Chaurasia Rajesh Kumar, Balakrishnan Sreedevi, Kunwar Amit, Yadav Usha, Bhat Nagesh, Anjaria Kshiti, Nairy Rajesha, Sapra Balvinder Kaur, Jain Vimal Kumar, Priyadarsini K Indira
Radiological Physics and Advisory Division, Bhabha Atomic Research Centre, Mumbai 400085, India.
Radiological Physics and Advisory Division, Bhabha Atomic Research Centre, Mumbai 400085, India.
Mutat Res Genet Toxicol Environ Mutagen. 2014 Nov 1;774:8-16. doi: 10.1016/j.mrgentox.2014.08.007. Epub 2014 Sep 6.
Our previous study showed that 3,3'-diselenodipropionic acid (DSePA), a simple, stable, and water-soluble organoselenium exhibiting glutathione peroxidase (GPx)-like activity offered good radioprotection under in vitro and in vivo conditions. Herein, we investigated the anti-genotoxic effect of DSePA in model cellular systems such as Chinese Hamster Ovary (CHO) cell line and human peripheral lymphocytes after exposure to γ-radiation. The measurements on the induction of γ-H2AX foci and micronuclei frequency in the cell nuclei indicated that pretreatment with DSePA significantly prevented the radiation induced DNA damage or genotoxicity and subsequent cytotoxicity without exerting its own toxicity. The maximum protective effect of DSePA was seen at a pre-treatment concentration of 3 μg/ml. The mechanistic investigations in CHO cells revealed that DSePA pretreatment prevented the radiation induced ROS generation, lipid peroxidation and subsequent apoptosis in these cells. Further, it was seen to augment the mRNA expressions of GPx2 significantly and GPx4 marginally without causing much change in the total GPx activity after radiation exposure. These results suggested the roles of GPx2 and GPx4 in DSePA mediated radioprotection. In conclusion our results confirm the nongenotoxic nature of the DSePA and validate its radioprotective efficacy and mechanisms of action in model cellular systems.
我们之前的研究表明,3,3'-二硒代二丙酸(DSePA)是一种简单、稳定且水溶性的有机硒,具有谷胱甘肽过氧化物酶(GPx)样活性,在体外和体内条件下均能提供良好的辐射防护作用。在此,我们研究了DSePA在诸如中国仓鼠卵巢(CHO)细胞系和人外周血淋巴细胞等模型细胞系统中,在暴露于γ辐射后的抗遗传毒性作用。对细胞核中γ-H2AX焦点诱导和微核频率的测量表明,用DSePA预处理可显著预防辐射诱导的DNA损伤或遗传毒性以及随后的细胞毒性,且不会产生自身毒性。在预处理浓度为3μg/ml时观察到DSePA的最大保护作用。对CHO细胞的机制研究表明,DSePA预处理可预防辐射诱导的这些细胞中ROS的产生、脂质过氧化和随后的细胞凋亡。此外,还发现它可显著增强GPx2的mRNA表达,并略微增强GPx4的表达,而在辐射暴露后总GPx活性没有太大变化。这些结果表明GPx2和GPx4在DSePA介导的辐射防护中发挥作用。总之,我们的结果证实了DSePA的非遗传毒性性质,并验证了其在模型细胞系统中的辐射防护功效和作用机制。