Scarr Elizabeth, Dean Brian
Centre for Neuroscience, University of Melbourne, Parkville, VIC, Australia.
Expert Rev Neurother. 2009 Jan;9(1):73-86. doi: 10.1586/14737175.9.1.73.
Schizophrenia is a devastating psychiatric disorder; the diagnosis probably encompasses a number of illnesses with similar clinical presentations, complicating both treatment and studies into the pathology of the disorder. The development of antipsychotic medications revolutionized treatment for the disorder. However, there are still symptom domains that are relatively untouched by the drugs currently available; these are the cognitive deficits and the negative symptoms. Basic research strongly supports a role of acetylcholine in cognitive processes, making it a primary target for drugs designed to improve this most impairing symptom. In addition, the fact that acetylcholine can modulate dopamine release makes the cholinergic system a target for novel antipsychotic drugs, ideally without the side-effect profiles that contribute to patient noncompliance seen with current antipsychotic drugs. Thus far, the results of clinical trials with cholinomimetics have been equivocal; where beneficial effects are seen they are, by and large, modest rather than compelling. These trials and studies investigating the role of both nicotinic and muscarinic receptors in the pathology of the disorder, published during the last 5 years, are reviewed to ascertain whether there is a role for the cholinergic system in the treatment of schizophrenia.
精神分裂症是一种极具破坏性的精神障碍;该诊断可能涵盖多种具有相似临床表现的疾病,这使得针对该疾病的治疗及病理研究都变得复杂。抗精神病药物的发展彻底改变了对该疾病的治疗方式。然而,目前仍有一些症状领域相对未受现有药物影响;这些症状包括认知缺陷和阴性症状。基础研究有力地支持了乙酰胆碱在认知过程中的作用,使其成为旨在改善这一最具损害性症状的药物的主要靶点。此外,乙酰胆碱可调节多巴胺释放这一事实,使得胆碱能系统成为新型抗精神病药物的靶点,理想情况下这类药物不会出现当前抗精神病药物所导致的、致使患者不依从治疗的副作用。到目前为止,拟胆碱药的临床试验结果并不明确;即便观察到有益效果,总体而言也较为有限而非令人信服。本文对过去5年中发表的、研究烟碱受体和毒蕈碱受体在该疾病病理过程中作用的这些试验和研究进行综述,以确定胆碱能系统在精神分裂症治疗中是否发挥作用。