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Reduction of DNA damage in older healthy adults by Tri E Tocotrienol supplementation
Siok-Fong Chin1, Noor Aini Abdul Hamid, Azian Abdul Latiff
1Department of Biochemistry, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Objective:
The free radical theory of aging (FRTA) suggests that free radicals are the leading cause of deteriorating physiologic function during senescence. Free radicals attack cellular structures or molecules such as DNA resulting in various modifications to the DNA structures. Accumulation of unrepaired DNA contributes to a variety of disorders associated with the aging process.
Methods:
A randomized, double-blinded placebo-controlled study was undertaken to evaluate the effect of Tri E Tocotrienol on DNA damage. Sixty four subjects 37-78 y old completed the study. A daily dose of 160 mg of Tri E Tocotrienol was given for 6 months. Blood samples were analyzed for DNA damage using comet assay, frequency of sister chromatid exchange (SCE), and chromosome 4 aberrations.
Results:
Results showed a significant reduction in DNA damage as measured by comet assay after 3 mo (P < 0.01) and remained low at 6 mo (P < 0.01). The frequency of SCE was also reduced after 6 mo of supplementation (P < 0.05), albeit more markedly in the >50 y-old group (P < 0.01) whereas urinary 8-hydroxy-2'-deoxyguanosine (8-OHdG) levels were significantly reduced (P < 0.05). A strong positive correlation was observed between SCE with age, whereas weak positive correlations were observed in DNA damage and 8-OHdG, which were reduced with supplementation. However, no translocation or a stable insertion was observed in chromosome 4.
Conclusion:
Tri E Tocotrienol supplementation may be beneficial by reducing DNA damage as indicated by a reduction in DNA damage, SCE frequency, and urinary 8-OHdG.
Insights
Tri E Tocotrienol supplementation significantly reduced DNA damage and markers of aging, including sister chromatid exchange (SCE) and 8-hydroxy-2'-deoxyguanosine (8-OHdG). This suggests a potential benefit in mitigating age-related cellular damage.
Area of Science:
- Gerontology and Molecular Biology
- Biochemistry and Oxidative Stress
Background:
- The free radical theory of aging (FRTA) posits that accumulated cellular damage from free radicals contributes to age-related decline.
- DNA damage is a key factor in aging, leading to various age-associated disorders.
Purpose of the Study:
- To investigate the efficacy of Tri E Tocotrienol in mitigating DNA damage in humans.
- To evaluate the impact of Tri E Tocotrienol on biomarkers of oxidative stress and DNA integrity.
Main Methods:
- A 6-month randomized, double-blinded, placebo-controlled study involving 64 participants aged 37-78.
- Daily administration of 160 mg of Tri E Tocotrienol.
- Analysis of DNA damage using comet assay, sister chromatid exchange (SCE) frequency, and chromosome 4 aberrations in blood samples.
Main Results:
- Significant reduction in DNA damage (comet assay) observed at 3 and 6 months (P < 0.01).
- Reduced SCE frequency after 6 months (P < 0.05), with a more pronounced effect in individuals over 50 (P < 0.01).
- Significant decrease in urinary 8-hydroxy-2 -deoxyguanosine (8-OHdG) levels (P < 0.05), a marker of oxidative DNA damage.
Conclusions:
- Tri E Tocotrienol supplementation demonstrates a beneficial effect in reducing DNA damage.
- The observed reductions in DNA damage, SCE, and 8-OHdG suggest potential anti-aging properties.
- Further research may explore Tri E Tocotrienol's role in managing age-related conditions.
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