4.2 Article

Long-term effects of caloric restriction or exercise on DNA and RNA oxidation levels in white blood cells and urine in humans

期刊

REJUVENATION RESEARCH
卷 11, 期 4, 页码 793-799

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/rej.2008.0712

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资金

  1. NIH [AG20487]
  2. NIH General Clinical Research Center [RR00036]
  3. Diabetes Research Training Center [DK20579]
  4. NIH Clinical Nutrition Research Unit [DK56341]
  5. National Institute on Aging [AG17994, AG21042]
  6. University of Florida Institute on Aging
  7. Claude D. Pepper Older Americans Independence Center NIH [1 P30 AG028740]
  8. General Clinical Research Centre (GCRC) [M01-RR00082]

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Excessive adiposity is associated with increased oxidative stress and accelerated aging. Weight loss induced by negative energy balance reduces markers of oxidation in experimental animals and humans. The long-term effects of weight loss induced by calorie restriction or increased energy expenditure induced by exercise on measures of oxidative stress and damage have not been studied in humans. The objective of the present study was to compare the effects of 20% caloric restriction or 20% exercise alone over I year on oxidative damage to DNA and RNA, as assessed through white blood cell and urine analyses. Eighteen men and women aged 50 to 60 years with a body mass index (BMI) between 23.5 to 29.9 kg/m(2) were assigned to one of two conditions 20% CR (n = 9) or 20% EX (n = 9) - which was designed to produce an identical energy deficit through increased energy expenditure. Compared to baseline, both interventions significantly reduced oxidative damage to both DNA (48.5% and 49.6% reduction for the CR and EX groups, respectively) and RNA (35.7% and 52.1% reduction for the CR and EX groups, respectively) measured in white blood cells. However, urinary levels of DNA and RNA oxidation products did not differ from baseline values following either 12-month intervention program. Data from the present study provide evidence that negative energy balances induced through either CR or EX result in substantial and similar improvements in markers of DNA and RNA damage to white blood cells, potentially by reducing systemic oxidative stress.

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