Steiner Heinz, Hrabak Michael, Bolaños-Guzmán Carlos A
Stanson Toshok Center for Brain Function and Repair, Rosalind Franklin University of Medicine and Science, North Chicago, IL 60064, USA; Discipline of Cellular and Molecular Pharmacology, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL 60064, USA.
Stanson Toshok Center for Brain Function and Repair, Rosalind Franklin University of Medicine and Science, North Chicago, IL 60064, USA.
Neurosci Biobehav Rev. 2025 Oct;177:106344. doi: 10.1016/j.neubiorev.2025.106344. Epub 2025 Aug 18.
Selective serotonin reuptake inhibitor (SSRI) antidepressants are used in combination with the medical psychostimulant methylphenidate (Ritalin), a dopamine reuptake inhibitor, in a variety of treatments in children and adults. Unintended co-exposure to these medications also occurs in patients on SSRIs who abuse methylphenidate as a "cognitive enhancer" or recreational drug. This review summarizes a series of studies on the neurobehavioral effects of such drug combinations, administered either orally (mimicking clinical doses) or intraperitoneally (abuse doses), in adolescent rats. Prototypical SSRIs such as fluoxetine (Prozac) given together with methylphenidate produce various behavioral changes, including facilitated acquisition of cocaine self-administration and increased reinstatement of cocaine seeking (model for relapse). Consistent with these behavioral effects, prototypical (but not novel atypical) SSRIs potentiate abuse/addiction-associated gene regulation by methylphenidate in dopamine target areas such as the striatum. Studies investigating the mechanisms underlying these effects revealed that 5-HT1A and 5-HT1B serotonin receptors inhibit and facilitate, respectively, such gene regulation. These findings indicate that combining methylphenidate with prototypical SSRIs may increase the abuse/addiction liability for psychostimulants, and that 5-HT1A and 5-HT1B receptors may serve as pharmacological targets to alleviate this risk.
选择性5-羟色胺再摄取抑制剂(SSRI)类抗抑郁药与医学用精神兴奋药哌醋甲酯(利他林)联合使用,后者是一种多巴胺再摄取抑制剂,用于儿童和成人的多种治疗。在滥用哌醋甲酯作为“认知增强剂”或消遣性药物的服用SSRI的患者中,也会意外发生这两种药物的共同暴露。本综述总结了一系列关于此类药物组合对青春期大鼠神经行为影响的研究,这些药物组合通过口服(模拟临床剂量)或腹腔注射(滥用剂量)给药。典型的SSRI如氟西汀(百忧解)与哌醋甲酯一起使用会产生各种行为变化,包括促进可卡因自我给药的习得以及增加对可卡因觅求行为的恢复(复发模型)。与这些行为效应一致,典型的(而非新型非典型的)SSRI在多巴胺靶区域如纹状体中增强了哌醋甲酯对滥用/成瘾相关基因的调控。对这些效应潜在机制的研究表明,5-HT1A和5-HT1B 5-羟色胺受体分别抑制和促进此类基因调控。这些发现表明,将哌醋甲酯与典型的SSRI联合使用可能会增加精神兴奋药的滥用/成瘾倾向,并且5-HT1A和5-HT1B受体可能作为减轻这种风险的药理学靶点。