Salim Mahmood Ahmed, Ammoo Afaq M, Ali Mayssam Hussein Mohammed, Hameed Tiba M, Al-Hussaniy Hany A, Aljumaili Abdulla Amer Abbas, Al-Fallooji Mohammed Hussein Alaa, Kadhim Ali Hakim
Department of Pharmacy, Al-Rasheed University, Baghdad 10001, Iraq.
Department of Pharmacy, Bilad Alrafidain University College, Diyala 32001, Iraq.
Pharmaceuticals (Basel). 2022 Nov 26;15(12):1468. doi: 10.3390/ph15121468.
NeuroAid II, a folk Chinese Medicine, is currently used in Asia for the treatment of stroke. An experimental study demonstrated that NeuroAid enables neuronal cells to be more resistant to glutamate toxicity. This research was constructed to evaluate the efficacy of NeuroAid in the prevention of epilepsy (EP). Forty healthy adult male mice were used and divided into four groups (10 mice/group): normal control group; positive control group; NeuroAid-treated group (10 mg/kg); topiramate-treated group (10 mg/kg). The treatment continued for 7 days, and on the last day, EP was induced using strychnine at a dose of 2 mg/kg via intraperitoneal (ip) administration. Seizure severity, latency to the seizure onset, the number of seizures, and the duration of each seizure episode were observed for one hour. The death and protection rates over the next twenty-four hours were recorded. Brain specimens from surviving animals were extracted and examined pathologically for quantification of glutamate receptor (GluR) gene expression in the isolated hippocampus employing real-time PCR analysis. Treatment with NeuroAid resulted in a significant reduction in seizure severity, prolonged the onset of seizures, decreased the number and duration of episodes, reduced brain insult, and decreased mortality rate. Reductions in the gene expression of GluRs in the hippocampus with minor histopathological changes were observed in the NeruoAid- and topiramate-treated groups. It is concluded that NeuroAid has a potential antiepileptic effect (EP) with the ability to prevent convulsion through its effect on the glutamate receptor.
中药醒脑再造丸(NeuroAid II)目前在亚洲用于治疗中风。一项实验研究表明,醒脑再造丸能使神经元细胞对谷氨酸毒性更具抵抗力。本研究旨在评估醒脑再造丸预防癫痫(EP)的疗效。选用40只健康成年雄性小鼠,分为四组(每组10只):正常对照组;阳性对照组;醒脑再造丸治疗组(10mg/kg);托吡酯治疗组(10mg/kg)。治疗持续7天,最后一天,通过腹腔注射(ip)2mg/kg的士的宁诱导癫痫发作。观察一小时内的癫痫发作严重程度、发作起始潜伏期、发作次数和每次发作持续时间。记录接下来24小时内的死亡率和保护率。提取存活动物的脑标本,采用实时PCR分析对分离海马体中的谷氨酸受体(GluR)基因表达进行病理定量检测。醒脑再造丸治疗可显著降低癫痫发作严重程度,延长发作起始时间,减少发作次数和持续时间,减轻脑损伤,并降低死亡率。在醒脑再造丸和托吡酯治疗组中,观察到海马体中GluRs基因表达降低,组织病理学变化轻微。结论是,醒脑再造丸具有潜在的抗癫痫作用(EP),能够通过对谷氨酸受体的作用预防惊厥。