Yamada Jun, Sugimoto Yumi
Department of Pharmacology, Kobe Pharmaceutical University, Motoyamakita-machi, Higashinada-ku, Kobe 658-8558, Japan.
Brain Res. 2002 Dec 20;958(1):161-5. doi: 10.1016/s0006-8993(02)03684-3.
The effects of the 5-HT(2) receptor antagonist, LY 53857 on the effects of noradrenaline and serotonin reuptake inhibitors were investigated using the forced swimming test. LY 53857 enhanced anti-immobility effects of clomipramine and maprotiline, which can inhibit reuptake of noradrenaline. However, LY 53857 did not affect the immobility time of mice treated with the selective serotonin reuptake inhibitors (SSRIs) fluoxetine and fluvoxamine. These results suggest that antagonism of the 5-HT(2) receptor leads to potentiation of the antidepressant effects of noradrenaline reuptake inhibitors but not SSRIs and that LY 53857 may modify the activity of noradrenergic neurons.
使用强迫游泳试验研究了5-羟色胺(5-HT)2受体拮抗剂LY 53857对去甲肾上腺素和5-羟色胺再摄取抑制剂作用的影响。LY 53857增强了氯米帕明和马普替林的抗不动效应,这两种药物可抑制去甲肾上腺素的再摄取。然而,LY 53857对用选择性5-羟色胺再摄取抑制剂(SSRI)氟西汀和氟伏沙明治疗的小鼠的不动时间没有影响。这些结果表明,5-HT2受体拮抗作用导致去甲肾上腺素再摄取抑制剂而非SSRI的抗抑郁作用增强,且LY 53857可能改变去甲肾上腺素能神经元的活性。