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The effects of antioxidants on gene expression following gamma-radiation (GR) and proton radiation (PR) in mice in vivo

机译:抗氧化剂对小鼠体内伽马辐射(GR)和质子辐射(PR)后基因表达的影响

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摘要

Ionizing radiation (IR) generates free radicals that interact randomly with a range of intracellular biomolecules that can result in lethal cellular injury. Therefore, IR-inflicted damage is a highly complex interplay of vastly different pathophysiological processes, including inflammation, epithelial regeneration, tissue remodeling, and fibrosis. The development of safe and effective radioprotectors that protect normal tissues following IR exposure is highly desirable. It was previously shown that dietary supplementation with an antioxidant (AOX) diet containing SeM (0.06 μg/g diet), α-lipoic acid (85.7 μg/g diet), NAC (171.4 μg/g diet), sodium ascorbate (142.8 μg/g diet), and vitamin E succinate (71.4μg/g diet) was an effective countermeasure to lethality in mice following γ-radiation (GR) and proton radiation (PR). Here we are examining the effect of the AOX diet on global gene expression following RBE-weighted doses of GR (7.0 Gy) and PR (6.4 Gy) in an attempt to gain further insight into the molecular mechanism of action of AOX diet in the context of radiation exposure. The AOX diet altered the expression pattern of several pro- and anti-apoptotic genes. Our data suggest that the AOX diet may alter IL6 signaling following GR and completely block the expression of the prokineticin PROK2, the ligand to the G protein-coupled receptors PROKR1 and PROKR2, which are involved in a number of pathophysiological processes.
机译:电离辐射(IR)产生的自由基与一系列细胞内生物分子随机相互作用,从而导致致命的细胞损伤。因此,IR造成的损害是极为不同的病理生理过程(包括炎症,上皮再生,组织重塑和纤维化)的高度复杂相互作用。迫切需要开发安全有效的辐射防护剂,以保护IR暴露后的正常组织。先前显示膳食补充了抗氧化剂(AOX)饮食,其中包含SeM(0.06μg/ g饮食),α-硫辛酸(85.7μg/ g饮食),NAC(171.4μg/ g饮食),抗坏血酸钠(142.8μg) / g饮食)和维生素E琥珀酸酯(71.4μg/ g饮食)是对抗γ辐射(GR)和质子辐射(PR)后小鼠致死率的有效对策。在这里,我们正在研究ROX加权剂量GR(7.0 Gy)和PR(6.4 Gy)后AOX饮食对全球基因表达的影响,以试图进一步了解AOX饮食在此背景下的分子机制。辐射暴露。 AOX饮食改变了一些促凋亡和抗凋亡基因的表达模式。我们的数据表明,AOX饮食可能会改变GR后的IL6信号,并完全阻断前动力蛋白PROK2(G蛋白偶联受体PROKR1和PROKR2的配体)的表达,PROKR1和PROKR2参与许多病理生理过程。

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