Khadir Fatemeh, Pouramir Mahdi, Joorsaraee Seyyed Gholamali, Feizi Farideh, Sorkhi Hadi, Yousefi Fatemeh
Department of Biochemistry, Babol University of Medical Sciences, Babol, Iran.
Cellular and Molecular Biology Research Center, Babol University of Medical Sciences, Babol, Iran.
Caspian J Intern Med. 2015 Fall;6(4):196-200.
Cyclosporine A (CsA) is a potent immunosuppressant drug with therapeutic and toxic actions. The use of CsA is limited by its toxicity. Several researchers had proposed that oxidative stress could play an important role in CsA-induced toxicity. Arbutin has recently been shown to possess antioxidative and free radical scavenging abilities. The present study was designed to investigate the in vivo effects of arbutin on lipid peroxidation and antioxidant capacity in the serum of cyclosporine treated rats.
Adult male Wistar rats were divided into six groups (n=8/group): (I) control (no CsA and arbutin administration), (II and III) were treated subcutaneously (Sc) with arbutin (50,100 mg/kg/bw), respectively, (IV) administered CsA (25 mg/kg/bw) intraperitoneally (IP), (V and VI) received the combination of CsA (25 mg/kg/bw) i.p and arbutin (50,100 mg/kg/bw) Sc daily, respectively. At the end of the treatment (after3 weeks), serum lipid peroxidation was measured by thiobarbituric acid-reacting substances (TBARS) and serum total antioxidant capacity (ferric reducing ability of plasma [FRAP]) was assayed based on spectrophotometric method.
TBARS had been significantly increased by CsA administration compared with control rats. Arbutin (50mg/kg/bw) completely prevented this effect, but arbutin (100 mg/kg/bw) alone or in combination with CsA significantly increased lipid peroxidation compared with controls.
Our data indicate that arbutin (50mg/kg/bw) had protective effect in the CsA-induced toxicity but high concentration of arbutin (100mg/kg/bw) showed meaningful oxidative and lipoperoxidative effects.
环孢素A(CsA)是一种具有治疗作用和毒性作用的强效免疫抑制剂。CsA的使用因其毒性而受到限制。一些研究人员提出氧化应激可能在CsA诱导的毒性中起重要作用。最近有研究表明熊果苷具有抗氧化和清除自由基的能力。本研究旨在探讨熊果苷对环孢素处理大鼠血清脂质过氧化和抗氧化能力的体内影响。
成年雄性Wistar大鼠分为六组(每组n = 8):(I)对照组(不给予CsA和熊果苷),(II和III)分别皮下注射(Sc)熊果苷(50、100mg/kg体重),(IV)腹腔注射(IP)CsA(25mg/kg体重),(V和VI)分别每日腹腔注射CsA(25mg/kg体重)和皮下注射熊果苷(50、100mg/kg体重)。在治疗结束时(3周后),通过硫代巴比妥酸反应物质(TBARS)测定血清脂质过氧化,并基于分光光度法测定血清总抗氧化能力(血浆铁还原能力[FRAP])。
与对照大鼠相比,CsA给药显著增加了TBARS。熊果苷(50mg/kg体重)完全阻止了这种作用,但单独使用熊果苷(100mg/kg体重)或与CsA联合使用时,与对照组相比显著增加了脂质过氧化。
我们的数据表明,熊果苷(50mg/kg体重)对CsA诱导的毒性具有保护作用,但高浓度的熊果苷(100mg/kg体重)显示出明显的氧化和脂质过氧化作用。