首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Inactivation of kupffer cells by gadolinium chloride protects murine liver from radiation-induced apoptosis.
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Inactivation of kupffer cells by gadolinium chloride protects murine liver from radiation-induced apoptosis.

机译:氯化g使枯否氏细胞失活可保护鼠肝免受辐射诱导的细胞凋亡。

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PURPOSE: To determine whether the inhibition of Kupffer cells before radiotherapy (RT) would protect hepatocytes from radiation-induced apoptosis. MATERIALS AND METHODS: A single 30-Gy fraction was administered to the upper abdomen of Sprague-Dawley rats. The Kupffer cell inhibitor gadolinium chloride (GdCl3; 10 mg/kg body weight) was intravenously injected 24 h before RT. The rats were divided into four groups: group 1, sham RT plus saline (control group); group 2, sham RT plus GdCl3; group 3, RT plus saline; and group 4, RT plus GdCl3. Liver tissue was collected for measurement of apoptotic cytokine expression and evaluation of radiation-induced liver toxicity by analysis of liver enzyme activities, hepatocyte micronucleus formation, apoptosis, and histologic staining. RESULTS: The expression of interleukin-1beta, interleukin-6, and tumor necrosis factor-alpha was significantly attenuated in group 4 compared with group 3 at 2, 6, 24, and 48 h after injection (p <0.05). At early points after RT, the rats in group 4 exhibited significantly lower levels of liver enzyme activity, apoptotic response, and hepatocyte micronucleus formation compared with those in group 3. CONCLUSION: Selective inactivation of Kupffer cells with GdCl3 reduced radiation-induced cytokine production and protected the liver against acute radiation-induced damage.
机译:目的:确定放疗(RT)前对Kupffer细胞的抑制是否能保护肝细胞免受辐射诱导的凋亡。材料与方法:对Sprague-Dawley大鼠的上腹部施用单一的30-Gy组分。在RT前24小时静脉内注射Kupffer细胞抑制剂氯化ado(GdCl3; 10 mg / kg体重)。将大鼠分为四组:第1组,假RT加生理盐水(对照组);第2组。第2组,假RT加GdCl3;第3组,放疗加生理盐水;第4组,RT加GdCl3。通过分析肝酶活性,肝细胞微核形成,细胞凋亡和组织学染色,收集肝组织以测量凋亡细胞因子的表达并评估辐射诱导的肝毒性。结果:与第3组相比,注射后2、6、24和48 h,第4组白细胞介素-1β,白细胞介素-6和肿瘤坏死因子-α的表达明显减弱(p <0.05)。在放疗后早期,第4组的大鼠与第3组相比,肝酶活性,凋亡反应和肝细胞微核形成水平显着降低。结论:GdCl3对Kupffer细胞的选择性失活减少了辐射诱导的细胞因子产生和保护肝脏免受急性辐射引起的损害。

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