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胡晓霞, 王艳, 王妮. p38MAPK、NF-B与氧化应激在肝纤维化中作用[J]. 中国公共卫生, 2013, 29(6): 834-836. DOI: 10.11847/zgggws2013-29-06-17
引用本文: 胡晓霞, 王艳, 王妮. p38MAPK、NF-B与氧化应激在肝纤维化中作用[J]. 中国公共卫生, 2013, 29(6): 834-836. DOI: 10.11847/zgggws2013-29-06-17
HU Xiao-xia, WANG Yan, WANG Ni. Effect of p38MAPK,NF-B and oxidative stress in liver fibrosis[J]. Chinese Journal of Public Health, 2013, 29(6): 834-836. DOI: 10.11847/zgggws2013-29-06-17
Citation: HU Xiao-xia, WANG Yan, WANG Ni. Effect of p38MAPK,NF-B and oxidative stress in liver fibrosis[J]. Chinese Journal of Public Health, 2013, 29(6): 834-836. DOI: 10.11847/zgggws2013-29-06-17

p38MAPK、NF-B与氧化应激在肝纤维化中作用

Effect of p38MAPK,NF-B and oxidative stress in liver fibrosis

  • 摘要: 目的观察p38丝裂原活化蛋白激酶(p38MAPK)、核因子-κBp50(NF-κBp50)在肝纤维化发生发展中作用。方法选取SD大鼠30只,随机分为对照组、肝纤维化4、8周组,每组各10只;肝纤维化组按0.3 mL/100g皮下注射40% CCl4,隔3 d注射1次,造模时间分别为4和8周;于相应时间点处死大鼠并收集肝组织,观察肝组织病理学改变;采用比色法检测肝组织中丙二醛(MDA)及超氧化物歧化酶(SOD)含量;采用免疫组化及western blot检测肝组织中p38MAPK、NF-κBp50蛋白表达变化。结果与对照组比较,肝纤维化4周组大鼠肝组织中p38MAPK(7.9±2.3)、NF-κBp50(16.3±8.1)、MDA(1.8±0.9) nmol/mgprot及肝纤维化8周组大鼠肝组织中p38MAPK(11.5±6.8)、NF-κBp50(24.6±13.5)和MDA(2.9±1.3) nmol/mgprot的含量均升高(P<0.05);与对照组比较,肝纤维化4、8周组大鼠肝组织中SOD酶活性(40.6±5.8)、(34.4±3.1) μ/mgprot均降低(P<0.01)。结论p38MAPK、NF-κBp50及氧化应激可能在肝纤维化的发生发展过程中发挥重要作用。

     

    Abstract: ObjectiveTo observe the changes of p38 mitogen-activated protein kinase (p38MAPK) and nuclear factor-κ Bp 50 (NF-κBp50) in carbon tetrachloride (CCl4) induced liver fibrosis and to explore their effects on hepatic fibrosis. MethodsThirty Sprague-Dawley rats were randomly divided into normal control group,4 weeks liver fibrosis group and 8 weeks liver fibrosis group.Liver fibrosis model was induced by hypodermic injection of 40% CCl4 at the dosage of 0.3 ml/100 g body weight.The levels of malondialdehyde (MDA) and superoxide dismutase (SOD) in liver tissue were measured with colormtric method and the expressions of p38MAPK and NF-κBp50 protein were detected with immunohistochemical techniques and western blot. ResultsCompared with the normal control group,the levels of p38MAPK(7.9±2.3),NF-κBp50(16.3±8.1),and MDA(1.8±0.9 nmol/mgprot) in 4 weeks liver fibrosis group and the levels of p38MAPK(11.5±6.8),NF-κBp50(24.6±13.5),and MDA(2.9±1.3 nmol/mgprot) in 8 weeks liver fibrosis group were increased,while the activityies of SOD (40.6±5.8,34.4±3.1 u/mgprot) in 4 weeks and 8 weeks liver fibrosis groups were decreased. Conclusionp38MAPK,NF-κBp50 and oxidative stress may play important roles in CCl4 induced liver fibrosis.

     

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