4.5 Article

Preventive effect of neutropenia on carbon tetrachloride-induced hepatotoxicity in rats

Journal

JOURNAL OF APPLIED TOXICOLOGY
Volume 26, Issue 2, Pages 178-186

Publisher

WILEY
DOI: 10.1002/jat.1122

Keywords

carbon tetrachloride; hepatotoxicity (rat); neutropenia; myeloperoxidase; reduced glutathione; superoxide dismutase; xanthine oxidase; reactive oxygen species metabolism

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The preventive effect of neutropenia on carbon tetrachloride (CCI4)-induced hepatotoxicity was examined in rats. In rats treated once with CCI4 (1 ml kg(-1), i.p.), the serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST), indices of liver cell damage, and the hepatic activity of myeloperoxidase (MPO), an index of tissue neutrophil infiltration, increased at 6 h after the intoxication and further increased at 24 h. The liver of CCI4-treated rats showed an increase in the concentration of thiobarbituric acid reactive substances (TBARS), an index of lipid peroxidation, and decreases in superoxide dismutase (SOD) activity and reduced glutathione (GSH) concentration at 6 h after the intoxication followed by a further increase in TBARS concentration and further decreases in SOD activity and GSH concentration at 24 h with increased xanthine oxidase (XO) activity at 24 h. Neutropenic treatment with anti-rat neutrophil antiserum (2 ml kg(-1), i.p.) at 0.5 h after CCI4 intoxication attenuated the increases in serum ALT and AST activities and hepatic NIPO activity and TBARS concentration and the decreases in hepatic SOD activity and GSH concentration found at 6 and 24 h after CCI4 intoxication and the increase in hepatic XO activity found at 24 h after the intoxication. This neutropenia reduced the necrotic and degenerative changes with inflammatory cell infiltration in the liver cell of CCI4- treated rats. These results indicate that neutropenia prevents CCI4-induced hepatotoxicity in rats by attenuating the disruption of hepatic reactive oxygen species metabolism mediated by neutrophils accumulating in the liver tissue. Copyright (c) 2005 John Wiley & Sons, Ltd.

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