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瑞士小鼠骨髓中微核红细胞自发频率及外周血DNA损伤的年龄依赖性变化。

Age-dependent changes in spontaneous frequency of micronucleated erythrocytes in bone marrow and DNA damage in peripheral blood of Swiss mice.

作者信息

Bhilwade Hari N, Jayakumar S, Chaubey R C

机构信息

Radiation Biology and Health Sciences Division, Bhabha Atomic Research Centre, Mumbai 400085, India.

Radiation Biology and Health Sciences Division, Bhabha Atomic Research Centre, Mumbai 400085, India.

出版信息

Mutat Res Genet Toxicol Environ Mutagen. 2014 Aug;770:80-4. doi: 10.1016/j.mrgentox.2014.04.026. Epub 2014 Jun 9.

Abstract

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.

摘要

在雄性和雌性瑞士小鼠中,研究了骨髓(一种自我增殖组织)中以自发出现的微核红细胞形式存在的染色体损伤的年龄依赖性变化,以及外周血中的DNA损伤。在骨髓中的红细胞群体中,多色(未成熟)红细胞的微核频率随小鼠年龄(1 - 20个月)的增加而显著升高。正色(成熟)红细胞中微核频率的增加较少。在所检查的所有年龄组中,雌性小鼠的微核频率高于雄性小鼠。然而,总红细胞以及多色红细胞中微核频率的雌雄比随年龄下降。在不同年龄组(1、6、12和18个月)小鼠外周血的单细胞凝胶电泳中,以尾矩衡量的DNA损伤随年龄逐渐增加。雌性小鼠比1个月和18个月大的雄性小鼠表现出更多的DNA损伤。总之,这些结果表明,衰老过程中小鼠骨髓中的遗传损伤和外周血中的DNA损伤会累积,并且雌性比雄性表现出更多的变化。

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