Protective effect of diallyl trisulfide against naphthalene-induced oxidative stress and inflammatory damage in mice
Author(s) -
Fang Zhang,
Yongchun Zhang,
Kaiming Wang,
Guangpu Liu,
Min Yang,
Zhongxi Zhao,
Shanzhong Li,
Cai J.,
JiMin Cao
Publication year - 2016
Publication title -
international journal of immunopathology and pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.724
H-Index - 53
eISSN - 2058-7384
pISSN - 0394-6320
DOI - 10.1177/0394632015627160
Subject(s) - oxidative stress , malondialdehyde , superoxide dismutase , chemistry , myeloperoxidase , glutathione , diallyl trisulfide , nitric oxide , tumor necrosis factor alpha , pharmacology , biochemistry , medicine , inflammation , enzyme , apoptosis , organic chemistry
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.
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