Pinar Neslihan
Department of Pharmacology, Faculty of Medicine, Mustafa Kemal University, Hatay, Turkey.
Neurol India. 2021 Mar-Apr;69(2):426-429. doi: 10.4103/0028-3886.314542.
Epilepsy is a common neurological disease, although its etiology and pathophysiology are not yet fully understood. Oxidative stress plays a key role in the pathogenesis of many neurological diseases, including epilepsy, and there have been many studies reporting that antiepileptic medicines with neuroprotective and antioxidant activity inhibit free oxygen radicals. This study evaluates the effects of tempol on epileptic activity through behavioral parameters in acute picrotoxin (Ptx) models.
This experimental study was conducted on 42 adult male Wistar Albino rats weighing 450-500 g. Ptx (2.5 mg/kg) was injected i.p. as a single dose and observed for one hour to establish the acute Ptx model. Following injection, the animals were observed for 30 min in glass observation cages measuring 35 cm x 35 cm x 35 cm.
In picrotoxin-induced epilepsy, the total number of seizures and the total duration of seizures were decreased significantly with Ptx + tempol 100 mg/kg and Ptx + Tempol 150 mg/kg. The seizure phases were reduced significantly by Ptx + tempol 150 mg/kg (P < 0.05).
Tempol 100 mg/kg and tempol 150 mg/kg are found to be effective in epilepsy models caused by Ptx, with tempol 150 mg/kg found especially to be more effective.
癫痫是一种常见的神经系统疾病,尽管其病因和病理生理学尚未完全明确。氧化应激在包括癫痫在内的许多神经系统疾病的发病机制中起关键作用,并且有许多研究报道具有神经保护和抗氧化活性的抗癫痫药物可抑制游离氧自由基。本研究通过急性匹鲁卡品(Ptx)模型中的行为参数评估tempol对癫痫活动的影响。
本实验研究使用了42只体重450 - 500克的成年雄性Wistar白化大鼠。以2.5毫克/千克的单剂量腹腔注射Ptx以建立急性Ptx模型,并观察一小时。注射后,将动物置于尺寸为35厘米×35厘米×35厘米的玻璃观察笼中观察30分钟。
在匹鲁卡品诱发的癫痫中,Ptx + 100毫克/千克tempol和Ptx + 150毫克/千克tempol组的癫痫发作总数和癫痫发作总时长均显著降低。Ptx + 150毫克/千克tempol组的癫痫发作阶段显著减少(P < 0.05)。
发现100毫克/千克tempol和150毫克/千克tempol对Ptx引起的癫痫模型有效,其中150毫克/千克tempol尤其更有效。