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Age-related increases in human lymphocyte DNA damage: is there a role of aerobic fitness?

Title
Age-related increases in human lymphocyte DNA damage: is there a role of aerobic fitness?
Type
Article in International Scientific Journal
Year
2013
Authors
soares, jp
(Author)
Other
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mota, mp
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
collins, a
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
gaivao, i
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Journal
Vol. 31
Pages: 743-748
ISSN: 0263-6484
Publisher: Wiley-Blackwell
Scientific classification
FOS: Natural sciences > Biological sciences
Other information
Authenticus ID: P-006-JA5
Abstract (EN): Oxidative stress has been advanced as one of the major causes of damage to DNA and other macromolecules. Although physical exercise may also increase oxidative stress, an important role has been recognized for regular exercise in improving the overall functionality of the body, as indicated by an increase in maximal aerobic uptake (VO2max), and in resistance to cell damage. The aims of this study were 1) to evaluate the association between DNA damage in human lymphocytes and age and 2) to evaluate the association between DNA damage in human lymphocytes and VO2max. The sample was composed of 36 healthy and nonsmoking males, aged from 20 to 84 years. VO2max was evaluated through the Bruce protocol with direct measurement of oxygen consumption. The comet assay was used to evaluate the DNA damage, strand breaks and formamidopyrimidine DNA glycosylase (FPG)-sensitive sites. We found a positive correlation of age with DNA strand breaks but not with FPG-sensitive sites. VO2max was significantly inversely related with DNA strand breaks, but this relation disappeared when adjusted for age. A significantly positive relation between VO2max and FPG-sensitive sites was verified. In conclusion, our results showed that younger subjects have lower DNA strand breaks and higher VO2max compared with older subjects and FPG-sensitive sites are positively related with VO2max, probably as transient damage due to the acute effects of daily physical activity. Copyright (c) 2013 John Wiley & Sons, Ltd.
Language: English
Type (Professor's evaluation): Scientific
Contact: jotafps@gmail.com
No. of pages: 6
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