Crow T J, Deakin J F, Longden A
Psychol Med. 1977 May;7(2):213-21. doi: 10.1017/s0033291700029287.
The hypothesis that neuroleptic drugs exert their therapeutic effects by blocking dopaminergic transmission has been investigated by examining the effects of 3 neuroleptic drugs on dopamine turnover in 2 dopaminergically innervated regions of brain--the neostriatum and nucleus accumbens. The drugs chlorpromazine, thioridazine and fluphenazine, known to be therapeutically active in the treatment of schizophrenia, but to have differing incidences of extrapyramidal side effects, were administered to rats in dose ratios approximating to those effective in man. All 3 drugs induced a similar rise in the content of the dopamine metabolite homovanillic acid (HVA) in the nucleus accumbens, whilst the changes in HVA observed in the neostriatum were in the rank order in which these drugs produce extrapyramidal side effects. While the concentrations of dopamine metabolites in the frontal cortex were too low to assess the possibility that neuroleptic drugs have actions at this level, our results are consistent with the hypothesis that these drugs exert their therapeutic effects by dopamine receptor blockade in the nucleus accumbens.
抗精神病药物通过阻断多巴胺能传递发挥治疗作用这一假说,已通过研究3种抗精神病药物对脑内两个多巴胺能神经支配区域——新纹状体和伏隔核中多巴胺周转的影响进行了探究。已知在治疗精神分裂症方面具有治疗活性但锥体外系副作用发生率不同的氯丙嗪、硫利达嗪和氟奋乃静,以接近对人体有效的剂量比例给予大鼠。所有3种药物均使伏隔核中多巴胺代谢产物高香草酸(HVA)含量出现类似升高,而在新纹状体中观察到的HVA变化顺序与这些药物产生锥体外系副作用的顺序一致。虽然额叶皮质中多巴胺代谢产物的浓度过低,无法评估抗精神病药物在此水平发挥作用的可能性,但我们的结果与这些药物通过阻断伏隔核中的多巴胺受体发挥治疗作用这一假说相符。