Mesripour Azadeh, Golbidi Mojgan, Hajhashemi Valiollah
Department of Pharmacology and Toxicology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, I.R. Iran.
Isfahan Pharmaceutical Sciences Research Center, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, I.R. Iran.
Res Pharm Sci. 2020 Oct 19;15(5):447-453. doi: 10.4103/1735-5362.297847. eCollection 2020 Oct.
Cyclosporine (Cyc) is a calcineurin inhibitor used in immunosuppressive therapy that may cause psychological problems such as depression. Previous investigations have shown the positive antidepressant effects of dextromethorphan (Dxt). Therefore, the aim of this study was the evaluation of the Dxt effect on Cyc-induced depression in an animal model of despair in two separate cohorts.
Male albino mice were used, first total activity was evaluated by the locomotor test, and then after that, the immobility time during the forced swimming test was measured as an indicator of depression. Cyc, Dxt, and fluoxetine (the reference antidepressant drug) were all administered IP. Tests were performed either 4 h after injection (cohort 4 h) or in separate groups 24 h after injection (cohort 24 h).
FINDINGS/RESULTS: Cyc reduced total activity measured after 4 h in the locomotor test and it was normalized after 24 h. Immobility time dose-dependently increased during the forced swimming test and remained so after 24 h (cohort 24 h; Cyc 10, 20, and 40 mg/kg, 157 ± 22, 180 ± 8, and 228 ± 4 s, respectively; Cyc 40 mg/kg < 0.001 control 142 ± 13 s) that indicated Cyc induced depressive-like behavior. Dxt (30 mg/kg) like fluoxetine reduced the immobility time when co-administered with Cyc compared with Cyc and remained effective after 24 h (cohort 24 h; 120 ± 30, < 0.001 Cyc 40 mg/kg alone).
Dxt was a useful drug for preventing Cyc-induced depression that remained effective for 24 h in mice. Since interpretation from animal studies to humans must be done with caution further clinical studies on the effect of Dxt in patients suffering from psychological side effects of Cyc may be reasonable.
环孢素(Cyc)是一种用于免疫抑制治疗的钙调神经磷酸酶抑制剂,可能会引发如抑郁等心理问题。先前的研究已表明右美沙芬(Dxt)具有积极的抗抑郁作用。因此,本研究的目的是在两个独立的队列中,评估Dxt对绝望动物模型中Cyc诱导的抑郁的影响。
使用雄性白化小鼠,首先通过自主活动试验评估总活动量,然后在强迫游泳试验中测量不动时间作为抑郁指标。Cyc、Dxt和氟西汀(参考抗抑郁药物)均通过腹腔注射给药。试验在注射后4小时(4小时队列)进行,或在注射后24小时在不同组中进行(24小时队列)。
Cyc降低了自主活动试验中4小时后测得的总活动量,并在24小时后恢复正常。在强迫游泳试验中,不动时间呈剂量依赖性增加,并在24小时后保持不变(24小时队列;Cyc 10、20和40mg/kg,分别为157±22、180±8和228±4秒;Cyc 40mg/kg与对照组142±13秒相比,P<0.001),这表明Cyc诱导了抑郁样行为。与单独使用Cyc相比,Dxt(30mg/kg)与氟西汀一样,在与Cyc联合给药时可减少不动时间,并在24小时后仍有效(24小时队列;120±30秒,与单独使用Cyc 40mg/kg相比,P<0.001)。
Dxt是预防Cyc诱导的抑郁的有效药物,在小鼠中24小时内仍有效。由于从动物研究到人类的推断必须谨慎进行,因此进一步开展关于Dxt对患有Cyc心理副作用患者影响的临床研究可能是合理的。