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

xlomafota13 shared this article with you from Inoreader Hesperetin attenuates silica-induced lung injury by reducing oxidative damage and inflammatory response Via Experimental and therapeutic medicine Exp Ther Med. 2021 Apr;21(4):297. doi: 10.3892/etm.2021.9728. Epub 2021 Jan 28. ABSTRACT 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 malondiald ehyde (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-β1, reduce the production of pro-inflammatory cytokines IL-1β, IL-4, TNF-α and increase the levels of anti-inflammatory factors IFN-γ and IL-10. The current study demonstrated that HSP can effectively attenuate silica-induced lung injury by reducing oxidative damage and the inflammatory response. PMID:3371724 0 | PMC:PMC7885076 | DOI:10.3892/etm.2021.9728 View on the web Inoreader. Take back control of your news feed. Follow us on Twitter and Facebook.