Goudarzi Mehdi, Khodayar Mohammad Javad, Hosseini Tabatabaei Seyed Mohammad Taghi, Ghaznavi Habib, Fatemi Iman, Mehrzadi Saeed
Department of Toxicology, School of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Pediatric Nephrology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Fundam Clin Pharmacol. 2017 Dec;31(6):625-635. doi: 10.1111/fcp.12303. Epub 2017 Jul 31.
Cyclophosphamide (CP) is widely used in treatment of different cancers. Nephrotoxicity is one of the dose-limiting side effects of CP. This study was carried out to investigate the effect of melatonin (MEL) on CP-induced nephrotoxicity in mice. In this study, 50 Swiss albino mice (20-25 g) were randomly divided into five groups. Mice were pretreated with MEL intraperitoneally (i.p) in doses of 5, 10 and 20 mg/kg for five consecutive days, and CP (200 mg/kg, i.p) was administrated on the 5th day 1 h after the last dose of MEL. Then on day 6, blood samples were collected to determine serum creatinine (Cr) and blood urea nitrogen (BUN) levels. The kidneys were used for histological examination, biochemical assays and real-time PCR studies. Malondialdehyde (MDA), glutathione (GSH), protein carbonyl (PC), nitric oxide (NO) level, catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx) and myeloperoxidase (MPO) activity were assessed in renal tissue. In addition, the expression of SOD2 and PGx1 was measured using real-time PCR method in renal tissue. Results showed that CP administration significantly increases Cr, BUN, MDA, PC, NO level and MPO activity. It also decreases renal GSH level, SOD, GPx and CAT activity. Pretreatment with MEL (especially 20 mg/kg, i.p.) for 5 days prevented these changes; however, it did not affect the SOD activity. Our results revealed that MEL might be useful for prevention of the nephrotoxicity induced by CP through ameliorative effects on biochemical indices and oxidative stress parameters.
环磷酰胺(CP)广泛用于治疗多种癌症。肾毒性是CP的剂量限制性副作用之一。本研究旨在探讨褪黑素(MEL)对CP诱导的小鼠肾毒性的影响。在本研究中,50只瑞士白化小鼠(20 - 25克)被随机分为五组。小鼠连续5天腹腔注射(i.p)剂量为5、10和20毫克/千克的MEL进行预处理,在最后一剂MEL后1小时,于第5天腹腔注射CP(200毫克/千克)。然后在第6天,采集血样以测定血清肌酐(Cr)和血尿素氮(BUN)水平。取肾脏进行组织学检查、生化分析和实时PCR研究。评估肾组织中的丙二醛(MDA)、谷胱甘肽(GSH)、蛋白质羰基(PC)、一氧化氮(NO)水平、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)活性。此外,使用实时PCR方法测定肾组织中SOD2和PGx1的表达。结果显示,给予CP显著增加了Cr、BUN、MDA、PC、NO水平和MPO活性。它还降低了肾组织中的GSH水平、SOD、GPx和CAT活性。用MEL(特别是20毫克/千克,腹腔注射)预处理5天可预防这些变化;然而,它不影响SOD活性。我们的结果表明,MEL可能通过改善生化指标和氧化应激参数对预防CP诱导的肾毒性有用。