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Published in: Metabolic Brain Disease 2/2013

01-06-2013 | Original Paper

Microglia contribute to ammonia-induced astrocyte swelling in culture

Authors: Kakulavarapu V. Rama Rao, Monica Brahmbhatt, Michael D. Norenberg

Published in: Metabolic Brain Disease | Issue 2/2013

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Abstract

Brain edema, a lethal complication of acute liver failure (ALF), is believed to be largely cytotoxic due to the swelling of astrocytes. Ammonia, a principal neurotoxin in ALF, has been strongly implicated in the development of the brain edema. It was previously shown that treatment of cultured astrocytes with ammonia (5 mM NH4Cl) results in cell swelling. While ammonia continues to exert a direct effect on astrocytes, it is possible that ammonia can affect other neural cells, particularly microglia. Microglia are capable of evoking an inflammatory response, a process known to contribute to the brain edema. We therefore examined the potential role of microglia in the mechanism of ammonia-induced astrocyte swelling. Conditioned media (CM) derived from ammonia-treated cultured microglia when added to cultured astrocytes resulted in significant cell swelling. Such swelling was synergistically increased when astrocytes were additionally treated with 5 mM ammonia. CM from ammonia-treated microglia also showed significant release of oxy-radicals and nitric oxide into the CM. CM from ammonia-treated microglia containing Tempol (a superoxide scavenger) or uric acid (a peroxynitrite scavenger) when added to astrocytes resulted in marked reduction in the cell swelling. Together, these studies indicate that microglia contribute to the ammonia-induced astrocyte swelling by a mechanism involving oxidative/nitrosative stress.
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Metadata
Title
Microglia contribute to ammonia-induced astrocyte swelling in culture
Authors
Kakulavarapu V. Rama Rao
Monica Brahmbhatt
Michael D. Norenberg
Publication date
01-06-2013
Publisher
Springer US
Published in
Metabolic Brain Disease / Issue 2/2013
Print ISSN: 0885-7490
Electronic ISSN: 1573-7365
DOI
https://doi.org/10.1007/s11011-012-9339-1

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