Fluoxetine potentiates methylphenidate-induced behavioral responses: Enhanced locomotion or stereotypies and facilitated acquisition of cocaine self-administration

Lorissa Lamoureux , Joel A. Beverley , Michela Marinelli , Heinz Steiner
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引用次数: 1

Abstract

The medical psychostimulant methylphenidate (MP) is used to treat attention-deficit hyperactivity disorder and recreationally as a “cognitive enhancer”. MP is a dopamine reuptake inhibitor, but does not affect serotonin. Serotonin contributes to addiction-related gene regulation and behavior. Previously, we showed that enhancing serotonin action by adding a selective serotonin reuptake inhibitor, fluoxetine (FLX), to MP potentiates MP-induced gene regulation in striatum and nucleus accumbens, mimicking cocaine effects. Here, we investigated the behavioral consequences of MP+FLX treatment. Young adult male rats received MP (5 mg/kg, i.p.) or MP+FLX (5 mg/kg each) daily for 6-8 days. Behavioral effects were assessed in an open-field test during the repeated treatment. Two weeks later the motor response to a cocaine challenge (25 mg/kg) and the rate of acquisition of cocaine self-administration behavior were determined. Our results demonstrate that FLX potentiates effects of MP on open-field behavior. However, we found differential behavioral responses to MP+FLX treatment, as approximately half of the rats developed high rates of focal stereotypies (termed “MP+FLX/high reactivity” group), whereas the other half did not, and only showed increased locomotion (“MP+FLX/low reactivity” group). Two weeks later, cocaine-induced locomotion and stereotypies were positively correlated with MP+FLX-induced behavior seen at the end of the repeated MP+FLX treatment. Moreover, the MP+FLX/high reactivity group, but not the low reactivity group, showed facilitated acquisition of cocaine self-administration. These results demonstrate that repeated MP+FLX treatment can facilitate subsequent cocaine taking behavior in a subpopulation of rats. These findings suggest that MP+FLX exposure in some individuals may increase the risk for psychostimulant use later in life.

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氟西汀增强哌甲酯诱导的行为反应:增强运动或刻板印象,促进可卡因自我给药的获得
药物精神刺激剂哌甲酯(MP)用于治疗注意力缺陷多动障碍,并作为“认知增强剂”用于娱乐。MP是一种多巴胺再摄取抑制剂,但不影响血清素。血清素有助于成瘾相关的基因调节和行为。此前,我们发现,通过在MP中添加选择性血清素再摄取抑制剂氟西汀(FLX)来增强血清素的作用,可以增强MP诱导的纹状体和伏隔核的基因调节,模仿可卡因的作用。在这里,我们调查了MP+FLX治疗的行为后果。年轻成年雄性大鼠每天接受MP(5mg/kg,i.p.)或MP+FLX(各5mg/kg),持续6-8天。在重复治疗过程中,通过开放场地测试评估行为影响。两周后,测定了对可卡因激发(25mg/kg)的运动反应和可卡因自我给药行为的获得率。我们的研究结果表明,FLX增强了MP对开放场行为的影响。然而,我们发现对MP+FLX治疗有不同的行为反应,因为大约一半的大鼠出现了高比例的局灶性刻板印象(称为“MP+FLX/高反应性”组),而另一半则没有,只表现出运动增加(“MP+FLEX/低反应性”小组)。两周后,可卡因诱导的运动和刻板印象与重复MP+FLX治疗结束时观察到的MP+FLX诱导的行为呈正相关。此外,MP+FLX/高反应性组(而非低反应性组)显示出可卡因自给药的获取便利。这些结果表明,重复MP+FLX治疗可以促进大鼠亚群随后的可卡因吸食行为。这些发现表明,一些人暴露于MP+FLX可能会增加日后使用精神刺激剂的风险。
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来源期刊
Addiction neuroscience
Addiction neuroscience Neuroscience (General)
CiteScore
1.30
自引率
0.00%
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0
审稿时长
118 days
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