Henan Medical Key Laboratory of Translational Research on Psychiatric Diseases, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, China.
The Illawarra Health and Medical Research Institute and School of Medicine, University of Wollongong, Wollongong, Australia.
Med Res Rev. 2019 Jan;39(1):386-403. doi: 10.1002/med.21512. Epub 2018 May 22.
Although antipsychotic drugs are mainly used for treating schizophrenia, they are widely used for treating various psychiatric diseases in adults, the elderly, adolescents and even children. Today, about 1.2% of the worldwide population suffers from psychosis and related disorders, which translates to about 7.5 million subjects potentially targeted by antipsychotic drugs. Neurites project from the cell body of neurons and connect neurons to each other to form neural networks. Deficits in neurite outgrowth and integrity are implicated in psychiatric diseases including schizophrenia. Neurite deficits contribute to altered brain development, neural networking and connectivity as well as symptoms including psychosis and altered cognitive function. This review revealed that (1) antipsychotic drugs could have profound effects on neurites, synaptic spines and synapse, by which they may influence and regulate neural networking and plasticity; (2) antipsychotic drugs target not only neurotransmitter receptors but also intracellular signaling molecules regulating the signaling pathways responsible for neurite outgrowth and maintenance; (3) high doses and chronic administration of antipsychotic drugs may cause some loss of neurites, synaptic spines, or synapsis in the cortical structures. In addition, confounding effects causing neurite deficits may include elevated inflammatory cytokines and antipsychotic drug-induced metabolic side effects in patients on chronic antipsychotic therapy. Unraveling how antipsychotic drugs affect neurites and neural connectivity is essential for improving therapeutic outcomes and preventing aversive effects for patients on antipsychotic drug treatment.
虽然抗精神病药物主要用于治疗精神分裂症,但它们也广泛用于治疗成人、老年人、青少年甚至儿童的各种精神疾病。如今,全世界约有 1.2%的人口患有精神病和相关障碍,这意味着约有 750 万人可能需要使用抗精神病药物。神经突从神经元的细胞体伸出,将神经元彼此连接起来形成神经网络。神经突的生长和完整性缺陷与包括精神分裂症在内的精神疾病有关。神经突缺陷导致大脑发育、神经网络和连接改变以及精神病和认知功能改变等症状。本综述揭示了:(1)抗精神病药物可能对神经突、突触棘和突触产生深远影响,从而可能影响和调节神经网络和可塑性;(2)抗精神病药物的作用靶点不仅是神经递质受体,还包括调节负责神经突生长和维持的信号通路的细胞内信号分子;(3)高剂量和慢性给予抗精神病药物可能导致皮质结构中神经突、突触棘或突触的一些丢失。此外,导致神经突缺陷的混杂效应可能包括慢性抗精神病治疗患者中升高的炎症细胞因子和抗精神病药物诱导的代谢副作用。阐明抗精神病药物如何影响神经突和神经连接对于改善治疗效果和预防患者对抗精神病药物治疗的不良反应至关重要。