Seabrook J M, Nolan P L
Eur J Pharmacol. 1983 Apr 22;89(1-2):131-5. doi: 10.1016/0014-2999(83)90617-9.
The action of 5-hydroxytryptamine (5-HT) to potentiate vasoconstrictor responses to noradrenaline has been studied using the rat isolated perfused mesenteric artery. Receptor antagonists have been employed to compare the vascular receptors which mediate the vasoconstrictor and potentiating actions of 5-HT. In preparations pretreated with methysergide (1 mumol X 1(-1)), cyproheptadine (1 mumol X 1(-1)) or fluoxetine (1 mumol X 1(-1)) the vasoconstrictor response to 5-HT (1 mumol X 1(-1)) was abolished, while ketanserin (1 nmol X 1(-1)) antagonized the response by 90%. In contrast, only methysergide antagonized the sensitizing effect of 5-HT, while the other three antagonists exerted no effect on this action. In view of the different sensitivities of the vasoconstrictor and potentiating effects of 5-HT to antagonist drugs, it is suggested that the vascular receptors which mediate these actions are different.
利用大鼠离体灌注肠系膜动脉,研究了5-羟色胺(5-HT)增强去甲肾上腺素血管收缩反应的作用。已使用受体拮抗剂来比较介导5-HT血管收缩和增强作用的血管受体。在用麦角新碱(1 μmol×1⁻¹)、赛庚啶(1 μmol×1⁻¹)或氟西汀(1 μmol×1⁻¹)预处理的制剂中,对5-HT(1 μmol×1⁻¹)的血管收缩反应被消除,而酮色林(1 nmol×1⁻¹)使反应拮抗90%。相比之下,只有麦角新碱拮抗5-HT的致敏作用,而其他三种拮抗剂对该作用无影响。鉴于5-HT的血管收缩和增强作用对拮抗剂药物的敏感性不同,提示介导这些作用的血管受体不同。