Co-administration of modafinil, atomoxetine, and citalopram increases exploratory behavior, produces withdrawal signs, and enhances self-administration of this drug mixture

Jorge Juárez, Amanda C. Hernandez De la Torre, Jesús E. Yepez
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Abstract

The monoaminergic systems are necessary for the motor and reinforcing effects of addictive psychostimulants such as cocaine and amphetamines. The participation of the dopaminergic system (DA) in relation to these properties has been studied extensively, but the role of the noradrenergic (NA) and serotoninergic (5-HT) systems has not been clarified. Clinical psychostimulants like modafinil have not shown clear evidence of addictive effects, perhaps due to differential activity in the latter two systems. The aim of this study was to determine the effect of monotherapies with modafinil (MOD, a drug with main activity in the inhibition of dopamine reuptake), atomoxetine (ATX, a selective norepinephrine reuptake inhibitor), and citalopram (CIT, a selective serotonin reuptake inhibitor), and coadministration (MOD+ATX+CIT), on locomotor activity, signs of anhedonia after drug withdrawal and self-administration of MOD and the mixture of these substances. Male Wistar rats were treated chronically (16 days) via the endogastric route with ATX at 2 mg/kg, CIT at 3 mg/kg, MOD at 60 mg/kg, or a combination (2ATX+3CIT+60MOD). The co-administered rats (COAD) increased exploratory behavior and showed signs of anhedonia post-withdrawal. The MOD and COAD groups showed higher MOD intake after being water-deprived for 12 h, while a sensitization of exploratory behavior was observed in the COAD group after consuming the ATX+CIT+MOD mixture. Higher seeking self-administration of the mixture was noted only in the COAD group. Results suggest that early simultaneous activation of the DA, NA, and 5-HT systems produces plastic changes that favor the posterior self-administration and rewarding effects of drugs that activate these three neurotransmission systems.
莫达非尼、托莫西汀和西酞普兰的联合用药增加了探索性行为,产生戒断症状,并增强了这种药物混合物的自我给药能力
单胺能系统对于上瘾的精神兴奋剂如可卡因和安非他明的运动和强化作用是必需的。多巴胺能系统(DA)在这些特性中的作用已被广泛研究,但去甲肾上腺素能(NA)和5-羟色胺能(5-HT)系统的作用尚未明确。临床使用的精神兴奋剂如莫达非尼并没有显示出明显的成瘾效应,这可能是由于后两个系统的活性不同。本研究的目的是确定莫达非尼(MOD,一种主要抑制多巴胺再摄取的药物)、托莫西汀(ATX,一种选择性去甲肾上腺素再摄取抑制剂)和西酞普兰(CIT,一种选择性5 -羟色胺再摄取抑制剂)单一治疗和共给药(MOD+ATX+CIT)对运动活性、停药后快感缺乏的症状、MOD和这些物质的混合物的自我给药的影响。雄性Wistar大鼠经胃内途径慢性治疗(16天),ATX剂量为2 mg/kg, CIT剂量为3 mg/kg, MOD剂量为60 mg/kg,或2ATX+3CIT+60MOD的组合。共同给药的大鼠(COAD)增加了探索行为,并表现出戒断后快感缺乏的迹象。MOD和COAD组在失水12 h后MOD摄入量增加,而COAD组在摄入ATX+CIT+MOD混合物后观察到探索行为的敏化。仅在COAD组中注意到较高的自我给药寻求。结果表明,早期同时激活DA、NA和5-HT系统会产生可塑性变化,有利于激活这三种神经传递系统的药物的后向自我给药和奖励效应。
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