Enhanced expression of parvalbumin and perineuronal nets in the medial prefrontal cortex after extended-access cocaine self-administration in rats

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Addiction Biology Pub Date : 2023-10-02 DOI:10.1111/adb.13334
Jereme C. Wingert, Jonathan N. Anguiano, Jonathan D. Ramos, Jordan M. Blacktop, Angela E. Gonzalez, Lynn Churchill, Barbara A. Sorg
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Abstract

The medial prefrontal cortex (mPFC) drives cocaine-seeking behaviour in rodent models of cocaine use disorder. Parvalbumin (PV)-containing GABAergic interneurons powerfully control the output of the mPFC, yet few studies have focused on how these neurons modulate cocaine-seeking behaviour. Most PV neurons are surrounded by perineuronal nets (PNNs), which regulate the firing of PV neurons. We examined staining intensity and number of PV and PNNs after long-access (6 h/day) cocaine self-administration in rats followed by either 8–10 days extinction ± cue-induced reinstatement or short-term (1–2 days) or long-term (30–31 days) abstinence ± cue-induced reinstatement. The intensity of PNNs was increased in the prelimbic and infralimbic PFC after long-term abstinence in the absence of cue reinstatement and after cue reinstatement following both daily extinction sessions and after a 30-day abstinence period. PV intensity was increased after 30 days of abstinence in the prelimbic but not infralimbic PFC. Enzymatic removal of PNNs with chondroitinase ABC (ABC) in the prelimbic PFC did not prevent incubation of cue-induced reinstatement but decreased cocaine-seeking behaviour at both 2 and 31 days of abstinence, and this decrease at 31 days was accompanied by reduced c-Fos levels in the prelimbic PFC. Increases in PNN intensity have generally been associated with the loss of plasticity, suggesting that the persistent and chronic nature of cocaine use disorder may in part be attributed to long-lasting increases in PNN intensity that reduce the ability of stimuli to alter synaptic input to underlying PV neurons.

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大鼠延长可卡因自给药后内侧前额叶皮层细小白蛋白和会阴神经网的表达增强。
内侧前额叶皮层(mPFC)驱动可卡因使用障碍啮齿动物模型中的可卡因寻求行为。含有Parvalbumin(PV)的GABA能中间神经元有力地控制mPFC的输出,但很少有研究关注这些神经元如何调节可卡因寻求行为。大多数PV神经元被会神经网络(PNN)包围,PNN调节PV神经元的放电。我们检测了大鼠长时间(6小时/天)自行给药可卡因后8-10天消退后PV和PNN的染色强度和数量 ± 提示诱导的恢复或短期(1-2天)或长期(30-31天) 天)禁欲 ± 提示诱导的恢复。在没有线索恢复的情况下长期禁欲后,以及在每日消退期后和30天禁欲期后线索恢复后,脊髓前和边缘下PFC的PNN强度增加。PV强度在30后增加 在角膜前但不是角膜下PFC中禁欲的天数。在角膜前PFC中用软骨素酶ABC(ABC)酶法去除PNN并不能阻止线索诱导的恢复,但在2岁和31岁时都降低了可卡因寻求行为 禁欲天数,在31天时有所减少 天时,脑脊髓炎前PFC中的c-Fos水平降低。PNN强度的增加通常与可塑性的丧失有关,这表明可卡因使用障碍的持续和慢性性质可能部分归因于PNN强度持续增加,从而降低了刺激改变对潜在PV神经元的突触输入的能力。
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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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