Evaluation of Renoprotective Effect of Lipoic Acid and Bosentan Against Diclofenac-Induced Acute Renal Failure

L. B. Qasim, G. A. Jasim, Ihsan Rabeea
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Abstract

Acute renal failure also known as acute kidney injury (AKI) is a complex health condition related to significant morbidity and mortality. In hospitalized patients, around 19-33 percent of AKI episodes are linked to drug induced nephrotoxicity. Although considered safe, NSAIDs such as diclofenac have gained special attention over the past few years due to the potential risk of renal injury. The direct effect of diclofenac-induced renal injury depends on targeting the mitochondria in kidney tissue, and formation of reactive oxygen species (ROS) resulting in oxidative stress. Secondly, diclofenac inhibit renal prostaglandin production, limiting renal afferent arteriole vasodilation, increasing afferent resistance; thus decreasing the glomerular capillary pressure below normal values and glomerular filtration rate will decrease resulting in AKI. Alpha-Lipoic acid (ALA) has beneficial effects in prevention or relief of symptoms of oxidative stress- related diseases, as it acts as antioxidant and anti-inflammatory micronutrient. Bosentan is a competitive antagonist with dual endothelin-1 receptors, as renal vascular ET-1 system is upregulated under many pathophysiological situations. In present study, we investigated the effect of lipoic acid and bosentan in diclofenac induced acute renal failure in male rats. We observed that diclofenac increased serum levels of urea, creatinine, malondialdehyde, KIM-1, TGFβ1 and fibronectin significantly (p>0.05) in the induction group compared to control group. While, SOD significantly (p>0.05) reduced in the induction group compared to control group. Both of lipoic acid and bosentan alone didn’t significantly protect against diclofenac induced AKI. However, the combination group showed a significant protection against AKI. Pearson correlation analysis showed a significant positive correlation between (urea and KIM-1) and between (creatinine and KIM-1) (r2=0.792 and r2=0.677 respectively). Furthermore, there was a significant positive correlation between fibronectin and urea (r2= 0.498, p>0.01) and fibronectin and creatinine (r2=0.356, p>0.05). Interestingly, KIM-1 showed a significant positive correlation with fibronectin (r2=0.536, p>0.01). ROC curve test was performed for KIM-1 and fibronectin biomarkers. The AUC for KIM-1 was 0.986 and for fibronectin was 0.829. We concluded that combination therapy of lipoic acid and bosentan showed a significant protective effect against diclofenac-induced AKI. In addition, fibronectin could be a promising biomarker for detection and diagnosis of acute kidney injury. Key words: Diclofenac, oxidative stress, alpha- lipoic acid, endothelin-1, bosentan
硫辛酸和波生坦对双氯芬酸致急性肾功能衰竭的肾保护作用评价
急性肾功能衰竭也称为急性肾损伤(AKI),是一种复杂的健康状况,具有很高的发病率和死亡率。在住院患者中,大约19- 33%的AKI发作与药物引起的肾毒性有关。尽管非甾体抗炎药(如双氯芬酸)被认为是安全的,但由于其潜在的肾损伤风险,在过去几年中,双氯芬酸等非甾体抗炎药受到了特别的关注。双氯芬酸诱导肾损伤的直接作用依赖于靶向肾组织线粒体,形成活性氧(ROS)导致氧化应激。其次,双氯芬酸抑制肾前列腺素生成,限制肾传入小动脉血管舒张,增加传入阻力;从而使肾小球毛细血管压力低于正常值,肾小球滤过率降低,导致AKI。α -硫辛酸(ALA)作为抗氧化和抗炎的微量营养素,在预防或缓解氧化应激相关疾病的症状方面具有有益的作用。波生坦是一种具有双内皮素-1受体的竞争性拮抗剂,因为肾血管ET-1系统在许多病理生理情况下上调。本研究探讨了硫辛酸和波生坦在双氯芬酸诱导的雄性大鼠急性肾功能衰竭中的作用。我们观察到双氯芬酸诱导组血清尿素、肌酐、丙二醛、KIM-1、tgf - β1和纤维连接蛋白水平显著高于对照组(p>0.05)。诱导组SOD显著低于对照组(p>0.05)。单用硫辛酸和波生坦对双氯芬酸诱导的AKI均无显著保护作用。然而,联合组显示出对AKI的显著保护。Pearson相关分析显示,尿素与KIM-1、肌酐与KIM-1呈正相关(r2=0.792、r2=0.677)。纤连蛋白与尿素呈显著正相关(r2= 0.498, p>0.01),纤连蛋白与肌酐呈显著正相关(r2=0.356, p>0.05)。有趣的是,KIM-1与纤连蛋白呈显著正相关(r2=0.536, p>0.01)。对KIM-1和纤维连接蛋白生物标志物进行ROC曲线检验。KIM-1的AUC为0.986,纤连蛋白的AUC为0.829。我们得出结论,硫辛酸和波生坦联合治疗对双氯芬酸诱导的AKI具有显著的保护作用。此外,纤维连接蛋白可能是一种有前景的检测和诊断急性肾损伤的生物标志物。关键词:双氯芬酸,氧化应激,α -硫辛酸,内皮素-1,波生坦
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