Pharmaceutical Sciences Research Center, Mazandaran University of Medical Sciences, Sari, Iran.
Department of Toxicology and Pharmacology, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Biol Trace Elem Res. 2017 Sep;179(1):102-109. doi: 10.1007/s12011-017-0944-z. Epub 2017 Jan 25.
Valproic acid (VPA) is an antiepileptic drug, which its usage is limited due to its hepatotoxicity. The present study was conducted to investigate the efficacy of zinc (Zn) and selenium (Se), necessary trace elements, against VPA-induced hepatotoxicity in Wistar rats. The animals were divided into five groups: control, VPA 200 mg/kg, VPA + Zn (100 mg/kg), VPA + Se (100 mg/kg), and VPA + Zn + Se. The administration of VPA for four consecutive weeks resulted in decrease in serum level of Zn in rats. Also, an increase in liver marker enzymes (ALT and AST) and also histological changes in liver tissue were shown after VPA administration. Oxidative stress was evident in VPA group by increased lipid peroxidation (LPO), protein carbonyl (PCO), glutathione (GSH) oxidation, and reducing total antioxidant capacity. Zn and Se (100 mg/kg) administration was able to protect against deterioration in liver enzyme, abrogated the histological change in liver tissue, and suppressed the increase in oxidative stress markers. Zn and combination of Zn plus Se treatment showed more protective effects than Se alone. These results imply that Zn and Se should be suggested as effective supplement products for the prevention of VPA-induced hepatotoxicity.
丙戊酸(VPA)是一种抗癫痫药物,但由于其肝毒性,其应用受到限制。本研究旨在探讨必需微量元素锌(Zn)和硒(Se)对 Wistar 大鼠 VPA 诱导的肝毒性的疗效。动物分为五组:对照组、VPA 200mg/kg 组、VPA+Zn(100mg/kg)组、VPA+Se(100mg/kg)组和 VPA+Zn+Se 组。连续四周给予 VPA 导致大鼠血清 Zn 水平降低。此外,VPA 给药后还显示肝脏标记酶(ALT 和 AST)升高和肝组织学变化。VPA 组脂质过氧化(LPO)、蛋白羰基(PCO)、谷胱甘肽(GSH)氧化和总抗氧化能力降低,表明氧化应激明显。Zn 和 Se(100mg/kg)给药能够防止肝酶恶化,消除肝组织的组织学变化,并抑制氧化应激标志物的增加。Zn 和 Zn 加 Se 联合治疗的保护作用比单独使用 Se 更明显。这些结果表明,Zn 和 Se 应作为预防 VPA 诱导的肝毒性的有效补充产品。