期刊文献+

10种黄酮类化合物对糖尿病致病机制中重要通路的抑制作用 被引量:8

Inhibitory effects of 10 flavonoid glycosides on the pathways of diabetic pathogenesis
原文传递
导出
摘要 目的:观察10种黄酮类化合物对糖尿病致病机制中4条重要通路的多靶点抑制作用,发挥中药多靶点、综合治疗的优势。方法:从正常大鼠脑组织中提取半纯化的蛋白激酶C(PKC)、肾脏组织中提取醛糖还原酶(AR)粗酶,Fenton试剂体外激发正常大鼠脑组织脂质过氧化生成丙二醛(MDA)及体外合成高级糖化终产物(AGEs),将上述酶或合成物与10种黄酮类化合物(终浓度为1 mg.mL-1)作用,观察黄酮类化合物对上述酶或合成物的抑制作用。结果:黄芩苷和灯盏花素对AR,PKC,AGEs及MDA均有不同程度的抑制作用。结论:上述结果提示此两种黄酮类化合物可以通过抑制上述4条通路来预防糖尿病及其并发症的发生,为进一步的机制研究及临床应用提供良好的实验依据。 Objective:To estimate the inhibitory effects of 10 flavonoid glycosides on the 4 important pathways in diabetic pathogenesis,and to find new and effective extracts of Chinese herbs for treatment of diabetes.Methods:Semi-purified protein kinase C(PKC) was extracted from brains of normal rats,and crude aldose reductase(AR) was from kidneys.Malondialdehyde(MDA) was produced by activating brain tissue with Fenton reagent.Advanced glycation end products(AGEs) were synthetized in vitro.The effects of flavonoid glycosides(1 mg·mL^-1) on the enzymes or their products were observed.Results:Baicalin and breviscapine showed inhibitory effects on AR,PKC,AGEs and MDA with different degrees of activity.Conclusion:Among 10 flavonoid glycosides,baicalin and breviscapine have potentially preventing effects for diabetic pathogenesis by inhibiting the 4 important pathways.
作者 程丽艳 史红
出处 《中国新药杂志》 CAS CSCD 北大核心 2010年第9期793-796,共4页 Chinese Journal of New Drugs
基金 浙江省中医药管理局青年基金(2007YA022)
关键词 活性黄酮 糖尿病 并发症 active flavanoid diabetes complication
  • 相关文献

参考文献11

  • 1LIN D, LOBELL S, JEWELL A,et al. Differential phosphorylation of connexin46 and connexin50 by H2O2 activation of protein kinase Cγ[J]. Mol Vis ,2004 ,10 :688 -695. 被引量:1
  • 2AGARWAL R,CHASE SD. Rapid,fluorimetric-liquid chromatographic determination of malondialdehyde in biological samples [J]. J Chromatogr B Analyt Technol Biomed Life Sci,2002,775(1):121 -126. 被引量:1
  • 3HA TS,SONG CJ,LEE JH. Effects of advanced glycosylation end products on perlecan core protein of glomerular epithelium [ J]. Pediatric nephrology,2004,19( 11 ) :1219 - 1224. 被引量:1
  • 4DAS B, SRIVASTAVA SK. Purification and properties of aldose reductase and aldehyde reductase II from human erythrocyte [ J ]. Arch Biochem Biophys, 1985,238 (2) :670 - 679. 被引量:1
  • 5HERRMANN RK,KADOR PF, KINOSHITA JH. Rat lens aldose reductase:rapid purification and comparison with human placental aldose reductase [ J ]. Experimental Eye Research, 1983,37 (5) :467 -474. 被引量:1
  • 6IWAHORI Y, ENOMOTO S, OKADA Y,et al. Naturally occurring substances for prevention of complications of diabetes. IV. screening of seavegetables for inhibitory effect on aldose reductase [J]. Nat Med,1999 ,53( 3 ) :138 -140. 被引量:1
  • 7ROBERT Y, SHINJI T, NAOFUMI M. Identification of phenolic compounds isolated from pigmented rices and their aldose reductase inhibitory activities[ J]. Food Chem,2007,101 (4) :1616 - 1625. 被引量:1
  • 8LOGENDRA S, RIBNICKY DM, YANG H,et al. Bioassay-guided fractionation and isolation of aldose reduetase inhibitors from Artemisia dracunculus[ J]. Phytochemistry,2006,67 ( 14 ) : 1539 - 1546. 被引量:1
  • 9PRADHAN SC,GIRISH C. Hepatoprotective herbal drug,silymarin from experimental pharmacology to clinical medicine[ J]. Indian J Med Res,2006,124( 5 ) :491 -504. 被引量:1
  • 10JUNG UJ, LEE MK,PARK YB,et al. Effect of citrus flavonoids on lipid metabolism and glucose-regulating enzyme mRNA levels in type-2 diabetic mices[ J]. lnt J Biochem Cell Biol,2006,38 (7) :1134 - 1145. 被引量:1

同被引文献108

引证文献8

二级引证文献67

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