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Efficacy of poly(adenosine diphosphate-ribose) polymerase inhibition in extracorporeal shock wave-induced renal injury

机译:聚腺苷二磷酸核糖聚合酶抑制作用在体外冲击波诱发的肾损伤中的作用

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Objectives: Extracorporeal shock wave lithotripsy (ESW) induces renal damage by excessive production of free oxygen radicals. Free Oxygen radicals cause cellular injury by inducing nicks in DNA. The enzyme poly(adenosine diphosphate-ribose) polymerase (PARP) involved in the process of repair of DNA in damaged cells. However, its activation in damaged cells can lead to adenosine triphosphate depletion and death. Thus, we designed a study to evaluate the efficacy of 3-aminobenzamide (3-AB), a PARP inhibitor, against extracorporeal shock wave induced renal injury. Methods: Twenty-four Sprague-Dawley rats were divided into three groups: control, ESW, ESW + 3-AB groups. All groups except control group were subjected to ESW procedure. ESW + 3-AB group received 20 mg/kg/day 3-aminobenzamide intraperitoneally at 2 h before ESW and continued once a day for consecutive 3 days. The surviving animals were sacrificed at the 4th day and their kidneys were harvested for biochemical and histopathologic analysis. Blood samples from animals were also obtained. Results: Serum ALT and AST levels, serum neopterin and tissue oxidative stress parameters were increased in the ESW group and almost came to control values in the treatment group (p<0.05, ESW vs. ESW + 3-AB). Histopathological injury score were significantly lower in treatment group than the ESW group (p<0.05, ESW vs. ESW + 3-AB). Conclusion: Our data showed that PARP inhibition protected renal tissue against ESW induced renal injury. These findings suggest that it would be possible to improve the outcome of ESW induced renal injury by using PARP inhibitors as a preventive therapy.
机译:目的:体外冲击波碎石术(ESW)会通过过量产生游离氧自由基来引起肾脏损害。游离氧自由基通过在DNA中诱导缺口而引起细胞损伤。聚(腺苷二磷酸核糖)聚合酶(PARP)参与了受损细胞DNA修复的过程。然而,其在受损细胞中的活化可导致三磷酸腺苷耗竭并死亡。因此,我们设计了一项研究以评估PARP抑制剂3-氨基苯甲酰胺(3-AB)对体外冲击波诱发的肾损伤的疗效。方法:将24只Sprague-Dawley大鼠分为三组:对照组,ESW,ESW + 3-AB组。除对照组外,所有组均接受ESW治疗。 ESW + 3-AB组在ESW前2小时腹膜内接受20 mg / kg /天的3-氨基苯甲酰胺,并连续3天每天一次。在第4天处死存活的动物,并收获它们的肾脏以进行生化和组织病理学分析。还获得了动物的血样。结果:ESW组血清ALT和AST水平,血清新蝶呤和组织氧化应激参数增加,治疗组几乎达到对照值(p <0.05,ESW vs. ESW + 3-AB)。治疗组的组织病理学损伤评分显着低于ESW组(p <0.05,ESW vs. ESW + 3-AB)。结论:我们的数据表明,PARP抑制作用可保护肾脏组织免受ESW致肾损伤。这些发现表明,通过使用PARP抑制剂作为预防性疗法,可以改善ESW诱发的肾损伤的预后。

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