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可卡因诱导的树突重塑发生在伏隔核中表达 D1 和 D2 多巴胺受体的神经元中。

Cocaine-induced dendritic remodeling occurs in both D1 and D2 dopamine receptor-expressing neurons in the nucleus accumbens.

机构信息

Department of Pathophysiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.

出版信息

Neurosci Lett. 2012 May 31;517(2):118-22. doi: 10.1016/j.neulet.2012.04.040. Epub 2012 Apr 23.

Abstract

Repeated exposure to cocaine can induce persistent alterations in the brain's reward system, including increases in the number of dendrites and spine density on medium-sized spiny neurons (MSNs) in the nucleus accumbens (NAc). The structural remodeling of dendrites and spines in the NAc is thought to play a critical role in cocaine addiction. MSNs in the NAc can be classified by expression of either D1 or D2 dopamine receptors, which are localized to the direct and indirect pathway, respectively. It is unknown whether the dendritic changes induced by repeated cocaine treatment occur in MSNs of the direct or indirect pathway. Because the traditional Golgi-Cox impregnation of neurons precludes identifying particular subpopulations of MSNs, we performed dendritic morphology analysis after biocytin-labeling and Golgi-Cox impregnation. We found that the biocytin staining MSNs showed higher dendritic spine density and higher number of dendrites than that in Golgi impregnation group. In addition, we found that the increasing spine density induced by repeated cocaine treatment in female mice was higher than that in male mice. Next we used biocytin staining and dynorphin/D2 receptor colocalization to determine which cell type(s) displayed dendritic changes after repeated cocaine treatment. We found that cocaine-induced changes in dendritic parameters occurred in MSNs of both the direct (D1-expressing) and indirect (D2-expressing) pathways.

摘要

反复接触可卡因会导致大脑奖励系统的持续改变,包括伏隔核(NAc)中型棘突神经元(MSNs)树突和棘突密度的增加。NAc 中树突和棘突的结构重塑被认为在可卡因成瘾中起着关键作用。NAc 中的 MSNs 可以通过表达 D1 或 D2 多巴胺受体来分类,它们分别位于直接和间接途径。尚不清楚反复可卡因处理引起的树突改变是否发生在直接或间接途径的 MSNs 中。由于神经元的传统高尔基-考克斯浸渍法排除了对 MSNs 特定亚群的鉴定,因此我们在生物胞素标记和高尔基-考克斯浸渍后进行了树突形态分析。我们发现,生物胞素染色的 MSNs 比高尔基浸渍组具有更高的树突棘密度和更多的树突。此外,我们发现,雌性小鼠中反复可卡因处理诱导的棘突密度增加高于雄性小鼠。接下来,我们使用生物胞素染色和强啡肽/D2 受体共定位来确定反复可卡因处理后哪种细胞类型显示树突变化。我们发现,可卡因诱导的树突参数变化发生在直接(表达 D1)和间接(表达 D2)途径的 MSNs 中。

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