期刊文献+

中药方剂对肝纤维化大鼠肝脏ALR基因表达的影响 被引量:2

Effect of Chinese herbs on ALR mRNA expression in liver of the hepatic fibrosis rats
下载PDF
导出
摘要 目的从分子水平探测中药治疗肝纤维化的作用机制。方法利用CCL4复合因素建立SD大鼠肝纤维化模型。实验动物分成正常对照组、模型组、中药治疗组3组,分别检测各组生化、肝纤维化指标和肝组织中ALR mRNA表达变化。结果ALT、AST、A/G、HA、PCⅢ、LN、PLD各指标:模型组均高于对照组(P<0.01),中药治疗组低于模型组(P<0.01),且HA、PCⅢ、LN、PLD的降低与病理组织反应肝纤维化的好转程度一致;肝组织中ALR mRNA的相对表达量:中药治疗组、模型组明显高于对照组(P<0.01),中药治疗组高于模型组(P<0.01)。结论本中药方剂可显著升高肝纤维化大鼠肝组织ALR mRNA表达。 Objective To study the molecular mechanism of treatment by Chinese herbs on the hepatic fibrosis of rats. Methods Hepatic fibrosis model of rats was established with CCL4. Then the rats were divided into control; model and Chinese herbs treated groups. The level of ALR mRNA expression, biochemical and hepatic fibrosis parameters were observed, from different groups. Results The concentrations of ALT, AST, A/G, HA, LN, PLD and PCⅢ in model group were higher than those in control group (P 〈 0.01 ); those in Chinese herbs treated group were lower than in model group (P 〈 0,01). The decrease of the levels of HA, LN, PLD and PCⅢ in Chinese herbs treated group were correlated with the improvement of hepatic fibrosis observed by pathology. The level of ALR mRNA expression both in Chinese herbs treated group and model group were significantly higher than that in control group (P〈0.01). After treatment by Chinese herbs, the level of ALR mRNA expression in liver tissues was higher than that of control group (P 〈 0.01 ). Conclusions Our Chinese herbs significantly enhanced the ALR mRNA expression in liver of hepatic fibrosis rats.
出处 《疾病控制杂志》 2006年第4期335-338,共4页 Chinese Journal of Disease Control and Prevention
基金 河北省科技厅博士基金(04547002D-4)
关键词 基因表达调控 Gene expression regulation
  • 相关文献

参考文献9

  • 1Alcolado R, Arthar MJ, Iredale JP. Pathogenesis of liver fibrosis[J]. Clin Sci, 1997,92(2):103-112.
  • 2Pinzani M, Marra F, Carloni V. Singal transduction in hepatic stellate cells [J]. Liver, 1998,18(1): 2-13.
  • 3Hagiya M, Francarilla A, Polimeno L, et al. Cloning and sequence analysis of the rat augmenter of liver regeneration (ALR) gene: expression of biologically active recombinant ALR and demonstration of tissue distribution [J]. Proc Natl Acad Sci USA, 1994,91(17):8142-8146.
  • 4杨晓明,谢玲,邱兆华,宫锋,吴祖泽,贺福初.肝再生增强因子的cDNA克隆、表达及表达产物的生物活性研究[J].生物化学杂志,1997,13(2):130-135. 被引量:32
  • 5Van Gossum A, Never J. Low selenium status in alcoholic cirrhosis is correlated with aminopyrine breath test. Preliminary effects of selenium supplementation [J]. Biol Trace Elem Res, 1995,47(1-3):201-207.
  • 6Michelson AM. Selenium glutathione perxidase: some aspects inman [J]. J Environ Pathol Toxicol Oncol, 1998,17(3-4):233-239.
  • 7Burk RF, Early DS, Hill KE, et al. Plasma selenium in patients with cirrhosis [J]. Hepatology, 1998,27(3):794-798.
  • 8杨晓明,贺福初,谢玲,胡志远,王清明,邱兆华,吴祖泽.新型人肝再生增强因子的分子克隆及其性能研究[J].新消化病学杂志,1997,5(5):335-335. 被引量:29
  • 9张丽梅,刘殿武,杨洁.大鼠肝再生增强因子真核表达质粒对急性肝损伤的治疗作用[J].疾病控制杂志,2004,8(5):425-428. 被引量:7

二级参考文献13

共引文献60

同被引文献13

引证文献2

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部