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首页> 外文期刊>Saudi Pharmaceutical Journal >Adjuvant role of Ocimum sanctum hydroalcoholic extract with carbamazepine and phenytoin in experimental model of acute seizures
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Adjuvant role of Ocimum sanctum hydroalcoholic extract with carbamazepine and phenytoin in experimental model of acute seizures

机译:在急性癫痫发作实验模型中,在急性癫痫发作模型中与血红素醇提取物的佐剂作用

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Purpose This study assessed adjuvant potential of Ocimum sanctum hydroalcoholic extract (OSHE) with antiepileptic drugs (AEDs) carbamazepine (CBZ) and phenytoin (PHT) in maximal electroshock seizure (MES) model in male Wistar rats. Material and Methods Pharmacodynamic effect of OSHE (1000?mg/kg) was assessed through seizure protection potential, neurobehavioral tests and oxidative stress estimation in MES model after 14?days administration of OSHE alone or combination with maximal (M) and sub-maximal (SM) dose of CBZ or PHT. Pharmacokinetic interaction of OSHE with AEDs was also assessed after 14?days of drug treatment. Results OSHE per se showed 50% protection against MES-induced seizures. Combination of OSHE with AEDs’ SM dose enhanced its seizure protection potential. Significant reduction in duration of tonic hind limb extension was observed in CBZ-SM? ?OSHE as compared to control group (p?=?0.006). Among neurobehavioral tests in Morris water maze test rats of CBZ-M? ?OSHE took significantly less time to reach the platform (p?=?0.022) and spent more time in target quadrant (p?=?0.016) as compared to other groups. Similarly, rats of PHT-SM? ?OSHE group spent significantly more time in the target quadrant (p?=?0.013). In elevated plus maze test, CBZ-M? ?OSHE had significantly decreased transfer latency compared to other groups (p?=?0.013). OSHE alone treated group had significantly lower oxidative stress as compared to other groups. No significant pharmacokinetic interaction was observed between OSHE and AEDs (CBZ, PHT). Conclusion Ocimum’s potential of enhanced seizure protection and neuroprotection along with minimal drug interaction with AEDs substantiate its adjuvant role in the management of epilepsy.
机译:目的,该研究评估了在雄性Wistar大鼠中最大电孔癫痫发作(MES)模型中的抗癫痫药物(AED)CARBAMAZEPINE(CBZ)和苯妥汀(PHT)的辅助和乳氨基醇提取物(OSHE)的辅助潜力。通过癫痫潜在保护潜力,神经表达试验和MES模型中的癫痫潜力,神经兽性试验和氧化应激估计来评估材料和方法的药物动力学效应于14.天施用OSHE单独或与最大(M)和Sub-Maximal组合( SM)CBZ或PHT的剂量。在14天的药物治疗后,还评估了OSHE与AEDs的药代动力学相互作用。结果OSHE本身表明,对MES诱导的癫痫发作的保护率为50%。 OSHE与AEDS SM剂量的组合增强了其癫痫发作潜力。在CBZ-SM中观察到滋补后肢延伸期持续时间显着降低? ?oshe与对照组相比(p?= 0.006)。在莫里斯水迷宫测试大鼠CBZ-M中的神经麻烦试验中?OSHE了显著更少的时间到达平台(P?=?0.022)和目标象限花更多的时间(P?=?0.016)相比于其他群体。同样地,PHT-SM的大鼠? ?Oshe Group在目标象限中花费了更多的时间(p?= 0.013)。在升高的加迷宫测试中,CBZ-M?与其他群体相比,oshe显着降低了转移等待时间(P?= 0.013)。与其他基团相比,Oshe单独治疗组氧化应激显着降低。在OSHE和AED(CBZ,PHT)之间没有观察到显着的药代动力学相互作用。结论目的,具有增强癫痫发作保护和神经保护作用的潜力以及对AED的最小药物相互作用证实了癫痫管理中的佐剂作用。

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