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Skin wound trauma, following high-dose radiation exposure, amplifies and prolongs skeletal tissue loss

机译:大剂量放射线照射后,皮肤伤口创伤会扩大并延长骨骼组织的损失

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The present study investigated the detrimental effects of non-lethal, high-dose (whole body) gamma-irradiation on bone, and the impact that radiation combined with skin trauma (i.e. combined injury) has on long-term skeletal tissue health. Recovery of bone after an acute dose of radiation (RI; 8 Gy), skin wounding (15-20% of total body skin surface), or combined injury (RI + Wound; Cl) was determined 3, 7, 30, and 120 days post-irradiation in female B6D2F1 mice and compared to non-irradiated mice (SHAM) at each time-point. Cl mice demonstrated long-term (day 120) elevations in serum TRAP 5b (osteoclast number) and sclerostin (bone formation inhibitor), and suppression of osteocalcin levels through 30 days as compared to SHAM (p < 0.05). Radiation-induced reductions in distal femur trabecular bone volume fraction and trabecular number through 120 days post-exposure were significantly greater than non-irradiated mice (p < 0.05) and were exacerbated in Cl mice by day 30 (p < 0.05). Negative alterations in trabecular bone microarchitecture were coupled with extended reductions in cancellous bone formation rate in both RI and CI mice as compared to Sham (p < 0.05). Increased osteoclast surface in Cl animals was observed for 3 days after irradiation and remained elevated through 120 days (p < 0.01). These results demonstrate a long-term, exacerbated response of bone to radiation when coupled with non-lethal wound trauma. Changes in cancellous bone after combined trauma were derived from extended reductions in osteoblast-driven bone formation and increases in osteoclast activity. Published by Elsevier Inc.
机译:本研究调查了非致死性大剂量(全身)γ射线对骨骼的有害影响,以及放射线与皮肤创伤(即合并损伤)的结合对长期骨骼组织健康的影响。在3、7、30和120时确定了急性剂量放射(RI; 8 Gy),皮肤受伤(占全身皮肤表面的15-20%)或合并损伤(RI +伤口; Cl)后骨骼的恢复在雌性B6D2F1小鼠接受辐照后的第二天,并在每个时间点与未辐照的小鼠(SHAM)进行比较。与SHAM相比,C1小鼠表现出血清TRAP 5b(破骨细胞数)和硬化素(骨形成抑制剂)长期(第120天)升高,并且骨钙蛋白水平抑制了30天(p <0.05)。辐射引起的股骨远端骨小梁骨体积分数和骨小梁数目的减少,经过暴露后120天明显大于未辐照的小鼠(p <0.05),而在Cl小鼠中则在第30天加剧(p <0.05)。与假手术相比,RI和CI小鼠的小梁骨微结构的负面变化与松质骨形成速率的持续降低相结合(p <0.05)。辐照后3天观察到C1动物的破骨细胞表面增加,并在120天内保持升高(p <0.01)。这些结果表明,在与非致命性伤口创伤相结合时,骨对放射线的长期,加剧反应。合并创伤后松质骨的变化源自成骨细胞驱动的骨形成的持续减少和破骨细胞活性的增加。由Elsevier Inc.发布

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