中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Cardio-Protection of Salvianolic Acid B through Inhibition of Apoptosis Network

文献类型:期刊论文

作者Xu, Lingling1; Deng, Yanping1; Feng, Lixin1; Li, Defang1; Chen, Xiaoyan1; Ma, Chao1; Liu, Xuan1; Yin, Jun2; Yang, Min1; Teng, Fukang1,2
刊名PLOS ONE
出版日期2011-09-06
卷号6期号:9
ISSN号1932-6203
DOI10.1371/journal.pone.0024036
文献子类Article
英文摘要Targeting cellular function as a system rather than on the level of the single target significantly increases therapeutic potency. In the present study, we detect the target pathway of salvianolic acid B (SalB) in vivo. Acute myocardial infarction (AMI) was induced in rats followed by the treatment with 10 mg/kg SalB. Hemodynamic detection and pathological stain, 2-dimensional electrophoresis, MALDI-TOF MS/MS, Western blot, pathway identification, apoptosis assay and transmission electron microscope were used to elucidate the effects and mechanism of SalB on cardioprotection. Higher SalB concentration was found in ischemic area compared to no-ischemic area of heart, correlating with improved heart function and histological structure. Thirty-three proteins regulated by SalB in AMI rats were identified by biochemical analysis and were classified as the components of metabolism and apoptosis networks. SalB protected cardiomyocytes from apoptosis, inhibited poly (ADP-ribose) polymerase-1 pathway, and improved the integrity of mitochondrial and nucleus of heart tissue during AMI. Furthermore, the protective effects of SalB against apoptosis were verified in H9c2 cells. Our results provide evidence that SalB regulates multi-targets involved in the apoptosis pathway during AMI and therefore may be a candidate for novel therapeutics of heart diseases.
WOS关键词MOLECULAR NETWORKS ; DRUG DISCOVERY ; HEART-FAILURE ; PATHWAY ; DEATH ; CELLS
资助项目National Science and Technology Major Project for "Key New Drug Creation and Manufacturing Program"[2009ZX09308-005] ; National Science and Technology Major Project for "Key New Drug Creation and Manufacturing Program"[2009ZX09102-122] ; National Science and Technology Major Project for "Key New Drug Creation and Manufacturing Program"[2009ZX090304-002] ; National Science and Technology Major Project for "Key New Drug Creation and Manufacturing Program"[2009ZX09311-001] ; National Science and Technology Major Project for "Key New Drug Creation and Manufacturing Program"[2009ZX09502-020]
WOS研究方向Science & Technology - Other Topics
语种英语
WOS记录号WOS:000294689200016
出版者PUBLIC LIBRARY SCIENCE
源URL[http://119.78.100.183/handle/2S10ELR8/278406]  
专题上海中药现代化研究中心
通讯作者Xu, Lingling
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 200031, Peoples R China;
2.Shenyang Pharmaceut Univ, Shenyang, Peoples R China
推荐引用方式
GB/T 7714
Xu, Lingling,Deng, Yanping,Feng, Lixin,et al. Cardio-Protection of Salvianolic Acid B through Inhibition of Apoptosis Network[J]. PLOS ONE,2011,6(9).
APA Xu, Lingling.,Deng, Yanping.,Feng, Lixin.,Li, Defang.,Chen, Xiaoyan.,...&Guo, Dean.(2011).Cardio-Protection of Salvianolic Acid B through Inhibition of Apoptosis Network.PLOS ONE,6(9).
MLA Xu, Lingling,et al."Cardio-Protection of Salvianolic Acid B through Inhibition of Apoptosis Network".PLOS ONE 6.9(2011).

入库方式: OAI收割

来源:上海药物研究所

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