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Podophyllotoxin and rutin in combination prevents oxidative stress mediated cell death and advances revival of mice gastrointestine following lethal radiation injury

机译:毒鼠毒素和芦丁组合可防止氧化应激介导的细胞死亡,并进入致命辐射损伤后的小鼠胃肠的复苏

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Intestinal injury is inevitable during exposure to high radiation doses and is a common side effect observed during abdominal/pelvic radiotherapy. Yet, no radiation countermeasures are available for gastrointestine (GI) injury management. The aim of this study is to determine the effects of podophyllotoxin and rutin in combination (G-003M) on ionising radiation induced GI injury. We prophylactically administered G-003M to C57BL/6J mice exposed to 9 Gy total body radiation (TBI) and assessed for morphological changes, loss in absorption, fluid retention, biochemical alterations, immunohistochemical analysis to study cPARP, caspase-3, PCNA expression, and TUNEL staining. The irradiated intestine demonstrated extensive loss in crypts and villi, disrupted mucosal lining with reduced xylose uptake and enhanced fluid level post 7-day radiation. Mice receiving G-003M before radiation showed significant protection to intestinal epithelium, better allocation of secretory goblet cells, recovery in absorption, and reduced intestinal oedema. Additionally, G-003M administration also prevented radiation induced ROS generation, lipid peroxidation (MDA levels) and maintained the intestinal glutathione pool compared to the irradiated animals. G-003M supplementation also resulted in restoration of intestinal mitochondrial membrane potential, which was otherwise depolarised by radiation treatment. Immunohistochemical analysis demonstrated decrease in c-PARP and caspase-3 expression in jejuna cross sections and upregulation of PCNA in G-003M treated crypt cells as compared to 9 Gy irradiated mice. Our findings show that G-003M augment survival of mice against lethal radiation by promoting structural and functional regeneration in intestinal tissue. This combination therefore can be effectively explored for preventing radiation induced GI toxicity. ?2018 Informa UK Limited, trading as Taylor & Francis Group.
机译:在暴露于高辐射剂量期间肠道损伤是不可避免的,并且是在腹部/盆腔放射治疗期间观察到的常见副作用。然而,没有辐射对策可用于胃肠道(GI)伤害管理。该研究的目的是确定鼠霉素毒素和芦丁在电离辐射诱导的GI损伤中的组合(G-003M)的影响。我们预防性施用的G-003M至C57BL / 6J小鼠暴露于9 Gy总体辐射(TBI)并评估形态变化,吸收损失,流体保留,生化改变,免疫组化分析研究CPARP,Caspase-3,PCNA表达,和tunel染色。辐照的肠道在隐窝和绒毛中展现了广泛的损失,扰乱了粘膜衬里,具有减少的木糖摄取和增强的液位7天辐射。在辐射之前接受G-003M的小鼠对肠上皮进行显着保护,更好地分配分泌脚耳细胞,吸收中的恢复和降低的肠道水肿。另外,G-003M给药还防止了辐射诱导的ROS生成,脂质过氧化(MDA水平)并与辐照动物相比将肠谷胱甘肽池保持。 G-003M补充还导致肠道线粒体膜电位恢复,其被辐射处理另有溶解。免疫组织化学分析在Jejuna横截面中表现出C-PARP和Caspase-3表达的降低,与9GY照射小鼠相比,G-003M处理的隐窝细胞中的PCNA的上调。我们的研究结果表明,通过在肠组织中促进结构和功能再生,G-003M增强小鼠的存活率免受致死的辐射。因此,可以有效地探索这种组合以防止辐射诱导的GI毒性。 ?2018年Informa UK Limited,贸易为泰勒和弗朗西斯集团。

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