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  4. The Gastroprotective Effect of Naringenin against Ethanol-Induced Gastric Ulcers in Mice through Inhibiting Oxidative and Inflammatory Responses
 
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The Gastroprotective Effect of Naringenin against Ethanol-Induced Gastric Ulcers in Mice through Inhibiting Oxidative and Inflammatory Responses

Journal
International Journal of Molecular Sciences
Journal Volume
22
Journal Issue
21
Pages
11985
Date Issued
2021-11
Author(s)
Wei-Sung Li  
Shih-Chao Lin
Chien-Hui Chu
Yu-Kang Chang
Xiang Zhang
Chi-Chien Lin
Yu-Tang Tung
DOI
10.3390/ijms222111985
URI
https://www.mdpi.com/1422-0067/22/21/11985
https://scholars.tari.gov.tw/handle/123456789/16409
Abstract
Naringenin is a major flavanone found in grapes, tangelos, blood oranges, lemons, pummelo, and tangerines. It is known to have anti-inflammatory, antioxidant, anticancer, antimutagenic, antifibrogenic, and antiatherogenic pharmacological properties. This study aims to investigate the anti-inflammatory effects of naringenin in ethanol-induced gastric damage in vivo and ethanol-stimulated KATO III cells in vitro. Our results showed that pretreatment with naringenin significantly protected mice from ethanol-induced hemorrhagic damage, epithelial cell loss, and edema with leucocytes. It reduced gastric ulcers (GU) by suppressing ethanol-induced nuclear factor-kappa B (NF-kappa B) activity and decreasing the levels of nitric oxide (NO), malondialdehyde (MDA), tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), interleukin-8 (IL-8), and myeloperoxidase (MPO). In addition, pretreatment with naringenin might inhibit the secretion of TNF-alpha, IL-6, and IL-8, as well as the proteins cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) via the suppression of NF-kappa B and mitogen-activated protein kinase (MAPK) signaling in ethanol-stimulated stomach epithelial KATO III cells. Together, the results of this study highlight the gastroprotective effect of naringenin in GU of mice by inhibiting gastric secretion and acidity, reducing inflammation and oxidative stress, suppressing NF-kappa B activity, and restoring the histological architecture. These findings suggested that naringenin has therapeutic potential in the alleviation of ethanol-induced GU.
Subjects
gastric ulcers
naringenin
ethanol
inflammation
oxidative stress
Publisher
MDPI
Description
This article belongs to the Special Issue Plant-Food-Derived Bioactives for Disorders Related to Oxidative Stress and Inflammation
Type
journal article

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