Department of Pharmacology, Bharati Vidyapeeth Medical College, Pune, India.
Indian J Pharmacol. 2009 Dec;41(6):268-72. doi: 10.4103/0253-7613.59926.
To study the effect of oral magnesium oxide supplementation alone and on the activity of standard anti-epileptic drugs in the animal models of maximal electroshock seizures (MES) and chemically (pentylenetetrazole [PTZ])-induced seizures.
Healthy male albino rats were given magnesium oxide (MgO) supplementation orally in various doses (500, 750 and 1000 mg/kg /day) for 4 weeks (day 1 to day 28). On day 0 and day 29, response to MES (180 mA for 0.2 s) was tested 1 h after pre-administration of phenytoin or carbamazepine orally. Similarly, in the other groups, the response to PTZ 40 mg/kg i.p. was tested 1 h after pre-administration of oral sodium valproate.
Oral administration of MgO in a low dose (500 mg/kg) for 4 weeks in healthy rats appears to exert protective effect against MES. High oral doses of MgO (750 and 1000 mg/kg) appear to enhance the activity of phenytoin and carbamazepine in the MES model. MgO supplementation was seen to decrease the latency of PTZ-induced seizures.
The dose of oral MgO appears to have an inverse relation with the protective effect in MES-induced seizure model. High doses of MgO supplementation given orally appear to enhance the activity of standard anti-epileptic drugs in the MES-induced seizure model.
研究单独口服氧化镁补充剂以及对标准抗癫痫药物在最大电休克发作(MES)和化学(戊四氮[PTZ])诱导发作的动物模型中的活性的影响。
健康雄性白化大鼠在 4 周内(第 1 天至第 28 天)每天口服给予不同剂量的氧化镁(MgO)(500、750 和 1000 mg/kg)。在第 0 天和第 29 天,在口服苯妥英或卡马西平给药前 1 小时测试对 MES(180 mA,0.2 s)的反应。同样,在其他组中,在口服丙戊酸钠给药前 1 小时测试对 40 mg/kg i.p. PTZ 的反应。
在健康大鼠中,4 周内低剂量(500 mg/kg)口服 MgO 似乎对 MES 具有保护作用。口服高剂量的 MgO(750 和 1000 mg/kg)似乎增强了 MES 模型中苯妥英和卡马西平的活性。MgO 补充剂可降低 PTZ 诱导的癫痫发作的潜伏期。
口服 MgO 的剂量似乎与 MES 诱导的癫痫发作模型中的保护作用呈反比。口服给予高剂量的 MgO 补充剂似乎增强了 MES 诱导的癫痫发作模型中标准抗癫痫药物的活性。