Abraham Suresh K, Khandelwal Nidhi
School of Life Sciences, Jawaharlal Nehru University, New Delhi 110067, India.
Mutat Res Genet Toxicol Environ Mutagen. 2013 Oct 9;757(2):167-72. doi: 10.1016/j.mrgentox.2013.08.004. Epub 2013 Aug 22.
We investigated whether combinations of ascorbic acid (AA) plus dietary polyphenols can protect in vivo against genotoxic damage induced by endogenous nitrosation. A nitrosation reaction mixture consisting of methylurea (MU) plus sodium nitrite (SN), which can react to form N-nitroso-N-methylurea in the stomach, was administered orally to mice, together with AA and one of the dietary polyphenols ferulic acid (FA), gallic acid (GA), chlorogenic acid (CA), or epigallocatechin gallate (EGCG). Genotoxic damage in bone marrow cells was assessed by measuring micronucleated polychromatic erythrocytes (Mn PCEs) and metaphase chromosome aberrations. When compared to damage induced by MU plus SN alone, co-administration with AA, FA, GA, CA, or EGCG resulted in significant protective effects. Combinations of AA plus EGCG or AA plus CA showed a further protective effect. Reduction in the frequency of Mn PCEs to the control level was obtained following co-administration of a combination of AA, FA, GA, and CA with MU plus SN. A similar trend was observed for metaphase chromosome aberrations. Co-administration of AA, FA, GA, or CA with N-nitroso-N-methylurea (MNU) did not show any significant reduction in genotoxicity, indicating the absence of a protective effect against a preformed N-nitroso compound. Our work demonstrates the protective effects of the 'antinitrosating' combination of AA and dietary polyphenols FA, GA, or CA against genotoxic damage induced by an endogenously formed N-nitroso compound.
我们研究了抗坏血酸(AA)与膳食多酚的组合是否能在体内保护机体免受内源性亚硝化诱导的遗传毒性损伤。将由甲基脲(MU)和亚硝酸钠(SN)组成的亚硝化反应混合物口服给予小鼠,该混合物在胃中可反应生成N-亚硝基-N-甲基脲,同时给予AA以及膳食多酚阿魏酸(FA)、没食子酸(GA)、绿原酸(CA)或表没食子儿茶素没食子酸酯(EGCG)中的一种。通过测量微核多染红细胞(Mn PCEs)和中期染色体畸变来评估骨髓细胞中的遗传毒性损伤。与单独由MU加SN诱导的损伤相比,同时给予AA、FA、GA、CA或EGCG可产生显著的保护作用。AA加EGCG或AA加CA的组合显示出进一步的保护作用。AA、FA、GA和CA与MU加SN联合给药后,Mn PCEs的频率降低至对照水平。中期染色体畸变也观察到类似趋势。AA、FA、GA或CA与N-亚硝基-N-甲基脲(MNU)联合给药未显示遗传毒性有任何显著降低,表明对预先形成的N-亚硝基化合物没有保护作用。我们的研究表明,AA与膳食多酚FA、GA或CA的“抗亚硝化”组合对由内源性形成的N-亚硝基化合物诱导的遗传毒性损伤具有保护作用。