Samanin R, Mennini T, Ferraris A, Bendotti C, Borsini F
Eur J Pharmacol. 1980 Jan 25;61(2):203-6. doi: 10.1016/0014-2999(80)90167-3.
28-day treatment with d-fenfluramine, a serotonin (5HT) releaser and uptake inhibitor, caused significant reduction (23%) of 3H-5HT binding sites (Bmax) in the rat cortex. These sites were significantly increased (31%) in cortical membranes of rats which had received metergoline, a potent serotonin antagonist, for 28 days. Parallel changes were found in the anorectic activity of metachlorophenylpiperazine (m-CPP), a potent central 5HT agonist: chronic treatment with d-fenfluramine or metergoline caused respectively a decrease and in the effect of m-CPP on food intake. The data show that changes in 5HT central receptor number and sensitivity may occur after chronic treatment with drugs acting on brain serotonin.
用d-芬氟拉明(一种血清素(5HT)释放剂和摄取抑制剂)进行28天治疗,导致大鼠皮层中3H-5HT结合位点(Bmax)显著减少(23%)。在接受强效血清素拮抗剂美替拉酮28天的大鼠皮层膜中,这些位点显著增加(31%)。在强效中枢5HT激动剂间氯苯哌嗪(m-CPP)的厌食活性方面发现了平行变化:用d-芬氟拉明或美替拉酮进行慢性治疗分别导致m-CPP对食物摄入的作用降低和增强。数据表明,在用作用于脑血清素的药物进行慢性治疗后,5HT中枢受体数量和敏感性可能会发生变化。