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Enhanced hippocampus‐dependent memory and reduced anxiety in mice over‐expressing human catalase in mitochondria
Author(s) -
Olsen Reid H. J.,
Johnson Lance A.,
Zuloaga Damian G.,
Limoli Charles L.,
Raber Jacob
Publication year - 2013
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/jnc.12187
Subject(s) - catalase , oxidative stress , reactive oxygen species , hippocampus , mitochondrion , lipid peroxidation , endocrinology , elevated plus maze , synaptic plasticity , glutathione , medicine , oxidative phosphorylation , biology , psychology , anxiety , neuroscience , chemistry , microbiology and biotechnology , biochemistry , enzyme , psychiatry , receptor
Abstract Oxidative stress ( OS ) and reactive oxygen species ( ROS ) play a modulatory role in synaptic plasticity and signaling pathways. Mitochondria ( MT ), a major source of ROS because of their involvement in energy metabolism, are important for brain function. MT ‐generated ROS are proposed to be responsible for a significant proportion of OS and are associated with developmental abnormalities and aspects of cellular aging. The role of ROS and MT function in cognition of healthy individuals is relatively understudied. In this study, we characterized behavioral and cognitive performance of 5‐ to 6‐month‐old mice over‐expressing mitochondrial catalase ( MCAT ). MCAT mice showed enhancements in hippocampus‐dependent spatial learning and memory in the water maze and contextual fear conditioning, and reduced measures of anxiety in the elevated zero maze. Catalase activity was elevated in MCAT mice in all brain regions examined. Measures of oxidative stress (glutathione, protein carbonyl content, lipid peroxidation, and 8‐hydroxyguanine) did not significantly differ between the groups. The lack of differences in these markers of oxidative stress suggests that the differences observed in this study may be due to altered redox signaling. Catalase over‐expression might be sufficient to enhance cognition and reduce measures of anxiety even in the absence of alteration in levels of OS .

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