Das Ujjal, Manna Krishnendu, Khan Amitava, Sinha Mahuya, Biswas Sushobhan, Sengupta Aaveri, Chakraborty Anindita, Dey Sanjit
a Department of Physiology , Centre for Nanoscience and Nanotechnology and Centre with Potential for Excellence in Particular Area (CPEPA), University of Calcutta , Kolkata , West Bengal , India.
b Division of Radiation Biology , UGC-DAE CSR Center Kolkata , Kolkata , West Bengal , India.
Free Radic Res. 2017 Jan;51(1):47-63. doi: 10.1080/10715762.2016.1267345. Epub 2017 Jan 11.
The present study was aimed to evaluate the radioprotective effect of ferulic acid (FA), a naturally occurring plant flavonoid in terms of DNA damage and damage related alterations of repair pathways by gamma radiation. FA was administered at a dose of 50 mg/kg body weight for five consecutive days prior to exposing the swiss albino mice to a single dose of 10 Gy gamma radiation. Ionising radiation induces oxidative damage manifested by decreased expression of Cu, Zn-SOD (SOD stands for super oxide dismutase), Mn-SOD and catalase. Gamma radiation promulgated reactive oxygen species (ROS) mediated DNA damage and modified repair pathways. ROS enhanced nuclear translocation of p53, activated ATM (ataxia telangiectasia-mutated protein), increased expression of GADD45a (growth arrest and DNA-damage-inducible protein) gene and inactivated Non homologous end joining (NHEJ) repair pathway. The comet formation in irradiated mice peripheral blood mononuclear cells (PBMC) reiterated the DNA damage in IR exposed groups. FA pretreatment significantly prevented the comet formation and regulated the nuclear translocation of p53, inhibited ATM activation and expression of GADD45a gene. FA promoted the nuclear translocation of nuclear factor (erythroid-derived 2)-like 2 (Nrf2) and activated NHEJ repair pathway to overcome ROS mediated oxidative stress and DNA damage. Therefore, the current study stated that FA can challenge the oxidative stress by (i) inducing nuclear translocation of Nrf2, (ii) scavenging ROS, and (iii) activating NHEJ DNA repair process.
本研究旨在评估阿魏酸(FA)的辐射防护作用。阿魏酸是一种天然存在的植物类黄酮,研究其对γ辐射造成的DNA损伤及损伤相关修复途径改变的影响。在将瑞士白化小鼠暴露于单次10 Gy γ辐射之前,连续五天以50 mg/kg体重的剂量给予阿魏酸。电离辐射会诱导氧化损伤,表现为铜锌超氧化物歧化酶(SOD代表超氧化物歧化酶)、锰超氧化物歧化酶和过氧化氢酶的表达降低。γ辐射引发活性氧(ROS)介导的DNA损伤并改变修复途径。ROS增强p53的核转位,激活共济失调毛细血管扩张突变蛋白(ATM),增加生长停滞和DNA损伤诱导蛋白(GADD45a)基因的表达,并使非同源末端连接(NHEJ)修复途径失活。照射小鼠外周血单个核细胞(PBMC)中彗星形成再次证明了辐射暴露组中的DNA损伤。阿魏酸预处理显著预防了彗星形成,并调节了p53的核转位,抑制了ATM激活和GADD45a基因的表达。阿魏酸促进核因子(红系衍生2)样2(Nrf2)的核转位并激活NHEJ修复途径,以克服ROS介导的氧化应激和DNA损伤。因此,当前研究表明,阿魏酸可以通过(i)诱导Nrf2的核转位、(ii)清除ROS和(iii)激活NHEJ DNA修复过程来应对氧化应激。