膳食补充抗氧化剂可降低衰老小鼠脾细胞hprt突变频率

A.I. Gaziev , A.Ja. Podlutsky , B.M. Panfilov , R. Bradbury
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引用次数: 36

摘要

在幼龄(8 - 14周龄)和老年(102 - 110周龄)雄性C57BL/6小鼠脾细胞中,研究了经抗氧化剂混合物(维生素C、E、β -胡萝卜素、芦丁、硒、锌)预处理的不同年龄小鼠的次黄嘌呤-鸟嘌呤磷酸核糖基转移酶(hprt)位点的自发和γ辐射诱导突变水平以及这些突变频率的降低。102 ~ 110周龄小鼠脾细胞自发突变频率比8 ~ 14周龄小鼠高68 ~ 88%。在小鼠γ辐照(0.5 ~ 5.0 Gy)条件下,老龄小鼠的辐射诱发突变(Vf测定)频率比幼龄小鼠高2.3 ~ 3.6倍(取决于剂量)。在辐照前每日向小鼠饮食中补充一种抗氧化剂混合物显示出抗诱变作用。2.0 Gy和5.0 Gy γ辐照前6周,14 - 110周龄小鼠的突变频率降低因子(MFRF)分别为5.4和3.7。抗氧化剂预防或不预防辐射诱发突变的频率在老年小鼠中比在年轻小鼠中要高得多。
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Dietary· supplements of antioxidants reduce hprt mutant frequency in splenocytes of aging mice

The level of spontaneous and gamma-radiation-induced mutations in the hypoxanthine-guanine phosphoribosyl-transferase (hprt) locus as well as the decrease in frequency of these mutations in mice of various age pretreated with dietary supplements of an antioxidant mixture (vitamins C, E, beta-carotene, rutin, selenium, zinc) were studied in splenocytes of young (8–14-week-old) and aged (102–110-week-old) male C57BL/6 mice.

The frequency of spontaneous mutations in splenocytes of 102–110-week-old mice was higher by 68–88% than that in mice aged 8–14 weeks. On gamma-irradiation (0.5–5.0 Gy) of mice, the frequency of radiation-induced mutations (Vf assay) in aged mice was 2.3 to 3.6 times (depending on dose) higher than in young ones.

Daily supplements of an antioxidant mixture to the diet of mice prior to irradiation showed an antimutagenic effect. The values of mutant frequency reduction factor (MFRF) for 14–110-week-old mice fed with dietary antioxidants during 6 weeks prior to gamma-irradiation with doses of 2.0 and 5.0 Gy were 5.4 and 3.7, respectively. The frequency of radiation-induced mutations prevented or not prevented by antioxidants was much higher in aged mice than in young ones.

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Publisher's note Editorial An accessory protein enhances both DNA binding and activity of DNA polymerase α isolated from normal, but not transformed, human fibroblasts Differences in the spectrum of spontaneous mutations in the hprt gene between tumor cells of the microsatellite mutator phenotype Spermatid micronucleus analysis of aging effects in hamsters
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