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通过微核试验评估福美锌、福美双和代森锰锌对小鼠骨髓细胞的影响。

Effect of Ziram, Thiram, and Dithane M-45 on bone marrow cells of mice-assessed by micronucleus test.

作者信息

Hemavathi E, Rahiman M A

机构信息

Department of Biosciences, Mangalore University, Mangalagangotri, D. Karnataka, India.

出版信息

Bull Environ Contam Toxicol. 1996 Feb;56(2):190-6. doi: 10.1007/s001289900029.

Abstract

Micronucleus test is an extensively used protocol to assess the mutagenicity of environmental chemicals. This was developed by Schmid and his co-workers (Matter and Schmid, 1971; Ledebur and Schmid, 1973). The micronucleus test is simple, quick and as sensitive as the chromosome aberration analysis. It is based on the principle that during anaphase, acentric chromatid and chromosome fragments lag behind, where as centric elements move towards the spindle pole. After telophase both the undamaged chromosomes and the centric fragments give rise to the daughter nuclei. The lagging elements are transferred into one or several secondary nuclei, which are as a rule much smaller than the main nucleus, and therefore called micronucleus (Schmid, 1973). The clastogenic effect of various chemicals is measured by micronucleus test. Erythrocytes are two types, the younger ones are polychromatic erythrocytes (PCE), which stain bluish and the older, the normo chromatic erythrocytes (NCE) which stain reddish. A few hours after the completion of last mitosis the erythroblasts expel their nucleus for unknown reasons and the micronucleus alone remains in the cytoplasm of the Polychromatic erythrocytes, and they are easily recognisable. Erythrocyte micronucleus represents the consequence of chromosomal aberrations induced during preceding mitotic division of erythrocytes (Matter and Grauwiler, 1974).

摘要

微核试验是一种广泛用于评估环境化学物质致突变性的实验方案。它由施密德及其同事开发(马特和施密德,1971年;莱德布尔和施密德,1973年)。微核试验简单、快速,且与染色体畸变分析一样灵敏。其原理是在后期,无着丝粒染色单体和染色体片段滞后,而着丝粒元件则移向纺锤极。末期后,未受损的染色体和着丝粒片段都形成子核。滞后元件被转移到一个或几个次级核中,这些次级核通常比主核小得多,因此被称为微核(施密德,1973年)。各种化学物质的致断裂效应通过微核试验来测定。红细胞有两种类型,较年轻的是嗜多色性红细胞(PCE),呈蓝色染色,较老的是正染色红细胞(NCE),呈红色染色。在最后一次有丝分裂完成后的几个小时,成红细胞因不明原因排出其细胞核,仅微核留在嗜多色性红细胞的细胞质中,且易于识别。红细胞微核代表了红细胞在前一次有丝分裂期间诱导的染色体畸变的结果(马特和格劳维勒,1974年)。

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