Effect of ischemia-reperfusion injury on elafin levels in rat liver.

Abdullah Hilmi Yılmaz, Ugur Dogan, Halit Özgül, Yunus Uzmay, Hamit Yasar Ellidag, Senay Yıldırım, Arif Aslaner
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Abstract

Background: The aim of this study was to quantify serum levels of elafin, a serine protease inhibitor, and to assess its effects on histopathological and biochemical parameters in hepatic ischemia-reperfusion injury.

Methods: Forty female Wistar albino rats were divided into five groups: Group 1 served as the control group. Liver ischemia was induced for 30 minutes in the other four groups. An additional 1-hour, 2-hour, and 3-hour reperfusion was induced in Groups 3, 4, and 5, respectively. At the end of the experiment, intracardiac blood samples were obtained for biochemical examination, and tissue samples from the liver were taken for histopathological examination. Levels of elafin, ischemia-modified albumin (IMA), total antioxi-dant status (TAS), and total oxidant status (TOS) were also examined.

Results: Serum elafin levels decreased beginning from Group 2, with the lowest level reached in Group 5 (p<0.01). The IMA level was the lowest in the control group and the highest in Group 5 (p<0.01). TOS, aspartate aminotransferase (AST), and alanine amino-transferase (ALT) levels were lowest in the control group and highest in Group 5 (p<0.01). Group 5 had the highest IMA/albumin ratio, although no significant differences were found between these four groups. The lowest TAS level was found in the control group, but a stable and significant increase was not detected in the other groups. No significant differences were found between the groups in terms of alkaline phosphatase (ALP) and albumin levels. A negative correlation was observed between serum elafin levels and AST, ALT, and TOS levels (p<0.01). The number of Grade 1 histopathological results was found to be higher in the groups with reperfusion (Groups 3, 4, 5). In histopathological subgroup analysis, while the elafin level was lower in Grade 1 group, AST, ALT, and TOS levels were higher (p<0.01). Additionally, the IMA/albumin ratio was found to be higher in the Grade 1 group (p=0.02).

Conclusion: In hepatic ischemia-reperfusion injury, elafin levels decreased as the reperfusion time increased. As the reperfusion time increased, both hepatocyte damage and oxidant capacity increased, with a negative correlation observed between these findings and elafin levels. Therefore, elafin may play a protective role in hepatic ischemia-reperfusion injury and could assist clinicians in assessing liver injury.

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缺血再灌注损伤对大鼠肝脏中elafin水平的影响
研究背景本研究旨在定量检测血清中丝氨酸蛋白酶抑制剂依拉芬的水平,并评估其对肝缺血再灌注损伤的组织病理学和生化指标的影响:方法:将 40 只雌性 Wistar 白化大鼠分为 5 组:第 1 组为对照组。其他四组诱导肝缺血 30 分钟。第 3 组、第 4 组和第 5 组分别再进行 1 小时、2 小时和 3 小时的再灌注。实验结束后,采集心内血液样本进行生化检查,并采集肝脏组织样本进行组织病理学检查。此外,还检测了依拉芬、缺血修饰白蛋白(IMA)、总抗氧化剂状态(TAS)和总氧化剂状态(TOS)的水平:结果:从第 2 组开始,血清中依拉芬的水平下降,第 5 组达到最低水平(p):结论:在肝缺血再灌注损伤中,随着再灌注时间的延长,依拉芬水平下降。随着再灌注时间的延长,肝细胞损伤和氧化能力都会增加,这些结果与依拉芬水平呈负相关。因此,依拉芬可能在肝脏缺血再灌注损伤中起到保护作用,并能帮助临床医生评估肝脏损伤。
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