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Neurochem Int. 2014 Apr;69:35-40. doi: 10.1016/j.neuint.2014.02.008. Epub 2014 Mar 7.

Systemic injection of LPS induces region-specific neuroinflammation and mitochondrial dysfunction in normal mouse brain.

Author information

1
Department of Molecular & Life Sciences, Hanyang University, Republic of Korea.
2
Department of Molecular & Life Sciences, Hanyang University, Republic of Korea. Electronic address: hseo@hanyang.ac.kr.

Abstract

Lipopolysaccharide (LPS) administration may be used to induce an in vivo model for neuroinflammation or neurodegeneration. We examined the regional distribution of inflammatory markers induced by LPS in the brain of young mice. Criteria for inflammation included measures of cytokines and microglial activation. Levels of IL-1β mRNA increased in the frontal cortex, parietal cortex, hippocampus, and striatum following systemic treatment with LPS. Levels of SRA mRNA increased in the frontal cortex and striatum and levels of TLR2 and TLR4 mRNAs increased in the frontal cortex and cerebellum. Iba1-positive microglial cells increased in the striatum, medial septum, frontal cortex, and hippocampus after LPS treatment. In addition, glutathione (GSH) levels decreased and mitochondrial complex II/III activities increased after systemic LPS injection. Although LPS treatment did not significantly alter cellular ATP levels, these levels correlated with levels of IL-1β and TLR4 in the LPS-treated mice. The region-specific inflammatory response to LPS in the brain may serve to create a model for studies of neurodegenerative disease.

KEYWORDS:

LPS; Mitochondrial dysfunction; Neuroinflammation

PMID:
24607701
DOI:
10.1016/j.neuint.2014.02.008
[Indexed for MEDLINE]

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