School of Psychology, Victoria University of Wellington, P.O. Box 600, Wellington, New Zealand.
Neuropharmacology. 2012 Mar;62(3):1371-80. doi: 10.1016/j.neuropharm.2011.03.013. Epub 2011 Mar 21.
Antipsychotic drugs for the treatment of schizophrenia arrived in the clinic in the fifties of the previous century and have since been the most effective treatment for patients with this devastating disorder. In spite of the more than half a century of clinical experience, and the introduction of a large number of chemical divers antipsychotic drugs, several recent large, multi-center studies have shown that, although novel (second generation) antipsychotics seem to be tolerated somewhat better (especially in relation to neurological side effects), their therapeutic potential is comparable to that of first generation antipsychotics. Hence there is still an urgent need for better pharmacological tools to treat schizophrenic patients. The current paper reviews the benefits and shortcomings of the currently available drugs, and gives an outlook towards the drugs and targets that are currently being pursued in clinical trials. Given the uncertainty of the drug discovery process and the relatively poor predictive validity of the currently available animal models, it is, at present, impossible to predict which of these drugs will ultimately become available for treating schizophrenic patients.
抗精神病药物于上世纪五十年代在临床上用于治疗精神分裂症,自此成为治疗这种严重疾病最有效的方法。尽管有半个多世纪的临床经验,以及引入了大量化学结构不同的抗精神病药物,最近的几项大型、多中心研究表明,虽然新型(第二代)抗精神病药物似乎耐受性更好(尤其是在神经副作用方面),但它们的治疗潜力与第一代抗精神病药物相当。因此,仍然迫切需要更好的药理学工具来治疗精神分裂症患者。本文综述了目前可用药物的优缺点,并展望了目前正在临床试验中探索的药物和靶点。鉴于药物发现过程的不确定性以及目前可用的动物模型的预测有效性相对较差,目前无法预测哪些药物最终将可用于治疗精神分裂症患者。