期刊文献+

丹黄方对大鼠肝再生过程中PC3、c-fos、LRF-1影响的实验研究 被引量:6

The experiment research of Danhuangfang influence expression of PC3 mRNA,c-fos mRNA,LRF-1 mRNA in rat liver regenerative process
下载PDF
导出
摘要 目的:探讨丹黄方对大鼠肝切除肝再生模型中促肝细胞再生的作用机制。方法:采用肝部分切除肝再生模型,用丹黄方进行干预,通过RT-PCR、电泳凝胶等方法检测与肝再生密切相关因子PC3 mRNA、c-fos mRNA、LRF-1 mRNA的表达,观察丹黄方对肝细胞再生的影响。结果:丹黄方对肝再生模型大鼠肝组织PC3 mRNA、c-fos mRNA的表达有增强作用,与模型比较,差异有显著性意义;对肝组织LRF-1 mRNA表达的影响不显著。结论:丹黄方可能是通过增强肝组织PC3 mRNA、c-fos mRNA的表达而促进肝细胞的增殖。 To approach the function mechanism of Danhuangfang (DHF) promoting the liver cell regenerate on the liver partial excision of liver regeneration model in rats. Methods: To adopt the liver partial excision of liver regeneration model in rats, carry on the intervention with DHF, examine the correlation factor which close liver regeneration expression of PC3 mRNA, c-fos mRNA, LRF-1 mRNA by gel electrophoresis and RT-PCR, observe the effectiveness which DHF influence liver regeneration. Results: DHF could enhance the hepatic tissue expression of PC3 mRNA, c-fos mRNA, LRF-1 mRNA in rats liver regeneration model, the DHF group had the significance difference comparing with the model group ; the DHF effected the hepatic tissue expression of LRF-1 mRNA which not to be remarkable. Conclusion: DHF can possibly promote the liver cell multiplication through enhancing the hepatic tissue expression of PC3 mRNA, c-fos mRNA.
出处 《中西医结合肝病杂志》 CAS 2008年第1期32-34,37,共4页 Chinese Journal of Integrated Traditional and Western Medicine on Liver Diseases
基金 国家中医药管理局中医药科学技术研究专项(No.06-07JP25) 湖北省科技厅科技攻关计划项目(No.2005AA301C12)
关键词 丹黄方 肝再生 抗增殖相关分泌蛋白 细胞癌基因fos 肝再生因子-1 DanHuangFang (DHF) liver regeneration PC3 c-fos LRF-1
  • 相关文献

参考文献13

  • 1Higgins GM, Anderson RM. Eeperimental pathology of the liverregeneration fo the liver by the white rat foiling parital suricai ronoval. Arch Pathol, 1931, 12:186-189
  • 2Panis Y, Lomri N, Emond JC. Early gene expression associated with regeneration is intact after massive hepatectomy in rats. J Surg Res, 1998, 2:103-106
  • 3王阁,张晓荣,胡辂,王军,冷恩仁,房殿春,杨晓明,张咏,贺福初.肝细胞生成素及肝部分切除诱导肝再生基因PC3的表达[J].中华肝脏病杂志,2002,10(4):256-259. 被引量:6
  • 4Bradbury A, Possenti R, Shooter EM, et al. Molecular cloning of PC3, a putatively secreted protein whose mRNA is induced by nerve growth factor and depolarization. Proc Natl Acad Sci USA, 1991, 88: 3353- 3357
  • 5Corral ML, Tichonick C, Guguen-Guillouzo D, et al. Expression of c- fos during hepatocarcinogenesis, liver regeneration and in synchronized HTC cells. Exp Cell Res, 1985, 160:427-431
  • 6Hunter Tony, Cooperation between oncogenes. Cell, 2001, 64: 249- 453
  • 7Jui Chou Hsu, Thomas Laz, Kenneth L, et al. Identification of LRF-1, a leucine-zipper protein that is rapidly and highly induced in regenerating liver. Prec. Natl. Acad Sci. USA, 1991, 88:3511-3514
  • 8杨晓明,王爱民,周平,王清明,吴祖泽,贺福初.人肝再生增强因子促肝增殖及其抗肝损伤作用[J].科学通报,1998,43(6):616-620. 被引量:22
  • 9Mohn KL, Melby AE, Tewari DS, et al. The gene encoding rat insulin- like growth factor-binding protein 1 is rapidly and highly induced in regenerating liver. Mol Cell Biol, 1991, 11:1393-1396
  • 10Hsu JC, Bravo R, Taub R. Interactions among LRF-1, Jung B, c-Jun and c-fos define a regulatory G1 phase of liver regeneration. Mol Cell, 1992, 4654-4658

二级参考文献20

  • 1武希润 郭文栋 等.大黄对暴发性肝衰竭肝损伤及肝再生的影响[J].中华肝脏病杂志,1999,7(3):179-179.
  • 2FUJIWARA K, OGATA I, TOMIYA T, et al. Insulin and glucogen therapy of acute hepatic failure[J]. Dig Dis Sei,1991,36:8093.
  • 3WOLF H K, MICHALOPOULOS G K. Hepatocyte regeneration in acute fulminant and nonfulminant hepatitia:a study of proliferation cell nucier antigen expression[J]. Hepatology, 1992,15:707.
  • 4杨晓明,生物物理与生物化学学报,1997年,4期,421页
  • 5杨晓明,中国科学.C,1997年,27卷,5期,463页
  • 6谢玲,中国应用生理杂志,1996年,12卷,4期,324页
  • 7He Fucho,Hepatology,1993年,17卷,225页
  • 8涂强,中国病理生理学杂志,1991年,7卷,5期,537页
  • 9Panis Y, Lomri N,Emond JC. Early gene expression associated with regeneration is intact after massive hepatectomy in rats. J Surg Res, 1998,2:103~108
  • 10Fromowitz FB, Voila MV, Chao S, et al. Ras P21 Ras P21 expression in the progession of breast cancer. Hum Pathol,1987,18:1268~1275

共引文献59

同被引文献77

引证文献6

二级引证文献17

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