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作 者:张武山[1]
机构地区:[1]太原市中心医院
出 处:《山西临床医药》1999年第4期251-253,共3页Shanxi Clinical Medicine
摘 要:要⑶目的⑶观察小剂量内毒素⒉ L P S⒕预处理对大鼠肝脏缺血再灌注损伤⒉ I/ R⒕模型⒚方法⑶小剂量内毒素预处理组于术前 24h 给予 L P S⒙分别于复灌后 60m in⒙90m in⒙120m in 测定血中肝功能酶活性及肝组织中肿瘤坏死因子⒉ T N Fα⒕及前列腺素 E1 ⒉ P G E1 ⒕含量⒙并与缺血再灌注组比较⒚结果⑶ L P S预处理组在各采样时点肝功能酶活性组织 T N Fα含量均显著低于 I/ R 组⒙⒉ P< 0.05⒕⒚而组织中 P G E 含量则明显高于 I/ R组⒉ P< 0.05⒕⒚结论⑶小剂量 L P S预处理可能系通过刺激巨噬细胞合成 P G E1 ⒙而对大鼠肝脏 I/ RObjective:To study the protective effect of preconditioning with LPS on ischemia-reperfusion injury in rat liver.Methods:LPS was injected 24 hours before operation,the serum GOT,GPT activity and tissue TNFα,PGE 1 content of LPS preconditioning group were detected and compared with that of I/R group at 60min,90min and 120min when reperfused.Results:the enzyme activity and TNFα are significantly lower in LPS preconditioning group than that in I/R group(P<0.05),however,the content of PGE 1 is higher in LPS group than in I/R group(P<0.05).Con clusion:LPS can stimulate the macrophage cell to produce PGE,Which led to the protective effect of preconditioning on I/R injury in rat liver.
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