Webster J P, Lamberton P H L, Donnelly C A, Torrey E F
Department of Zoology, University of Oxford South Parks Road, Oxford OX1 3SY, UK.
Proc Biol Sci. 2006 Apr 22;273(1589):1023-30. doi: 10.1098/rspb.2005.3413.
With increasing pressure to understand transmissible agents, renewed recognition of infectious causation of both acute and chronic diseases is occurring. Epidemiological and neuropathological studies indicate that some cases of schizophrenia may be associated with environmental factors, such as exposure to the ubiquitous protozoan Toxoplasma gondii. Reasons for this include T. gondii's ability to establish persistent infection within the central nervous system, its ability to manipulate intermediate host behaviour, the occurrence of neurological and psychiatric symptoms in some infected individuals, and an association between infection with increased incidence of schizophrenia. Moreover, several of the medications used to treat schizophrenia and other psychiatric disease have recently been demonstrated in vitro to possess anti-parasitic, and in particular anti-T. gondii, properties. Our aim here was thus to test the hypothesis that the anti-psychotic and mood stabilizing activity of some medications may be achieved, or at least augmented, through their in vivo inhibition of T. gondii replication and invasion in infected individuals. In particular we predicted, using the epidemiologically and clinically applicable rat-T. gondii model system, and following a previously described and neurologically characterized 'feline attraction' protocol that haloperidol (an anti-psychotic used in the treatment of mental illnesses including schizophrenia) and/or valproic acid (a mood stabilizer used in the treatment of mental illnesses including schizophrenia), would be, at least, as effective in preventing the development of T. gondii-associated behavioural and cognitive alterations as the standard anti-T. gondii chemotherapeutics pyrimethamine with Dapsone. We demonstrate that, while T. gondii appears to alter the rats' perception of predation risk turning their innate aversion into a 'suicidal' feline attraction, anti-psychotic drugs prove as efficient as anti-T. gondii drugs in preventing such behavioural alterations. Our results have important implications regarding the aetiology and treatment of such disorders.
随着了解可传播病原体的压力不断增加,人们对急性和慢性疾病的感染病因有了新的认识。流行病学和神经病理学研究表明,某些精神分裂症病例可能与环境因素有关,例如接触无处不在的原生动物弓形虫。原因包括弓形虫在中枢神经系统内建立持续感染的能力、操纵中间宿主行为的能力、一些受感染个体出现神经和精神症状,以及感染与精神分裂症发病率增加之间的关联。此外,最近在体外证明,用于治疗精神分裂症和其他精神疾病的几种药物具有抗寄生虫特性,尤其是抗弓形虫特性。因此,我们的目的是检验这样一种假设,即某些药物的抗精神病和情绪稳定活性可能通过其在体内抑制感染个体中弓形虫的复制和侵袭来实现,或者至少得到增强。特别是,我们使用流行病学和临床适用的大鼠 - 弓形虫模型系统,并遵循先前描述的具有神经学特征的“猫吸引力”方案进行预测,即氟哌啶醇(一种用于治疗包括精神分裂症在内的精神疾病的抗精神病药物)和/或丙戊酸(一种用于治疗包括精神分裂症在内的精神疾病的情绪稳定剂),至少在预防弓形虫相关行为和认知改变的发展方面,与标准抗弓形虫化疗药物乙胺嘧啶和氨苯砜一样有效。我们证明,虽然弓形虫似乎会改变大鼠对捕食风险的感知,将它们天生的厌恶变成“自杀性”的猫吸引力,但抗精神病药物在预防这种行为改变方面与抗弓形虫药物一样有效。我们的结果对这些疾病的病因和治疗具有重要意义。