Maĭsov N I, Gankina E M, Voronina T A
Farmakol Toksikol. 1985 Jul-Aug;48(4):46-50.
The authors investigated the ability of psychotropic drugs of different classes (psychostimulants, antidepressants and tranquilizers) to inhibit the reverse synaptosomal uptake of monoamine neurotransmitters in the rat brain. The psychostimulants amphetamine and cocaine (50 microM) powerfully suppressed noradrenaline, dopamine and serotonin transport without influencing GABA uptake. Phenazepam (50 microM) negligibly decreased the reverse synaptosomal uptake chiefly of noradrenaline. Studies of the antidepressants evidenced that inkazan is a highly selective inhibitor of the reverse uptake of serotonin, whereas other antidepressants such as zimelidine, imipramine and norzimelidine were discovered to inhibit the uptake of serotonin to a larger extent than that of other transmitters. The antidepressants pyrazidol and viloxazine turned out to be non-selective inhibitors of the transport of all monoamines tested. Iproniazide and moclobamide appeared inactive as regards the reverse uptake of monoamine neurotransmitters.
作者研究了不同种类精神药物(精神兴奋剂、抗抑郁药和镇静剂)抑制大鼠脑中单胺神经递质逆向突触体摄取的能力。精神兴奋剂苯丙胺和可卡因(50微摩尔)强烈抑制去甲肾上腺素、多巴胺和5-羟色胺的转运,而不影响γ-氨基丁酸的摄取。非那西泮(50微摩尔)对主要是去甲肾上腺素的逆向突触体摄取的降低作用可忽略不计。抗抑郁药的研究表明,印卡赞是5-羟色胺逆向摄取的高度选择性抑制剂,而其他抗抑郁药如齐美利定、丙咪嗪和去甲丙咪嗪被发现对5-羟色胺摄取的抑制作用比对其他递质的抑制作用更大。抗抑郁药吡嗪醇和维洛沙嗪被证明是所有测试单胺转运的非选择性抑制剂。异烟肼和吗氯贝胺在单胺神经递质的逆向摄取方面似乎没有活性。