Acquired alterations in nucleus accumbens responsiveness to a cocaine-paired discriminative stimulus preceding rats’ daily cocaine consumption

David J. Estrin , Julianna M. Kulik , Nicholas J. Beacher , Anthony P. Pawlak , Samuel D. Klein , Mark O. West
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Abstract

Resumption of drug taking is a primary focus for substance use disorder research and can be triggered by drug-associated environmental stimuli. The Nucleus Accumbens (NAc) is a key brain region which guides motivated behavior and is implicated in resumption. Yet, there remains a pressing need to characterize NAc neurons’ responsiveness to drug associated stimuli during withdrawal and abstinence. We recorded discriminative stimulus (DS) induced NAc activity via in vivo single-unit electrophysiology in rats that self-administered cocaine. Male and female rats implanted with a jugular catheter and a microwire array in NAc Core and Shell self-administered cocaine under control of a 30s auditory DS for 6 hours per session across 14 consecutive days. Rats acquired tone discrimination within 4 sessions. To exclude pharmacological effects of circulating cocaine from all neuronal analyses, we studied changes in DS-induced firing only for trials preceding the first infusion of cocaine in each of the 14 sessions, which were defined as “pre-drug trials.” NAc neuron responses were assessed prior to tone-evoked movement onset. Responsiveness to the DS tone was exhibited throughout all sessions by the NAc Core population, but only during Early sessions by the NAc Shell population. Both Core and Shell responded selectively to the DS, i.e., more strongly on drug taking trials, or Hits, than on Missed opportunities. These findings suggest that NAc Core and Shell play distinct roles in initiating cocaine seeking prior to daily cocaine consumption, and align with reports suggesting that as drug use becomes chronic, cue-evoked activity shifts from NAc Shell to NAc Core.

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在大鼠每日吸食可卡因之前,获得性改变伏隔核对可卡因配对的鉴别刺激的反应
恢复吸毒是物质使用障碍研究的主要焦点,可由与药物相关的环境刺激引发。伏隔核(NAc)是一个关键的大脑区域,指导动机行为,并涉及恢复。然而,仍然迫切需要表征NAc神经元在戒断和戒断期间对药物相关刺激的反应性。我们通过体内单单位电生理记录了自我给药的大鼠的辨别性刺激(DS)诱导NAc活性。在NAc Core和Shell中植入颈静脉导管和微丝阵列的雄性和雌性大鼠,在30秒听觉DS控制下,连续14天,每次6小时,自我给药可卡因。大鼠在4次实验中获得了音调辨别能力。为了从所有神经元分析中排除循环可卡因的药理作用,我们只研究了14次试验中第一次注射可卡因之前ds诱导放电的变化,这被定义为“药物前试验”。在声调诱发运动开始前评估NAc神经元的反应。NAc核心人群在所有的会话中都表现出对DS音调的响应性,但NAc外壳人群只在早期会话中表现出对DS音调的响应性。Core和Shell对DS的反应都是有选择性的,即对药物试验(hit)的反应比错失机会的反应更强烈。这些发现表明,在每日可卡因消费之前,NAc核心和Shell在开始寻求可卡因方面发挥着不同的作用,并且与报告表明,随着吸毒成为慢性吸毒,线索诱发的活动从NAc外壳转移到NAc核心。
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来源期刊
Addiction neuroscience
Addiction neuroscience Neuroscience (General)
CiteScore
1.30
自引率
0.00%
发文量
0
审稿时长
118 days
期刊最新文献
Opioid drug seeking after early-life adversity: a role for delta opioid receptors Contents Editorial Board Corrigendum to “Xylazine is an agonist at kappa opioid receptors and exhibits sex-specific responses to opioid antagonism” [Addiction Neuroscience, Volume 11, June 2024, 100155] Neurokinin-1 receptors in the nucleus accumbens shell influence sensitivity to social defeat stress and stress-induced alcohol consumption in male mice
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