Çalışkan Hasan, Akat Fırat, Dursun Ali Doğan, Zaloğlu Nezahet
Department of Physiology, School of Medicine, Balıkesir University, Balıkesir, Turkey.
Department of Physiology, Faculty of Medicine, Ankara University, Ankara, Turkey.
BMC Pharmacol Toxicol. 2024 Oct 1;25(1):72. doi: 10.1186/s40360-024-00794-y.
Pregabalin is an antiepileptic drug that binds to the alpha-2/delta unit at presynaptic voltage-dependent calcium channels. We aimed to investigate the effect of acute and chronic pregabalin administration on anxiety and depression-like behaviors.
Fifty-six male Wistar albino rats were divided into seven groups: control, vehicle, and five different dose groups (5, 10, 30, 60, and 100 mg/kg). Pregabalin was administered for two weeks. Depression-like behaviors were evaluated by Forced swimming test. Anxiety-like behavior (ALB) was evaluated by Open field test (OFT), Elevated Plus Maze (EPM), and light-dark box. Subjects underwent the forced swimming test (FST) after the first dose, while the open field test (OFT), elevated plus maze (EPM), and light-dark box (LDB) were performed after two weeks of treatment. Further sucrose preference test was conducted to evaluate anhedonia until the end of the experiment.
In the forced swimming test, depression-like behaviors increased after acute single-dose administration of 10, 30, 60, 100 mg/kg pregabalin. According to OFT results, chronic 100 mg/kg pregabalin showed anxiolytic effects by decreasing grooming, and freezing behaviors. In addition, 100 mg/kg chronic pregabalin administration significantly increased the time spent in the central region, the number of entries to the center, and the unsupported rearing number without causing any change in locomotor activity. According to EPM results, both chronic 60 and 100 mg/kg pregabalin treatments showed anxiolytic effects by increasing open arm time and head dipping behavior. In addition, 60 and 100 mg/kg chronic pregabalin administration significantly decreased stretch attend posture. All pregabalin administrations between 5 and 100 mg/kg displayed anxiolytic effects in the LDB. Sucrose preference was above 65% for the duration of all experiments and subjects did not show anhedonia.
Acute pregabalin treatment triggered depression-like behaviors. Anhedonia, which may be associated with depression, was not observed during chronic treatment. Moreover, chronic treatment with pregabalin revealed potent anxiolytic effects in different behavior patterns and doses for all tests of unconditional anxiety. In particular, 100 mg/kg chronic pregabalin administration decreased anxiety-like behaviors in all experiment setups. Although the anxiolytic effect was demonstrated in chronic treatment, acute treatment of pregabalin induced depression-like behaviors, and thus in clinical practice should be done with caution, especially in patients with anxiety-depression comorbidity.
普瑞巴林是一种抗癫痫药物,可与突触前电压依赖性钙通道的α-2/δ亚基结合。我们旨在研究急性和慢性给予普瑞巴林对焦虑和抑郁样行为的影响。
将56只雄性Wistar白化大鼠分为七组:对照组、溶剂组和五个不同剂量组(5、10、30、60和100mg/kg)。给予普瑞巴林两周。通过强迫游泳试验评估抑郁样行为。通过旷场试验(OFT)、高架十字迷宫(EPM)和明暗箱评估焦虑样行为(ALB)。在首次给药后对受试者进行强迫游泳试验(FST),而在治疗两周后进行旷场试验(OFT)、高架十字迷宫(EPM)和明暗箱(LDB)试验。在实验结束前进一步进行蔗糖偏好试验以评估快感缺失。
在强迫游泳试验中,急性单次给予10、30、60、100mg/kg普瑞巴林后,抑郁样行为增加。根据OFT结果,慢性给予100mg/kg普瑞巴林通过减少修饰和僵住行为显示出抗焦虑作用。此外,慢性给予100mg/kg普瑞巴林显著增加了在中央区域停留的时间、进入中央区域的次数和无支撑站立次数,而不引起运动活动的任何变化。根据EPM结果,慢性给予60和100mg/kg普瑞巴林均通过增加开放臂时间和探头行为显示出抗焦虑作用。此外,慢性给予60和100mg/kg普瑞巴林显著减少了伸展注意姿势。5至100mg/kg的所有普瑞巴林给药在明暗箱中均显示出抗焦虑作用。在所有实验期间,蔗糖偏好均高于65%,受试者未表现出快感缺失。
急性普瑞巴林治疗引发抑郁样行为。在慢性治疗期间未观察到可能与抑郁相关的快感缺失。此外,普瑞巴林的慢性治疗在所有无条件焦虑测试中,在不同行为模式和剂量下均显示出有效的抗焦虑作用。特别是,慢性给予100mg/kg普瑞巴林在所有实验设置中均降低了焦虑样行为。尽管在慢性治疗中证明了抗焦虑作用,但普瑞巴林的急性治疗诱导了抑郁样行为,因此在临床实践中应谨慎使用,尤其是在伴有焦虑抑郁共病的患者中。