Soliman Mohamed Mohamed, Elshehawei Ahmed M, Althobaiti Saed, Sayed Samy M
Clinical Laboratory Sciences Department, Turabah University College, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Department of Bitechnology, College of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Toxicol Res (Camb). 2023 Jul 22;12(4):685-692. doi: 10.1093/toxres/tfad058. eCollection 2023 Aug.
Current study examined the boosting impacts of leaf extract from Taif area (high-altitude area) against hepatic and renal toxicity induced by diclofenac in experimental rats. Withania is highly grown on Taif area as environmental herb with multiple functions. Diclofenac is non-steroidal medication used for treatment of pain but over dose has severe side effects. Thirty-two adult Wistar rats of male type were subdivided into 4 groups. The control rats (group 1) received saline. Second group received diclofenac (50 mg/kg BW intraperitoneally) at days 4 and 5. Third group received leaf extract (250 mg /kg body weight) for 6 days. The fourth protective group, received leaf extract plus diclofenac for 6 days as shown in groups 2 and 3. Diclofenac significantly increased serum AST, ALT, and decreased albumin and total proteins levels. It also increased serum concentrations of uric acid and creatinine. In addition, it increased lipid peroxidation, and decreased reduced glutathione and superoxide dismutase levels. Diclofenac increased inflammatory cytokines secretion and up-regulated hepatic oxidative stress genes (HO-1; hemoxygenase-1 and Nrf2nuclear factor erythroid 2-related factor 2 (Nrf2) and renal inflammatory transcriptional markers (TGF-β1; transforming growth factor-beta1 and COX-2; cycloxygenas-2). In parallel, hepatic caspase-3 expression was up-regulated as an apoptotic marker, while Bcl2; (B-cell lymphoma 2) mRNA expression was down regulated as anti-apoptotic marker. pre-administration in the protective group ameliorated the altered parameters induced by diclofenac. In conclusion, leaf extract has the potential to antagonize side effects of diclofenac by regulating the pathways of oxidative stress, inflammation, and apoptosis/antiapoptosis.
当前研究考察了来自塔伊夫地区(高海拔地区)的叶提取物对双氯芬酸诱导的实验大鼠肝毒性和肾毒性的增强作用。假人参在塔伊夫地区作为具有多种功能的环境草本植物大量生长。双氯芬酸是一种用于治疗疼痛的非甾体类药物,但过量服用会有严重的副作用。32只成年雄性Wistar大鼠被分为4组。对照组大鼠(第1组)接受生理盐水。第二组在第4天和第5天接受双氯芬酸(50毫克/千克体重,腹腔注射)。第三组接受叶提取物(250毫克/千克体重),持续6天。第四保护组,如第2组和第3组所示,接受叶提取物加双氯芬酸,持续6天。双氯芬酸显著增加血清天冬氨酸转氨酶、丙氨酸转氨酶,并降低白蛋白和总蛋白水平。它还增加了血清尿酸和肌酐浓度。此外,它增加了脂质过氧化,并降低了还原型谷胱甘肽和超氧化物歧化酶水平。双氯芬酸增加了炎性细胞因子的分泌,并上调了肝脏氧化应激基因(血红素加氧酶-1;HO-1和核因子红细胞2相关因子2;Nrf2)以及肾脏炎性转录标志物(转化生长因子-β1;TGF-β1和环氧化酶-2;COX-2)。同时,肝脏半胱天冬酶-3表达作为凋亡标志物被上调,而B细胞淋巴瘤2;(Bcl2)mRNA表达作为抗凋亡标志物被下调。保护组的预先给药改善了双氯芬酸诱导的参数变化。总之,叶提取物有潜力通过调节氧化应激、炎症和凋亡/抗凋亡途径来拮抗双氯芬酸的副作用。