High-dose atorvastatin reduces oxidative stress of ischemia/reperfusion injury after isogeneic kidney transplantation in rats: in vivo, preclinical, case–control, open-label study

IF 0.9 Q4 UROLOGY & NEPHROLOGY
Giacomo Cusumano, Edoardo Cola, Gionata Spagnoletti, Anna Severino, Simona Giubilato, Egidio Stigliano, Maria Emiliana Caristo, Gisella Vischini, Giovanna Liuzzo, Maria Paola Salerno, Filippo Crea, Jacopo Romagnoli
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引用次数: 0

Abstract

Abstract Background Renal ischemia/reperfusion injury is an unavoidable event in transplantation in which free radical-mediated injury determines release of pro-inflammatory cytokines and activation of innate immunity. In addition to their cholesterol-lowering action, statins have shown dose-dependent pleiotropic effects on inflammatory pathways and oxidative stress. We investigated the effects of high-dose atorvastatin (atorvastatin 40 mg/kg) in preventing ischemia/reperfusion injury in an animal model of kidney transplant. Methods Forty female rats underwent left nephrectomy and orthotopic autotransplantation. Animals were divided in four groups: A = Transplant only; B = high-dose atorvastatin + Transplant; C = right nephrectomy + Transplant; D = high-dose atorvastatin + right nephrectomy + Transplant. Bilateral nephrectomy was performed 24 h post-transplant. Oxidative stress was assessed measuring malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GPx) and myeloperoxidase (MPO) activity on renal tissue; ischemia/reperfusion injury was also evaluated by histology. Donor pre-treatment with high-dose atorvastatin improved oxidative stress. Results MDA levels were lower in group B versus A ( p = 0.002) and D ( p = 0.004). High-dose atorvastatin pre-treated rats displayed higher GPx activity in group B versus A ( p = 0.009) and D ( p = 0.005). SOD scavenger activity was also higher in group B versus A ( p < 0.001) D ( p < 0.001) and C ( p = 0.003). MPO activity was lower in group B versus A ( p = 0.02), C ( p = 0.007) and D ( p = 0.03). Histology revealed significantly lower rate of intratubular casts and luminal congestion in Group D versus C ( p = 0.02 and p = 0.008, respectively). Conclusions High-dose atorvastatin pre-treatment reduces oxidative stress and inflammation in a model of kidney transplant in the rat.
大剂量阿托伐他汀降低大鼠异基因肾移植后缺血/再灌注损伤的氧化应激:体内、临床前、病例对照、开放标签研究
肾缺血/再灌注损伤是移植中不可避免的事件,自由基介导的损伤决定了促炎细胞因子的释放和先天免疫的激活。除了降低胆固醇的作用外,他汀类药物在炎症途径和氧化应激方面也显示出剂量依赖性的多效性作用。我们研究了大剂量阿托伐他汀(阿托伐他汀40 mg/kg)对肾移植动物模型缺血再灌注损伤的预防作用。方法40只雌性大鼠行左肾切除术和原位自体肾移植。动物分为四组:A =仅移植;B =大剂量阿托伐他汀+移植;C =右肾切除+移植;D =大剂量阿托伐他汀+右肾切除术+移植。移植后24小时行双侧肾切除术。通过测定肾组织丙二醛(MDA)、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)活性来评估氧化应激;组织病理学评价缺血再灌注损伤。供体大剂量阿托伐他汀预处理可改善氧化应激。结果B组MDA水平低于A组(p = 0.002)和D组(p = 0.004)。高剂量阿托伐他汀预处理组大鼠GPx活性高于A组(p = 0.009)和D组(p = 0.005)。SOD清除剂活性B组高于A组(p <0.001) D (p <0.001)和C (p = 0.003)。MPO活性B组低于A组(p = 0.02)、C组(p = 0.007)和D组(p = 0.03)。组织学显示,D组小管内铸型和管腔充血率明显低于C组(p = 0.02和p = 0.008)。结论大剂量阿托伐他汀预处理可降低大鼠肾移植模型的氧化应激和炎症反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Renal Replacement Therapy
Renal Replacement Therapy Medicine-Transplantation
CiteScore
1.70
自引率
8.30%
发文量
57
审稿时长
19 weeks
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