De Vries P, Villalón C M, Heiligers J P, Saxena P R
Department of Pharmacology, Faculty of Medicine and Health Sciences, Erasmus University Rotterdam, The Netherlands.
Naunyn Schmiedebergs Arch Pharmacol. 1997 Jul;356(1):90-9. doi: 10.1007/pl00005034.
It has been suggested that the late hypotensive response to serotonin (5-hydroxytryptamine; 5-HT) in vagosympathectomized rats is mediated by '5-HT1-like' receptors since this effect is mimicked by 5-carboxamidotryptamine (5-CT), is not modified by cyproheptadine, ketanserin or MDL 72222, but it is blocked by methysergide. The present study was set out to reanalyze this suggestion in terms of the classification schemes proposed in 1994 and 1996 by the NC-IUPHAR subcommittee on the classification and nomenclature of 5-HT receptors. I.v. bolus injections of 5-CT (0.01-0.3 microg x kg(-1)), 5-HT (1-30 microg x kg(-1)) and 5-methoxytryptamine (5-MeO-T; 1-30 microg x kg(-1)) produced dose-dependent hypotensive responses with a rank order of agonist potency: 5-CT >> 5-HT > 5-methoxytryptamine with sumatriptan (30-1000 microg x kg(-1)) inactive. The depressor responses to 5-HT and 5-CT were not attenuated by i.v. GR127935 (300-3000 microg x kg(-1)) or equivalent volumes of saline. In contrast, lisuride, methiothepin, mesulergine, metergoline and clozapine dose-dependently antagonized the responses to 5-HT and 5-CT; the rank order of apparent pA2 values against 5-HT and 5-CT, respectively, was: lisuride (7.7; 7.8) > methiothepin (6.8; 7.0) > or = mesulergine (6.4; 6.6) > clozapine (5.7; 5.8); metergoline displayed variable potencies (5.6; 6.4). Except for lisuride, which also affected isoprenaline-induced hypotension, the antagonism by the other drugs was selective. Based upon the above rank order of agonist potency, the blockade by a series of drugs showing high affinity for the cloned 5-ht7 receptor and the lack of blockade by GR127935, our results indicate that the 5-HT receptor mediating hypotension in vagosympathectomized rats is operationally similar to other putative 5-ht7 receptors mediating vascular and non-vascular responses (e.g. relaxation of the rabbit femoral vein, canine coronary and external carotid arteries and guinea-pig ileum as well as feline tachycardia).
有人提出,去迷走交感神经大鼠对血清素(5-羟色胺;5-HT)的延迟降压反应是由“5-HT1样”受体介导的,因为5-羧酰胺色胺(5-CT)可模拟这种效应,而赛庚啶、酮色林或MDL 72222对此无影响,但麦角新碱可阻断该效应。本研究旨在根据1994年和1996年NC-IUPHAR 5-HT受体分类和命名小组委员会提出的分类方案重新分析这一观点。静脉推注5-CT(0.01 - 0.3μg·kg⁻¹)、5-HT(1 - 30μg·kg⁻¹)和5-甲氧基色胺(5-MeO-T;1 - 30μg·kg⁻¹)产生剂量依赖性降压反应,激动剂效力顺序为:5-CT >> 5-HT > 5-甲氧基色胺,舒马曲坦(30 - 1000μg·kg⁻¹)无活性。静脉注射GR127935(300 - 3000μg·kg⁻¹)或等量生理盐水对5-HT和5-CT的降压反应无减弱作用。相比之下,利舒脲、甲硫噻嗪、美舒麦角、美替戈林和氯氮平剂量依赖性地拮抗对5-HT和5-CT的反应;分别针对5-HT和5-CT的表观pA2值顺序为:利舒脲(7.7;7.8)>甲硫噻嗪(6.8;7.0)≥美舒麦角(6.4;6.6)>氯氮平(5.7;5.8);美替戈林效力不一(5.6;6.4)。除利舒脲也影响异丙肾上腺素诱导的低血压外,其他药物的拮抗作用具有选择性。基于上述激动剂效力顺序、一系列对克隆的5-ht7受体具有高亲和力的药物的阻断作用以及GR12793未见阻断作用,我们的结果表明,介导去迷走交感神经大鼠低血压的5-HT受体在功能上与其他介导血管和非血管反应(如兔股静脉、犬冠状动脉和颈外动脉及豚鼠回肠松弛以及猫心动过速)的假定5-ht7受体相似。