首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Downregulation of mGluR2/3 receptors during morphine withdrawal in rats impairs mGluR2/3-and NMDA receptor-dependent long-term depression in the nucleus accumbens
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Downregulation of mGluR2/3 receptors during morphine withdrawal in rats impairs mGluR2/3-and NMDA receptor-dependent long-term depression in the nucleus accumbens

机译:在大鼠吗啡戒断期间MGLUR2 / 3受体的下调损害核心尿液中的MGLUR2 / 3-and NMDA受体依赖性的长期凹陷

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摘要

Drugs of abuse modify synaptic long-term potentiation and long-term depression (LTD) in the nucleus accumbens, and the impairment of synaptic plasticity in this brain region may be a universal feature of drug addiction. It is unknown whether metabotropic glutamate receptors (mGluRs) play a role in synaptic plasticity induced by drugs such as morphine. The neurochemical, electrophysiological, and Western blotting experiments reported here reveal a novel form of LTD in synapses of the shell region of the nucleus accumbens induced in vivo by low-frequency stimulation of the medial prefrontal cortex. This plasticity required the activation of N-methyl-D-aspartate receptors and mGluR2/3 but not mGluR5. The expression of mGluR2/3 was downregulated during withdrawal from repeated morphine exposure (10 days after the last injection), resulting in impaired low-frequency stimulation-induced LTD. These results indicate that withdrawal-induced mGluR2/3 downregulation alters neural plasticity after morphine exposure, which may be a mechanism contributing to drug addiction.
机译:滥用药物在细胞核中修饰突触长期增强和长期凹陷(LTD),并且该脑区中突触塑性的损害可能是吸毒成瘾的普遍特征。尚不清楚代谢谷氨酸受体(MGLURS)是否在药物如吗啡诱导的突触塑性中发挥作用。这里报道的神经化学,电生理学和蛋白质印迹实验揭示了一种新的LTD形式,其在通过内侧前额叶皮质的低频刺激在体内诱导的细胞核壳区域的壳区域的突出形式。这种可塑性需要活化N-甲基-D-天冬氨酸受体和MGLUR2 / 3但不是MGLUR5。在退出反复吗啡暴露(最后一次注射后10天)期间,MGLUR2 / 3的表达是下调的,导致低频刺激引起的有限公司受损。这些结果表明,取代诱导的MGLUR2 / 3下调改变了吗啡暴露后的神经可塑性,这可能是有助于吸毒成瘾的机制。

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