Vlastos D, Stephanou G, Demopoulos N A
Department of Biology, University of Patras, Greece.
Skin Pharmacol Appl Skin Physiol. 1998 Mar-Apr;11(2):104-10. doi: 10.1159/000029815.
The ability of cetirizine dihydrochloride, an antihistaminic agent, to induce chromosome aberrations as well as sister chromatid exchanges (SCEs) was evaluated in human lymphocyte cultures treated in vitro. The following concentrations were tested: 25, 50, 75, 100 and 200 micrograms/ml. The results of our study revealed that cetirizine dihydrochloride is capable of inducing chromosome aberrations, at least at the higher concentrations studied, 100 and 200 micrograms/ml. The majority of aberrations was of chromatid type. Cetirizine is also a weak inducer of SCEs. Further studies are now warranted in order to define the in vivo cytogenetic activity of cetirizine in humans.
在体外处理的人淋巴细胞培养物中,评估了抗组胺药盐酸西替利嗪诱导染色体畸变以及姐妹染色单体交换(SCE)的能力。测试了以下浓度:25、50、75、100和200微克/毫升。我们的研究结果表明,盐酸西替利嗪至少在所研究的较高浓度(100和200微克/毫升)下能够诱导染色体畸变。大多数畸变是染色单体类型。西替利嗪也是SCE的弱诱导剂。现在有必要进行进一步研究,以确定西替利嗪在人体内的体内细胞遗传学活性。