Gao Lina, Yang Shuang, Liu Junting, Liu Libo
School of Forensic Medicine, China Medical University, Shenyang 110001, Liaoning, China. Corresponding author: Liu Libo, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2015 Apr;27(4):246-9. doi: 10.3760/cma.j.issn.2095-4352.2015.04.004.
To investigate the protective effects of 5-hydroxy-1-methylhyantoin (HM ) on paraquat (PQ)-induced nephrotoxicity in rat and its possible mechanism.
Twenty-four male Sprague-Dawley (SD) rats were randomly divided into four groups: namely control, PQ, vitamin C and HMH groups, with 6 rats in each group. The rats in control group were given an injection of 2 mg/kg of normal saline intraperitoneally. The rats in PQ group were given an injection of 50 mg/kg of PQ intraperitoneally. The rats in vitamin C and HMH groups were given 1 mmol/kg of vitamin C or HMH through gastric tube right after PQ injection. The hydroxyl free radical scavenging ability of HMH and vitamin C was determined by Fenton method. Blood sample was collected after 24 hours of PQ treatment, then the animals were sacrificed and renal tissues were harvested. Blood urea nitrogen (BUN), serum creatinine (SCr), protein content of renal cortex, blood malondialdehyde (MDA), reduced glutathione (GSH) and superoxide dismutase (SOD) activity were determined.
Both vitamin C and HMH showed a very good ability to scavenge hydroxyl radicals, and the 50% inhibiting concentration (IC₅₀) was both 4.02 mg/mL. Compared with control group, serum BUN, SCr and MDA in renal tissue were significantly increased in PQ group, and the protein, GSH contents and SOD activity were significantly decreased [BUN (mmol/L): 40.80 ± 2.49 vs. 13.67 ± 1.58, SCr (μmol/L): 163.46 ± 8.67 vs. 51.80 ± 4.37, MDA (nmol/g): 7.51 ± 0.23 vs. 4.52 ± 0.33, protein (μmol/L): 0.94 ± 0.14 vs. 1.35 ± 0.10, GSH (mg/g): 1.08 ± 0.48 vs. 3.30 ± 0.44, SOD (kU/L): 70.74 ± 6.42 vs. 112.89 ± 8.72, all P < 0.01 ]. Compared with PQ group, serum BUN and SCr and MDA in kidney tissue in vitamin C and HMH groups were significantly decreased, and GSH content and SOD activity in kidney tissue were significantly elevated [BUN mmol/L): 22.64 ± 2.36, 18.71 ± 5.23 vs. 40.80 ± 2.49, SCr (μmol/L): 97.28 ± 4.81, 89.20 ± 6.72 vs. 163.46 ± 8.67, MDA (nmol/g): 4.67 ± 0.31, 4.21 ± 0.42 vs. 7.51 ± 0.23, GSH (mg/g): 1.78 ± 0.10, 1.86 ± 0.39 vs. 1.08 ± 0.48, SOD (kU/L): 98.69 ± 5.43, 103.76 ± 4.45 vs. 70.74 ± 6.42, all P < 0.01]. Compared with vitamin C group, HMH could significantly reduce SCr contents P < 0.05). There were no differences in reduction PQ-induced BUN, MDA content, and effect on GSH content and SOD activity between vitamin C group and HMH group (all P > 0.05).
HMH can protect the kidney against PQ-induced nephrotoxicity, and the mechanism of which maybe attributed to its anti-oxidation property and ability to scavenge hydroxyl radical.
探讨5-羟基-1-甲基乙内酰脲(HM)对百草枯(PQ)诱导的大鼠肾毒性的保护作用及其可能机制。
将24只雄性Sprague-Dawley(SD)大鼠随机分为四组:即对照组、PQ组、维生素C组和HMH组,每组6只。对照组大鼠腹腔注射2mg/kg生理盐水。PQ组大鼠腹腔注射50mg/kg PQ。维生素C组和HMH组大鼠在PQ注射后立即经胃管给予1mmol/kg维生素C或HMH。采用Fenton法测定HMH和维生素C清除羟自由基的能力。PQ处理24小时后采集血样,然后处死动物并收集肾组织。测定血尿素氮(BUN)、血清肌酐(SCr)、肾皮质蛋白含量、血丙二醛(MDA)、还原型谷胱甘肽(GSH)和超氧化物歧化酶(SOD)活性。
维生素C和HMH均表现出很好的清除羟自由基能力,50%抑制浓度(IC₅₀)均为4.02mg/mL。与对照组相比,PQ组血清BUN、SCr和肾组织MDA显著升高,蛋白、GSH含量和SOD活性显著降低[BUN(mmol/L):40.80±2.49 vs. 13.67±1.58,SCr(μmol/L):163.46±8.67 vs. 51.80±4.37,MDA(nmol/g):7.51±0.23 vs. 4.52±0.33,蛋白(μmol/L):0.94±0.14 vs. 1.35±0.10,GSH(mg/g):1.08±0.48 vs. 3.30±0.44,SOD(kU/L):70.74±6.42 vs. 112.89±8.72,均P<0.01]。与PQ组相比,维生素C组和HMH组血清BUN、SCr和肾组织MDA显著降低,肾组织GSH含量和SOD活性显著升高[BUN(mmol/L):22.64±2.36,18.71±5.23 vs. 40.80±2.49,SCr(μmol/L):97.28±4.81,89.20±6.72 vs. 163.46±8.67,MDA(nmol/g):4.67±0.31,4.21±0.42 vs. 7.51±0.23,GSH(mg/g):1.78±0.10,1.86±0.39 vs. 1.08±0.48,SOD(kU/L):98.69±5.43,103.76±4.45 vs. 70.74±6.42,均P<0.01]。与维生素C组相比,HMH能显著降低SCr含量(P<0.05)。维生素C组和HMH组在降低PQ诱导的BUN、MDA含量以及对GSH含量和SOD活性的影响方面无差异(均P>0.05)。
HMH可保护肾脏免受PQ诱导的肾毒性,其机制可能与其抗氧化性能和清除羟自由基的能力有关。