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环境富集增强对GBR 12935诱导活性的敏感性,并降低内侧前额叶皮质中的多巴胺转运体功能。

Environmental enrichment enhances sensitization to GBR 12935-induced activity and decreases dopamine transporter function in the medial prefrontal cortex.

作者信息

Zhu Jun, Green Thomas, Bardo Michael T, Dwoskin Linda P

机构信息

College of Pharmacy, University of Kentucky, Lexington, KY 40536, USA.

出版信息

Behav Brain Res. 2004 Jan 5;148(1-2):107-17. doi: 10.1016/s0166-4328(03)00190-6.

Abstract

Rats raised in an enriched condition (EC) during development display increased hyperactivity to the effect of acute amphetamine compared to rats raised in an impoverished condition (IC). The present study determined whether environmental enrichment differentially alters the effects of GBR 12935 administration, a selective dopamine transporter (DAT) inhibitor. Acutely, EC rats showed a greater, dose-dependent GBR 12935-induced increase in activity compared to IC rats; however, basal activity for EC rats was lower than for IC rats. After repeated GBR 12935, only EC rats exhibited behavioral sensitization. Kinetic analysis of DAT function in medial prefrontal cortex (mPFC) revealed that the maximal velocity of [3H]dopamine ([3H]DA) uptake in EC rats was less than in IC rats (4.9 +/- 0.6 and 7.7 +/- 0.6 pmol/min/mg, respectively), but not in striatum or nucleus accumbens. Furthermore, GBR 12935-induced inhibition of DAT function, [3H]GBR 12935 binding density and DA content in mPFC, striatum and nucleus accumbens were not different between EC and IC rats. However, dihydroxyphenylacetic acid content in mPFC was lower in EC than IC rats, whereas no differences were found in striatum and nucleus accumbens. These results suggest that EC-induced changes in activity may be due to decreased DAT function and decreased DA metabolism in the mPFC.

摘要

与在贫瘠环境(IC)中饲养的大鼠相比,在发育过程中处于丰富环境(EC)中的大鼠对急性苯丙胺的作用表现出更高的多动性。本研究确定环境丰富化是否会差异地改变选择性多巴胺转运体(DAT)抑制剂GBR 12935给药的效果。急性给药时,与IC大鼠相比,EC大鼠在GBR 12935诱导下的活动增加更大且呈剂量依赖性;然而,EC大鼠的基础活动低于IC大鼠。重复给予GBR 12935后,只有EC大鼠表现出行为敏化。内侧前额叶皮质(mPFC)中DAT功能的动力学分析表明,EC大鼠中[3H]多巴胺([3H]DA)摄取的最大速度低于IC大鼠(分别为4.9±0.6和7.7±0.6 pmol/min/mg),但在纹状体或伏隔核中并非如此。此外,GBR 12935诱导的mPFC、纹状体和伏隔核中DAT功能抑制、[3H]GBR 12935结合密度和DA含量在EC和IC大鼠之间没有差异。然而,EC大鼠mPFC中的二羟基苯乙酸含量低于IC大鼠,而在纹状体和伏隔核中未发现差异。这些结果表明,EC诱导的活动变化可能是由于mPFC中DAT功能降低和DA代谢减少所致。

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