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β-胡萝卜素在体内的诱变修饰作用

[Mutagen-modifying effects of beta-carotene in vivo].

作者信息

Durnev A D, Tiurina L S, Guseva N V, Oreshchenko A V, Seredenin S B

出版信息

Genetika. 1997 May;33(5):717-20.

PMID:9273322
Abstract

A chromosome aberration test on bone marrow cells of C57B1/6 mice showed that beta-carotene (BC) applied by oral administration as a E160a food dye (30% oil suspension) at doses of 0.5, 5, and 50 mg/kg simultaneously with cyclophosphamide (CPA) and dioxidine (DN) injected intraperitoneally for a period of 24 h did not modify their clastogenic effects. If the animals were pretreated with perorally administrated beta-carotene dye at doses of 5 and 50 mg/kg (corresponding to 1.5 and 15 mg/kg of BC) for 5 consecutive days, a statistically significant reduction in the clastogenic effect of the DN injected for 24 h but not the CPA was observed. In another set of experiments, E160a and clastogens were administered simultaneously for 5 consecutive days, and the animals were killed 6 h after the last treatment. In this case, BC at the dose of 0.15-15 mg/kg statistically significantly reduced the clastogenicity of DN at all doses used, and of CPA at doses of 1.5 and 15 mg/kg.

摘要

对C57B1/6小鼠骨髓细胞进行的染色体畸变试验表明,以E160a食用色素(30%油悬液)形式口服给予β-胡萝卜素(BC),剂量为0.5、5和50 mg/kg,同时腹腔注射环磷酰胺(CPA)和二氧化嘧啶(DN),持续24小时,并未改变它们的致断裂效应。如果动物连续5天经口给予剂量为5和50 mg/kg(相当于1.5和15 mg/kg的BC)的β-胡萝卜素染料进行预处理,观察到注射24小时的DN的致断裂效应有统计学意义的降低,但CPA没有。在另一组实验中,E160a和致断裂剂连续5天同时给药,在最后一次处理后6小时处死动物。在这种情况下,剂量为0.15 - 15 mg/kg的BC在统计学上显著降低了所有使用剂量的DN以及1.5和15 mg/kg剂量的CPA的致断裂性。

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