Anticonvulsive and Antioxidant Effects of Pioglitazone on Pentylenetetrazole-induced Seizures in Rats

Y. Ghiasi, S. Rostamian, E. Aali, Y. Naderi
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引用次数: 1

Abstract

Background: Epilepsy is a neurologic dysfunction caused by abnormal electrical activity in the brain. Oxidative stress is involved in the seizure-induced brain damage. Objective: This study aimed to evaluate the anticonvulsant and antioxidant effects of pioglitazone (a peroxisome proliferator-activated receptor gamma agonist used for treatment of type 2 diabetes) on Pentylenetetrazole (PTZ)-induced seizure in rats. Methods: In this experimental study, 28 rats weighing 20-30 g were divided into four groups of control, pioglitazone, PTZ, and treatment. For treatment, PTZ (85 mg/kg) or normal saline was injected intraperitoneally and 4 hours later, pioglitazone (80 mg/kg) was administrated orally. Carboxymethylcellulose was administered orally in the control and PTZ groups, instead of pioglitazone. One hour after PTZ injection, seizure severity was assessed using Racine scale. Then, the rats were decapitated and the Malondialdehyde (MDA) level and the activity of Catalase (CAT) and Superoxide Dismutase (SOD) in their hippocampus samples were measured by standard methods. Findings: Pioglitazone administration significantly increased the latency to the onset of seizure stages 1-4 and prevented the stage 5. It significantly reduced the lipid peroxidation caused by PTZ-induced seizure and increased the activity of CAT and SOD enzymes in the hippocampus of rats. Conclusion: Antioxidant effects of pioglitazone may play a role in preventing stable PTZ-induced seizures and protecting neurons from seizure-caused damage.
吡格列酮对戊四唑致大鼠癫痫发作的抗惊厥和抗氧化作用
背景:癫痫是一种由大脑异常电活动引起的神经功能障碍。氧化应激与癫痫发作引起的脑损伤有关。目的:本研究旨在评价吡格列酮(一种用于治疗2型糖尿病的过氧化物酶体增殖物激活受体γ激动剂)对戊四唑(PTZ)诱导的大鼠癫痫发作的抗惊厥和抗氧化作用。方法:本实验将28只体重20~30g的大鼠分为对照组、吡格列酮组、PTZ组和治疗组。为了治疗,腹膜内注射PTZ(85mg/kg)或生理盐水,4小时后口服吡格列酮(80mg/kg)。对照组和PTZ组口服羧甲基纤维素代替吡格列酮。PTZ注射后1小时,使用拉辛量表评估癫痫发作的严重程度。然后,将大鼠斩首,用标准方法测定海马样品中丙二醛(MDA)水平、过氧化氢酶(CAT)和超氧化物歧化酶(SOD)活性。研究结果:吡格列酮给药显著增加了发作1-4期的潜伏期,并阻止了发作5期。显著降低PTZ致癫痫大鼠的脂质过氧化,提高海马CAT和SOD酶活性。结论:吡格列酮的抗氧化作用可能在预防稳定的PTZ诱导的癫痫发作和保护神经元免受癫痫损伤中发挥作用。
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