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大鼠在长期获取可卡因自我给药戒断2个月期间伏隔核树突棘的动态变化

Dynamic Alterations of Rat Nucleus Accumbens Dendritic Spines over 2 Months of Abstinence from Extended-Access Cocaine Self-Administration.

作者信息

Christian Daniel T, Wang Xiaoting, Chen Eugenia L, Sehgal Lakshya K, Ghassemlou Michael N, Miao Julia J, Estepanian Derenik, Araghi Cameron H, Stutzmann Grace E, Wolf Marina E

机构信息

Department of Neuroscience, The Chicago Medical School at Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.

出版信息

Neuropsychopharmacology. 2017 Feb;42(3):748-756. doi: 10.1038/npp.2016.168. Epub 2016 Aug 24.

Abstract

Chronic cocaine exposure influences the density and morphology of dendritic spines on medium spiny neurons (MSNs) in the nucleus accumbens (NAc), a critical brain region for cocaine craving. However, the relationship between spine plasticity and craving remains unclear. To study this relationship, we trained rats to self-administer cocaine using an extended-access regimen (6 h per day, 10 days); controls self-administered saline. Previously, a time-dependent intensification (incubation) of cue-induced cocaine craving has been demonstrated after withdrawal from this regimen; furthermore, Ca-permeable AMPA receptors (CP-AMPARs) increase in the NAc core after ~1 month of withdrawal and thereafter mediate the expression of incubated craving. Although neither craving nor CP-AMPAR levels were measured in the present study, we killed rats at four withdrawal day (WD) time-points (WD14, WD25, WD36, or WD60) selected to span the rising phase of incubation and the transition from low to high CP-AMPAR levels. MSNs were iontophoretically filled with Lucifer yellow and spines were analyzed with NeuronStudio software. Compared with saline controls, cocaine rats showed no changes in spine density or morphology in the NAc core on WD14 or WD25. On WD36, approximately the withdrawal time when stable elevation of CP-AMPAR levels is detected, the cocaine group exhibited increased density of thin spines in the NAc core. By WD60, however, this effect had reversed: the density of thin spines was lower in cocaine rats compared with saline rats. In contrast, craving and CP-AMPAR levels remain high on WD60. We also assessed spine density on WD36 in the dorsolateral striatum, a region that is not implicated in incubation of cocaine craving and does not undergo CP-AMPAR plasticity. Here, the cocaine group exhibited a small leftward shift in the distribution of spine densities plotted as a cumulative distribution, opposite to the effect found in the NAc core. Overall, our results demonstrate changes in NAc core spines over 2 months of withdrawal but no simple relationship between the time dependency of these spine changes and the previously demonstrated time course of incubation of cocaine craving. However, they raise the possibility that CP-AMPAR accumulation in the NAc core occurs in a population of thin spines that emerges after ~1 month of withdrawal.

摘要

长期接触可卡因会影响伏隔核(NAc)中中等棘状神经元(MSN)树突棘的密度和形态,伏隔核是与可卡因渴望密切相关的关键脑区。然而,树突棘可塑性与渴望之间的关系仍不清楚。为了研究这种关系,我们训练大鼠采用延长获取方案(每天6小时,共10天)自行注射可卡因;对照组自行注射生理盐水。此前已证明,从该方案撤药后,线索诱导的可卡因渴望会出现时间依赖性增强(潜伏期延长);此外,撤药约1个月后,伏隔核核心区钙通透性AMPA受体(CP-AMPARs)增加,此后介导潜伏期延长的渴望的表达。尽管本研究未测量渴望程度和CP-AMPAR水平,但我们在四个撤药日(WD)时间点(WD14、WD25、WD36或WD60)处死大鼠,这些时间点涵盖了潜伏期延长的上升阶段以及CP-AMPAR水平从低到高的转变。通过离子电泳法用荧光黄填充MSN,并使用NeuronStudio软件分析树突棘。与生理盐水对照组相比,可卡因处理组大鼠在WD14或WD25时伏隔核核心区的树突棘密度或形态没有变化。在WD36时,大约是检测到CP-AMPAR水平稳定升高的撤药时间,可卡因组伏隔核核心区细树突棘的密度增加。然而,到WD60时,这种效应发生了逆转:与生理盐水处理组大鼠相比,可卡因处理组大鼠细树突棘的密度更低。相比之下,在WD60时,渴望程度和CP-AMPAR水平仍然很高。我们还评估了WD36时背外侧纹状体的树突棘密度,该区域与可卡因渴望的潜伏期延长无关,也不会发生CP-AMPAR可塑性变化。在这里,可卡因组在以累积分布绘制的树突棘密度分布上出现了小幅左移,这与在伏隔核核心区发现的效应相反。总体而言,我们的结果表明,撤药2个月内伏隔核核心区的树突棘发生了变化,但这些树突棘变化的时间依赖性与先前证明的可卡因渴望潜伏期延长的时间进程之间没有简单的关系。然而,这些结果增加了一种可能性,即伏隔核核心区CP-AMPAR的积累发生在撤药约1个月后出现的一群细树突棘中。

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