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评估阿替洛尔对人外周血淋巴细胞的遗传毒性:染色体脆性与微核含量的相关性。

Assessment of the genotoxicity of atenolol in human peripheral blood lymphocytes: correlation between chromosomal fragility and content of micronuclei.

机构信息

Dpto. Genética, Antropología Física y Fisiología Animal, Facultad de Ciencia y Tecnología, Universidad del País Vasco, Bilbao, Spain.

出版信息

Mutat Res. 2010 Jan;695(1-2):46-54. doi: 10.1016/j.mrgentox.2009.02.015. Epub 2009 Nov 20.

Abstract

The antihypertensive drug atenolol was found to induce chromosome loss, detected as micronuclei in the peripheral lymphocytes of treated patients. The fundamental question which chromosomes the micronuclei were derived from remains to be answered. Analysis of structural chromosomal aberrations (CAs) and expression of fragile sites (FS) were pursued in this study. They revealed a significantly higher incidence of chromosomal aberrations (chromatid and chromosome breaks) in patients compared with controls, where 10 FS emerged as specific. Also, the band 17q12-21, where known fragile sites have not been reported, was only expressed in atenolol-treated patients. Fluorescence in situ hybridization using chromosome-specific probes revealed the preferential involvement of chromosomes 7, 11, 17 and X in the micronuclei (MN) of patients. The results also suggest a correlation between chromosomal fragility and content of MN, and support the findings for a linkage between hypertension and a locus on chromosome 17.

摘要

降压药阿替洛尔被发现可诱导染色体丢失,在接受治疗的患者的外周血淋巴细胞中检测到微核。微核源自哪些染色体的基本问题仍有待解答。本研究对结构染色体畸变(CAs)和脆性位点(FS)的表达进行了分析。结果显示,与对照组相比,患者的染色体畸变(染色单体和染色体断裂)发生率显著升高,其中 10 个 FS 为特异性表达。此外,已知脆性位点未报道的 17q12-21 带仅在阿替洛尔治疗的患者中表达。使用染色体特异性探针的荧光原位杂交显示,微核(MN)中优先涉及染色体 7、11、17 和 X。结果还提示染色体脆性与 MN 含量之间存在相关性,并支持高血压与 17 号染色体上的一个基因座之间存在关联的发现。

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