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吲哚雷酯对食物摄入的影响:与芬氟拉明和苯丙胺的比较。

Effects of indorenate on food intake: a comparison with fenfluramine and amphetamine.

作者信息

Velázquez Martínez D N, Valencia Flores M, López Cabrera M, Villarreal J E

机构信息

Departamento de Psicofisiología, Facultad de Psicología, Universidad Nacional Autónoma de México, México D.F.

出版信息

Psychopharmacology (Berl). 1995 Jan;117(1):91-101. doi: 10.1007/BF02245103.

DOI:10.1007/BF02245103
PMID:7724707
Abstract

Indorenate (TR3369, 5-methoxytryptamine b-methylcarboxylate HCl) is a 5-HT1-like receptor agonist with hypotensive activity. Here, we describe that indorenate also decreases food intake (ED50 26.1 mg/kg) without an appreciable effect in water intake (the estimated ED50 for water was 589.8 mg/kg). The anorectic activity of indorenate was compared to the effects of amphetamine and other serotonin agonists; the effect of indorenate was smaller than those of the other compounds; however, the effect of indorenate was specific to food, whereas all the other drugs also produced significant decrements in water intake. The serotonin antagonists cinanserin, cyproheptadine, methergoline and methysergide effectively prevented the decrease in food intake produced by indorenate and fenfluramine. Haloperidol, a dopaminergic antagonist, was ineffective in preventing the effect of indorenate although it prevented the anorectic effect of amphetamine. The present results suggest the participation of serotoninergic, but not dopaminergic mechanisms, in the decrease in food intake produced by indorenate.

摘要

吲哚雷尼(TR3369,5-甲氧基色胺盐酸β-甲酯)是一种具有降压活性的5-HT1样受体激动剂。在此,我们描述吲哚雷尼还能减少食物摄入量(半数有效量为26.1毫克/千克),而对水摄入量没有明显影响(估计水的半数有效量为589.8毫克/千克)。将吲哚雷尼的厌食活性与苯丙胺和其他血清素激动剂的作用进行了比较;吲哚雷尼的作用小于其他化合物;然而,吲哚雷尼的作用对食物具有特异性,而所有其他药物也会使水摄入量显著减少。血清素拮抗剂辛那色林、赛庚啶、麦角苄酯和甲基麦角新碱可有效防止吲哚雷尼和芬氟拉明引起的食物摄入量减少。多巴胺能拮抗剂氟哌啶醇虽然能防止苯丙胺的厌食作用,但对防止吲哚雷尼的作用无效。目前的结果表明,血清素能机制而非多巴胺能机制参与了吲哚雷尼引起的食物摄入量减少。

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本文引用的文献

1
The central vasomotor effects of 5-hydroxytryptamie.5-羟色胺的中枢血管舒缩效应。
Br J Pharmacol Chemother. 1959 Dec;14(4):411-4. doi: 10.1111/j.1476-5381.1959.tb00943.x.
2
Lowering of blood pressure by direct- and indirect-acting serotonin agonists in spontaneously hypertensive rats.直接和间接作用的5-羟色胺激动剂对自发性高血压大鼠血压的降低作用
Clin Exp Hypertens (1978). 1981;3(3):497-508. doi: 10.3109/10641968109033678.
3
The effect of altered dopaminergic activity on food intake in the rat: evidence for an optimal level of dopaminergic activity for behavior.
氟哌啶醇和氯氮平拮抗苯丙胺诱导的条件性味觉厌恶潜伏抑制的破坏。
Psychopharmacology (Berl). 2003 Nov;170(3):263-270. doi: 10.1007/s00213-003-1544-5. Epub 2003 Jul 25.
4
Pharmacological approaches for the treatment of obesity.治疗肥胖症的药理学方法。
Drugs. 2002;62(6):915-44. doi: 10.2165/00003495-200262060-00005.
多巴胺能活性改变对大鼠食物摄入量的影响:行为存在多巴胺能活性最佳水平的证据
Prog Neuropsychopharmacol. 1980;4(4-5):351-62. doi: 10.1016/0364-7722(80)90005-3.
4
Tryptophan analogues. 1. Synthesis and antihypertensive activity of positional isomers.色氨酸类似物。1. 位置异构体的合成与降压活性
J Med Chem. 1982 Jun;25(6):723-30. doi: 10.1021/jm00348a022.
5
Differential effects of pharmacological agents acting on monoaminergic systems on drug-induced anorexia.作用于单胺能系统的药物制剂对药物性厌食的不同影响。
Prog Neuropsychopharmacol. 1980;4(4-5):327-39. doi: 10.1016/0364-7722(80)90003-x.
6
Anorexigenic effects of fenfluramine hydrochloride in rats, guinea pigs, and dogs.盐酸芬氟拉明对大鼠、豚鼠和犬的厌食作用。
Toxicol Appl Pharmacol. 1969 Jan;14(1):182-91. doi: 10.1016/0041-008x(69)90178-1.
7
Comparative study of the anorectic activity of phenindamine d-amphetamine and fenfluramine in different species.非尼拉敏、右旋苯丙胺和芬氟拉明在不同物种中的食欲抑制活性比较研究。
Arch Int Pharmacodyn Ther. 1970 Dec;188(2):271-83.
8
The effect of cyproheptadine on food consumption in the fasted rat.赛庚啶对禁食大鼠食物摄入量的影响。
Br J Pharmacol. 1970 May;39(1):229P-230P.
9
[Modification of the cerebral serotonin level in the rat by trifluoromethyl-2-phenyl ethyl aminopropane (Fenfluramine 768 S)].[三氟甲基-2-苯基乙胺丙烷(芬氟拉明768 S)对大鼠脑5-羟色胺水平的影响]
Arch Int Pharmacodyn Ther. 1967 Dec;170(2):276-86.
10
The effect of cyproheptadine on water and food intake and on body weight in the fasted adult and weanling rats.赛庚啶对禁食成年大鼠和断奶大鼠水和食物摄入量及体重的影响。
Br J Pharmacol. 1973 Jun;48(2):328P-329P.