慢性普瑞巴林治疗可减少大鼠的焦虑,而急性普瑞巴林治疗可增加大鼠的抑郁样行为。

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY BMC Pharmacology & Toxicology Pub Date : 2024-10-01 DOI:10.1186/s40360-024-00794-y
Hasan Çalışkan, Fırat Akat, Ali Doğan Dursun, Nezahet Zaloğlu
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引用次数: 0

摘要

背景:普瑞巴林是一种抗癫痫药物,能与突触前电压依赖性钙通道的α-2/δ单元结合。我们旨在研究急性和慢性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 7 组:对照组、药物组和 5 个不同剂量组(5、10、30、60 和 100 mg/kg)。普瑞巴林给药两周。通过强迫游泳测试评估抑郁样行为。焦虑样行为(ALB)通过开阔地测试(OFT)、高架迷宫(EPM)和光-暗箱进行评估。受试者在首次服药后进行强迫游泳测试(FST),两周后进行开阔地测试(OFT)、高架迷宫测试(EPM)和光暗箱测试(LDB)。实验结束前还进行了蔗糖偏好测试以评估失神:结果:在强迫游泳试验中,急性单剂量给药 10、30、60、100 毫克/千克普瑞巴林后,抑郁样行为增加。根据OFT结果,长期服用100毫克/千克普瑞巴林可减少梳理和冻结行为,从而显示出抗焦虑作用。此外,长期服用100毫克/千克普瑞巴林可显著增加在中心区域停留的时间、进入中心的次数和无支撑饲养次数,而不会导致运动活动发生任何变化。根据EPM结果,60毫克/千克和100毫克/千克普瑞巴林的慢性给药都有抗焦虑作用,增加了张臂时间和头下垂行为。此外,每公斤 60 毫克和 100 毫克普瑞巴林的长期用药可显著减少伸展出席姿势。5 至 100 毫克/千克的普瑞巴林剂量均对低密度脂蛋白有抗焦虑作用。在所有实验期间,蔗糖偏好度均高于 65%,受试者未表现出失神:结论:急性普瑞巴林治疗会引发类似抑郁症的行为。结论:急性普瑞巴林治疗会引发类似抑郁症的行为,但在慢性治疗过程中并未观察到可能与抑郁症相关的失乐症。此外,在所有无条件焦虑测试中,普瑞巴林的慢性治疗在不同行为模式和剂量下都显示出强烈的抗焦虑作用。尤其是在所有实验设置中,100 毫克/千克的普瑞巴林长期用药可减少焦虑样行为。虽然普瑞巴林的抗焦虑作用在慢性治疗中得到了证实,但其急性治疗会诱发类似抑郁的行为,因此在临床实践中应谨慎使用,尤其是对合并焦虑-抑郁的患者。
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Chronic pregabalin treatment reduced anxiety, and acute pregabalin treatment increased depression-like behaviors in rats.

Background: 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.

Methods: 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.

Results: 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.

Conclusion: 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.

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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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