Suppr超能文献

副交感神经节兴奋剂和胃泌素样多肽对豚鼠回肠乙酰胆碱释放的影响

Acetylcholine release from guinea-pig ileum by parasympathetic ganglion stimulants and gastrin-like polypeptides.

作者信息

Vizi E S

出版信息

Br J Pharmacol. 1973 Apr;47(4):765-77. doi: 10.1111/j.1476-5381.1973.tb08203.x.

Abstract
  1. The release of acetylcholine by parasympathetic ganglion stimulants from the nerve terminals of the guinea-pig longitudinal muscle strip was studied. The acetylcholine released was collected in the presence of physostigmine sulphate.2. Nicotine and 1,1-dimethyl-4'-phenylpiperazinium iodide (DMPP) released acetylcholine. Tetrodotoxin (50 ng/ml) and hexamethonium completely prevented their action on acetylcholine release, indicating that their effect is on nicotinic receptors of cell bodies. Noradrenaline (1 mug/ml), excess magnesium, and calcium withdrawal inhibited the acetylcholine release induced by nicotine or by DMPP.3. There was rapid tachyphylaxis to the acetylcholine releasing action of both nicotine and DMPP.4. The octapeptide amide of cholecystokinin and caerulein (10(-9)M) enhanced the acetylcholine release without producing tachyphylaxis. Tetrodotoxin completely inhibited acetylcholine release. However, hexamethonium or desensitization with 5-hydroxytryptamine did not prevent their action. In the early phase of nicotine action the polypeptides studied failed to increase acetylcholine release. However, a few minutes later the tissue became sensitive to polypeptides despite the fact that the tissue was still exposed to nicotine. These data suggest the presence in the parasympathetic ganglion cells of separate gastrointestinal hormone-sensitive receptors.5. Noradrenaline inhibited the acetylcholine releasing action of polypeptides. This effect was mediated via alpha-adrenoceptors since phentolamine prevented its action.6. Excess magnesium (9.3 mM) also reduced the acetylcholine release in response to the polypeptides.
摘要
  1. 研究了豚鼠纵行肌条神经末梢的副交感神经节兴奋剂释放乙酰胆碱的情况。在硫酸毒扁豆碱存在的情况下收集释放的乙酰胆碱。

  2. 尼古丁和1,1 - 二甲基 - 4'- 苯基哌嗪碘化物(DMPP)释放乙酰胆碱。河豚毒素(50纳克/毫升)和六甲铵完全阻止了它们对乙酰胆碱释放的作用,表明它们的作用是作用于细胞体的烟碱受体。去甲肾上腺素(1微克/毫升)、过量镁和去除钙抑制了尼古丁或DMPP诱导的乙酰胆碱释放。

  3. 对尼古丁和DMPP的乙酰胆碱释放作用存在快速耐受性。

  4. 胆囊收缩素八肽酰胺和蛙皮素(10⁻⁹摩尔/升)增强了乙酰胆碱释放且未产生耐受性。河豚毒素完全抑制了乙酰胆碱释放。然而,六甲铵或用5 - 羟色胺脱敏并不能阻止它们的作用。在尼古丁作用的早期阶段,所研究的多肽未能增加乙酰胆碱释放。然而,几分钟后,尽管组织仍暴露于尼古丁,组织对多肽变得敏感。这些数据表明在副交感神经节细胞中存在独立的胃肠激素敏感受体。

  5. 去甲肾上腺素抑制多肽的乙酰胆碱释放作用。这种作用是通过α - 肾上腺素受体介导的,因为酚妥拉明阻止了其作用。

  6. 过量镁(9.3毫摩尔/升)也减少了对多肽的乙酰胆碱释放反应。

相似文献

引用本文的文献

2
Mediation of the Acute Stress Response by the Skeleton.骨骼对急性应激反应的介导作用。
Cell Metab. 2019 Nov 5;30(5):890-902.e8. doi: 10.1016/j.cmet.2019.08.012. Epub 2019 Sep 12.

本文引用的文献

8
The inhibition of the peristaltic reflex by sympathomimetic amines.拟交感胺对蠕动反射的抑制作用。
Br J Pharmacol Chemother. 1954 Jun;9(2):131-7. doi: 10.1111/j.1476-5381.1954.tb00831.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