期刊文献+

Exendin-4与神经退行性疾病的关系 被引量:1

Relationship between exendin-4 and neurodegenerative diseases
下载PDF
导出
摘要 Exendin-4是一种糖尿病新药,也是胰高血糖素样肽-1(GLP-1)类似物,能激活GLP-l受体,上调cAMP发挥生理活性。GLP-1受体与神经元可塑性及存活密切联系。Exendin-4还能激活多条信号通路,调节胞内钙离子(Ca2+)稳态,减轻兴奋性毒性,抑制细胞凋亡,促进神经元增生、分化,对神经退行性疾病有治疗作用。该文旨在阐明exendin-4的神经保护机制,为神经退行性疾病的预防与治疗提供新思路。 Exendin-4,a peptide analogue of glucagon-like peptide-1(GLP-1),is presently in clinical trials as a therapy for type 2 diabetes mellitus.Exendin-4 selectively acts on GLP-1 receptors,which are coupled to the cAMP nucleotide second messenger pathway to enhance the survival and plasticity of neurons in the brain.Exendin-4 has potent effects on homeostasis of Ca2+,on multiple targets to block apoptotic signaling pathways,and on neuronal proliferation and differentiation.It has also been demonstrated to possess properties against oxidative stress and excitotoxicity.In this review the functions of exendin-4 on central nerve system and the potentia therapeutic effects on neurodegenerative diseases will be involved.
作者 柳超 郭军
出处 《中国药理学通报》 CAS CSCD 北大核心 2010年第5期566-569,共4页 Chinese Pharmacological Bulletin
基金 国家自然科学基金资助项目(No30871200) 江苏省卫生厅自然科学基金资助项目(NoH200749)
关键词 EXENDIN-4 GLP-1受体 CAMP 神经退行性疾病 exendin-4 GLP-1 receptor cAMP neurodegenerative diseases
  • 相关文献

参考文献22

  • 1Eng J,Kleinman W A,Singh L,et al.Isolation and characterization of exendin-4,an exendin-3 analogue from Heloderma suspectum venom[J].J Biol Chem,1992,267(11):7402-5.
  • 2VanDeKoppel S,Choe H M,Sweet B V.Managed care perspective on three new agents for type 2 diabetes[J].J Manag Care Pharm,2008,14(4):363-80.
  • 3Goke R,Fehmann H C,Linn T,et al.Exendin-4 is a high potency agonist and truncated exendin-(9-39)-amide an antagonist at the glucagon-like peptide 1-(7-36)-amide receptor of insulin-secreting beta-cells[J].J Biol Chem,1993,268(26):19650-5.
  • 4Al-Sabah S,Donnelly D.A model for receptor-peptide binding at the glucagon-like peptide-1(GLP-1)receptor through the analysis of truncated ligands and receptors[J].Br J Pharmacol,2003,140(2):339-46.
  • 5Robles G I,Singh-Franco D.A review of exenatide as adjunctive therapy in patients with type 2 diabetes[J].Drug Des Devel Ther,2009,21(3):219-40.
  • 6光红梅,杜冠华.cAMP反应元件结合蛋白与神经退行性疾病[J].中国药理学通报,2006,22(3):262-266. 被引量:4
  • 7Pedersen W A,Wan R,Zhang P,et al.Urocortin,but not urocortinⅡ,protects cultured hippocampal neurons from oxidative and excitotoxic cell death via corticotropin-releasing hormone receptor typeⅠ[J].J Neurosci,2002,22(2):404-12.
  • 8Ferdaoussi M,Abdelli S,Yang J Y,et al.Exendin-4 protects β-cells from interleukin-1β induced apoptosis by interfering with the c-Jun NH2-Terminal kinase pathway[J].Diabetes,2008,57(5):1205-15.
  • 9潘静,陈生弟.JNK信号通路与神经退行性疾病[J].中国药理学通报,2008,24(8):999-1001. 被引量:6
  • 10Noma T,Yoon Y S,Nakazawa A.Overexpression of NeuroD in PC12 cells alters morphology and enhances expression of the adenylate kinase isozyme 1 gene[J].Brain Res Mol Brain Res,1999,67(1):53-63.

二级参考文献21

  • 1李军,曹红,连庆泉,王耀岐,曾因明.JNK通路在缺血预处理诱导海马神经元保护中的作用[J].中国药理学通报,2007,23(3):346-350. 被引量:4
  • 2Yang D D, Kuan C Y, Whitmarsh A J,et al. Absence of excitotoxicity-induced apoptosis in the hippocampus of mice lacking the Jnk3 gene [ J ]. Nature, 1997,389 ( 6653 ) :865 - 70.
  • 3Kuan C Y,Yang D D,Samanta Roy D R,et al. The Jnkl and Jnk2 protein kinases are required for regional specific apoptosis during early brain development [ J ]. Neuron, 1999,22 (4) :667 - 76.
  • 4Li G, Xiang Y, Sabapathy K, et al. An apoptotic signaling pathway in the interferon antiviral response mediated by RNase L and c-Jun NH2-terminal kinase [ J ]. J Biol Chem,2004,279 ( 2 ) : 1123 - 31.
  • 5Bogoyevitch M A ,Kobe B. Uses for JNK:the many and varied substrates of the c-Jun N-terminal kinases[ J]. Microbiol Mol Biol Rev, 2006,70(4) :1061 -95.
  • 6Ho D T, Bardwell A J, Grewal S, et al. Interacting JNK-docking sites in MKK7 promote binding and activation of JNK mitogen-activated protein kinases[ J]. J Biol Chem,2006,281 ( 19 ) : 13169 - 79.
  • 7Zou H, Li Q, Lin S C, et al. Differential requirement of MKK4 and MKK7 in JNK activation by distinct scaffold proteins [ J ]. FEBS Lett ,2007,581 ( 2 ) : 196 - 202.
  • 8Zhang J Y,Adams A E ,Ridky T W,et al. Tumor necrosis factor receptor 1/c-Jun-NH2-kinase signaling promotes human neoplasia [ J ]. Cancer Res, 2007,67 ( 8 ) : 3827 - 34.
  • 9Pan J,Wang G,Yang H Q,et al. K252a prevents nigral dopaminergic cell death induced by 6-hydroxydopamine through inhibition of both mixed-lineage kinase 3/c-Jun NH2-terminal kinase 3 ( JNK3 ) and apoptosis-inducing kinase 1/JNK3 signaling pathways [ J ]. Mol Pharmacol. 2007,72 ( 6 ) : 1607 - 18.
  • 10Mooney L M, Whitmarsh A J. Docking interactions in the c-Jun N- terminal kinase pathway[ J]. J Biol Chem ,2004,279 ( 12 ) : 11843 - 52.

共引文献8

同被引文献1

引证文献1

二级引证文献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