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评估突触前和突触后5-羟色胺能受体在电休克治疗中的作用。

Evaluation of the role of pre- and postsynaptic serotonergic receptors in electroconvulsive shock therapy.

作者信息

Schoups A A, Beeckman N, Lauwers M C, De Potter W P

机构信息

Department of Medicine, Wilrijk, Belgium.

出版信息

Biol Psychiatry. 1988 Apr 15;23(8):807-17. doi: 10.1016/0006-3223(88)90069-8.

Abstract

Despite the well-established clinical efficacy of electroconvulsive therapy (ECT) in the treatment of affective disorders, there is no generally accepted theory regarding its mode of action. Pre- and postsynaptic serotonin (5-hydroxytryptamine, 5-HT) receptors were studied following treatment of rabbits with electroconvulsive therapy (8 shocks). No change was observed in the binding at the postsynaptic 5-HT2 receptor in frontoparietal cortex, as indicated by an unchanged affinity and by the total number of receptors. In control rabbits, exogenously added serotonin and metitepin modulated the electrically evoked 3H-serotonin release, probably by acting on a presynaptic serotonin autoreceptor. Following electroconvulsive therapy, exogenous serotonin still inhibited the 3H-serotonin release, whereas metitepin had lost its enhancing effect. This observation provides evidence for a decreased amount of endogenous neurotransmitter present in the synaptic cleft at stimulation. The results indicate that postsynaptic receptor changes following antidepressant treatments are related to the presynaptic autoreceptor changes.

摘要

尽管电休克疗法(ECT)在治疗情感障碍方面具有公认的临床疗效,但关于其作用方式尚无普遍接受的理论。在用电休克疗法(8次电击)治疗兔子后,对突触前和突触后5-羟色胺(5-羟色胺,5-HT)受体进行了研究。额叶顶叶皮质突触后5-HT2受体的结合未观察到变化,这表现为亲和力和受体总数未变。在对照兔子中,外源性添加的5-羟色胺和甲硫替平可能通过作用于突触前5-羟色胺自身受体来调节电诱发的3H-5-羟色胺释放。电休克疗法后,外源性5-羟色胺仍抑制3H-5-羟色胺释放,而甲硫替平则失去了其增强作用。该观察结果为刺激时突触间隙中内源性神经递质数量减少提供了证据。结果表明,抗抑郁治疗后突触后受体变化与突触前自身受体变化有关。

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