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维拉帕米作用下急性心梗大鼠比较蛋白质组学研究
引用本文:李莹,王毅,瞿海斌,程翼宇.维拉帕米作用下急性心梗大鼠比较蛋白质组学研究[J].高等学校化学学报,2008,29(3):515-518.
作者姓名:李莹  王毅  瞿海斌  程翼宇
作者单位:浙江大学中药科学与工程学系,杭州,310058
基金项目:国家重点基础研究发展计划(973计划) , 教育部跨世纪优秀人才培养计划
摘    要:以急性心梗大鼠为研究对象, 应用双向凝胶电泳法(2-DE)分析比较了维拉帕米作用下急性心梗大鼠心肌蛋白表达的差异, 从蛋白质水平探讨了维拉帕米心肌保护作用的发生机制. 结果表明, 与假手术组及模型组相比, 维拉帕米给药组心肌组织中有8个蛋白点表达显著上调, 7个蛋白点表达显著下调. 采用质谱(MALDI-TOF-MS)分析结合数据库检索, 共鉴定了其中的15种蛋白质, 可按功能分为如下4类: (1) 能量代谢及线粒体功能相关蛋白; (2) 氧化应激相关蛋白; (3) 细胞骨架蛋白; (4) 其它蛋白. 研究结果表明, 维拉帕米的心肌保护作用与恢复心肌损伤过程中的能量供应及对抗氧化应激等作用有关.

关 键 词:维拉帕米  蛋白质组  双向电泳
文章编号:0251-0790(2008)03-0515-04
收稿时间:2007-08-14
修稿时间:2007年8月14日

Proteome Study of Differential Protein Expression in Acute Infracted Rat Heart after Verapamil Treatment
LI Ying,WANG Yi,QU Hai-Bin,CHENG Yi-Yu.Proteome Study of Differential Protein Expression in Acute Infracted Rat Heart after Verapamil Treatment[J].Chemical Research In Chinese Universities,2008,29(3):515-518.
Authors:LI Ying  WANG Yi  QU Hai-Bin  CHENG Yi-Yu
Institution:Department of Chinese Medicine Science &; Engineering, Zhejiang University, Hangzhou 310058, China
Abstract:To explore the protein-level action mechanism of verapamil in acute myocardial infracted rats,the myocardial proteome was analyzed by two-dimensional electrophoresis(2-DE).In comparison with the sham-operated group and the infracted group,the result shows that eight proteins expressions in verapamil treated group were up-regulated,and seven proteins expression in this group were down-regulated significantly.By using MALDI-TOF-MS,15 proteins with significant changes were identified by database searching.These proteins can be divided into four groups via their biological function:(1) energy metabolism and mitochondrial function related proteins;(2) oxidative stress-induced proteins;(3) cytoskeletal proteins;(4) other proteins.The findings show that the myocardial protective effects of verapamil in myocardial damage process were related to the recovery of energy supply as well as anti-oxidative stress property.
Keywords:Verapamil  Proteomics  Two-dimensional electrophoresis(2-DE)
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