Hesperetin attenuates silica-induced lung injury by reducing oxidative damage and inflammatory response

被引:16
|
作者
Li, Shuxian [1 ]
Shao, Linlin [2 ]
Fang, Jinguo [3 ]
Zhang, Juan [1 ]
Chen, Yanqin [1 ]
Yeo, Abrey J. [4 ]
Lavin, Martin F. [4 ]
Yu, Gongchang [1 ]
Shao, Hua [1 ]
机构
[1] Shandong First Med Univ & Shandong Acad Med Sci, Shand Acad Occupat Hlth & Occupat Med, 18877 Jingshi Rd, Jinan 250062, Shandong, Peoples R China
[2] Shandong First Med Univ, Shandong Prov Hosp, Dept Neurol, Jinan 250021, Shandong, Peoples R China
[3] Linqing Hlth Bur, Primary Hlth Dept, Linqing 252600, Shandong, Peoples R China
[4] Univ Queensland, Ctr Clin Res, Brisbane, Qld 4072, Australia
基金
美国国家科学基金会;
关键词
silica; hesperetin; lung injury; fibrosis; oxidative stress; inflammatory response; rat;
D O I
10.3892/etm.2021.9728
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Oxidative stress and the inflammatory response are two important mechanisms of silica-induced lung injury. Hesperetin (HSP) is a natural flavonoid compound that is found in citrus fruits and has been indicated to exhibit strong antioxidant and anti-inflammatory properties. The current study evaluated the protective effect of HSP on lung injury in rats exposed to silica. The results indicated that the degree of alveolitis and pulmonary fibrosis in the HSP-treated group was significantly decreased compared with the silica model group. The content of hydroxyproline (HYP) was also revealed to decrease overall in the HSP treated group compared with the silica model group, indicating that the degree of pulmonary fibrosis was decreased compared with the silica model group. The present study also demonstrated that HSP reduced oxidation levels of malondialdehyde (MDA) and increased the activities of antioxidant enzymes superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GSH-PX). Total antioxidant capacity (T-AOC) was also increased following HSP treatment, indicating that HSP can alleviate oxidative stress in the lung tissue of silica-exposed rats. In addition, HSP was revealed to inhibit the synthesis and secretion of fibrogenic factor TGF-beta 1, reduce the production of pro-inflammatory cytokines IL-1 beta, IL-4, TNF-alpha and increase the levels of anti-inflammatory factors IFN-gamma and IL-10. The current study demonstrated that HSP can effectively attenuate silica-induced lung injury by reducing oxidative damage and the inflammatory response.
引用
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页数:11
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