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- Title
Brain gene expression, metabolism, and bioenerg, interrelationships in murine models of cerebral and noncerebral malaria.
- Authors
Rae, Caroline; McQuillan, James A.; Parekh, Sapan B.; Bubb, William A.; Weiser, Silvia; Balcar, Vladimir J.; Hansen, Anna M.; Ball, Helen J.; Hunt, Nicholas H.
- Abstract
Malaria infection can cause cerebral symptoms without parasite invasion of brain tissue. We examined the relationships between brain biochemistry, bioenergetics, and gene expression in murine models of cerebral (Plasmodium berghei ANKA) and noncerebral (P. berghei K173) malaria using multinuclear NMR spectroscopy, neuropharmacological approaches, and real-time RT-PCR. In cerebral malaria caused by P. berghei ANKA infection, we found biochemical changes consistent with increased glutamatergic activity and decreased flux through the Krebs cycle, followed by increased production of the hypoxia markers lactate and alanine. This was accompanied by compromised brain bioenergetics. There were few significant changes in expression of mRNA for metabolic enzymes or transporters or in the rate of transport of glutamate or glucose. However, in keeping with a role for endogenous cytokines in malaria cerebral pathology, there was significant up-regulation of mRNAs for TNF-α, interferon-γ, and lymphotoxin, These changes are consistent with a state of cytopathic hypoxia. By contrast, in P. berghei K173 infection the brain showed increased metabolic rate, with no deleterious effect on bioenergetics. This was accompanied by mild up-regulation of expression of metabolic enzymes. These changes are consistent with benign hypermetabolism whose cause remains a subject of speculation.
- Subjects
MALARIA; BRAIN; LABORATORY mice; BIOENERGETICS; HYPOXEMIA
- Publication
FASEB Journal, 2004, Vol 18, Issue 3, p499
- ISSN
0892-6638
- Publication type
Article
- DOI
10.1096/fj.03-0543com