Faghihi Nastaran, Mohammadi Mohammad Taghi
Department of Physiology and Biophysics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Adv Pharm Bull. 2017 Jun;7(2):291-298. doi: 10.15171/apb.2017.035. Epub 2017 Jun 30.
The pleiotropic effects of statins (antioxidant and anti-inflammation) have been reported by previous studies. Therefore, we aimed to determine whether pitavastatin has protective effects against pentylenetetrazol (PTZ)-induced kindling in mice and also whether pitavastatin improves the brain antioxidant capacity and attenuates the oxidative injuries in kindled mice. Twenty-four mice were randomly divided into four groups (each group n=6); control, PTZ-kindling and PTZ-kindled rats treated with pitavastatin (1&4 mg/kg). PTZ kindling seizures were induced by repetitive intraperitoneal injections of PTZ (65 mg/kg) every 48 hours till day twenty-one. Animals received daily oral pitavastatin for twenty-one days. Latency, score and duration of the seizures were recorded. The activities of catalase (CAT) ad superoxide dismutase (SOD), and likewise the contents of malondialdehyde (MDA) and nitrate were assessed in the brains of all rats. There was a progressive reduction in latency of the kindled rats in the next injections of PTZ. Pitavastatin reduced this value (latency) particularly at higher dose. Seizures duration and score also decreased in treatment groups. SOD and CAT activities significantly decreased in PTZ-kindling group by 62% and 64%, respectively, but pitavastatin did not significantly change the SOD and CAT activities. Brain MDA and nitrate significantly increased in PTZ-kindling group by 53% and 30%, respectively. Pitavastatin at higher dose significantly decreased the MDA and nitrate contents of PTZ-kindling rats by 45% and 32%, respectively. Our findings revealed that pitavastatin can improve the behavioral expression of the PTZ-kindling rats and attenuate the seizure-induced oxidative/nitrosative damage.
先前的研究报道了他汀类药物的多效性作用(抗氧化和抗炎)。因此,我们旨在确定匹伐他汀是否对小鼠戊四氮(PTZ)诱导的点燃具有保护作用,以及匹伐他汀是否能提高大脑抗氧化能力并减轻点燃小鼠的氧化损伤。将24只小鼠随机分为四组(每组n = 6);对照组、PTZ点燃组以及用匹伐他汀(1和4 mg/kg)治疗的PTZ点燃大鼠组。每48小时重复腹腔注射PTZ(65 mg/kg)直至第21天以诱导PTZ点燃性癫痫发作。动物每日口服匹伐他汀,持续21天。记录癫痫发作的潜伏期、评分和持续时间。评估所有大鼠大脑中过氧化氢酶(CAT)和超氧化物歧化酶(SOD)的活性,以及丙二醛(MDA)和硝酸盐的含量。在接下来的PTZ注射中,点燃大鼠的潜伏期逐渐缩短。匹伐他汀降低了这一值(潜伏期),尤其是在较高剂量时。治疗组的癫痫发作持续时间和评分也有所降低。PTZ点燃组中SOD和CAT活性分别显著降低了6