Deniz Esra, Topcu Atilla, Ozturk Aykut, Ozturk Seda Duman, Akyildiz Kerimali
Department of Pharmacology, Faculty of Medicine, Recep Tayyip Erdogan University, Rize 53100, Turkey.
Department of Pharmacology, Faculty of Medicine, Recep Tayyip Erdogan University, Rize 53100, Turkey.
Tissue Cell. 2025 Oct;96:102967. doi: 10.1016/j.tice.2025.102967. Epub 2025 May 15.
Methotrexate (MTX)-induced hepatotoxicity is linked to oxidative damage and inflammatory processes. Hedera helix folium (HHF) extract protects cells against oxidative damage. We investigated the role of HHF extract in tumor necrosis factor alpha (TNF-α) and interleukin-10 (IL-10)-associated inflammation and oxidative stress in the pathology of MTX-associated liver injury in rats. Forty male rats were divided into one of five equal groups: Control, HHF, MTX, H+MTX and H+MTX. HHF extract was administered via the oral route at 100 mg/kg or 200 mg/kg once daily for seven days, while MTX was administered as a single dose of 20 mg/kg intraperitoneally. Intracardiac blood samples and liver tissue samples were collected at the conclusion of the experiment. Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels increased due to MTX. Increased ALT levels were significantly reduced by low-dose HHF and increased AST levels were significantly reduced by high-dose HHF administration. The application of MTX significantly increased malondialdehyde (MDA) and TNF-α levels, while significantly reducing those of glutathione (GSH) and IL-10. High-dose HHF also significantly lowered MDA and TNF-α levels, while significantly increasing those of GSH and IL-10. Histopathological damage findings observed due to MTX were significantly attenuated with high-dose HHF. In addition, the increased caspase-3, p53, and Bcl2 levels caused by MTX decreased with high-dose HHF administration. HHF extract can alleviate liver damage induced by MTX. This extract, which has the ability to reduce damage due to oxidative stress and inflammation, may represent an alternative approach to preventing MTX-induced liver damage.
甲氨蝶呤(MTX)诱导的肝毒性与氧化损伤和炎症过程有关。常春藤叶提取物(HHF)可保护细胞免受氧化损伤。我们研究了HHF提取物在大鼠MTX相关性肝损伤病理过程中肿瘤坏死因子α(TNF-α)和白细胞介素-10(IL-10)相关炎症及氧化应激中的作用。40只雄性大鼠被分为五个相等的组之一:对照组、HHF组、MTX组、H+MTX组和H+MTX组。HHF提取物以100mg/kg或200mg/kg的剂量经口给药,每日一次,共七天,而MTX以20mg/kg的单剂量腹腔注射。实验结束时采集心内血样和肝组织样本。MTX导致血清丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)水平升高。低剂量HHF可显著降低升高的ALT水平,高剂量HHF给药可显著降低升高的AST水平。MTX的应用显著增加了丙二醛(MDA)和TNF-α水平,同时显著降低了谷胱甘肽(GSH)和IL-10水平。高剂量HHF也显著降低了MDA和TNF-α水平,同时显著增加了GSH和IL-10水平。MTX导致的组织病理学损伤结果在高剂量HHF作用下显著减轻。此外,MTX引起的半胱天冬酶-3、p53和Bcl2水平升高在高剂量HHF给药后降低。HHF提取物可减轻MTX诱导的肝损伤。这种具有减轻氧化应激和炎症损伤能力的提取物可能代表了一种预防MTX诱导肝损伤的替代方法。