Naik Prashantha, Vijayalaxmi K K
Department of Post-Graduate Studies and Research in Biosciences, Mangalore University, Mangalagangothri 574 199, D.K., India.
Mutat Res. 2009 May 31;676(1-2):106-12. doi: 10.1016/j.mrgentox.2009.04.010. Epub 2009 Apr 22.
Bisphenol-A (BP-A) is a xenobiotic estrogenic compound used in a wide range of consumer products. BP-A was tested for its genotoxicity by employing three cytogenetic assays, viz., chromosomal aberration test, micronucleus assay and test for c-mitotic effects in Swiss albino mice. Studies were carried out for three doses, 10, 50 and 100 mg/kg in single oral exposure and 10 mg/kg in repeated oral exposure (for 5 days). It is evident from the present investigation that although BP-A failed to induce conventional chromosomal aberrations and micronuclei, its genotoxic potential was manifested in the form of achromatic lesion and c-mitotic effects in the bone marrow cells. It can also be speculated from the results that the threshold concentration of BP-A required for the formation of MN is much higher than that for the induction of c-mitotic effects.
双酚A(BP-A)是一种用于多种消费品的外源性雌激素化合物。通过采用三种细胞遗传学检测方法,即染色体畸变试验、微核试验和瑞士白化小鼠的c-有丝分裂效应试验,对BP-A的遗传毒性进行了检测。在单次口服暴露中,对10、50和100mg/kg三个剂量进行了研究,在重复口服暴露(持续5天)中,对10mg/kg剂量进行了研究。从目前的研究中可以明显看出,尽管BP-A未能诱导传统的染色体畸变和微核,但它的遗传毒性潜力以骨髓细胞中的无色病变和c-有丝分裂效应的形式表现出来。从结果中还可以推测,形成微核所需的BP-A阈值浓度远高于诱导c-有丝分裂效应所需的浓度。