Kłodzińska A, Chojnacka-Wójcik E
Institute of Pharmacology, Polish Academy of Sciences, Kraków.
Pol J Pharmacol Pharm. 1990 Jan-Feb;42(1):13-7.
1-[3-(trifluoromethyl) phenyl] piperazine (TFMPP), a putative 5-HT1B, 5-HT1C and 5-HT2 agonist decreased dose-dependently food intake over 4 h in freely feeding rats. The TFMPP-induced anorexia was blocked by mesulergine (a 5-HT1C and 5-HT2 antagonist), metergoline (a 5-HT1A, 5-HT1B, 5-HT1C and 5-HT2 antagonist), mianserin (a 5-HT1C and 5-HT2 antagonist) and attenuated by ketanserin and ritanserin (5-HT2 antagonists). The examined anorexia was not antagonized by cyanopindolol and compound 21009 (5-HT1A and 5-HT1B antagonists). These results indicate that the TFMPP-induced anorexia in freely feeding rats is probably mediated by 5-HT2--and, may be also by 5-HT1C receptors.
1-[3-(三氟甲基)苯基]哌嗪(TFMPP),一种假定的5-羟色胺1B、5-羟色胺1C和5-羟色胺2激动剂,在自由进食的大鼠中,4小时内剂量依赖性地减少食物摄入量。TFMPP诱导的厌食症被美舒麦角(一种5-羟色胺1C和5-羟色胺2拮抗剂)、美替戈林(一种5-羟色胺1A、5-羟色胺1B、5-羟色胺1C和5-羟色胺2拮抗剂)、米安色林(一种5-羟色胺1C和5-羟色胺2拮抗剂)阻断,并被酮色林和利坦色林(5-羟色胺2拮抗剂)减弱。所检测的厌食症未被氰吲哚洛尔和化合物21009(5-羟色胺1A和5-羟色胺1B拮抗剂)拮抗。这些结果表明,TFMPP在自由进食大鼠中诱导的厌食症可能由5-羟色胺2介导,也可能由5-羟色胺1C受体介导。