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长期给予典型和非典型抗精神病药物后大鼠纹状体体积的变化。

Striatal volume changes in the rat following long-term administration of typical and atypical antipsychotic drugs.

作者信息

Andersson Candace, Hamer Robert M, Lawler Cindy P, Mailman Richard B, Lieberman Jeffrey A

机构信息

Department of Psychiatry, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Neuropsychopharmacology. 2002 Aug;27(2):143-51. doi: 10.1016/S0893-133X(02)00287-7.

Abstract

Striatal enlargement has been consistently reported in schizophrenics receiving chronic neuroleptic treatment although the results following atypical antipsychotic treatment have been equivocal. In order to disentangle patient illness from a possible drug effect on brain structure, young adult rats were administered either haloperidol, risperidone, clozapine, olanzapine, or vehicle daily for four or eight months via drinking water. Significant increases in caudate-putamen volumes were seen in animals receiving either haloperidol or clozapine when compared with control animals following eight months of drug administration. Conversely, olanzapine-treated animals showed significant decreases in caudate-putamen volumes when compared with control animals after eight months of drug. Thus, converging evidence indicates that the neuroplastic response of the striatum following neuroleptic exposure causes volumetric increases, whereas atypical antipsychotics affect the basal ganglia differentially. The current data suggests that such differential responses may be due to both the pharmacological properties and the relative doses of the atypical agents.

摘要

一直有报告称,接受长期抗精神病药物治疗的精神分裂症患者纹状体增大,不过非典型抗精神病药物治疗后的结果并不明确。为了区分患者疾病与药物对脑结构可能产生的影响,通过饮水方式,对成年幼鼠每日给予氟哌啶醇、利培酮、氯氮平、奥氮平或赋形剂,持续4个月或8个月。给药8个月后,与对照动物相比,接受氟哌啶醇或氯氮平治疗组动物的尾状核-壳核体积显著增加。相反,给药8个月后,与对照动物相比,奥氮平治疗组动物的尾状核-壳核体积显著减小。因此,越来越多的证据表明,抗精神病药物暴露后纹状体的神经可塑性反应会导致体积增加,而非典型抗精神病药物对基底神经节的影响则有所不同。目前的数据表明,这种不同的反应可能是由于非典型药物的药理特性和相对剂量所致。

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