安非他酮对多巴胺受体的调节:与抗抑郁药和中枢神经系统兴奋剂的比较。

A Vassout, A Bruinink, J Krauss, P Waldmeier, S Bischoff
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引用次数: 24

摘要

抗抑郁药安非他酮急性治疗大鼠体内增加[3H]spiperone与D2受体的结合。这种剂量和时间依赖性作用在纹状体中最大,在小脑和垂体中最小。在同样的大鼠身上发生了平行的行为刺激。在21种抗抑郁药和中枢神经系统兴奋剂的测试中,只有激活多巴胺(DA)传递的药物有相似的效果:诺米芬、氨奈丁、哌醋甲酯、d -安非他明、氨苯酸、可卡因、苯托品和GBR 12909。利血平加α -甲基-对酪氨酸降低DA传递,阻止了安非他酮的作用。最后,安非他酮在体内外均无活性。因此,我们提出安非他酮和其他da增强剂通过干预D2受体的动态调节来改变[3H]spiperone结合的特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of dopamine receptors by bupropion: comparison with antidepressants and CNS stimulants.

Acute treatment of rats with the antidepressant bupropion increased [3H]spiperone binding to D2 receptors in vivo. This dose- and time-dependent effect was greatest in striatum and minimal in cerebellum and pituitary. A parallel behavioral stimulation occurred in the same rats. Among 21 antidepressants and CNS stimulants tested, only those that activate dopamine (DA) transmission had similar effects: nomifensine, amineptine, methylphenidate, D-amphetamine, amfonelic acid, cocaine, benztropine and GBR 12909. Decreasing DA transmission with reserpine plus alpha-methyl-p-tyrosine prevented the action of bupropion. Finally, bupropion was inactive in vitro and ex-vivo. Therefore, we propose that bupropion and other DA-enhancing agents modify the characteristics of [3H]spiperone binding through the intervention of a dynamic regulation of the D2 receptors by the neurotransmitter itself.

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