Poirier M F, Loo H, Benkelfat C, Sechter D, Zarifian E, Galzin A M, Schoemaker H, Segonzac A, Langer S Z
Eur J Pharmacol. 1984 Nov 27;106(3):629-33. doi: 10.1016/0014-2999(84)90069-4.
In platelets of normal volunteers taking chlorimipramine (50 mg/day) for one week, the saturable uptake of [3H]5HT was fully inhibited at day 8, but returned to control values at day 15. The Bmax of [3H]imipramine binding was decreased by 65% at day 8 and remained significantly below control values at day 15. If the present findings can be extrapolated to other antidepressants, the reported decreases in [3H]imipramine binding in depression may partly reflect residual treatment effects. It cannot be excluded that, in depression, the platelet [3H]imipramine receptor already is down-regulated maximally which would preclude a further down-regulation due to antidepressant drug therapy.
在正常志愿者服用氯米帕明(50毫克/天)一周的血小板中,[3H]5HT的可饱和摄取在第8天被完全抑制,但在第15天恢复到对照值。[3H]丙咪嗪结合的Bmax在第8天下降了65%,并在第15天仍显著低于对照值。如果目前的研究结果可以外推到其他抗抑郁药,那么报道的抑郁症中[3H]丙咪嗪结合的减少可能部分反映了残留的治疗效果。不能排除在抑郁症中,血小板[3H]丙咪嗪受体已经最大程度地下调,这将排除由于抗抑郁药物治疗导致的进一步下调。