Biochemistry Department, Faculty of Science, Alexandria University, Alexandria, Egypt.
Department of Medical Biotechnology, Genetic Engineering, and Biotechnology Research Institute, City for Scientific Research and Technology Applications (SRTA-City), New Borg EL-Arab, Alexandria 21934, Egypt.
Biomed Pharmacother. 2024 Apr;173:116340. doi: 10.1016/j.biopha.2024.116340. Epub 2024 Feb 29.
The current study investigated the ameliorating impact of GA water extract (GAE) on CCl-induced nephrotoxicity in renal cells and tissue by comparing its effectiveness with the Ketosteril (Ks) drug in restoring oxidative stress and necroinflammation. The cell morphology, necrosis, and redox state were evaluated in Vero cells. The influence of GAE on CCl-induced oxidative stress, inflammation, and necrosis was examined in rats. The predicted inhibitory mechanism of GAE phenolic constituents against COX-2 and iNOS was also studied. The results revealed that GAE contains crucial types of phenolic acids, which are associated with its antiradical activities. GAE improved CCl-induced Vero cell damage and restored renal architecture damage, total antioxidant capacity, ROS, TBARS, NO, GSH, GPX, SOD, and MPO in rats. GAE downregulated the gene expression of renal NF-κB, TNF-α, iNOS, and COX-2, as well as kidney injury molecule-1 (KIM-1) in rats. The GAE improved blood urea, creatinine, cholesterol, and reducing power. The computational analysis revealed the competitive inhibitory mechanism of selected phenolic composites of GAE on COX-2 and iNOS activities. The GAE exhibited higher potency than Ks in most of the studied parameters, as observed by the heatmap plots. Thus, GAE is a promising extract for the treatment of kidney toxicity.
本研究通过比较 GA 水提取物 (GAE) 与 Ketosteril (Ks) 药物在恢复氧化应激和坏死性炎症方面的效果,研究了 GAE 对 CCl 诱导的肾细胞和组织毒性的改善作用。在 Vero 细胞中评估了细胞形态、坏死和氧化还原状态。在大鼠中研究了 GAE 对 CCl 诱导的氧化应激、炎症和坏死的影响。还研究了 GAE 酚类成分对 COX-2 和 iNOS 的预测抑制机制。结果表明,GAE 含有重要类型的酚酸,这与其抗自由基活性有关。GAE 改善了 CCl 诱导的 Vero 细胞损伤,并恢复了大鼠的肾组织结构损伤、总抗氧化能力、ROS、TBARS、NO、GSH、GPX、SOD 和 MPO。GAE 下调了大鼠肾组织 NF-κB、TNF-α、iNOS 和 COX-2 以及肾损伤分子-1 (KIM-1) 的基因表达。GAE 改善了血液尿素、肌酐、胆固醇和还原力。计算分析揭示了 GAE 中选定酚类化合物对 COX-2 和 iNOS 活性的竞争性抑制机制。从热图图中可以看出,GAE 在大多数研究参数中的作用强于 Ks。因此,GAE 是一种有前途的治疗肾毒性的提取物。