Abstract | BACKGROUND/AIMS: METHODS: MMP-9 and its proform were assayed using SDS-PAGE and in situ gelatin zymographies. Brain extravasation was assessed with Evans blue. Brain water was determined by specific gravity and astrocytic endfoot swelling by electron microscopy. FHF in mice was induced by azoxymethane. MMP inhibitor GM6001 and MMP-9 monoclonal antibody were used. RESULTS: Active MMP-9 was significantly increased at the onset of coma and brain extravasation in FHF mice. Blocking MMP-9 with either GM6001 or MMP-9 monoclonal antibody significantly attenuated brain extravasation, astrocytic endfoot swelling, and brain edema. Brains of FHF mice did not show MMP-9 activity. In contrast, livers of these animals showed marked up-regulation of MMP-9 activity. CONCLUSIONS: Our findings suggest that MMP-9 contributes to the pathogenesis of brain extravasation and edema in FHF. The necrotic liver is the source of MMP-9 in FHF. Inhibition of MMP-9 may protect against the development of brain edema in FHF.
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Authors | Justin H Nguyen, Satoshi Yamamoto, Jeffery Steers, Daniel Sevlever, Wenlang Lin, Naoki Shimojima, Monica Castanedes-Casey, Petrina Genco, Todd Golde, Elliott Richelson, Dennis Dickson, Michael McKinney, Christopher B Eckman |
Journal | Journal of hepatology
(J Hepatol)
Vol. 44
Issue 6
Pg. 1105-14
(Jun 2006)
ISSN: 0168-8278 [Print] Netherlands |
PMID | 16458990
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Matrix Metalloproteinase Inhibitors
- Evans Blue
- Matrix Metalloproteinase 9
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Topics |
- Animals
- Brain
(enzymology)
- Brain Edema
(enzymology)
- Capillary Permeability
- Evans Blue
(metabolism)
- Liver
(enzymology, pathology)
- Liver Failure, Acute
(enzymology)
- Male
- Matrix Metalloproteinase 9
(genetics, physiology)
- Matrix Metalloproteinase Inhibitors
- Mice
- Mice, Inbred C57BL
- Up-Regulation
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