Ca2+和5-羟色胺拮抗剂多他嗪和氟桂利嗪的记忆效应。

V D Petkov, E Konstantinova, V V Petkov, S Belcheva, R Kehayov, J Vaglenova
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引用次数: 0

摘要

在Wistar和Long Evans大鼠实验中,新合成的具有Ca2+和5-羟色胺拮抗作用的二苯基甲基哌嗪衍生物多他嗪(DOT)以50和10 mg/kg的剂量反复口服,在某些情况下,采用被动(降伏和穿越)和主动(穿梭箱双向回避和惩罚强化)行为方法改善记忆过程。在相同的实验条件下,化学相关的多塔利嗪Ca2+拮抗剂氟桂利嗪显著促进保留。大剂量DOT对老龄大鼠(Long Evans和Wistar)的学习判据值有降低作用。这可能是药物固有的具有促智作用的“治疗窗口”的表现。同一和其他作者的早期研究表明,5 -羟色胺能神经传递参与了药物DOT记忆效应的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Memory effects of the Ca2+ and 5-HT antagonists dotarizine and flunarizine.

In experiments on Wistar and Long Evans rats, using behavioral methods for passive (step-down and step-through) and active (shuttle-box two-way avoidance with punishment reinforcement) the newly synthesized diphenyl-methyl-piperazine derivative with Ca2+ and 5-HT antagonistic action dotarizine (DOT) administered repeatedly at oral doses of 50 and 10 mg/kg in some cases improve memory process. Under the same experimental conditions the chemically related to dotarizine Ca2+ antagonist flunarizine significantly facilitated retention. In old (Long Evans and Wistar) rats DOT in large dose decreases values of learning criterion. Probably this is a manifestation of the inherent to drugs with nootropic action "therapeutic window". Earlier investigations of the same and other authors suggest the participation of serotonergic neurotransmission in the mechanism of the memory effects of the drug DOT.

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