Behavioral Neuropharmacology and Neuroimaging Laboratory (BNNL), Clinical Research Institute on Addictions, Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14051, USA.
Department of Psychology, University at Buffalo, Buffalo, NY, 14203, USA.
Curr Pharm Biotechnol. 2023;24(10):1307-1314. doi: 10.2174/1389201024666221028092342.
Attention Deficit Hyperactivity Disorder (ADHD) can be comorbid with depression, often leading to the prescription of both methylphenidate (MP) and selective serotonin reuptake inhibitor (SSRI) antidepressants, such as fluoxetine (FLX). Moreover, these drugs are often misused as cognitive enhancers. This study examined the effects of chronic oral co-administration of MP and FLX on depressive- and anxiety-like behaviors.
Adolescent rats received daily either water (control), MP, FLX, or the combination of MP plus FLX in their drinking water over the course of 4 weeks.
Data analysis shows a decrease in food consumption and body weight for rats exposed to FLX or the combination of MP and FLX. Sucrose consumption was significantly greater in FLX or MP+FLX groups compared to controls. FLX-treated rats showed no effect in the elevated plus maze (EPM; open arm time) and forced swim test (FST; latency to immobility). However, rats treated with the combination (MP+FLX) showed significant anxiolytic-like and anti-depressive-like behaviors (as measured by EPM and FST), as well as significant increases in overall activity (distance traveled in open field test). Finally, the combined MP+FLX treatment induced a decrease in anxiety and depressive- like behaviors significantly greater than the response from either of these drugs alone.
These behavioral results characterize the long-term effects of these drugs (orally administered) that are widely co-administered and co-misused and provide important insight into the potential neurobiological and neurochemical effects. Future research will determine the potential risks of the long-term use of MP and FLX together.
注意力缺陷多动障碍(ADHD)可能与抑郁症共病,通常导致同时开处哌醋甲酯(MP)和选择性 5-羟色胺再摄取抑制剂(SSRI)抗抑郁药,如氟西汀(FLX)。此外,这些药物经常被滥用于认知增强剂。本研究检查了慢性口服共给予 MP 和 FLX 对抑郁和焦虑样行为的影响。
青春期大鼠在 4 周的时间内每天通过饮用水接受水(对照)、MP、FLX 或 MP 加 FLX 的组合。
数据分析显示,暴露于 FLX 或 MP+FLX 的大鼠的食物消耗和体重减少。与对照组相比,FLX 或 MP+FLX 组的蔗糖消耗明显更大。FLX 处理的大鼠在高架十字迷宫(EPM;开臂时间)和强迫游泳试验(FST;不动潜伏期)中没有效果。然而,用组合(MP+FLX)治疗的大鼠表现出明显的抗焦虑和抗抑郁样行为(如 EPM 和 FST 测量),以及总体活动(旷场试验中行进的距离)的显著增加。最后,联合 MP+FLX 治疗诱导的焦虑和抑郁样行为的减少显著大于这些药物单独治疗的反应。
这些行为结果描述了这些药物(口服给予)的长期影响,这些药物广泛共同给予和共同滥用,并为潜在的神经生物学和神经化学效应提供了重要的见解。未来的研究将确定长期联合使用 MP 和 FLX 的潜在风险。