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典型和非典型抗精神病药物对大鼠纹状体中神经肽Y样免疫反应性及神经肽Y mRNA表达的影响。

Influence of typical and atypical antipsychotics on neuropeptide Y-like immunoreactivity and NPY mRNA expression in rat striatum.

作者信息

Obuchowicz E, Turchan J

机构信息

Department of Clinical Pharmacology, Silesian University School of Medicine, Katowice, Poland.

出版信息

Neuropeptides. 1998 Oct;32(5):473-80. doi: 10.1016/s0143-4179(98)90074-9.

Abstract

Striatal neuropeptide Y-like immunoreactivity (NPY-LI) levels were investigated in naive rats after acute, subchronic (14 days) or chronic (28 days) intraperitoneal (i.p.) treatment with chlorpromazine (2 or 10mg/kg), haloperidol (0.5 or 2 mg/kg), (+/-)sulpiride (50 or 100 mg/kg) or clozapine (10 or 25 mg/kg), and in chronically treated rats after 8-day drug withdrawal. The most pronounced changes in NPY-LI levels were found 24 h after acute chlorpromazine or haloperidol administration (a decrease) and after withdrawal of chlorpromazine, haloperidol or sulpiride (an increase). The effect of clozapine on NPY-LI differed from those of the other antipsychotics: both single doses had no effect, the higher chronic dose increased NPY-LI levels, and its withdrawal resulted in their decrease. No significant alterations were detected in the hybridization signal of NPY mRNA in response to acute or subchronic administration of haloperidol or clozapine. Our results suggest that the effects of antipsychotics are in part mediated by blockade of dopamine D2-like (D2/D3) or serotonin 5HT2A receptors but not dopamine D1, D4 or alpha1-adrenergic receptors. The antipsychotic-induced changes in NPY system activity has been discussed in connection with adaptive alterations in the dopamine system.

摘要

在未用药的大鼠中,研究了腹腔注射(i.p.)氯丙嗪(2或10mg/kg)、氟哌啶醇(0.5或2mg/kg)、(±)舒必利(50或100mg/kg)或氯氮平(10或25mg/kg)急性、亚慢性(14天)或慢性(28天)后纹状体神经肽Y样免疫反应性(NPY-LI)水平,以及在长期用药后停药8天的大鼠中的NPY-LI水平。在急性给予氯丙嗪或氟哌啶醇后24小时(降低)以及氯丙嗪、氟哌啶醇或舒必利停药后(升高)发现NPY-LI水平最明显的变化。氯氮平对NPY-LI的作用与其他抗精神病药物不同:单次给药均无作用,较高的慢性剂量可增加NPY-LI水平,停药后则导致其降低。急性或亚慢性给予氟哌啶醇或氯氮平后,未检测到NPY mRNA杂交信号的显著改变。我们的结果表明,抗精神病药物的作用部分是通过阻断多巴胺D2样(D2/D3)或5-羟色胺5HT2A受体介导的,而不是通过多巴胺D1、D4或α1-肾上腺素能受体。已结合多巴胺系统的适应性改变讨论了抗精神病药物诱导的NPY系统活性变化。

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