کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2147916 | 1548591 | 2014 | 5 صفحه PDF | دانلود رایگان |
• Ageing enhanced the bone-marrow micronucleated erythrocytes in mice.
• As compared to males, females showed higher micronuclei frequency with age.
• Enhancement of DNA damage was also observed with age in mice.
Age-dependent changes in chromosomal damage in bone marrow – a self-proliferating tissue – in the form of spontaneously occurring micronucleated erythrocytes, and DNA damage in peripheral blood were examined in male and female Swiss mice. In the erythrocyte population in the bone marrow, polychromatic (immature) erythrocytes showed a significant increase in the frequency of micronuclei as a function of age of the mice (1–20 months). The increase in micronucleus frequency was less in normochromatic (mature) erythrocytes. The female mice showed a higher frequency of micronuclei than the male mice in all the age groups examined. However, the female to male ratio of micronucleus frequencies in total erythrocytes as well as in polychromatic erythrocytes decreased with age. DNA damage, measured as tail moment in the single-cell gel electrophoresis in peripheral blood of different age groups of mice (1, 6, 12 and 18 months) showed a gradual increase with age. Female mice showed more DNA damage than 1-month and 18-month-old male mice. In conclusion, these results show that there is an accumulation of genetic damage in bone marrow and DNA damage in peripheral blood of mice during ageing, and that females show more alterations than males.
Journal: Mutation Research/Genetic Toxicology and Environmental Mutagenesis - Volume 770, August 2014, Pages 80–84