期刊文献+

App17肽对Tau蛋白超磷酸化表达的影响 被引量:7

THE EFFECT OF App17 PEPTIDE ON THE EXPRESSION OF HYPERPHOSPHORYLATED Tau PROTEIN
下载PDF
导出
摘要 目的 通过对 Tau蛋白磷酸化在脑内分布的观察 ,研究 App17肽对糖尿病小鼠脑神经元 Tau蛋白磷酸化的影响。 方法 用链脲佐菌素 (streptozotion,STZ)诱发小鼠糖尿病模型 ,并皮下注射 App17肽对糖尿病小鼠进行治疗 ,4周后取脑组织做 AT- 8、Tau- 1、蛋白磷酸酯酶 (PP- 2 B)脱磷酸后的 Tau- 1免疫组织化学染色。 结果 糖尿病小鼠脑内 AT- 8阳性反应神经元广泛分布于压后颗粒皮层、海马、丘脑、下丘脑等部位 ,胞浆深染 ,而正常小鼠及 App17肽保护的糖尿病小鼠脑内阳性反应细胞仅在海马和压后颗粒皮层表达 ,阳性细胞数目少 ,染色淡 ;用Tau- 1单染正常小鼠脑及 App17肽治疗的糖尿病小鼠脑的压后颗粒皮层及海马阳性反应神经元数目多 ,糖尿病小鼠只有用 PP- 2 B脱磷酸后阳性反应神经元数目及染色程度才与正常组接近。 结论 糖尿病小鼠脑内 Tau蛋白磷酸化广泛表达 ,App17肽可改善糖尿病小鼠脑内 Tau蛋白磷酸化 ,从而改善学习与记忆。 Objective Through the observation on the distribution of hyperphosphorylated Tau,to investigate the connection between hyperphosphorylated Tau and learning, memory tasks. Furthermore, the treatment of App17 on brain tissues of diabetic mice. Methods Diabetic model mouse was produced in the use of streptozotion and App17 peptide as a curative was injected subcutaneously. Four weeks later, removed the brains. Immunohistochemical stainning was done with AT\|8, Tau\|1, again with Tau\|1 antibody after dephosphorylation. Results In the brains of diabetic mice positive AT\|8 reacting neurons were widely distribution in retrosplenial granular cortex, hippocampas, thalamus et al, the cytoplasm was darkly stained, while in normal mice and App17 peptide\|treated diabetic mice positive cells were localized in retrosplenial granular cortex, however, in hippocampas and RSG area, the cytoplasm were poorly stained. Conclusion Hyperphosphorylated Tau is widely expressed in brains of diabetic mice. App17 peptide can improve the hyperphosphorylated Tau in brains of diabetic mice, therefore, it may improve learning ability and memory.\;
出处 《解剖学报》 CAS CSCD 北大核心 2001年第1期30-33,T010,共5页 Acta Anatomica Sinica
基金 北京市科委资助项目!( 95 1890 60 0 )
关键词 APP17肽 糖尿病脑病 TAU蛋白 超磷酸化 小鼠 老年性痴呆 App17 peptide Diabetic encephalopathy Tau protein Hyperphosphorylation
  • 相关文献

参考文献3

二级参考文献2

  • 1Gong C X,FEBS Lett,1994年,341卷,94页
  • 2Becky Welsh,Lynn Wecker. Effects of streptozotocin-induced diabetes on acetylcholine metabolism in rat brain[J] 1991,Neurochemical Research(4):453~460

共引文献16

同被引文献16

  • 1徐杰,单国冰,姚志彬.脑内胰岛素研究进展[J].解剖科学进展,1995,1(2):183-188. 被引量:10
  • 2李文彬,韦丰,范明,张京立,张炳烈,马向晨,杨卫平,魏文.D-半乳糖在小鼠上诱导的拟脑老化效应[J].中国药理学与毒理学杂志,1995,9(2):93-95. 被引量:170
  • 3Sheng SHL. Alzheimer Disease: From Molecular Biology to Clinical Diagnosis and Treatment [M]. Beijing: Scientific and Technical Documents Publishing House, 1998: 222-224.盛树力.老年痴呆病:从分子生物学到临床治疗[M].北京:科学技术文献出版社,1998:222-224.
  • 4Soilu HM, Ekert P, Bucci T, et al. Nerve growth factor signaling through p75 induces apoptosis in Schwann cells via a Bcl-2-independent pathway[J]. Neurosci, 1999,19(12) :4828-4838.
  • 5Lindenboim L, Haviv R, Stein R. Bcl-xl inhibits different apoptosis pathways in rat PC 12 cells [J]. Neurosci Lett, 1998,253 (1): 37-40.
  • 6Yuan J, Yankner BA. Apoptosis in the nervous System[J]. Nature, 2000,407 (6805): 802-809.
  • 7Lambeng N, Michel PP, Brugg B, et al. Mechanisms of apoptosis in PC12cells irreversibly differentiated with nerve growth factor and cyclic AMP[J]. Brain Res, 1999,821(1);60-68.
  • 8Khwaja A. Akt is more than just a bad kinase[J]. Nature, 1999,401(6748): 33-34.
  • 9崔旭,李文彬,张炳烈,张洁.D-半乳糖脑老化模型的脂质过氧化机理[J].中国老年学杂志,1998,18(1):38-40. 被引量:83
  • 10赵咏梅,赵志炜,姬志娟,钱玉英,孙异临,晋志高,盛树力.APP17肽对糖尿病小鼠微管结构和tau蛋白磷酸化有关酶类的影响[J].中华老年医学杂志,1999,18(5):306-309. 被引量:12

引证文献7

二级引证文献32

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