Shifted Balance Between Ventral Striatal Prodynorphin and Proenkephalin Biases Development of Cocaine Place Avoidance

IF 2.6 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Amélia Nicot, Pavankumar Yecham, Ilana Serin, David J. Barker, Lauren K. Dobbs
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Abstract

Evidence from human self-report and rodent models indicate that cocaine can induce a negative affective state marked by panic and anxiety, which may reduce future cocaine use or promote co-use with opiates. Dynorphin-mediated signalling within the striatum is associated with negative affect following cocaine withdrawal and stress-induced cocaine seeking. Here, we used a trace conditioning procedure to first establish the optimum parameters to capture this transient cocaine negative affective state in wild-type mice, and then we investigated striatal opioid peptides as a substrate mediating cocaine conditioned place avoidance (CPA). Previous reports indicate that trace conditioning, where drug administration occurs after removal from the conditioning chamber, results in CPA to ethanol, nicotine and amphetamine. We tested different cocaine doses, conditioning session lengths and apparatus types to determine which combination yields the best cocaine CPA. Cocaine CPA was moderately larger at the highest cocaine dose (25 mg/kg), but this did not generalize across apparatus types and the effect was transient; thus, data were collapsed across all parameters. Cocaine conditioning scores were variable but also became more polarized across conditioning, with approximately equal proportions developing preference and avoidance. We then correlated cocaine CPA with striatal gene expression levels of the opioid peptides enkephalin (Penk) and dynorphin (Pdyn) using qPCR. Cocaine CPA was correlated with low Pdyn levels and a low Pdyn:Penk ratio in the ventral, but not dorsal, striatum. Consistent with this, mice with higher striatal Pdyn relative to Penk were more resistant to developing cocaine CPA compared with littermate controls. This approach revealed a subset of subjects sensitive to the aversive state immediately following cocaine administration. Our findings suggest that striatal dynorphin has opposing roles in mediating the aversion associated with acute cocaine intoxication versus cocaine withdrawal.

Abstract Image

腹侧纹状体前啡肽和前脑啡肽偏倚平衡的转移
来自人类自我报告和啮齿动物模型的证据表明,可卡因可以诱导以恐慌和焦虑为特征的消极情感状态,这可能会减少未来可卡因的使用或促进与阿片类药物的共同使用。纹状体中啡啡介导的信号与可卡因戒断和压力诱导的可卡因寻求后的负面影响有关。本研究采用微量条件反射法,首先在野生型小鼠中建立捕获瞬时可卡因负性情感状态的最佳参数,然后研究纹状体阿片肽作为介导可卡因条件下的场所回避(CPA)的底物。先前的报告表明,微量条件作用,即在离开条件作用室后给药,导致对乙醇、尼古丁和安非他明的CPA。我们测试了不同的可卡因剂量、调节时间长度和仪器类型,以确定哪种组合产生最好的可卡因CPA。可卡因CPA在可卡因最高剂量(25 mg/kg)时稍大,但这种效应并不适用于所有器官类型,而且这种效应是短暂的;因此,数据在所有参数上被折叠。可卡因条件反射得分是可变的,但在条件反射中也变得更加两极化,倾向和回避的比例大致相等。然后,我们使用qPCR将可卡因CPA与阿片肽脑啡肽(Penk)和啡肽(Pdyn)纹状体基因表达水平联系起来。可卡因CPA与腹侧纹状体的低Pdyn水平和低Pdyn:Penk比值相关,但与背侧纹状体无关。与此一致的是,纹状体Pdyn相对于Penk较高的小鼠,与同窝对照相比,对可卡因CPA的抗性更强。这种方法揭示了一小部分受试者在服用可卡因后立即对厌恶状态敏感。我们的研究结果表明纹状体运动啡在介导急性可卡因中毒与可卡因戒断相关的厌恶中具有相反的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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