Department of Pharmacology & Toxicology, Prof Dora Akunyili College of Pharmacy, Igbinedion University Okada, Benin City, Edo, Nigeria.
Department of Biochemistry, Faculty of Science, Obafemi Awolowo University, Ile Ife, Osun, Nigeria.
Metab Brain Dis. 2021 Apr;36(4):571-579. doi: 10.1007/s11011-021-00684-w. Epub 2021 Feb 9.
Epilepsy has been associated with several behavioral changes such as depression and anxiety while some antiepileptic drugs can precipitate psychiatric conditions in patients. This study evaluated the ameliorative effect of creatine on seizure severity and behavioral changes in pentylenetetrazole (PTZ) kindled mice. Mice were kindled by administering sub-convulsive doses of PTZ (35 mg/kg i.p.) at interval of 48 h. The naïve group (n = 7) constituted group 1, while successfully kindled mice were randomly assigned to five groups (n = 7). Group II served as vehicle treated group; groups III-V were treated with creatine 75, 150, and 300 mg/kg/day, p.o; Group V was given 25 mg/kg/day of phenytoin p.o. The treatment was for 15 consecutive days. The intensity of convulsion was scored according to a seven-point scale ranging from stage 0-7. Tail suspension test (TST) and Elevated plus maze (EPM) were utilized to assess depression and anxiety-like behavior respectively. After behavioral evaluation on day 15th, their brain was isolated and assayed for catalase, superoxide dismutase, reduced glutathione, and malondialdehyde. There was a significant (p < 0.05) reduction in the seizure scores, anxiety and depression-like behaviors in mice from the 5th day of treatment. The antioxidant assays revealed significant (p < 0.05) increase in catalase and reduced glutathione, and significant (p < 0.05) reduction in lipid peroxidation in treated mice. This study provides evidence for the seizure reducing property of creatine and its ameliorating potential on anxiety and depressive-like behaviors that follows seizure episodes.
癫痫与多种行为改变有关,如抑郁和焦虑,而一些抗癫痫药物会使患者出现精神疾病。本研究评估了肌酸对戊四氮(PTZ)点燃小鼠癫痫严重程度和行为改变的改善作用。通过给予亚惊厥剂量的 PTZ(35mg/kg 腹腔注射),每 48 小时间隔一次对小鼠进行点燃。未处理组(n=7)构成第 1 组,而成功点燃的小鼠被随机分为五组(n=7)。第 II 组为载体处理组;第 III-V 组分别给予肌酸 75、150 和 300mg/kg/天,口服;第 V 组给予 25mg/kg/天苯妥英,口服。治疗持续 15 天。根据 0-7 级的 7 分制对惊厥强度进行评分。利用悬尾试验(TST)和高架十字迷宫(EPM)分别评估抑郁和焦虑样行为。在第 15 天进行行为评估后,分离其大脑并测定其过氧化氢酶、超氧化物歧化酶、还原型谷胱甘肽和丙二醛。从第 5 天开始,治疗小鼠的癫痫评分、焦虑和抑郁样行为均显著(p<0.05)降低。抗氧化测定显示,治疗小鼠的过氧化氢酶和还原型谷胱甘肽显著(p<0.05)增加,脂质过氧化显著(p<0.05)降低。本研究为肌酸的抗癫痫作用及其对癫痫发作后焦虑和抑郁样行为的改善潜力提供了证据。