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

被引:14
|
作者
Telez, Mercedes [1 ]
Ortiz-Lastra, Eduardo [2 ]
Gonzalez, Adolfo J. [3 ]
Flores, Piedad [4 ]
Huerta, Iratxe [1 ]
Ramirez, Juan M. [1 ]
Barasoain, Maitane [1 ]
Criado, Begona [5 ]
Arrieta, Isabel [1 ]
机构
[1] Univ Basque Country, Dpto Genet Antropol Fis & Fisiol Anim, Fac Ciencias & Tecnol, E-48080 Bilbao, Spain
[2] Univ Basque Country, Dpto Especialidades Medicoquirurg, Fac Med & Odontol, E-48080 Bilbao, Spain
[3] Univ Basque Country, Dpto Med Interna, Fac Med & Odontol, E-48080 Bilbao, Spain
[4] Univ Basque Country, Dpto Farmacol Clin & Dietet, Escuela Enfermeria, E-48080 Bilbao, Spain
[5] Cooperat Ensino Super Politecn & Univ, Oporto, Portugal
关键词
Genotoxicity; Antihypertensives; Fragile sites; Content of micronuclei; CULTURED HUMAN-LYMPHOCYTES; IN-VITRO; X-CHROMOSOME; MOLECULAR CHARACTERIZATION; ESSENTIAL-HYPERTENSION; ABERRATIONS; FREQUENCY; IDENTIFICATION; LINKAGE; FEMALE;
D O I
10.1016/j.mrgentox.2009.02.015
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 54
页数:9
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