| Literature DB >> 26813860 |
Fang Zhang1, Yongchun Zhang2, Kaiming Wang1, Guangpu Liu1, Min Yang1, Zhongxi Zhao3, Shanzhong Li4, Jianhua Cai4, Jimin Cao4.
Abstract
The aim of this study was to investigate the possible protective effects of diallyl trisulfide (DATS) against naphthalene-induced oxidative and inflammatory damage in the livers and lungs of mice. Elevated serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels showed significant hepatic damage after the challenge with 100 mg/kg naphthalene. Hepatic malondialdehyde (MDA) contents and the activity of myeloperoxidase (MPO) increased significantly, accompanying a decrease in the hepatic activity of total superoxide dismutase (SOD) and glutathione (GSH) levels after the naphthalene damage. In addition, the serum levels of nitric oxide (NO), tumor necrosis factor α (TNF-α), and interleukin 8 (IL-8) increased significantly in the groups damaged with naphthalene. The main parameters related to oxidative stress and inflammatory responses in the lungs, including the NO, MPO, and GSH contents, were determined, and the histopathological and immunohistochemical changes in the lung and liver tissues were also observed. In the DATS-treated groups, all of the oxidative and inflammatory damage in the serum, liver, and lung tissues were significantly prevented.Entities:
Keywords: diallyl trisulfide; inflammatory; myeloperoxidase; naphthalene; nitric oxide; oxidative
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Year: 2016 PMID: 26813860 PMCID: PMC5806724 DOI: 10.1177/0394632015627160
Source DB: PubMed Journal: Int J Immunopathol Pharmacol ISSN: 0394-6320 Impact factor: 3.219