糖胺酮对肾缺血再灌注损伤的潜在保护作用。

IF 0.6 Q3 ANESTHESIOLOGY
Vildan Kölükçü, Mehtap Gürler Balta, Ahmet Tuğrul Şahin, Ali Genç, Velid Unsal, Fatih Fırat, Fikret Gevrek, Asiye Yancı, Ahmet Burak Gülpınar
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引用次数: 0

摘要

目的:探讨糖麦酮对肾组织缺血再灌注损伤的治疗作用。方法:21只Wistar白化雌性大鼠分为3组。第一组作为对照队列进行比较。第2、3组建立肾缺血再灌注模型。此外,在缺血停止后,第三组大鼠静脉注射糖胺酮,剂量为4 mg kg-1。随后采集血液和组织样本进行分析。结果:生化分析显示,3组的谷胱甘肽过氧化物酶和超氧化物歧化酶活性明显高于2组(P < 0.001和P=0.015)。此外,与2组相比,3组的丙二醛浓度显著降低(P=0.004)。与2组相比,3组肿瘤坏死因子- α、白细胞介素6和白细胞介素1 β水平明显降低(P=0.021、P=0.006和P=0.016)。组2中性粒细胞明胶酶相关脂钙蛋白和肾损伤分子-1含量最高(P < 0.001和P=0.015)。同样,组织病理学损伤以2组最显著(P < 0.001)。结论:糖玛德对肾组织缺血再灌注损伤具有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Potential Renoprotective Effect of Sugammadex in Renal Ischemia-reperfusion Injury.

Objective: We aimed to evaluate the effectiveness of sugammadex on renal tissue for against ischemia-reperfusion injury.

Methods: Twenty-one Wistar albino strain female rats were divided into three groups. The first group functioned as the control cohort for comparison. In Groups 2 and 3, a renal ischemia-reperfusion model was established. Moreover, following the cessation of ischemia, the rats in Group 3 were intravenously administered sugammadex at a dose of 4 mg kg-1. Blood and tissue samples were subsequently collected for analysis.

Results: Biochemical analyses revealed a notable increase in the enzymatic activities of glutathione peroxidase and superoxide dismutase in Group 3 relative to Group 2 (P < 0.001 and P=0.015, respectively). Additionally, the concentration of malondialdehyde was found to be significantly reduced in Group 3 relative to Group 2 (P=0.004). Group 3 exhibited a substantial decrease in tumor necrosis factor-alpha, interleukin 6, and interleukin 1 beta levels when compared to Group 2 (P=0.021, P=0.006, and P=0.016 respectively). Group 2 exhibited the highest concentrations of neutrophil gelatinase-associated lipocalin and kidney injury molecule-1 (P < 0.001 and P=0.015, respectively). Similarly, the histopathologic tissue damage was the most prominent in Group 2 (P < 0.001).

Conclusion: Sugammadex plays a protective role against ischaemia-reperfusion injury in renal tissue.

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