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首页> 外文期刊>Behavioural Brain Research: An International Journal >Gene expression of conditioned locomotion and context-specific locomotor sensitization controlled by morphine-associated environment.
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Gene expression of conditioned locomotion and context-specific locomotor sensitization controlled by morphine-associated environment.

机译:吗啡相关环境控制的条件运动和上下文特定运动敏化的基因表达。

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摘要

The nucleus accumbens (NAc) is involved in contextual drug associations, which might be particularly important for environmental cue-induced relapse to drug seeking. In the present study, rats were first administered repeated morphine for 5 days (5 mg/kg, i.p.) in a contextually paired and unpaired design. After reexposure to the morphine-associated environment, which induced conditioned locomotor activity in the morphine-paired group, we performed a rat 27k 70-mer oligo array to profile gene expression in the NAc. One hundred fifty-five upregulated and 88 downregulated genes were found in the paired group compared with the unpaired group. Eight gene transcripts were then selected to confirm their alterations by quantitative real-time polymerase chain reaction (qRT-PCR). The identified genes generally play important roles in neuroactive receptor-ligand interactions, synapse plasticity, ion transport, and protein phosphorylation. Furthermore, the expression of the eight selected genes that were identified and confirmed to show significant fold changes in the first microarray experiment were again measured with qRT-PCR after morphine challenge (2 mg/kg, i.p.). As expected, 2 mg/kg morphine-induced context-specific sensitization. Meanwhile, mRNA expression of the selected genes showed marked upregulation in the morphine-paired group compared with the unpaired and acute groups. These results suggest that alterations in the expression of the identified genes in the NAc may contribute to the neuroplasticity underlying contextual cue-induced relapse to drug use.
机译:伏伏核(NAc)参与情境药物关联,这对于环境提示诱发的寻求药物复发尤其重要。在本研究中,首先根据上下文配对和不配对的设计,对大鼠连续5天(5 mg / kg,腹腔注射)重复给予吗啡。在再次暴露于吗啡相关组的吗啡相关环境中后,我们在吗啡配对组中诱导了条件性运动活性,我们进行了大鼠27k 70-mer寡核苷酸阵列分析了NAc中的基因表达。与未配对组相比,配对组发现155个上调基因和88个下调基因。然后选择八个基因转录本,以通过定量实时聚合酶链反应(qRT-PCR)确认其改变。所鉴定的基因通常在神经活性受体-配体相互作用,突触可塑性,离子转运和蛋白质磷酸化中起重要作用。此外,在吗啡激发后(2mg / kg,i.p。)再次用qRT-PCR测量在第一个微阵列实验中被鉴定并证实显示出明显倍数变化的八个选定基因的表达。如预期的那样,2 mg / kg吗啡诱导的情境特异性致敏。同时,与未配对和急性组相比,吗啡配对组中所选基因的mRNA表达显示出明显的上调。这些结果表明,NAc中已鉴定基因表达的改变可能有助于背景可诱导的药物使用复发的神经可塑性。

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