期刊文献+

糖基化终末产物及相关药物研究进展 被引量:25

Advanced glycosylation end products and related drug development
下载PDF
导出
摘要 糖基化终末产物(AGEs)是蛋白质和脂类经非酶糖基化后生成的含多种结构分子的混合物,阻断AGEs的致病途径有望成为改善糖尿病慢性并发症,缓解衰老,治疗老年痴呆等的新途径。该文主要综述了体内AGEs的来源,病理生理学机制,及AGEs生成抑制剂,断裂剂及AGEs受体阻断剂的研究进展。 Glycosylation end products (AGEs) are a mixture containing various structural compounds, which are products of proteins and lipids through non-enzymatic glycosylation. Bloc- king the pathogenesis of AGEs is expected to be an effective new way to improve the chronic complications of diabetes, to treat Alzheimer' s disease, and to ease aging. This article reviews the major source of AGEs in vivo, pathophysiological mechanisms,and the drug development of AGE-inhibitors, AGE-breakers and receptor antagonist agents of progress.
出处 《中国药理学通报》 CAS CSCD 北大核心 2011年第9期1185-1188,共4页 Chinese Pharmacological Bulletin
基金 中国科技部-魁北克合作项目(No2008DFA31710) 科技部十一五"重大新药创制"科技重大专项(No2009ZX09102-123)
关键词 晚期糖基化终末产物 药物治疗 AGEs断裂剂 AGEs生成抑制剂 AGEs受体 糖尿病慢性并发症 老年痴呆 advanced glycosylation end products drug thera-py AGE-breaker AGE-inhibitor advanced glycosylation end-product receptor chronic complications of diabetes Alzheimer'sdisease
  • 相关文献

参考文献1

二级参考文献24

  • 1Thomalley P J. Glyoxalase I-structure, function and a critical role in the enzymatic defence against glycation [J].Biochem Soc Trans, 2003,31(6) :1343 -8.
  • 2Kuhla B, Boeck K, Luth H J, et al. Age-dependent changes of glyoxalase I expression in human brain [J].Neurobiol Aging, 2006,27(6) : 815 -22.
  • 3Kalousova M, Zima T,Tesar V, et al. Advanced glyeoxidation end products in chronic diseases clinical chemistry and genetic back- ground [ J ]. Murat Res,2005,579 ( 1 - 2 ) :37 - 46.
  • 4Fujimoto M, Uchida S, Watanuki T, et al. Reduced expression of glyoxalase-1 mRNA in mood disorder patients [ J ]. Neurosci Letters, 2008,438 ( 2 ) : 196 - 9.
  • 5Chen F,Wollmer M A, Hoerndli F,et al. Role for glyoxalase I in Alzheimer's disease[J].Proc Natl Acad Sci USA ,2004,101 ( 20 ) : 7687 - 92.
  • 6Cameron A D, Olin B, Ridderstron M, et al. Crystal structure of human glyoxalase I-evidence for gene duplication and 3D domain swapping[ J]. EMBO J, J 997,16 ( 12 ) :3386 - 95.
  • 7Ridderstrom M,Cameron A D, Jones T A, et al. Involvement of an active-site Zn^2 + ligand in the catalytic mechanism of human glyoxalase I[J]. Biol Chem,1998,273(34) :21623 -8.
  • 8Thornalley P J. Population genetics of human glyoxalases [ J ]. Heredity, 1991,67 ( Pt2 ) : 139 - 42.
  • 9Ranganathan S, Ciaccio P J,Walsh E S, et al. Genomic sequence of human glyoxalase-I:analysis of promoter activity and its regulation[J]. Gene, 1999,240( 1 ) : 149 - 55.
  • 10Kim N S, Sekine S, Kiuchi N, et al. cDNA cloning and characterization of human glyoxalase I isoforms from HT-1080 cells[J]. Biochem,1995,117(2) :359 -61.

共引文献10

同被引文献372

引证文献25

二级引证文献404

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