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2-氨基甲酸甲酯基苯并咪唑、己烯雌酚和雌二醇的致突变性:结构染色体畸变、姐妹染色单体交换、C-有丝分裂、多倍体和微核。

Mutagenicity of methyl 2-benzimidazolecarbamate, diethylstilbestrol and estradiol: structural chromosomal aberrations, sister-chromatid exchanges, C-mitoses, polyploidies and micronuclei.

作者信息

Banduhn N, Obe G

出版信息

Mutat Res. 1985 Jun;156(3):199-218. doi: 10.1016/0165-1218(85)90065-5.

Abstract

Methyl 2-benzimidazolecarbamate (MBC), diethylstilbestrol (DES) and estradiol were tested with regard to their ability to induce C-mitoses, polyploidies, micronuclei, structural chromosomal aberrations and sister-chromatid exchanges (SCE) in human peripheral lymphocytes in vitro. The compounds did not induce structural chromosomal aberrations either in the presence or absence of metabolic activation. MBC and estradiol were negative in the SCE test. DES induced SCE rates which were not even twice the control level and which were independent of dose and of metabolic activation. All compounds induced C-mitoses, polyploidies and micronuclei. The micronuclei are interpreted as resulting from errors in the anaphase distribution of chromosomes by spindle disturbances rather than from structural chromosomal aberrations.

摘要

对2-苯并咪唑氨基甲酸甲酯(MBC)、己烯雌酚(DES)和雌二醇进行了测试,以考察它们在体外诱导人外周血淋巴细胞C-有丝分裂、多倍体、微核、染色体结构畸变和姐妹染色单体交换(SCE)的能力。无论有无代谢活化,这些化合物均未诱导染色体结构畸变。MBC和雌二醇在SCE试验中呈阴性。DES诱导的SCE率甚至不到对照水平的两倍,且与剂量和代谢活化无关。所有化合物均诱导了C-有丝分裂、多倍体和微核。微核被解释为是由纺锤体干扰导致的染色体后期分布错误所致,而非染色体结构畸变。

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