University of Toronto, Toronto, Ontario, Canada.
Expert Rev Neurother. 2011 Apr;11(4):589-607. doi: 10.1586/ern.10.191.
Antipsychotics represent the first effective therapy for schizophrenia, with their benefits linked to dopamine D2 blockade. Schizophrenia was soon identified as a hyperdopaminergic disorder, and antipsychotics proved to be reasonably effective in controlling positive symptoms. However, over the years, schizophrenia has been reconceptualized more broadly, now defined as a heterogeneous disorder with multiple symptom domains. Negative and cognitive features, not particularly responsive to antipsychotic therapy, have taken on increased importance--current thinking suggests that these domains predate the onset of positive symptoms and are more closely tied to functional outcome. That they are better understood in the context of decreased dopamine activity suggests that schizophrenia may fundamentally represent a hypodopaminergic disorder. This shift in thinking has important theoretical implications from the standpoint of etiology and pathophysiology, but also clinically in terms of treatment and drug development.
抗精神病药物是精神分裂症的第一种有效治疗方法,其疗效与多巴胺 D2 阻断有关。精神分裂症很快被确定为一种多巴胺功能亢进障碍,抗精神病药物在控制阳性症状方面被证明是相当有效的。然而,多年来,精神分裂症的概念已经被更广泛地重新定义,现在被定义为一种具有多种症状领域的异质性障碍。阴性和认知特征对抗精神病药物治疗的反应不特别敏感,其重要性日益增加——目前的观点认为,这些领域先于阳性症状的出现,与功能结果更为密切相关。在多巴胺活性降低的情况下,这些领域更容易被理解,这表明精神分裂症可能从根本上代表一种低多巴胺能障碍。这种思维模式的转变从病因学和病理生理学的角度来看具有重要的理论意义,而且从治疗和药物开发的角度来看也具有临床意义。