White F J, Wang R Y
Science. 1983 Sep 9;221(4615):1054-7. doi: 10.1126/science.6136093.
Prolonged treatment with classical antipsychotic drugs decreased the number of spontaneously active dopamine neurons in both the substantia nigra (A9) and the ventral tegmental area (A10) of the rat brain. In contrast, treatment with atypical antipsychotic drugs selectively decreased the number of A10 dopamine neurons. Related drugs lacking antipsychotic efficacy failed to decrease dopamine activity. These findings suggest that the inability of atypical antipsychotic drugs to decrease A9 dopamine neuronal activity may be related to their lower potential for causing tardive dyskinesia and that the inactivation of A10 neurons may be involved in the delayed onset of therapeutic effects during treatment.
用经典抗精神病药物进行长期治疗会减少大鼠脑黑质(A9)和腹侧被盖区(A10)中自发活动的多巴胺能神经元数量。相比之下,用非典型抗精神病药物治疗会选择性地减少A10多巴胺能神经元数量。缺乏抗精神病疗效的相关药物未能降低多巴胺活性。这些发现表明,非典型抗精神病药物无法降低A9多巴胺能神经元活性可能与其导致迟发性运动障碍的可能性较低有关,并且A10神经元的失活可能参与治疗期间治疗效果的延迟出现。