Abdelall Ali M Ali, Khames Ali, Bekhit Amany Abdlrehim, Fathy Moustafa
Department of Biochemistry, Faculty of Pharmacy, Sohag University, Sohag, 82511, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Sohag University, Sohag, 82511, Egypt.
Inflammation. 2025 Aug;48(4):2407-2416. doi: 10.1007/s10753-024-02198-w. Epub 2024 Nov 27.
Numerous chemotherapeutic medications can have hazardous effects on the lungs, which can result in severe lung diseases. Methotrexate (MTX) is prescribed for cancer and inflammation-related disorders; nevertheless, it is exceptionally highly toxic and has multiple kinds of adverse reactions, including pulmonary injury. Our work was designed to demonstrate the ability of etoricoxib (ETO) to mitigate MTX-induced lung injury in experimental animals. Adult male Wistar rats were separated into four groups. The first group consisted of healthy controls that received carboxymethyl cellulose (1 ml/day, p.o.), the second group received a single dose of MTX (20 mg/kg/day, i.p.), the third group received ETO (10 mg/kg/day, p.o.) for three weeks, and the fourth group first received a single MTX (20 mg/kg, i.p.) and then was treated with ETO for three weeks. Concomitant treatment with ETO and MTX improved the histological structure of the lung tissue. It significantly altered the levels of oxidant/antioxidant markers, such as malondialdehyde (MDA), heme oxygenase-1 (HO-1), reduced glutathione (GSH), and nuclear factor erythroid 2-related factor 2 (Nrf-2), in favor of antioxidants. Moreover, ETO can normalize the proinflammatory cascade, which includes tumor necrosis factor-alpha (TNF-α) and interleukin-1 beta (IL-1β). At the molecular level, ETO downregulated the protein expression of toll-like receptor 4 (TLR4), nuclear factor kappa-B (NF-κB), and p38 mitogen-activated protein kinase (p38 MAPK) in inflamed rat lungs. In conclusion, our findings indicate that oral administration of ETO ameliorates MTX-induced lung injury by inhibiting oxidative stress and suppressing the TLR4/NF-κB and TLR4/p38-MAPK inflammatory signaling pathways.
许多化疗药物可对肺部产生有害影响,进而导致严重的肺部疾病。甲氨蝶呤(MTX)被用于治疗癌症及与炎症相关的病症;然而,它具有极高的毒性,并会引发多种不良反应,包括肺损伤。我们的研究旨在证明依托考昔(ETO)减轻实验动物中MTX诱导的肺损伤的能力。成年雄性Wistar大鼠被分为四组。第一组为健康对照组,给予羧甲基纤维素(1毫升/天,口服);第二组接受单次剂量的MTX(20毫克/千克/天,腹腔注射);第三组连续三周给予ETO(10毫克/千克/天,口服);第四组先接受单次MTX(20毫克/千克,腹腔注射),然后连续三周接受ETO治疗。ETO与MTX联合治疗改善了肺组织的组织结构。它显著改变了氧化/抗氧化标志物的水平,如丙二醛(MDA)、血红素加氧酶-1(HO-1)、还原型谷胱甘肽(GSH)和核因子红细胞2相关因子2(Nrf-2),使其向有利于抗氧化剂的方向变化。此外,ETO可使包括肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)在内的促炎级联反应恢复正常。在分子水平上,ETO下调了炎症大鼠肺组织中Toll样受体4(TLR4)、核因子κB(NF-κB)和p38丝裂原活化蛋白激酶(p38 MAPK)的蛋白表达。总之,我们的研究结果表明,口服ETO可通过抑制氧化应激和抑制TLR4/NF-κB以及TLR4/p38-MAPK炎症信号通路来改善MTX诱导的肺损伤。