期刊文献+

BALB/c、C57BL/6小鼠糖皮质激素效应差异机制研究 被引量:1

The study of glucocorticoid efficiency difference between BALB/c and C57BL/6 mice
下载PDF
导出
摘要 目的 观察BALB/c和C5 7BL/ 6两株小鼠的糖皮质激素 (Gc)效应差异 ,并对其分子机制进行初步探讨。方法 采用放免测定、Westernblot和EMSA方法检测两株小鼠即时应激前后血清皮质醇浓度、脑组织糖皮质激素受体 (GR)表达和脑组织GRE结合效率。结果 BALB/c和C5 7BL/ 6小鼠存在Gc GR信号通路效应差异 ,C5 7BL/ 6小鼠应激前、后GRE结合效率 (P <0 .0 1)和GR胞核 /胞浆比值 (P <0 .0 1)均高于BALB/c小鼠 ,但两株小鼠应激前后血清皮质醇浓度 (P >0 .0 5 )和胞浆内GR含量(P >0 .0 5 )相差不显著。结论 GR核转位量导致的GRE结合差异在两株小鼠Gc GR效应差异中扮演了重要角色。 Objective To observe the glucocorticoid efficiency difference between BALB/c and C57BL/6 mice and also to study its molecular mechanism. Methods RIA, Western blot and EMSA methods were used to detect serum concentration of cortisol, expression of glucocorticoid receptor (GR) and glucocorticoid response element (GRE) binding efficiency in brain tissue. Results The different efficiency of Gc GR pathway was confirmed between BALB/c and C57BL/6 mice. GRE binding efficiency and the ratio of nucleus/cytoplasm of GR in the brain tissue of C57BL/6 mice were significantly higher than those of BALB/c mice, while there was no significant difference of the concentration of cortisol and cytoplasmic GR in the brain tissue of the two strains of mice. Conclusion The difference of GR nucleic translocation may play an important role in the different efficiency of Gc GR pathway between BALB/c and C57BL/6 mice via regulating GRE binding.
出处 《重庆医学》 CAS CSCD 2003年第6期644-646,共3页 Chongqing medicine
基金 国家自然科学基金资助项目 (30 1 0 0 1 0 6) 全国优秀博士论文基金资助项目 (2 0 0 1 56)
关键词 糖皮质激素效应 信号转导 糖皮质激素反应元件 glucocorticoid efficiency signal transduction glucocorticoid response element
  • 相关文献

参考文献10

  • 1石汉平,李建珍,秦路平,缪明永,杨林,宋春桥,谭金兴,徐仁宝.失血大鼠肝、脑组织糖皮质激素受体的变化及其意义[J].中国危重病急救医学,1996,8(10):577-578. 被引量:8
  • 2冯刚,王正国,杨志焕,朱佩芳,周立雄,李晓炎,宁心,肖凯,张良,蒋建新.C57BL/6和BALB/C小鼠创伤反应差异性初步探讨[J].中华创伤杂志,2001,17(5):301-303. 被引量:14
  • 3Witchel SF, Smith RR. Glucocorticoid resistance in premature pubarche and adolescent hyperandrogenism[J].Mol Genet Metab, 1999,66(2) :137.
  • 4X Li, S Mohan, And W Gu,et al. Analysis of gene expression in the wound repair/regeneration process [J].Mammalian Genome, 2001,12(1) :52.
  • 5Ulett GC,Ketheesan N and Hirst RG. Cytokine gene expression in innately susceptible BALB/c mice and relatively resistant C57BL/6 mice during infection with virulent Burkholderia pseudomallei[J]. Infection Immunity,2000, 68(4): 2034.
  • 6Lewis S, Handy RD, Cordi B, et al. Stress proteins HSP's: methods of detection and their use as an environmental biomarker[J]. Ecotoxicology, 1999,8: 351.
  • 7X Li, Weikuan GU, and Godfred M, et al. Genetic control of the rate of wound healing in mice[J]. Heredity,2001, 86(Pt6): 668.
  • 8Amberts SW. The glucocorticoid insensitivity syndrome[J]. Horm Res,1996,45(Suppl 1) :2.
  • 9Jibard N, Meng X, Leclerc P, et al. Delimitation of two regions in the 90-kDa heat shock protein (Hsp90) able to interact with the glucocorticosteroid receptor (GR)[J].Exp Cell Res,1999,247(2),461.
  • 10Yan P, Xu J, Li Q, et al. Glucocorticoid receptor expression in the spinal cord after traumatic injury in adult rats[J], J Neurodci,1999, 19(21) :9355.

二级参考文献3

共引文献20

同被引文献5

  • 1Solit DB, Rosen N. Hsp90:a novel target for cancer therapy. Curt Top Med Chem,2006;6(11):1205-1214.
  • 2Ramesh Sathiyaa, Tracey Campbell, Mathilakath M. Cortisol modulates HSP90 mRNA expression in primary cultures of trout hepatocytes. Comp Biochem Physiol [B], 2001 ; 129 (2): 679-685.
  • 3Uehara Y. Natural product origins of Hsp90 inhibitors. Curr Cancer Drug Targets, 2003 ; 3 (5) : 325-330.
  • 4Workman P. Pharmacogenomics in cancer drug discovery and development: inhibitors of the Hsp90 molecular chaperone. Cancer Detect Prey ,2002 ; 26(6) :405-410.
  • 5周元国.加强创伤耐受性差异的分子基础研究,促进分子创伤学的发展[J].创伤外科杂志,2002,4(5):257-259. 被引量:2

引证文献1

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