| Literature DB >> 20005284 |
Glen E Kisby1, Steven G Kohama, Antoinette Olivas, Mona Churchwell, Daniel Doerge, Edward Spangler, Rafael de Cabo, Donald K Ingram, Barry Imhof, Gaobin Bao, Yoke W Kow.
Abstract
Apyrimidinic/apurinic endonuclease (APE) is a key protein involved in the base-excision DNA repair (BER) pathway of oxidative DNA lesions. Using a novel oligonucleotide substrate, we demonstrate that APE activity in the frontal/parietal cortex (F/PCTX), cerebellum, brainstem, midbrain and hypothalamus declined with age in rats on an ad libitum (AL) diet. In contrast, APE activity for these brain regions was approximately 1.5-3 times higher in young, caloric restricted (CR) rats. Despite continuous CR treatment in all animals since six weeks of age, APE activity in the CR group started to decline by middle-age and continued into old age. However, CR maintained APE activity at a level that was significantly higher than that in AL rats across age and in the brain regions examined. Because Western analysis of APE, DNA polymerase beta and DNA ligase III levels in the F/PCTX of both CR and AL rats remained unchanged with age, this suggests that the increased APE activity in CR rats is the result of differential post-translational modification of APE. Copyright 2009 Elsevier Inc. All rights reserved.Entities:
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Year: 2009 PMID： 20005284 PMCID： PMC2826610 DOI： 10.1016/j.exger.2009.12.003
Source DB: PubMed Journal: Exp Gerontol ISSN： 0531-5565 Impact factor: 4.032