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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Furazolidone Increases Survival of Mice Exposed to Lethal Total Body Irradiation through the Antiapoptosis and Antiautophagy Mechanism
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Furazolidone Increases Survival of Mice Exposed to Lethal Total Body Irradiation through the Antiapoptosis and Antiautophagy Mechanism

机译:Furazolidone通过抗痘病和抗畏缩机制增加暴露于致命总体辐射的小鼠的存活

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Exposure to total body irradiation (TBI) causes dose- and tissue-specific lethality. However, there are few effective and nontoxic radiation countermeasures for the radiation injury. In the current study, mice were pretreated with a traditional antimicrobial agent, FZD, before TBI; the protective effects of FZD on radiation injury were evaluated by using parameters such as the spleen index and thymus index, immunohistochemical staining of intestinal tissue, and frequency of micronuclei in polychromatophilic erythrocytes of bone marrow. The intestinal epithelial cell line IEC-6 was used to investigate the underlying mechanisms. Our results indicated that FZD administration significantly improved the survival of lethal dose-irradiated mice, decreased the number of micronuclei, upregulated the number of leukocytes and immune organ indices, and restored intestinal integrity in mice after TBI. TUNEL and western blot showed that FZD protected intestinal tissue by downregulating radiation-induced apoptosis and autophagy. Meanwhile, FZD protected IEC-6 cells from radiation-induced cell death by inhibiting apoptosis and autophagy. To sum up, FZD protected against radiation-induced cell death both in vitro and in vivo through antiapoptosis and antiautophagy mechanisms.
机译:暴露于总体辐射(TBI)导致剂量和组织特异性杀伤性。然而,辐射损伤几乎没有有效和无毒的辐射反应。在目前的研究中,用传统的抗微生物剂,在TBI之前预处理小鼠;通过使用诸如脾脏指数和胸腺组织的免疫组织化学染色,肠道组织的免疫组织化学染色,肠道组织的免疫组织化学染色以及骨髓的微核频率评估FZD对放射损伤的保护作用。肠上皮细胞系IEC-6用于研究潜在机制。我们的研究结果表明,FZD管理显着改善了致死剂量照射小鼠的存活,减少了微核的数量,上调了白细胞和免疫器官索引的数量,并在TBI后恢复了小鼠的肠完整性。 Tunel和Western印迹显示FZD通过下调辐射诱导的细胞凋亡和自噬受保护的肠组织。同时,通过抑制细胞凋亡和自噬来自辐射诱导的细胞死亡,FZD保护IEC-6细胞。总结,FZD通过抗痘病和抗畏缩机制在体外和体内保护辐射诱导的细胞死亡。

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