Sex, but not juvenile stress, affects reversal learning and DRL performance following cocaine administration

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
Tracie A. Paine, Caroline Pierotti , Evan S. Swanson , Zoë Martin del Campo , Sydney Kulkarni, Jeffrey Zhang
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引用次数: 0

Abstract

Introduction

Early adversity, impulsivity and sex all contribute to the risk of developing substance use disorder. Using rats, we examined how juvenile stress interacts with sex and cocaine to affect performance on a serial reversal task and a differential reinforcement of low rates 10 s (DRL10) task. The expression of dopamine-related proteins in several brain areas was also assessed.

Methods

From postnatal days (PND) 25–29, rats were exposed to a variable stress protocol. In adulthood, rats were trained on the reversal task and the effects of cocaine (0, 10, or 20 mg/kg, IP) on performance were assessed. Next, rats were trained on the DRL10 task and the effects of cocaine on performance were assessed. Finally, brains were extracted, and Western blot analyses conducted.

Results

Juvenile stress did not affect behavior. Sex did not affect baseline performance in either task. In the reversal task, cocaine decreased % high probability responses and the number of rewards earned in both sexes. Cocaine had sex-dependent effects on omissions, low probability responses and response latencies. In the DRL10 task, cocaine decreased the peak latency to respond and the number of rewards earned in both sexes. Cocaine had sex-dependent effects on peak rate of responding, response efficiency, burst responses and long responses. Female rats exhibited increased expression of DRD1 receptors in the striatum.

Discussion

These data contribute to the growing literature demonstrating sex differences in the behavioral effects of cocaine and suggest that DRD1 receptors could contribute to the observed behavioral sex differences.

性,但不是青少年的压力,会影响可卡因给药后的逆转学习和DRL表现。
引言:早期的逆境、冲动和性行为都会增加患药物使用障碍的风险。使用大鼠,我们研究了青少年压力如何与性和可卡因相互作用,以影响连续逆转任务和低比率10s(DRL10)任务的表现。还评估了多巴胺相关蛋白在几个大脑区域的表达。方法:从出生后第25-29天(PND),大鼠暴露于可变应激方案。成年后,对大鼠进行逆转任务训练,并评估可卡因(0、10或20 mg/kg,IP)对表现的影响。接下来,对大鼠进行DRL10任务训练,并评估可卡因对表现的影响。最后,提取大脑,并进行蛋白质印迹分析。结果:青少年压力不影响行为。性别对两项任务的基线表现都没有影响。在逆转任务中,可卡因降低了%的高概率反应和两性获得的奖励数量。可卡因对遗漏、低概率反应和反应潜伏期具有性别依赖性影响。在DRL10任务中,可卡因降低了男女反应的峰值潜伏期和获得的奖励数量。可卡因对峰值反应率、反应效率、突发反应和长期反应具有性别依赖性影响。雌性大鼠纹状体中DRD1受体的表达增加。讨论:这些数据有助于越来越多的文献证明可卡因行为影响的性别差异,并表明DRD1受体可能导致观察到的行为性别差异。
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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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