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新生大鼠中致断裂和非整倍体损伤的检测。

Detection of clastogenic and aneugenic damage in newborn rats.

作者信息

Udroiu Ion, Ieradi Luisa Anna, Cristaldi Mauro, Tanzarella Caterina

机构信息

Dipartimento di Biologia Animale e dell'Uomo, Università La Sapienza, 00161 Rome, Italy.

出版信息

Environ Mol Mutagen. 2006 Jun;47(5):320-4. doi: 10.1002/em.20209.

Abstract

The last 25 years have seen an ever-growing use of the erythrocyte micronucleus test for measuring damage to mammalian chromosomes in vivo. In addition, staining micronuclei with antikinetochore antibodies from CREST serum discriminates aneugenic from clastogenic damage. The use of the micronucleus test in rats, however, has been problematic because the spleen of adult rats efficiently removes micronucleated erythrocytes from the blood. In the present study, we have treated 5-day-old rats with either X-rays (a clastogen) or vinblastine (an aneugen) and measured micronuclei in erythrocytes from the blood and liver. Each treatment increased the frequency of micronuclei in both tissues, with the percentages of CREST-staining micronuclei reflecting the mechanism of micronucleus induction by the two agents. The results indicate that performing the micronucleus assay in the liver and peripheral blood of 5-day-old rats may be a useful approach for detecting the in vivo genotoxicity of chemical and physical agents.

摘要

在过去25年里,红细胞微核试验在体内检测哺乳动物染色体损伤方面的应用越来越广泛。此外,用来自CREST血清的抗动粒抗体对微核进行染色,可以区分非整倍体损伤和断裂剂损伤。然而,在大鼠中使用微核试验存在问题,因为成年大鼠的脾脏能有效地从血液中清除含微核的红细胞。在本研究中,我们用X射线(一种断裂剂)或长春碱(一种非整倍体剂)处理5日龄大鼠,并测量血液和肝脏中红细胞的微核。每种处理都增加了两个组织中微核的频率,CREST染色微核的百分比反映了这两种试剂诱导微核的机制。结果表明,在5日龄大鼠的肝脏和外周血中进行微核试验可能是检测化学和物理试剂体内遗传毒性的一种有用方法。

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