Elberry Ahmed A, Refaie Shereen M, Kamel Mohamed, Ali Tarek, Darwish Hatem, Ashour Osama
Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.
Ann Saudi Med. 2013 Jan-Feb;33(1):57-62. doi: 10.5144/0256-4947.2013.57.
The clinical use of cisplatin (CP) is highly limited because of its renal toxicity and the production of reactive oxygen species (ROS) that intensify the cytotoxic effects. Oxytocin (OT) was previously shown to have antioxidant activity.
Experimental study on male Wistar albino rats performed in the Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.
Forty-eight male Wistar albino rats were classified into four equal groups: a control group, OT only-treated group which received OT twice (500 micro g/kg intraperitoneally (ip) 30 minutes and just before saline administration), a CP-induced nephrotoxicity group that received a single dose of CP (7.5 mg/kg ip) and treated with saline, and CP+OT group treated with the same previous doses. Seventy-two hours after CP administration, the rats were sacrificed and blood was withdrawn for determination of urea, creatinine, albumin and lactate dehydrogenase (LDH). The kidneys were extracted for histopathological examination and determination of the tissue levels of reduced glutathione (GSH), thiobarbituric acid reactive substances (TBARS) and nitric oxide end product nitrite (NO(2)). Glutathione S-transferase (GST), catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx) and myeloperoxidase (MPO) activities were assessed.
CP-induced renal injury was evidenced histopathologically and manifested by a significant increase in serum LDH activity as well as urea and creatinine levels. Moreover, renal injury was associated with decreased renal tissue activities of CAT, SOD, GPx and GST as well as GSH level. On the other hand, renal tissue content of TBARS and NO(2) as well as the activity of MPO were increased. Alterations in these biochemical and histopathological indices due to CP were attenuated by OT.
OT protected rats from CP-induced nephrotoxicity. Such protection is attributed, at least in part, to its antioxidant activity.
顺铂(CP)的临床应用因肾毒性以及活性氧(ROS)的产生而受到极大限制,ROS会增强细胞毒性作用。此前研究表明催产素(OT)具有抗氧化活性。
在沙特阿拉伯吉达阿卜杜勒阿齐兹国王大学药学院对雄性Wistar白化大鼠进行的实验研究。
48只雄性Wistar白化大鼠被分为四组,每组数量相等:对照组、仅接受OT治疗的组(分别于腹腔注射生理盐水前30分钟和注射前腹腔注射500μg/kg OT两次)、CP诱导的肾毒性组(腹腔注射单次剂量CP,7.5mg/kg)并给予生理盐水治疗、CP + OT组给予与前相同剂量治疗。CP给药72小时后,处死大鼠,采集血液测定尿素、肌酐、白蛋白和乳酸脱氢酶(LDH)。取出肾脏进行组织病理学检查,并测定组织中还原型谷胱甘肽(GSH)、硫代巴比妥酸反应性物质(TBARS)和一氧化氮终产物亚硝酸盐(NO₂)的水平。评估谷胱甘肽S-转移酶(GST)、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)和髓过氧化物酶(MPO)的活性。
组织病理学证实CP诱导了肾损伤,表现为血清LDH活性以及尿素和肌酐水平显著升高。此外,肾损伤与肾组织中CAT、SOD、GPx和GST活性以及GSH水平降低有关。另一方面,肾组织中TBARS和NO₂含量以及MPO活性增加。OT减轻了CP引起的这些生化和组织病理学指标的改变。
OT保护大鼠免受CP诱导的肾毒性。这种保护作用至少部分归因于其抗氧化活性。