4.5 Article

Behavioral and metabolic characterization of heterozygous and homozygous POLG mutator mice

期刊

MITOCHONDRION
卷 13, 期 4, 页码 282-291

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.mito.2013.03.006

关键词

mtDNA polymerase gamma; mtDNA mutation; Parkinson's disease; Dopamine; Behavioral deficits; Metabolic deficits

资金

  1. National Institute on Aging [1R03AG035223-01]
  2. National Institute of Neurological Disorders and Stroke [1R21NS077758]

向作者/读者索取更多资源

The mitochondrial DNA (mtDNA) polymerase (POLG) mutator mice provide the first experimental evidence that high levels of somatic mtDNA mutations can be functionally significant. Here we report that older homozygous, but not heterozygous, POLG mice show significant reductions in striatal dopaminergic terminals as well as deficits in motor function. However, resting oxygen consumption, heat production, mtDNA content and mitochondrial electron transport chain activities are significantly decreased at older ages in both homozygous and heterozygous mice. These results indicate that high levels of somatic mtDNA mutations can contribute to dopaminergic dysfunction and to behavioral and metabolic deficits. (c) 2013 Elsevier B.V. and Mitochondria Research Society. All rights reserved.

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