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The effect of carbon irradiation is associated with greater oxidative stress in mouse intestine and colon relative to γ-rays

机译:碳辐射的效果与小鼠肠和结肠相对于γ射线的氧化应激相关

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Carbon irradiation due to its higher biological effectiveness relative to photon radiation is a concern for toxicity to proliferative normal gastrointestinal (GI) tissue after radiotherapy and long-duration space missions such as mission to Mars. Although radiation-induced oxidative stress is linked to chronic diseases such as cancer, effects of carbon irradiation on normal GI tissue have not been fully understood. This study assessed and compared chronic oxidative stress in mouse intestine and colon after different doses of carbon and ?radiation, which are qualitatively different. Mice (C57BL/6J) were exposed to 0.5 or 1.3 Gy of ?or carbon irradiation, and intestinal and colonic tissues were collected 2 months after irradiation. While part of the tissues was used for isolating epithelial cells, tissue samples were also fixed and paraffin embedded for 4 祄 thick sections as well as frozen for biochemical assays. In isolated epithelial cells, reactive oxygen species and mitochondrial status were studied using fluorescent probes and flow cytometry. We assessed antioxidant enzymes and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity in tissues and formalin-fixed tissue sections were stained for 4-hydroxynonenal, a lipid peroxidation marker. Data show that mitochondrial deregulation, increased NADPH oxidase activity, and decreased antioxidant activity were major contributors to carbon radiation-induced oxidative stress in mouse intestinal and colonic cells. When considered along with higher lipid peroxidation after carbon irradiation relative to ?rays, our data have implications for functional changes in intestine and carcinogenesis in colon after carbon radiotherapy as well as space travel. ?2018 Informa UK Limited, trading as Taylor & Francis Group.
机译:由于其相对于光子辐射的较高生物效能导致的碳辐射是对放疗后的增殖正常胃肠道(GI)组织的毒性和诸如MARS的长期空间任务的毒性。尽管辐射诱导的氧化应激与诸如癌症如慢性疾病相关的氧化胁迫,但碳辐射对正常GI组织的影响尚未得到完全理解。该研究评估并比较了小鼠肠道和结肠后的慢性氧化应激和在不同剂量的碳和辐射后的结肠,这与定性不同。小鼠(C57BL / 6J)暴露于0.5或1.3GY的α或碳辐照,辐射后2个月收集肠道和结肠组织。虽然部分组织用于分离上皮细胞,但是也固定组织样品并将石蜡嵌入4°厚的部分以及生物化学测定的冷冻。在孤立的上皮细胞中,使用荧光探针和流式细胞术研究活性氧物质和线粒体状态。我们评估了抗氧化酶和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶活性,染色于4-羟基的组织中的组织中的氧化酶活性,脂质过氧化标记物染色。数据表明,线粒体放松管制,增加的NADPH氧化酶活性和降低的抗氧化活性是对小鼠肠道和结肠细胞中碳辐射诱导的氧化应激的主要贡献者。当碳照射后含有更高的脂质过氧化时,我们的数据对碳放射治疗后结肠癌和癌症发生的功能变化以及空间行程具有影响。 ?2018年Informa UK Limited,贸易为泰勒和弗朗西斯集团。

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