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氯化镧对内毒素诱导巨噬细胞肿瘤坏死因子表达的影响
引用本文:汪泱,袁铿,曹勇,李国辉,戴育成,周水莲. 氯化镧对内毒素诱导巨噬细胞肿瘤坏死因子表达的影响[J]. 中华烧伤杂志, 2002, 18(2): 102-104
作者姓名:汪泱  袁铿  曹勇  李国辉  戴育成  周水莲
作者单位:1. 330006,南昌,江西医学院第一附属医院烧伤研究所
2. 江西省医学科学研究所
基金项目:国家自然科学基金资助项目 (3 98690 0 3 )
摘    要:
目的 探讨稀土化合物氯化镧对内毒素效应的影响。 方法 分离培养小鼠腹腔巨噬细胞 (M) ,用内毒素 (lipopolysaccharide ,LPS)对其进行诱导实验。采用ELISA法及SYBRGreen荧光定量RT PCR方法 ,观察氯化镧对LPS诱导的小鼠M肿瘤坏死因子α(TNFα)分泌及TNFαmRNA表达的影响。BALB/C小鼠随机分为 2组 ,分别给予致死量LPS及经氯化镧处理的LPS ,观察 7d内小鼠死亡率。 结果 经氯化镧处理的LPS诱导的小鼠 ,MTNFα分泌量及TNFαmRNA表达水平均明显低于LPS组 (P <0 .0 1)。经氯化镧处理的致死量LPS攻击小鼠 ,其死亡率明显低于LPS对照组。 结论 氯化镧具有降低内毒素毒性、抑制LPS诱导小鼠MTNFα分泌及TNFαmRNA表达的作用

关 键 词:内毒素类  金属  稀土  肿瘤坏死因子  巨噬细胞
修稿时间:2001-02-22

The influence of lanthanum chloride on the TNFα expression of murine peritoneal macrophages stimulated by lipopolysaccharide
WANG Yang,YUAN Keng,CAO Yong,LI Guohui,DA I Yucheng,ZHOU Shuilian. The influence of lanthanum chloride on the TNFα expression of murine peritoneal macrophages stimulated by lipopolysaccharide[J]. Chinese journal of burns, 2002, 18(2): 102-104
Authors:WANG Yang  YUAN Keng  CAO Yong  LI Guohui  DA I Yucheng  ZHOU Shuilian
Affiliation:Department of Burns, The First Affiliated Hospital, Jiangxi Medical College, Nanchang 330006 Jiang xi Province, P.R. China.
Abstract:
OBJECTIVE: To explore the influence of lanthanum chloride on the TNFalpha expression of murine peritoneal macrophages stimulated by lipopolysaccharide (LPS). METHODS: Murine peritoneal macrophages (Mphi) were isolated, cultured and then stimulated by LPS. The influence of lanthanum chloride on the TNFalpha secretion and TNFalphamRNA expression of murine Mphi stimulated by LPS was determined by ELISA method and SYBR green fluorescence quantitative RT-PCR. Forty BALB/C mice were randomly divided into two groups and were treated by lethal dose of LPS and lanthanum chloride processed LPS, respectively. The mortality within 7 days was observed. RESULTS: The TNFalpha secretion and TNFalphamRNA expression level of the Mphi from mice treated by lanthanum chloride processed LPS were obviously lower than those by LPS only (P < 0.01). The mortality of the mice treated by lethal dose of LPS which has been processed by lanthanum chloride was significantly lower than that by lethal dose of LPS only. CONCLUSION: Lanthanum chloride possessed the capacity of lowering down the toxicity of LPS and inhibiting the TNFalpha secretion and TNFalphamRNA expression in murine Mphi stimulated by LPS.
Keywords:Lipopolysaccharide  Lanthanum chloride  Tumor necrosis factor  Macrophage
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