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药理抗抑郁作用及噻奈普汀诱导的5-羟色胺摄取增加。

Pharmacological antidepressive effects and tianeptine-induced 5-HT uptake increase.

作者信息

Mocaër E, Rettori M C, Kamoun A

机构信息

Institut de Recherches Internationales Servier, Neuilly-sur-Seine, France.

出版信息

Clin Neuropharmacol. 1988;11 Suppl 2:S32-42.

PMID:3180116
Abstract

The antidepressant activity of tianeptine has been demonstrated using the classical screening tests of antagonism of reserpine-like compounds, rat behavioral despair (Porsolt's test), and aggressive behavior induced by isolation in mice. Tianeptine has novel behavioral effects. it is devoid of sedative effects. In rodents it induces slight stimulation of locomotor activity. In monkeys, tianeptine decreases aggressive and emotive states and improves individual behavior and group social interactions. Electroencephalographic studies in rats and monkeys have shown that tianeptine has no stimulant or sedative properties, and does not modify the overall distribution of wakefulness-sleep phases. Pharmacological studies have shown that tianeptine does not have anticholinergic effects and that it is also devoid of any effect on the cardiovascular and neuroendocrine systems. Tianeptine does not disturb memory. Tianeptine, in contrast to tricyclic antidepressants which inhibit 5-HT uptake, stimulates serotonin uptake ex vivo in the rat brain (cortex, hippocampus) and rat as well as human platelets following both acute and chronic administration. Tianeptine increases the firing rate of hippocampus pyramidal cells which could be consistent with tianeptine-induced serotonin uptake stimulation. Tianeptine allows us to examine the coexistence of a classical pharmacological profile and original neurochemical effects.

摘要

通过利血平样化合物拮抗作用的经典筛选试验、大鼠行为绝望试验(波索尔特试验)以及小鼠隔离诱导的攻击行为试验,已证实了噻奈普汀的抗抑郁活性。噻奈普汀具有新颖的行为效应。它没有镇静作用。在啮齿动物中,它会轻微刺激运动活性。在猴子中,噻奈普汀可降低攻击和情绪状态,并改善个体行为和群体社交互动。对大鼠和猴子的脑电图研究表明,噻奈普汀没有兴奋或镇静特性,也不会改变清醒 - 睡眠阶段的总体分布。药理学研究表明,噻奈普汀没有抗胆碱能作用,对心血管和神经内分泌系统也没有任何影响。噻奈普汀不会干扰记忆。与抑制5 - HT摄取的三环类抗抑郁药不同,噻奈普汀在急性和慢性给药后,均可在离体大鼠脑(皮层、海马体)以及大鼠和人类血小板中刺激5 - 羟色胺摄取。噻奈普汀可提高海马体锥体细胞的放电频率,这可能与噻奈普汀诱导的5 - 羟色胺摄取刺激作用一致。噻奈普汀使我们能够研究经典药理学特征与原始神经化学效应的共存情况。

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