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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Behavioral sensitization to amphetamine is not accompanied by changes in glutamate receptor surface expression in the rat nucleus accumbens.
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Behavioral sensitization to amphetamine is not accompanied by changes in glutamate receptor surface expression in the rat nucleus accumbens.

机译:对苯丙胺的行为敏化并不伴随伏伏大鼠核中谷氨酸受体表面表达的变化。

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We examined whether behavioral sensitization to amphetamine is associated with redistribution of glutamate receptors (GluR) in the rat nucleus accumbens (NAc) or dorsolateral striatum (DLSTR). Following repeated amphetamine treatment and 21 days of withdrawal, surface and intracellular levels of alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate (AMPA) or NMDA receptor subunits were determined using a protein cross-linking assay. In contrast to our previous results in cocaine-sensitized rats, we did not observe redistribution of GluR1 or GluR2 to the cell surface in the NAc after amphetamine withdrawal, although a small increase in total GluR1 was found in the shell subregion. Nor did we observe activation of signaling pathways associated with cocaine-induced AMPA receptor trafficking or changes in NMDA receptor subunits. No significant changes were observed in the DLSTR. We also investigated the effect of administering a challenge injection of amphetamine to amphetamine-sensitized rats 24 h prior tobiochemical analysis based on prior studies showing that cocaine challenge decreases AMPA receptor surface expression in the NAc of cocaine-sensitized rats. GluR1 and GluR2 were not significantly altered in either NAc or DLSTR, although a modest effect on GluR3 cannot be ruled out. Our results suggest that glutamate transmission in the NAc is dramatically different in rats sensitized to amphetamine versus cocaine.
机译:我们检查了对苯丙胺的行为敏感性是否与大鼠伏隔核(NAc)或背外侧纹状体(DLSTR)中的谷氨酸受体(GluR)的重新分布有关。经过反复的苯丙胺治疗和戒断21天后,使用蛋白质交联测定法确定了表面和细胞内α-氨基-3-羟基-5-甲基异恶唑-4-丙酸酯(AMPA)或NMDA受体亚基的水平。与我们先前在可卡因致敏大鼠中的研究结果相反,安非他明撤除后,虽然在壳亚区域发现总GluR1略有增加,但并未观察到GluR1或GluR2在NAc的细胞表面重新分布。我们也没有观察到与可卡因诱导的AMPA受体运输或NMDA受体亚基变化相关的信号通路的激活。 DLSTR中未观察到明显变化。我们还根据以前的研究显示,可卡因激发降低了可卡因致敏大鼠的NAc中AMPA受体表面的表达,因此,在生化分析之前24小时,我们还对生化分析前24小时对安非他命致敏的大鼠进行了安非他命激发注射的效果进行了研究。尽管不能排除对GluR3的适度影响,但NAc或DLSTR中的GluR1和GluR2均未显着改变。我们的结果表明,对苯丙胺和可卡因致敏的大鼠,NAc中的谷氨酸传递有显着差异。

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