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慢性抗精神病药物治疗可诱导大鼠前额叶皮质中fos和jun家族基因以及激活蛋白1复合物的长期表达。

Chronic antipsychotic drug treatment induces long-lasting expression of fos and jun family genes and activator protein 1 complex in the rat prefrontal cortex.

作者信息

Kontkanen Outi, Lakso Merja, Wong Garry, Castrén Eero

机构信息

A.I. Virtanen Institute, University of Kuopio, Kuopio, Finland.

出版信息

Neuropsychopharmacology. 2002 Aug;27(2):152-62. doi: 10.1016/S0893-133X(02)00289-0.

Abstract

We have characterized the effects of chronic clozapine and haloperidol treatments on the expression of fos (c-fos, fosB, fra-2) and jun (c-jun, junB, junD) family genes in the rat forebrain. The effects of chronic (17d) clozapine and haloperidol on mRNA expression were determined two hours, 24 hours, and six days after the last drug injection, and the DNA-binding activity of the activator protein-1 (AP-1) complex was studied after washout periods of 24 hours and six days. Chronic clozapine treatment with a 6 d washout period induced the expression of several fos and jun family genes in cortical regions, including the prefrontal cortex (PFC), and in the caudate putamen and nucleus accumbens. Moreover, the DNA-binding activity of the AP-1 complex was greatly increased in the anterior cingulate cortex-PFC in mobility shift assays already after 24 h, and remained increased after a 6d washout period. Chronic administration of haloperidol upregulated fos and jun family mRNA expression that was detectable 24 h and 6 d after cessation of the treatment mainly in the cortex. However, the DNA-binding activity of the AP-1 complex was not altered in the anterior cingulate cortex-PFC by chronic haloperidol administration at any of the time points studied. Thus, chronic treatments with clozapine and haloperidol induce a long-lasting enhancement of fos and jun family transcription factors that continues for several days after the cessation of the treatments in the cortex. These lasting effects might represent events that are potentially involved in the mechanisms of antipsychotic drug action.

摘要

我们已经描述了慢性氯氮平和氟哌啶醇治疗对大鼠前脑fos(c-fos、fosB、fra-2)和jun(c-jun、junB、junD)家族基因表达的影响。在最后一次药物注射后的两小时、24小时和六天,测定了慢性(17天)氯氮平和氟哌啶醇对mRNA表达的影响,并在24小时和六天的洗脱期后研究了激活蛋白-1(AP-1)复合物的DNA结合活性。经过6天洗脱期的慢性氯氮平治疗诱导了包括前额叶皮质(PFC)在内的皮质区域以及尾状壳核和伏隔核中几种fos和jun家族基因的表达。此外,在迁移率变动分析中,AP-1复合物的DNA结合活性在24小时后在前扣带回皮质-PFC中就大幅增加,并在6天洗脱期后仍保持增加。慢性给予氟哌啶醇上调了fos和jun家族mRNA表达,在治疗停止后的24小时和6天主要在皮质中可检测到。然而,在研究的任何时间点,慢性给予氟哌啶醇均未改变前扣带回皮质-PFC中AP-1复合物的DNA结合活性。因此,慢性氯氮平和氟哌啶醇治疗诱导了fos和jun家族转录因子的持久增强,在皮质中治疗停止后这种增强会持续数天。这些持久效应可能代表了潜在参与抗精神病药物作用机制的事件。

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