Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
Trends Pharmacol Sci. 2010 Aug;31(8):381-90. doi: 10.1016/j.tips.2010.05.004. Epub 2010 Jun 25.
Dopamine D(2) receptor antagonism is a unifying property of all antipsychotic drugs in use for schizophrenia. While often effective at ameliorating psychosis, these drugs are largely ineffective at treating negative and cognitive symptoms. Increasing attention is being focused on the complex genetics of the illness and the signaling pathways implicated in its pathophysiology. We review targeted approaches for pharmacotherapy involving the glutamatergic, GABAergic and cholinergic pathways. We also describe several of the major genetic findings that identify signaling pathways representing potential targets for novel pharmacological intervention. These include genes in the 22q11 locus, DISC1, Neuregulin 1/ErbB4, and components of the Akt/GSK-3 pathway.
多巴胺 D2 受体拮抗作用是所有用于治疗精神分裂症的抗精神病药物的共同特性。虽然这些药物通常在改善精神病方面非常有效,但它们在治疗阴性症状和认知症状方面效果不大。人们越来越关注这种疾病的复杂遗传学以及涉及它的病理生理学的信号通路。我们回顾了涉及谷氨酸能、γ-氨基丁酸能和胆碱能途径的靶向药物治疗方法。我们还描述了几项主要的遗传发现,这些发现确定了代表新的药理学干预潜在靶点的信号通路。这些包括 22q11 基因座、DISC1、神经调节蛋白 1/ErbB4 以及 Akt/GSK-3 途径的组成部分。