Abbaszadeh Mohammad Ebrahim, Khezri Mohammad Rafi, Ghasemnejad-Berenji Morteza
Department of Anatomical Sciences, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Urmia University of Medical Sciences, Urmia, Iran.
Adv Pharmacol Pharm Sci. 2025 Apr 6;2025:5227142. doi: 10.1155/adpp/5227142. eCollection 2025.
Bleomycin, an antibacterial antibiotic, is used in chemotherapy and is effective against various forms of human carcinomas. However, its use is limited due to its tendency to cause pulmonary fibrosis. Oxidative stress and excessive expression of TGF beta occur in pulmonary fibrosis, leading to cellular death, inflammation, and additional damage to lung tissue. Metformin has the ability to reduce oxidative stress and lower the level of TGF beta by activating AMPK. Additionally, ascorbic acid possesses potent antioxidant characteristics. Consequently, we decided to investigate the effects of these two medications on pulmonary fibrosis and compare with methyl prednisolone. Thirty-six adult mice were categorized into 6 distinct groups: Control, bleomycin (bleo), bleo + methyl prednisolone, bleo + metformin, bleo + ascorbic acid, bleo + metformin + ascorbic acid. Pulmonary fibrosis was induced by the administration of bleomycin in all groups, except for the control group. Subsequently, medications were administered for a duration of 14 days. Ultimately, the mice were sacrificed and lung tissues were obtained for biochemical and histological examination. As shown by biochemical and histological analysis, all treatment groups showed a decrease in oxidative stress factors, inflammation, and lung tissue fibrosis; however, the effects of administering metformin and ascorbic acid together were noticeable. Our study found that administering metformin and ascorbic acid over a period of 14 days, either alone or in combination, may contribute to the repair of pulmonary fibrosis. However, our data indicate that the combined therapy of these drugs provided a better result.
博来霉素是一种抗菌抗生素,用于化疗,对多种人类癌症有效。然而,由于其有导致肺纤维化的倾向,其应用受到限制。氧化应激和转化生长因子β(TGF-β)的过度表达在肺纤维化中出现,导致细胞死亡、炎症以及对肺组织的进一步损伤。二甲双胍有能力通过激活腺苷酸活化蛋白激酶(AMPK)来降低氧化应激并降低TGF-β水平。此外,抗坏血酸具有强大的抗氧化特性。因此,我们决定研究这两种药物对肺纤维化的影响,并与甲基强的松龙进行比较。36只成年小鼠被分为6个不同的组:对照组、博来霉素组(博来霉素)、博来霉素+甲基强的松龙组、博来霉素+二甲双胍组、博来霉素+抗坏血酸组、博来霉素+二甲双胍+抗坏血酸组。除对照组外,所有组均通过给予博来霉素诱导肺纤维化。随后,给药14天。最终,处死小鼠并获取肺组织进行生化和组织学检查。生化和组织学分析表明,所有治疗组的氧化应激因子、炎症和肺组织纤维化均有所降低;然而,同时给予二甲双胍和抗坏血酸的效果显著。我们的研究发现,单独或联合给予二甲双胍和抗坏血酸14天可能有助于肺纤维化的修复。然而,我们的数据表明,这些药物的联合疗法效果更好。