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GR43175,一种犬离体隐静脉中5-HT1样受体的选择性激动剂。

GR43175, a selective agonist for the 5-HT1-like receptor in dog isolated saphenous vein.

作者信息

Humphrey P P, Feniuk W, Perren M J, Connor H E, Oxford A W, Coates L H, Butina D

机构信息

Glaxo Group Research Limited, Ware, Hertfordshire.

出版信息

Br J Pharmacol. 1988 Aug;94(4):1123-32. doi: 10.1111/j.1476-5381.1988.tb11630.x.

Abstract
  1. We describe the actions of a novel and selective 5-HT1-like receptor agonist, GR43175, in a range of isolated tissue preparations containing different 5-hydroxytryptamine (5-HT) receptor types. 2. GR43175 was a potent agonist at 5-HT1-like receptors mediating contraction of the dog isolated saphenous vein and also at those inhibiting neuronally mediated contractions in the same preparations. For both actions, GR43175 was approximately four times weaker than 5-HT. 3. GR43175 was devoid of agonist properties at 5-HT1-like receptors mediating relaxation of the cat isolated saphenous vein. 4. GR43175 was devoid of agonist properties at 5-HT2 receptors mediating contraction of the rabbit isolated aorta, pig coronary artery, greyhound coronary artery and beagle femoral artery. 5. GR43175 was devoid of agonist properties at 5-HT3 receptors mediating depolarization of the rat isolated vagus nerve. 6. The contractile response to GR43175 in the dog isolated saphenous vein was selectively antagonized by methiothepin but was resistant to antagonism by the 5-HT2 receptor blocking drug ketanserin and the 5-HT3 receptor blocking drug MDL 72222. Methiothepin antagonized the contractile action of 5-HT and GR43175 to an equal extent suggesting that both agonists act at the same receptor. 7. The results demonstrate that GR43175 is a highly selective agonist for the 5-HT1-like receptors found in the dog saphenous vein. The absence of an action of GR43175 at 5-HT1-like receptors mediating relaxation of the cat isolated saphenous vein provides further evidence that 5-HT1-like receptors are heterogeneous.
摘要
  1. 我们描述了一种新型选择性5-羟色胺(5-HT)1样受体激动剂GR43175在一系列含有不同5-羟色胺(5-HT)受体类型的离体组织制剂中的作用。2. GR43175是一种强效激动剂,作用于介导犬离体隐静脉收缩的5-HT1样受体,以及在相同制剂中抑制神经介导收缩的受体。对于这两种作用,GR43175的效力约为5-HT的四分之一。3. GR43175对介导猫离体隐静脉舒张的5-HT1样受体无激动剂特性。4. GR43175对介导兔离体主动脉、猪冠状动脉、灵缇冠状动脉和比格犬股动脉收缩的5-HT2受体无激动剂特性。5. GR43175对介导大鼠离体迷走神经去极化的5-HT3受体无激动剂特性。6. 在犬离体隐静脉中,GR43175引起的收缩反应可被甲硫噻平选择性拮抗,但对5-HT2受体阻断药酮色林和5-HT3受体阻断药MDL 72222的拮抗作用具有抗性。甲硫噻平对5-HT和GR43175的收缩作用拮抗程度相同,表明这两种激动剂作用于同一受体。7. 结果表明,GR43175是犬隐静脉中发现的5-HT1样受体的高度选择性激动剂。GR43175对介导猫离体隐静脉舒张的5-HT1样受体无作用,进一步证明5-HT1样受体是异质性的。

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