Chronic oral methylphenidate plus fluoxetine treatment in adolescent rats increases cocaine self-administration

Daniela Senior , Madison McCarthy , Rania Ahmed , Shannon Klein , Wen Xuan Lee , Michael Hadjiargyrou , David Komatsu , Heinz Steiner , Panayotis K. Thanos
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引用次数: 2

Abstract

Background

Depression and attention deficit hyperactivity disorder are known to be comorbid. Treatment of these commonly coexisting diseases typically involves the combined prescription of methylphenidate (MP), a psychostimulant, and fluoxetine (FLX), a selective serotonin reuptake inhibitor (SSRI). MP and cocaine have similar mechanisms of action and this study examined the effects of chronic treatment of MP combined with FLX on cocaine consumption in rats.

Methods

Four groups of rats received access to drinking solutions of water (control), MP (30/60 mg/kg/day), FLX (20 mg/kg/day), or the combination of MP (30/60 mg/kg/day) plus FLX (20 mg/kg/day), during 8 h per day for one month. Following these drug treatments, rats were allowed to self-administer cocaine for 14 days.

Results

Our results showed that, during the first week of cocaine self-administration, the MP-treated rats had significantly greater numbers of active lever presses (plus 127%) and increased consumption of cocaine compared to the control rats. In contrast, during week two of cocaine self-administration, the rats treated with the MP + FLX combination showed significantly more lever presses (plus 198%) and significantly greater cocaine consumption (plus 84%) compared to the water controls.

Conclusion

Chronic oral treatment during adolescence with the combination of MP plus FLX resulted in increased cocaine use after 2 weeks of cocaine self-administration in rats. These novel findings suggest that the combined exposure to these two drugs chronically, during adolescence, may produce increased vulnerability towards cocaine abuse during young adulthood.

慢性口服哌甲酯加氟西汀治疗青春期大鼠增加可卡因自我给药
背景抑郁症和注意缺陷多动障碍是已知的共病。这些常见共存疾病的治疗通常包括哌醋甲酯(MP),一种精神兴奋剂和氟西汀(FLX),一种选择性血清素再摄取抑制剂(SSRI)的联合处方。MP和可卡因具有相似的作用机制,本研究考察了MP联合FLX慢性治疗对大鼠可卡因消耗的影响。方法4组大鼠分别给予水(对照组)、MP (30/60 mg/kg/d)、FLX (20 mg/kg/d)或MP (30/60 mg/kg/d)加FLX (20 mg/kg/d)的饮水溶液,每天8 h,连续1个月。在这些药物治疗之后,大鼠被允许自行服用可卡因14天。结果我们的研究结果表明,在自我给药的第一周,与对照组相比,mp处理的大鼠有明显增加的主动杠杆按压次数(增加127%)和增加的可卡因消耗量。相比之下,在可卡因自我给药的第二周,与水对照组相比,MP + FLX联合治疗的大鼠表现出明显更多的杠杆按压(增加198%)和明显更多的可卡因消耗(增加84%)。结论青春期长期口服MP + FLX可导致大鼠自给药2周后可卡因使用量增加。这些新发现表明,在青春期长期同时接触这两种药物,可能会增加青年时期对可卡因滥用的脆弱性。
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 neuroscience
Addiction neuroscience Neuroscience (General)
CiteScore
1.30
自引率
0.00%
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审稿时长
118 days
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