2。两种反应均被河豚毒素所消除,而无丛的制剂则不存在。3。用(+)-微管尿素,二甲基微管尿素或六甲铵对神经节进行阻滞,或使神经节麻痹剂量的尼古丁均不能降低反应。因此,兴奋的神经节前末端对这些反应的贡献可忽略不计。4。这两种反应均不是由于组胺,5-羟色胺(5-HT)或前列腺素的释放引起的,因为A和B均在存在美吡拉明,美塞麦肽和前列腺素拮抗剂SC-19220(1-乙酰基2(8 -氯-10,11-二氢二苯并[b,f] [1,4]氧杂氮杂-10-羰基肼).5。两种药物对这两种反应成分的影响不同。6。 0·1μg/ ml组胺可将反应A降低为B;烟碱1-2·5×10 -5 g / ml可特异性拮抗A中组胺敏感成分的这种选择性抑制作用。7。 0·1μg/ ml的5-HT和20-40μg/ ml的士丁宁也将响应A降低到B的水平,但是尼古丁没有拮抗这些选择性抑制作用8。 10μg/ ml苯海拉明通过压低A和增强B.9产生两个反应的相等性。上述药物的抑制作用不是由于儿茶酚胺的释放,因为它们在α+β肾上腺素受体被酚妥拉明和普萘太洛阻断后以及先前的豚鼠再固定化之后仍然存在。在豚鼠降结肠的纵向肌的含有肌萎缩神经丛的制剂中,在50 Hz和5 Hz引起的反应实际上是相等的,并且由于它们不受组胺,5-HT的抑制,因此看起来都是B型。或士的宁;苯海拉明产生强烈的收缩。

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