检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:段钢[1] 朱自强[1] 闫长明[1] 辛兵[2] 李高玉 王斌[1] 刘刚[1]
机构地区:[1]徐州医学院第二附属医院骨科,江苏省徐州市221002 [2]徐州医学院附属医院骨科
出 处:《中国煤炭工业医学杂志》2013年第11期1756-1758,共3页Chinese Journal of Coal Industry Medicine
摘 要:目的探讨脂多糖(LPS)促进人工关节松动的可能性。方法采用酶联免疫吸附法(ELISA)测定在不同剂量LPS作用下超高分子聚乙烯微粒(UHMWPE)诱导人外周血单核细胞(MOs),培养3,6,12,24,48h肿瘤坏死因子α(TNF-α)、白细胞介素6(IL-6)的含量变化。结果与空白对照组A组相比LPS组、UHMWPE组、及不同浓度的LPS联合UHMWPE刺激组刺激3h后TNF-α、IL-6显著升高(均P<0.05),12h达高峰,TNF-α、IL-6分泌与LPS呈现浓度依赖性,刺激12,24,48h F组TNF-α、IL-6分泌明显高于A、B、C、D、E组(P<0.05)。结论 LPS能有效地促进由于UHMWPE刺激MOs所致的TNF-α、IL-6的分泌,增强了人工关节置换术后由微粒诱导的骨溶解。Objective To investigate the possibility of Lipopolysaccharide (LPS) contribute to aseptic loosening of orthopedic implants. Methods Peripheral blood samples were obtained from healthy human donors. Monocytes (MOs) were isolated and assigned to 6 groups. Group A was treated with MOs alone, group B with MOs + LPS (100ng/ ml), group C with MOs + ultrahigh molecular weight polylethylene (UHMWPE), group D with MOs + UHMWPE + LPS (1ng/ml), group E with MOs + UHMWPE + LPS [10ng/ml), group F with MOs + UHMWPE + LPS [100ng/ml). The contents of TNF-α and IL -6 in the culture supernatant were measured by method of enzyme linked immunoadsorbent assay (ELISA). Results The released contents of TNF-α, IL- 6 from MOs were increased significantly compared with those before LPS or UHMWPE challenge(P〈0.05). And the content of TNF-α, IL- 6 were gradually increased by LPS with different concentrations(P(0.05). The content of targets above was little by little increased with stimulated time prolonging, then the peak of TNF-α, IL - 6 were appeared in 12h.Conclusions The inflammatory cytokine of TNF-α, IL- 6 are increased in the MOs stimulated by LPS. LPS and UHMWPE cooperative interact to enhance the biological effects of aseptic loosening.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:3.149.247.115