偏振多色非相干光(Bioptron®light)下小鼠外周血微核分析

Guillermo M. Zúñiga-González , Jesús O. Martínez-Sánchez , Ana L. Zamora-Perez , Martha P. Gallegos-Arreola , Blanca M. Torres-Mendoza , Juan E. Gutiérrez-Sevilla , María G. Sánchez-Parada , Angélica Barros-Hernández , Belinda C. Gómez-Meda
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摘要

近年来癌症发病率的上升表明,人们无意中接触到了导致基因损伤的物质。偏振多色非相干光Bioptron®灯用于加速愈合,在其他治疗应用中,其作为有丝分裂剂的潜在致癌作用尚未被探索。目的是通过对小鼠红细胞的微核测定来评价生物加速器光疗的遗传毒性。雄性SKH1无毛小鼠随机分为6组(每组5只);第一组:阴性对照组接受环境光;第二组:阳性对照暴露于紫外线灯A (UV-A)下80 min;实验组3 ~ 6分别在Bioptron灯下照射10、20、40、80 min。各组每天暴露一次,连续4天,每天进行血液涂片,连续5天,随后在配备有荧光的显微镜下读取。测定小鼠微核红细胞(MNE)、微核多染红细胞(MNPCE)及多染红细胞(PCE)比例。接受UV-A光的研究组是唯一一个MNE和MNPCE值增加的研究组,而暴露于Bioptron灯和阴性对照的组在任何采样日都没有显示出增加。综上所述,在本实验条件下,通过外周血微核试验,我们的结果表明,Bioptron灯的光不会对SKH1小鼠的遗传物质造成损害。
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Micronuclei analysis in mice peripheral blood exposed to polarized polychromatic noncoherent light (Bioptron® Light)

The increase in cancer in recent years suggests an inadvertent exposure to agents that cause genetic damage. The polarized polychromatic noncoherent light Bioptron® lamp is used to accelerate healing, among other therapeutic applications and its potential carcinogenic effects as a mitogenic agent have not been explored. The objective was to evaluate the genotoxicity of the Bioptron light therapy by means of the micronucleus assay in mouse erythrocytes. Male SKH1 hairless mice were randomly divided into six groups (5 mice/group); Group 1: negative control received ambient light; Group 2: positive control was exposed to ultraviolet light lamp A (UV-A) for 80 min; Experimental Groups 3–6 were exposed to the Bioptron lamp light for 10, 20, 40 and 80 min, respectively. Exposures in all groups were once a day for 4 days and blood smears were performed daily for 5 days and subsequently read with a microscope equipped with epifluorescence. The values of micronucleated erythrocytes (MNE), micronucleated polychromatic erythrocytes (MNPCE) and the proportion of polychromatic erythrocytes (PCE) were determined. The study group that received the UV-A light was the only one that increased MNE and MNPCE values, while in the groups exposed to the Bioptron lamp and the negative control did not show increases in any of the sampling days. In conclusion, under the conditions presented here, our results suggest that the light of the Bioptron lamp does not cause damage to the genetic material of SKH1 mice, by means of the micronucleus test in peripheral blood.

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