Ahuja Y R, Jaju M, Jaju M
Hum Genet. 1981;57(3):321-2. doi: 10.1007/BF00278953.
Antitubercular drugs in general are given in various combinations, one being isoniazid and thiacetazone. In the present study, was evaluated the in vivo chromosome-damaging effects of a combination of these two drugs in 72 h lymphocyte cultures. Chromosome aberrations were significantly increased in the patients treated with INH and thiacetazone as compared with two types of controls: (1) tuberculosis patients before starting the drug treatment and (2) individuals from the general population. The most frequently observed aberrations were chromatid breaks and gaps. It has been shown that individually, isoniazid may not be clastogenic on human chromosomes in therapeutic doses. The effects of thiacetazone on human chromosomes are not known. Consequently, the enhancement in chromosomal aberrations in the drug-exposed patients may be due to a synergistic effect of isoniazid and thiacetazone or to the clastogenic effects of thiacetazone alone.
抗结核药物通常以各种组合形式给药,其中一种是异烟肼和氨硫脲。在本研究中,评估了这两种药物组合在72小时淋巴细胞培养物中的体内染色体损伤作用。与两种类型的对照相比,接受异烟肼和氨硫脲治疗的患者染色体畸变显著增加:(1)开始药物治疗前的结核病患者;(2)普通人群个体。最常观察到的畸变是染色单体断裂和裂隙。已经表明,单独使用时,治疗剂量的异烟肼可能不会对人类染色体产生断裂作用。氨硫脲对人类染色体的影响尚不清楚。因此,药物暴露患者中染色体畸变的增加可能是由于异烟肼和氨硫脲的协同作用,或者仅仅是氨硫脲的断裂作用。