Anticonvulsant potential of rosuvastatin in combination with carbamazepine and valproate in animal models of epilepsy.

Vandana Tayal, Akash Mandal, Ijasul Haque M, Akhilesh Mishra, Bhupinder S Kalra, Vandana Roy
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Abstract

Background: Epilepsy impacts millions of people, with many not responding to existing treatments. Some evidence links neuroinflammatory processes to epilepsy. Statins exhibit anti-inflammatory and neuroprotective properties, potentially offering antiepileptic effects.

Aim: To evaluate the anticonvulsant effects of rosuvastatin in animal models of epilepsy.

Methods: Ninety-six albino mice were divided into 16 groups. In the maximal electroshock seizure (MES) model, eight groups received intraperitoneal vehicle, carbamazepine, rosuvastatin, or a combination. Outcomes measured included seizure protection [tonic hind limb extension (THLE)], duration of THLE, seizure duration, and mortality. In the pentylenetetrazol (PTZ) model, eight groups were pretreated with vehicle, valproate, rosuvastatin, or a combination, with outcomes measured as seizure latency, seizure duration, and mortality.

Results: In the MES model, rosuvastatin exhibited protection against THLE in a small percentage of mice. Rosuvastatin shortens the duration of THLE in a dose-dependent manner. However, none of these were statistically significant compared to the control group. The combination of rosuvastatin 10 mg/kg with carbamazepine 4 mg/kg resulted in a significant reduction in seizure duration compared to the control group, better than carbamazepine alone at 4 mg/kg and 6 mg/kg. In the PTZ model, rosuvastatin alone showed no significant effects on latency, duration of seizure, or mortality. However, rosuvastatin 10 mg/kg combined with valproate 100 mg/kg significantly delayed the onset of seizures, seizure duration and mortality percentage, better than valproate alone at 100 mg/kg.

Conclusion: Rosuvastatin enhanced the anticonvulsant effects of carbamazepine and valproate. Further studies are required to explore the antiepileptic potential of rosuvastatin at various doses, durations, dosage forms, routes and models.

瑞舒伐他汀联合卡马西平和丙戊酸在癫痫动物模型中的抗惊厥潜能。
背景:癫痫影响着数百万人,其中许多人对现有治疗无效。一些证据表明神经炎症过程与癫痫有关。他汀类药物具有抗炎和神经保护特性,可能具有抗癫痫作用。目的:评价瑞舒伐他汀在癫痫动物模型中的抗惊厥作用。方法:96只白化小鼠分为16组。在最大电休克发作(MES)模型中,8组接受腹腔注射载药、卡马西平、瑞舒伐他汀或联合用药。测量的结果包括癫痫发作保护[强直性后肢伸展(THLE)]、THLE持续时间、癫痫发作持续时间和死亡率。在戊四唑(PTZ)模型中,8组小鼠分别接受载药、丙戊酸盐、瑞舒伐他汀或联合治疗,观察癫痫发作潜伏期、癫痫发作持续时间和死亡率。结果:在MES模型中,瑞舒伐他汀对一小部分小鼠的THLE有保护作用。瑞舒伐他汀以剂量依赖的方式缩短THLE持续时间。然而,与对照组相比,这些都没有统计学意义。瑞舒伐他汀10 mg/kg联合卡马西平4 mg/kg与对照组相比,癫痫发作时间显著缩短,优于单独使用卡马西平4 mg/kg和6 mg/kg。在PTZ模型中,单独瑞舒伐他汀对潜伏期、癫痫发作持续时间或死亡率没有显著影响。然而,瑞舒伐他汀10 mg/kg联合丙戊酸100 mg/kg显著延迟癫痫发作、癫痫发作持续时间和死亡率,优于单独使用丙戊酸100 mg/kg。结论:瑞舒伐他汀可增强卡马西平和丙戊酸的抗惊厥作用。需要进一步的研究来探索瑞舒伐他汀在不同剂量、持续时间、剂型、途径和模型下的抗癫痫潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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