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生物胺及相关激动剂和拮抗剂对乌贼(Sepia officinalis L.)离体心脏的影响

Effects of biogenic amines and related agonists and antagonists on the isolated heart of the common cuttlefish Sepia officinalis L.

作者信息

Kling G, Schipp R

机构信息

Institut für Allgemeine und Spezielle Zoologie, Universität Giessen, FRG.

出版信息

Comp Biochem Physiol C Comp Pharmacol Toxicol. 1987;87(2):251-8. doi: 10.1016/0742-8413(87)90005-3.

Abstract
  1. Effects of noradrenaline and the related compounds adrenaline, dopamine, octopamine, tyramine, clonidine and isoprenaline were studied in isolated heart preparations from the cuttlefish Sepia officinalis L. 2. All analogues produced a positive inotropic affect, with noradrenaline being the most potent substance. The chronotropic effects of the tested compounds differed widely. 3. The action of substances of the phenylethanolamine group were not antagonized by propranolol but were partly antagonized by phentolamine. 4. Serotonin and its analogues also produced cardio-excitation. These effects were blocked by cyproheptadine but not by methysergide. 5. These results indicate the presence of two different receptors in the Sepia myocardium: one type reacting with noradrenaline most effectively and a second type being stimulated by serotonin.
摘要
  1. 研究了去甲肾上腺素及相关化合物肾上腺素、多巴胺、章鱼胺、酪胺、可乐定和异丙肾上腺素对乌贼(Sepia officinalis L.)离体心脏标本的作用。2. 所有类似物均产生正性肌力作用,其中去甲肾上腺素是最有效的物质。受试化合物的变时作用差异很大。3. 苯乙醇胺类物质的作用不受普萘洛尔拮抗,但部分受酚妥拉明拮抗。4. 血清素及其类似物也产生心脏兴奋作用。这些作用可被赛庚啶阻断,但不能被甲基麦角新碱阻断。5. 这些结果表明乌贼心肌中存在两种不同的受体:一种类型与去甲肾上腺素反应最有效,另一种类型受血清素刺激。

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