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Effects of atorvastatin and metformin on development of pentylenetetrazole-induced seizure in mice

机译:阿托伐他汀和二甲双胍对戊四唑诱发的小鼠癫痫发作的影响

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摘要

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.
机译:最近的研究表明,他汀类药物和二甲双胍可能通过不同的机制对癫痫发作具有有益作用。在本研究中,我们调查了二甲双胍,阿托伐他汀及其同时使用是否对戊四唑(PTZ)诱发的点燃有有益作用。将成年雄性C57BL / 6小鼠随机分为四个实验组,每组七只。第一组,对照组;第2组,接受二甲双胍(200 mg / kg,腹腔注射);第3组,接受阿托伐他汀(10 mg / kg,腹腔注射);第4组接受阿托伐他汀(10 mg / kg,腹膜内)和二甲双胍(200 mg / kg,腹膜内)。注射上述药物后20分钟,实验小鼠在隔日腹膜内接受37/5 mg / kg的PTZ。然后在每次PTZ注射后20分钟评估惊厥行为征象。与第2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)的第2阶段潜伏期参数有显着差异。对照组,而仅将第2、3和4组与除对照组以外的其他组进行比较,没有发现显着差异。与PTZ组相比,阿托伐他汀(p = 0.002,F = 33),阿托伐他汀+二甲双胍(p = 0.006,F = 20.77)和单独的二甲双胍预处理显着增加了5期潜伏期。同样,我们的结果表明,与对照组相比,用阿托伐他汀(p = 0.013,F = 14.48),二甲双胍(p = 0.015,F = 16.67)进行预处理,并同时使用它们可以显着减少第5阶段的持续时间。我们的发现清楚地表明,与单独使用这些药物相比,同时使用二甲双胍和阿托伐他汀对点燃的发生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的机制抑制点燃,我们认为这可能是通过调节自噬。

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