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首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >Radioprotective Effect of Kupffer Cell Depletion on Hepatic Sinusoidal Endothelial Cells
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Radioprotective Effect of Kupffer Cell Depletion on Hepatic Sinusoidal Endothelial Cells

机译:库普弗细胞耗竭对肝窦窦内皮细胞的辐射防护作用

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摘要

Radiation-induced liver injury remains a clinical problem and data suggest that sinusoidal endothelial cells (SECs) are an important target. The purpose of this study was to determine whether the inhibition of Kupffer cells before exposure would protect SECs from radiation-induced injury. Sprague-Dawley rats were intravenously injected 24 h before irradiation with Kupffer cell inhibitor gadolinium chloride (GdCl3) (10 mg/kg body weight). Three groups of animals were treated: 1. control group (saline and sham irradiation); 2. GdCl3 + 30 Gy radiation group and 3. 30 Gy radiation only group. Specimens were collected at 2, 6, 12, 24 and 48 h after completion of each treatment. Liver tissue was assessed for inflammatory cytokine expression and radiation-induced SEC injury based on serum hyaluronic acid (HA) level, apoptosis and ultrastructural and histological analyses. The results showed that radiation exposure caused apoptosis of SECs, but not hepatocytes. Inflammatory cytokine expression, including tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta) expression, was significantly attenuated in the GdCl3 + 30 Gy radiation group, compared with the 30 Gy radiation-only group (P < 0.05). The GdCl3 + radiation-treated rats exhibited significantly lower levels of HA and SEC apoptosis than the radiation-treated only rats at early time points, and radiation-induced liver injury was also attenuated. In conclusion, we hypothesize that selective Kupffer cell inhibition by gadolinium chloride was shown to reduce apoptosis in SECs caused by irradiation of the live and protected the liver against radiation-induced injury. (C) 2015 by Radiation Research Society
机译:辐射诱发的肝损伤仍然是一个临床问题,数据表明正弦血管内皮细胞(SEC)是重要的靶标。这项研究的目的是确定在暴露之前抑制Kupffer细胞是否可以保护SEC免受辐射诱导的损伤。在用Kupffer细胞抑制剂氯化g(GdCl3)(10 mg / kg体重)照射前24小时静脉注射Sprague-Dawley大鼠。治疗三组动物:1.对照组(盐水和假辐射); 2. GdCl3 + 30 Gy辐射组和3. 30 Gy仅辐射组。每种处理完成后的2、6、12、24和48小时收集标本。根据血清透明质酸(HA)水平,细胞凋亡以及超微结构和组织学分析评估肝脏组织的炎性细胞因子表达和辐射诱导的SEC损伤。结果表明,辐射暴露引起SECs凋亡,但不引起肝细胞凋亡。与仅使用30 Gy放射治疗的组相比,GdCl3 + 30 Gy放射治疗组的炎症细胞因子表达,包括肿瘤坏死因子-α(TNF-alpha)和白介素-1 beta(IL-1 beta)表达显着减弱( P <0.05)。与GdCl3 +辐射治疗的大鼠相比,在早期的时间点,其HA和SEC凋亡水平明显低于仅辐射治疗的大鼠,并且辐射诱发的肝损伤也有所减轻。总而言之,我们假设氯化selective对选择性Kupffer细胞的抑制作用可减少由活体辐射引起的SEC细胞凋亡,并保护肝脏免受辐射诱导的损伤。 (C)辐射研究学会2015年

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