Modulation of the gene expression in the protective effects of electroacupuncture against cerebral ischemia: A cDNA microarray study

被引:17
作者
Guo, JC [1 ]
Gao, HM
Chen, J
Zhao, P
Cao, XD
Li, Y
Cheng, JS
机构
[1] Fudan Univ, Shanghai Med Coll, Natl Key Lab Med Neurobiol, Shanghai 200032, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Inst Acupuncture Res, WHO,Collaborating Ctr Tradit Med, Shanghai 200032, Peoples R China
[3] Fudan Univ, Sch Life Sci, Inst Genet Res, Shanghai 200433, Peoples R China
关键词
cerebral ischemia; electroacupuncture (EA); microarray; monkey; middle cerebral artery occlusion (MCAO); insulin-like growth factor (IGF-1);
D O I
10.3727/036012904815901434
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
In the present study, a cDNA microarray technology was used to analyze the gene expression profile in ischemia and in electroacupuncture (EA)-treated ischemia. A focal cerebral ischemia/ reperfusion model on Macaca mulatta was performed with a modified middle cerebral artery occlusion method. Among the nearly 8,000 genes, approximately 8% of the total number of genes examined were affected after ischemia/ reperfusion injury. Major altered genes were downregulated. In EA-treated monkeys, approximately 10% of the total number of genes examined were affected. Major altered genes were upregulated, including signal transduction-, cell-cycle-, metabolism-, stress response-, DNA repair-related genes. One of the representative upregulated genes encodes insulin-like growth factor-1 (IGF-1) was confirmed using in situ hybridization. Results showed that after ischemia/ reperfusion injury, IGF-1 mRNA expression decreased in ipsilateral striatum, whereas increased in ipsilateral hippocampus. No expression changes were observed in cortex. EA treatment could obviously upregulate the IGF-1 mRNA expression in striatum, and further enhance its expression in hippocampus. Therefore, the data presented suggest a possible mediator underlying the mechanisms of anti-ischemic effect of acupuncture. In conclusion, the protective mechanisms of EA against stroke include several related pathways and gene expressions. Microarray analysis may provide a framework for understanding these complicated mechanisms and yield valuable, clinically relevant insights and potentially therapeutic targets of stroke.
引用
收藏
页码:173 / 186
页数:14
相关论文
共 20 条
[1]  
CHEN YH, 2000, ZHEN CI YAN JIU, V25, P165
[2]   The neuroprotective effects of electroacupuncture on focal cerebral ischemia in monkey [J].
Gao, HM ;
Guo, JC ;
Zhao, P ;
Cheng, JS .
ACUPUNCTURE & ELECTRO-THERAPEUTICS RESEARCH, 2002, 27 (01) :45-57
[3]   Expression of nuclear redox factor ref-1 in the rat hippocampus following global ischemia induced by cardiac arrest [J].
Gillardon, F ;
Böttiger, B ;
Hossmann, KA .
MOLECULAR BRAIN RESEARCH, 1997, 52 (02) :194-200
[4]   Gene expression analysis in N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine mice model of Parkinson's disease using cDNA microarray:: effect of R-apomorphine [J].
Grünblatt, E ;
Mandel, S ;
Maor, G ;
Youdim, MBH .
JOURNAL OF NEUROCHEMISTRY, 2001, 78 (01) :1-12
[5]   Insulin-like growth factor-1 reduces postischemic white matter injury in fetal sheep [J].
Guan, J ;
Bennet, L ;
George, S ;
Wu, D ;
Waldvogel, HJ ;
Gluckman, PD ;
Faull, RLM ;
Crosier, PS ;
Gunn, AJ .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2001, 21 (05) :493-502
[6]   Effect of taurine in combination with electroacupuncture on neuronal damage following transient focal cerebral ischemia in rats [J].
Guo, JC ;
Li, R ;
Zhao, P ;
Cheng, JS .
ACUPUNCTURE & ELECTRO-THERAPEUTICS RESEARCH, 2002, 27 (02) :129-136
[7]   Discovery and analysis of inflammatory disease-related genes using cDNA microarrays [J].
Heller, RA ;
Schena, M ;
Chai, A ;
Shalon, D ;
Bedilion, T ;
Gilmore, J ;
Woolley, DE ;
Davis, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2150-2155
[8]   Defining interactions between DNA-PK and ligase IV/XRCC4 [J].
Hsu, HL ;
Yannone, SM ;
Chen, DJ .
DNA REPAIR, 2002, 1 (03) :225-235
[9]  
JIN ZQ, 1998, SHANG HAI J ACUPUNCT, V5, P37
[10]   Inhibition of release of taurine and excitatory amino acids in ischemia and neuroprotection [J].
Kimelberg, HK ;
Nestor, NB ;
Feustel, PJ .
NEUROCHEMICAL RESEARCH, 2004, 29 (01) :267-274