ANTIOXIDATIVE ROLES OF METALLOTHIONEIN AND MANGANESE SUPEROXIDE-DISMUTASE INDUCED BY TUMOR-NECROSIS-FACTOR-ALPHA AND INTERLEUKIN-6
Citation
M. Sato et al., ANTIOXIDATIVE ROLES OF METALLOTHIONEIN AND MANGANESE SUPEROXIDE-DISMUTASE INDUCED BY TUMOR-NECROSIS-FACTOR-ALPHA AND INTERLEUKIN-6, Archives of biochemistry and biophysics, 316(2), 1995, pp. 738-744
Categorie Soggetti
Biology,Biophysics
SICI code
0003-9861(1995)316:2<738:AROMAM>2.0.ZU;2-G
Abstract
Antioxidative roles of metallothionein (MT) and manganese superoxide d
ismutase (Mn-SOD) induced by tumor necrosis factor (TNF) and interleuk
in 6 (IL-6) have been studied. Since pretreatment of rat with dexameth
asone, an inhibitor of cytokine production, prevented MT synthesis ind
uced by paraquat which is a typical superoxide generator, MT synthesis
by oxidative stress may be, at least partly, mediated through cytokin
es. Pretreatment of rat with TNF or IL-6 prevented liver damage and li
pid peroxidation caused by carbon tetrachloride. Administration of TNF
increased activity of mitochondrial Mn-SOD and concentrations of cyto
plasmic MT, but not activities of glutathione peroxidases and Cu,Zn-SO
D in the liver. The increment of the Mn-SOD activity and MT was due to
the de novo protein synthesis, because gene expression of mRNAs of Mn
-SOD and MT in the liver was also induced by TNF and IL-6. These data
strongly suggest that MT and Mn-SOD in the liver cooperatively play an
tioxidative roles. Pretreatment with TNF, however, did not affect the
increased levels of plasma fibrinogen and liver MT induced by the foll
owing paraquat treatment, although it did prevent lipid peroxidation i
n the liver. The data suggest that MT is not directly induced by oxyge
n free radicals. Cytokines may be released by paraquat in tissues othe
r than the liver and induce hepatic synthesis of acute phase proteins
including fibrinogen, MT, and Mn-SOD. MT and Mn-SOD induced by cytokin
es in the liver exert an antioxidative role during acute phase respons
e, therefore preventing tissues from injury by oxidative stress. (C) 1
995 Academic Press, Inc.