Egashira T, Goto S, Wada Y, Takayama F, Yamanaka Y
Department of Pharmacology, Oita Medical University, Japan.
Jpn J Pharmacol. 1995 Feb;67(2):177-9. doi: 10.1254/jjp.67.177.
We found that substances present in monkey cerebrospinal fluid (CSF) could inhibit [3H]-paroxetine binding in monkey brain preparations. The molecular weight of one of these inhibitory substances was approximately 2000, which is in agreement with earlier studies using human CSF. We also found that the inhibitory effect of the substances present in monkey CSF on [3H]-paroxetine binding decreased after 8 weeks of chronic fluvoxamine (5 mg/kg day, p.o.) treatment. These results suggest that the ability of a drug to decrease the activity of endogenous 5-HT uptake modulators may related to its antidepressive effects.
我们发现,猴脑脊液(CSF)中的物质能够抑制猴脑制剂中[3H]-帕罗西汀的结合。其中一种抑制性物质的分子量约为2000,这与早期使用人脑脊液的研究结果一致。我们还发现,在慢性氟伏沙明(5毫克/千克·天,口服)治疗8周后,猴脑脊液中物质对[3H]-帕罗西汀结合的抑制作用减弱。这些结果表明,药物降低内源性5-羟色胺摄取调节剂活性的能力可能与其抗抑郁作用有关。