Selenium supplementation decreases hepatic fibrosis in mice after chronic carbon tetrachloride administration

Ding, M; Potter, JJ; Liu, X; Torbenson, MS; Mezey, E

HERO ID

652482

Reference Type

Journal Article

Year

2010

Language

English

PMID

19488682

HERO ID 652482
In Press No
Year 2010
Title Selenium supplementation decreases hepatic fibrosis in mice after chronic carbon tetrachloride administration
Authors Ding, M; Potter, JJ; Liu, X; Torbenson, MS; Mezey, E
Journal Biological Trace Element Research
Volume 133
Issue 1
Page Numbers 83-97
Abstract Oxidative stress stimulates fibrogenesis, and selenium (Se) has antioxidant properties. This study determined whether Se supplementation affects CCl(4)-induced liver injury and fibrosis. Mice were administered CCl(4) over 4 weeks, while controls received olive oil. Se was provided as sodium selenite in the drinking water. Se increased liver Se-dependent glutathione peroxidase activity and decreased liver malondialdehyde after CCl(4). Se decreased liver inflammation but not necrosis caused by CCl(4). Se increased hepatocyte apoptosis after CCl(4) and the pro-apoptotic BAX and Bcl Xs/l proteins. Stellate cell apoptosis occurred only after CCl(4) in Se-supplemented mice. Se decreased stellate cell number and fibrosis after CCl(4). Liver matrix metalloproteinase-9 increased after CCl(4) with Se supplementation. In conclusion, Se supplementation decreased hepatic fibrosis after CCl(4) in the setting of decreased inflammation but increased apoptosis. The principal mechanisms for the decreased fibrosis are a lower number of collagen-producing stellate cells and increased collagen degradation.
Doi 10.1007/s12011-009-8414-x
Pmid 19488682
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword Animals; *Carbon Tetrachloride/toxicity; *Carbon Tetrachloride Poisoning; *Dietary Supplements; Liver/*drug effects/injuries; Liver Cirrhosis/chemically induced; Male; Mice; Mice, Inbred C57BL; Reference Standards; Selenium/administration & dosage/*pharmacology
Is Qa No