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抑郁症吲哚胺假说的重新评估。抗抑郁药降低中枢5-羟色胺系统功能活性的证据。

Reevaluation of the indoleamine hypothesis of depression. Evidence for a reduction of functional activity of central 5-HT systems by antidepressant drugs.

作者信息

Ogren S O, Fuxe K, Agnati L F, Gustafsson J A, Jonsson G, Holm A C

出版信息

J Neural Transm. 1979;46(2):85-103. doi: 10.1007/BF01250331.

Abstract

The effects of antidepressant drugs on central 5-HT receptor activity were studied in rats and mice. Antidepressant drugs were evaluated for their ability to displace 3H-5-HT and 3H-d-LSD from membrane binding sites in the dorsal neocortex of rats in vitro and for their ability to block 5-HTP and d-LSD induced behavioral effects in mice. The degree of blockade of head-twitches in mice produced by the antidepressants was highly correlated with their affinity for 3H-d-LSD binding sites. A number of antidepressant drugs such as amitriptyline, nortriptyline, mianserine, doxepine, nomifensine and dibenzepine appear to possess marked 5-HT receptor blocking activity at some type of 5-HT receptors in brain. New antidepressant drugs such as zimelidine, which specifically inhibit 5-HT reuptake and do not block 5-HT receptor sites, may after chronic treatment also reduce the functional activity of 5-HT systems by producing adaptive changes in postsynaptic 5-HT mechanisms. Thus, a new indoleamine hypothesis of depression is presented: the therapeutic action of antidepressant drugs may in part be due to a reduced functional acitivity of some central 5-HT systems.

摘要

在大鼠和小鼠中研究了抗抑郁药物对中枢5-羟色胺(5-HT)受体活性的影响。评估了抗抑郁药物在体外从大鼠背侧新皮质膜结合位点置换3H-5-HT和3H-d-麦角酰二乙胺(3H-d-LSD)的能力,以及它们阻断5-羟色胺酸(5-HTP)和d-LSD诱导的小鼠行为效应的能力。抗抑郁药物对小鼠头部抽搐的阻断程度与其对3H-d-LSD结合位点的亲和力高度相关。一些抗抑郁药物,如阿米替林、去甲替林、米安色林、多塞平、诺米芬辛和二苯氮䓬,似乎在脑内某些类型的5-HT受体上具有显著的5-HT受体阻断活性。新的抗抑郁药物,如齐美利定,它特异性抑制5-HT再摄取且不阻断5-HT受体位点,长期治疗后可能也会通过在突触后5-HT机制中产生适应性变化来降低5-HT系统的功能活性。因此,提出了一种新的抑郁症吲哚胺假说:抗抑郁药物的治疗作用可能部分归因于某些中枢5-HT系统功能活性的降低。

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