Neurochemistry and Biochemical Neuropharmacology Research Unit, Department of Biochemistry, University of Karachi, Karachi, Pakistan.
Neurochemistry and Biochemical Neuropharmacology Research Unit, Department of Biochemistry, University of Karachi, Karachi, Pakistan/Neuroscience Research Laboratory, Dr. Panjwani Center for Molecular Medicine and Drug Research, ICCBS, University of Karachi, Karachi, Pakistan.
Pak J Pharm Sci. 2021 Sep;34(5):1749-1757.
In the present study we have monitored effects of repeated coadministration of fluoxetine with midazolam; a benzodiazepine (CNS depressant). It is the primary drug of choice for procedural sedation, preoperative sedation, and in emergency departments. Repeated administration of this drug is reported to have abuse potential and may cause this by increasing dopaminergic neurotransmission. Since an important role of serotonin is there in the pathophysiology of anxiety and addiction, administration of midazolam may involve altered 5-HT metabolism as well. Present study was designed to monitor effects of repeated administration of fluoxetine with midazolam. Effects of fluoxetine and midazolam coadministration were monitored on motor activities in familiar and novel environments, hot plate test, forced swim test, conditioned place preference test and levels of dopamine, 5-HT and their metabolites. Both midazolam (2.5mg/kg) and fluoxetine (1mg/kg) were administered orally for 12 days. Conditioned place preference test was performed on day 13. Rats were decapitated and whole brain samples were collected and stored at -70°C until neurochemical analysis by HPLC-EC. Findings from the present study show attenuation of midazolam-induced reinforcement upon repeated co-administration of fluoxetine. These could be implicated to increased therapeutic utility of midazolam and related benzodiazepines.
在本研究中,我们监测了氟西汀与咪达唑仑(一种苯二氮䓬类药物(CNS 抑制剂))重复联合给药的影响。咪达唑仑是程序镇静、术前镇静和急诊科的首选药物。据报道,这种药物的重复给药有滥用的潜力,可能通过增加多巴胺能神经传递来引起这种情况。由于 5-羟色胺在焦虑和成瘾的病理生理学中起着重要作用,咪达唑仑的给药可能也涉及到 5-HT 代谢的改变。本研究旨在监测氟西汀与咪达唑仑重复给药的影响。监测氟西汀和咪达唑仑联合给药对熟悉和陌生环境中的运动活动、热板试验、强迫游泳试验、条件性位置偏好试验以及多巴胺、5-HT 及其代谢物水平的影响。咪达唑仑(2.5mg/kg)和氟西汀(1mg/kg)均口服给药 12 天。第 13 天进行条件性位置偏好试验。大鼠断头后收集全脑样本,储存在-70°C,直到通过 HPLC-EC 进行神经化学分析。本研究的结果表明,氟西汀重复给药可减弱咪达唑仑诱导的强化作用。这可能意味着咪达唑仑和相关苯二氮䓬类药物的治疗用途增加。