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:廖联琼 蒋兴亮[2] 刘素兰[2] 张均[2] 王光华[2]
机构地区:[1]广安市人民医院检验科,四川广安638000 [2]川北医学院附属医院检验科,四川南充637000
出 处:《四川医学》2010年第4期418-420,共3页Sichuan Medical Journal
基 金:四川省卫生厅科研课题(编号:2009042)
摘 要:目的探讨对氧磷酯酶1(PON1)活性在溃疡性结肠炎(UC)中的变化及临床意义。方法分别测定44例活动期UC患者、23例缓解期UC患者及32例健康对照者的血浆PON1、C-反应蛋白(CRP)及丙二醛(MDA)含量,分析其相关性。结果活动期及缓解期UC组血浆CRP、MDA含量显著高于对照组(P<0.05),血浆PON1活性显著低于对照组(P<0.05)。活动期患者组血浆CRP、MDA含量显著高于缓解期患者组(P<0.05),血浆PON1活性显著低于缓解期患者组(P<0.05)。UC患者组对氧磷酯酶1活性与MDA及CRP水平呈负相关(r=-0.358,P<0.01,r=-0.422,P<0.01)。结论UC患者PON1活性显著降低,增加的氧自由基(OFR)导致致氧化环境可能使血浆PON1活性显著降低。Objective To investigate the change of plasma antioxidant enzyme paraoxonase 1(PON1)activity in patients with ulcerative colitis(UC),as well as its clinical significances.Methods Plasma PON1 activity,malondiadehyde(MDA) and C-reactive protein(CRP) levels were analysed in 44 case of active ulcerative colitis,23 case of ulcerative colitis in remission and 32 case of control.Correlation analysis was made between these variables.Results Plasma PON1 activity was lower and MDA,CRP levels was higer in the active and remission patients groups than the control.When active subgroups were compared with the remission group,there was a statistically difference between each parameter.Plasma PON1 activity was significantly lower,while CRP and MDA levels was significantly higer in the active UC group than the remission UC group.The analysis of linear correlation showed PON1 was negatively correlated with MDA(r=-0.358,P0.01),CRP(r=-0.422,P0.01) in patients with ulcerative colitis.Conclusion Plasma PON1 activity was significantly decreased in patients with ulcerative colitis.Increased oxygen free radicals(OFR) levels in ulcerative colitis may result in a pro-oxidation environment,which in turn could result in decreased antioxidant paraoxonase 1 activity.
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:216.73.216.63