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Effects of aminoguanidine and melatonin on intestinal ischemia/reperfusion injury in rats: An assessor-blinded controlled experimental study

机译:氨基胍和褪黑激素对大鼠肠缺血/再灌注损伤的影响:评估者盲对照研究

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摘要

>Background: The reactive oxygen and nitrogen species generated during reperfusion of tissue are characteristic of intestinal ischemia and reperfusion (IIR) injury.>Objective: This study was designed to assess whether the administration of aminoguanidine (AG), a selective nitric oxide synthase inhibitor, and/or melatonin has protective potential in IIR injury.>Methods: Male Wistar albino rats (age, 3–4 weeks; weight, 100–150 g) were divided in a nonrandom fashion into 5 groups of equal size: group 1, IIR injury + AG 100 mg/kg; group 2, IIR injury + melatonin 10 mg/kg; group 3, IIR injury + AG 100 mg/kg + melatonin 10 mg/kg; group 4, sham operation; and group 5, IIR injury alone. Sixty minutes of intestinal ischemia and 4 hours of reperfusion were carried out in all but the sham-operation group. Ileal specimens were obtained from all rats to determine the extent of histologic changes, measure tissue concentrations of malondialdehyde (MDA) and protein carbonyl (PC), and assess the activity of superoxide dismutase (SOD) and glutathione peroxidase (GPx). Specimens were also assessed and scored by a pathologist blinded to the experiment and the data.Results: Forty rats were divided into 5 groups of 8 each; all 40 survived until study end. In the IIR injury-alone group, mean (SD) MDA concentration and PC content were significantly higher than that of the sham-operation group, and SOD and GPx activity were significantly lower: MDA concentration, 0.86 (0.03) versus 0.54 (0.01) mmol/g protein, respectively; PC content, 0.60 (0.02) versus 0.34 (0.01) mmol/g protein; SOD activity, 104.33 (43.14) versus 2954.72 (109.55) U/g protein; and GPx activity, 10.44 (0.63) versus 24.34 (1.77) U/g protein (all, P < 0.001). Administration of AG, melatonin, and the AG/melatonin combination was associated with significantly higher SOD (1802.31 [102.35], 1776.50 [58.41], and 1924.28 [98.10] U/g protein, respectively) and GPx (17.36 [1.23], 15.96 [1.08], and 18.06 [1.72] U/g protein) activity and significantly lower MDA concentration (0.62 [0.02], 0.64 [0.02], and 0.56 [0.01] mmol/g protein) and PC content (0.53 [0.03], 0.51 [0.01], and 0.49 [0.02] mmol/g protein) compared with the IIR injury-alone group (P < 0.001). Mean intestinal mucosal injury scores were significantly lower in the 3 treatment groups (2.12 [0.35], 1.75 [0.46], and 1.12 [0.35]) compared with the IIR injury-alone group (3.87 [0.35]; all, P < 0.001).>Conclusion: In this study, AG, melatonin, or both administered in combination were associated with improvements in oxidative markers in this rat model of IIR injury.
机译:>背景:组织再灌注过程中产生的活性氧和氮是肠道缺血和再灌注(IIR)损伤的特征。>目的:该研究旨在评估给药是否一氧化氮合酶抑制剂氨基胍(AG)和/或褪黑激素对IIR损伤具有保护潜力。>方法:雄性Wistar白化病大鼠(年龄3-4周;体重100-150岁) g)以非随机方式分为5组,大小相同:第1组,IIR损伤+ AG 100 mg / kg;第2组,IIR损伤+褪黑激素10 mg / kg;第3组,IIR损伤+ AG 100 mg / kg +褪黑激素10 mg / kg;第4组,假手术;第5组,仅IIR伤害。除假手术组外,其余各组均进行了60分钟的肠缺血和4小时的再灌注。从所有大鼠中获得回肠标本,以确定组织学变化的程度,测量丙二醛(MDA)和蛋白羰基(PC)的组织浓度,以及评估超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx)的活性。结果:40只大鼠被分成5组,每组8只。全部40例均存活至研究结束。仅IIR损伤组的MDA平均浓度和PC含量均明显高于假手术组,SOD和GPx活性明显低于假手术组:MDA浓度分别为0.86(0.03)和0.54(0.01)。分别为mmol / g蛋白; PC含量为0.60(0.02)对0.34(0.01)mmol / g蛋白; SOD活性为104.33(43.14)对2954.72(109.55)U / g蛋白; GPx活性分别为10.44(0.63)和24.34(1.77)U / g蛋白(全部,P <0.001)。施用AG,褪黑激素和AG /褪黑激素的组合分别显着提高了SOD(分别为1802.31 [102.35],1776.50 [58.41]和1924.28 [98.10] U / g蛋白)和GPx(17.36 [1.23],15.96) [1.08]和18.06 [1.72] U / g蛋白)活性,并显着降低MDA浓度(0.62 [0.02],0.64 [0.02]和0.56 [0.01] mmol / g蛋白)和PC含量(0.53 [0.03]),与单纯IIR损伤组相比,蛋白含量分别为0.51 [0.01]和0.49 [0.02] mmol / g(P <0.001)。与仅IIR损伤组(3.87 [0.35];所有,P <0.001)相比,三个治疗组(2.12 [0.35],1.75 [0.46]和1.12 [0.35])的平均肠粘膜损伤评分显着降低。 。>结论:在这项研究中,AG,褪黑激素或两者合用与这种IIR损伤大鼠模型中的氧化标志物改善有关。

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