期刊文献+

ZDY101和SZ201对α-分泌性淀粉样前体蛋白生成的影响 被引量:4

The Effect of ZDY101 and SZ201 on α-sAPP Generation
下载PDF
导出
摘要 目的探讨ZDY10 1和SZ2 0 1及二者不同配比联合应用对HEK2 93sw细胞生成α -分泌性淀粉样前体蛋白的影响。 方法用Westernblot法检测HEK2 93sw细胞生成的α -sAPP含量 ,观察ZDY10 1、SZ2 0 1及二者不同配比联合应用在 2 4~ 48h、48~ 72h时段内α -sAPP生成量的变化。 结果 2 4~ 48h时段的实验中 ,ZDY10 1和SZ2 0 1浓度分别为 1× 10 - 5mol L时 ,α -sAPP含量分别为 2 .0 6± 0 .73、2 .6 4± 1.2 1,明显高于DMSO对照组的 1.0 0(P <0 .0 1) ;48~ 72h时段的实验中 ,ZDY10 1和SZ2 0 1单独应用且浓度分别为 1× 10 5mol L时 ,α -sAPP含量也明显高于DMSO对照组的 1.0 0 (P <0 .0 1)。二者相加的效果高于ZDY 10 1、SZ2 0 1单独应用 (P <0 .0 5 )。如果二者联合应用 ,降低各自的浓度 ,总浓度仍为 1× 10 - 5mol L时 ,提高α -sAPP含量的效果不明显。 结论ZDY10 1、SZ2 0 1在一定浓度时 ,能增加α -sAPP的生成 ,二者联合应用效果更强。 Objective To study the effect of single or combined application of ZDY101 and SZ201 on the generation of α-sAPP by HEK293sw cells. Methods The levels of α-sAPP from HEK293sw cells were examined by Western blot and the effects of single or combined application of ZDY101 and SZ201 on generation of α-sAPP were observed from 24h to 48h or 48h to 72h. Results In the time period of 24h to 48h,when ZDY101 or SZ201 was applied separately at 1×10 -5mol/L,the level of α-sAPP was 2.06±0.73 and 2.64±1.21,respectively significantly higher than the DMSO control(1.00).In the time period of 48 to 72h,when the concentration of ZDY101 or SZ201 was 1×10 -5mol/L,the level of α-sAPP was 1.77±0.5 and 2.31±0.62,respectively also significantly higher than the DMSO control(1.00).When the two substances were used in combination,each at 1×10 -5mol/L,the level of α-sAPP was higher than that with single ZDY101 or SZ201 group.However,when the concentrations of both substances were lowered to make the total concentration equal to 1×10 -5mol/L,the elevation effect on α-sAPP was not significant. Conclusion ZDY101and SZ201 promote the generation of α-sAPP when the concentration of the substances reached certain level,combination of ZDY101, and SZ201 is more effective than ZDY101 or SZ201 alone.
出处 《上海第二医科大学学报》 CSCD 2002年第4期289-291,296,共4页 Acta Universitatis Medicinalis Secondae Shanghai
基金 国家自然科学基金资助项目 (30 0 70 92 6)
  • 相关文献

参考文献9

  • 1Christian H,Michael GS Albert YH,et al.Amyloid β-peptide is produced by cultured cells during normal metabolism[].Nature.1992
  • 2Tadatoshi K,Yasuko O,Hiroyuki S,et al.Arachidonate metabolites affect the secretion of an N-terminal fragment of AD amyloid precursor protein[].Biochemical and Biophysical Research Communications.1995
  • 3Van Nostrand WE,Schmaier AH,Farrow JS,et al.Protease nexin-Ⅱ(amyloidβ-protein precursor): A plateletα-granule protein[].Science.1990
  • 4Yan RQ,Michael JB,Mary ES,et al.Membrane - anchored aspartyl protease with Alzheimer’s disease β- secretase activity[].Nature.1999
  • 5Abbenante G,Kovacs DM,Leung DL,et al.Inhibitors of β-amyloid formation based on the β-secretase cleavage site[].Biochemical and Biophysical Research Communications.2000
  • 6Selkoe DJ.Cell biology of the amyloid β- protein precursor and the mechanism of Alzheimer’s disease[].Annual Review of Cell Biology.1994
  • 7Sinha S,Anderson JP,Barbour R,et al.Purification and cloning of amyloid precursor protein β-secretase from human brain[].Nature.1999
  • 8Citron M,Diehl TS,Capell A,et al.Inhibition of Amyloid β- protein production in Neural Cells by the serine protease inhibitor AEBSF[].Neuron.1996
  • 9Michael F,Christine E,Schnitzler NV,et al.BACE2, a β- secretase homolog, cleaves at the βsite and within the amyloid-βregion of the amyloid-βprecursor protein[].Proceedings of the National Academy of Sciences of the United States of America.2000

同被引文献27

引证文献4

二级引证文献22

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