Suppr超能文献

从奥尔巴赫神经丛释放出两种抗阿托品痉挛原的证据。

Evidence for the release of two atropine-resistant spasmogens from Auerbach's plexus.

作者信息

Ambache N, Verney J, Zar M A

出版信息

J Physiol. 1970 May;207(3):761-82. doi: 10.1113/jphysiol.1970.sp009093.

Abstract
  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 mug/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 x 10(-5) g/ml.7. 5-HT, 0.1 mug/ml., and strychnine, 20-40 mug/ml., also reduce response A to the level of B, but these selective inhibitions are not antagonized by nicotine.8. Diphenhydramine, 10 mug/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 alpha + beta 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.
摘要
  1. 通过对豚鼠回肠纵肌含神经丛标本进行交替电场刺激,分别施加50 Hz(反应A)和5 Hz(反应B)的等量脉冲,检测到了两种神经源性抗阿托品反应成分。当施加十个或更多脉冲串时,反应A总是大于反应B;A/B的比值(1.2 - 21.3)存在动物个体差异。

  2. 两种反应均被河豚毒素消除,且在无神经丛的标本中不存在。

  3. 用(+) - 筒箭毒碱、二甲基筒箭毒碱或六甲铵进行神经节阻断,或用麻痹神经节剂量的尼古丁处理,均不会降低这两种反应;因此,兴奋的节前末梢对这些反应的贡献可忽略不计。

  4. 两种反应均不是由组胺、5 - 羟色胺(5 - HT)或前列腺素释放引起的,因为在存在甲氧苄胺嘧啶、甲基麦角新碱和前列腺素拮抗剂SC - 19220(1 - 乙酰 - 2(8 - 氯 - 10,11 - 二氢二苯并[b,f][1,4]恶唑嗪 - 10 - 羰基)肼)的情况下,A和B反应均持续存在。

  5. 这两种反应成分受多种药物的影响不同。

  6. 0.1 μg/ml的组胺可将反应A降低至反应B的水平;1 - 2.5×10⁻⁵ g/ml的尼古丁可特异性拮抗A中组胺敏感成分的这种选择性抑制。

  7. 0.1 μg/ml的5 - HT和20 - 40 μg/ml的士的宁也可将反应A降低至反应B的水平,但这些选择性抑制不能被尼古丁拮抗。

  8. 10 μg/ml的苯海拉明通过抑制A并增强B使两种反应相等。

  9. 上述药物的抑制作用不是由于儿茶酚胺释放,因为在用酚妥拉明和丙萘洛尔阻断α + β肾上腺素受体后,以及在豚鼠预先用利血平处理后,这些作用仍然存在。

  10. 在豚鼠降结肠纵肌的阿托品化含神经丛标本中,50 Hz和5 Hz刺激所引发的反应实际上相等,且似乎均为B型反应,因为它们不受组胺、5 - HT或士的宁的抑制;苯海拉明会产生强烈收缩。

相似文献

3
An inhibitory action of histamine on the guinea-pig ileum.组胺对豚鼠回肠的抑制作用。
Br J Pharmacol. 1970 Jan;38(1):229-40. doi: 10.1111/j.1476-5381.1970.tb10352.x.

引用本文的文献

本文引用的文献

1
Compound 48/80: a potent histamine liberator.化合物48/80:一种强效组胺释放剂。
Br J Pharmacol Chemother. 1951 Sep;6(3):499-508. doi: 10.1111/j.1476-5381.1951.tb00661.x.
6
An inhibitory action of histamine on the guinea-pig ileum.组胺对豚鼠回肠的抑制作用。
Br J Pharmacol. 1970 Jan;38(1):229-40. doi: 10.1111/j.1476-5381.1970.tb10352.x.

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