Zeyghami Mohammad Ali, Hesam Ebrahim, Khadivar Parand, Hesam Halimeh Khaton, Ahmadnia Ali, Amini Abolfazl
Neuroscience Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Dept. Pharmacology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Heliyon. 2020 Apr 9;6(4):e03761. doi: 10.1016/j.heliyon.2020.e03761. eCollection 2020 Apr.
Recent studies have shown that statins and Metformin may have beneficial effects on seizure through different mechanisms In the current study, we investigated whether Metformin, Atorvastatin, and concomitant uses of them have beneficial effects on pentylenetetrazole (PTZ)-induced kindling. Adult male C57BL/6 mice were randomly divided into four experimental groups with seven mice in each group. Group 1, control group; group 2, received Metformin (200 mg/kg, i.p); group 3, received Atorvastatin (10 mg/kg, i.p.); group 4, received Atorvastatin (10 mg/kg, i.p.) plus Metformin (200 mg/kg, i.p.). Twenty minutes after injection of the mentioned drugs, the experimented mice received 37/5 mg/kg of PTZ intraperitoneally on alternating days. Then the convulsive behavior signs were evaluated for 20 min after each PTZ injection. There were significant differences in the stage 2 latency parameter among group 2 (p = 0.033, F = 8.46)/group 3 (p = 0.032, F = 10.42)/group 4 (p = 0.008, F = 24.57) as compared to the control group, while no significant differences were found comparing only group 2,3, and 4 with eachother excluding the control group. Pretreatment with Atorvastatin (p = 0.002, F = 33), Atorvastatin + Metformin (p = 0.006, F = 20.77), and Metformin alone increased stage 5 latency as compared to the PTZ group, significantly. Also, our results have shown that pretreatment with Atorvastatin (p = 0.013, F = 14.48), Metformin (p = 0.015, F = 16.67), and concomitant usage of them significantly decreased stage 5 duration as compared to the control group. Our findings clearly demonstrate that concomitant use of Metformin and Atorvastatin has no more protective effect against the development of kindling as compare to these drugs alone. Thus, we concluded that, these drugs may inhibit kindling via a similar mechanism and we suggested that it is probably through regulation of autophagy.
近期研究表明,他汀类药物和二甲双胍可能通过不同机制对癫痫发作产生有益影响。在本研究中,我们调查了二甲双胍、阿托伐他汀以及它们的联合使用对戊四氮(PTZ)诱导的点燃效应是否具有有益影响。成年雄性C57BL/6小鼠被随机分为四个实验组,每组七只。第1组为对照组;第2组腹腔注射二甲双胍(200mg/kg);第3组腹腔注射阿托伐他汀(10mg/kg);第4组腹腔注射阿托伐他汀(10mg/kg)加二甲双胍(200mg/kg)。注射上述药物20分钟后,实验小鼠每隔一天腹腔注射37.5mg/kg的PTZ。然后在每次PTZ注射后评估20分钟的惊厥行为体征。与对照组相比,第2组(p = 0.033,F = 8.46)/第3组(p = 0.032,F = 10.42)/第4组(p = 0.008,F = 24.57)在2期潜伏期参数上存在显著差异,而仅比较第2、3和4组(不包括对照组)之间未发现显著差异。与PTZ组相比,阿托伐他汀预处理(p = 0.002,F = 33)、阿托伐他汀+二甲双胍预处理(p = 0.006,F = 20.77)以及单独使用二甲双胍均显著增加了5期潜伏期。此外,我们的结果表明,与对照组相比,阿托伐他汀预处理(p = 0.013, F = 14.48)、二甲双胍预处理(p = 0.015, F = 16.67)以及它们的联合使用均显著缩短了5期持续时间。我们的研究结果清楚地表明,与单独使用这些药物相比,二甲双胍和阿托伐他汀的联合使用对点燃效应的发展并没有更多的保护作用。因此,我们得出结论,这些药物可能通过类似机制抑制点燃效应,并且我们认为这可能是通过自噬调节实现的。