Protective effect of luteolin against oxidative stress‑mediated cell injury via enhancing antioxidant systems

• Published in: Molecular medicine reports Vol. 30; no. 1
• Main Authors: Fernando, Pincha Devage Sameera Madushan, Ko, Dong Ok, Piao, Mei Jing, Kang, Kyoung Ah, Herath, Herath Mudiyanselage Udari Lakmini, Hyun, Jin Won
• Format: Journal Article
• Language: English
• Published: Greece Spandidos Publications 01.07.2024; D.A. Spandidos
• Subjects: Analysis; Animals; Antioxidants; Antioxidants - pharmacology; Apoptosis - drug effects; Cell Line; Cell Survival - drug effects; Cricetinae; Cricetulus; DNA damage; Fibroblasts - drug effects; Fibroblasts - metabolism; Hydrogen Peroxide - pharmacology; Hydrogen Peroxide - toxicity; Lipid peroxidation; Lipid Peroxidation - drug effects; Luteolin - pharmacology; Oxidative stress; Oxidative Stress - drug effects; Reactive oxygen species; Reactive Oxygen Species - metabolism; South Korea; antioxidant enzyme; lung fibroblast; luteolin; apoptosis; oxidative stress
• ISSN: 1791-2997; 1791-3004
• DOI: 10.3892/mmr.2024.13244

Physiological stress such as excessive reactive oxygen species (ROS) production may contribute normal fibroblasts activation into cancer‑associated fibroblasts, which serve a crucial role in certain types of cancer such as pancreatic, breast, liver and lung cancer. The present study aimed to examine the cytoprotective effects of luteolin (3',4',5,7‑tetrahydroxyflavone) against hydrogen peroxide (H O )‑generated oxidative stress in lung fibroblasts. To examine the effects of luteolin against H O ‑induced damages, cell viability, sub‑G cell population, nuclear staining with Hoechst 33342, lipid peroxidation and comet assays were performed. To evaluate the effects of luteolin on the protein expression level of apoptosis, western blot assay was performed. To assess the antioxidant effects of luteolin, detection of ROS using H DCFDA staining, O ‑ and ·OH using electron spin resonance spectrometer and antioxidant enzyme activity was performed. In a cell‑free chemical system, luteolin scavenges superoxide anion and hydroxyl radical generated by xanthine/xanthine oxidase and the Fenton reaction (FeSO /H O ). Furthermore, Chinese hamster lung fibroblasts (V79‑4) treated with H O showed a significant increase in cellular ROS. Intracellular ROS levels and damage to cellular components such as lipids and DNA in H O ‑treated cells were significantly decreased by luteolin pretreatment. Luteolin increased cell viability, which was impaired following H O treatment and prevented H O ‑mediated apoptosis. Luteolin suppressed active caspase‑9 and caspase‑3 levels while increasing Bcl‑2 expression and decreasing Bax protein levels. Additionally, luteolin restored levels of glutathione that was reduced in response to H O . Moreover, luteolin enhanced the activity and protein expressions of superoxide dismutase, catalase, glutathione peroxidase, and heme oxygenase‑1. Overall, these results indicated that luteolin inhibits H O ‑mediated cellular damage by upregulating antioxidant enzymes.