Brain substrates activated by electroacupuncture of different frequencies .1. Comparative study on the expression of oncogene c-fos and genes coding for three opioid peptides

被引:67
作者
Guo, HF
Tian, JH
Wang, XM
Fang, Y
Hou, YP
Han, JS
机构
[1] BEIJING MED UNIV,CTR RES NEUROSCI,BEIJING 100083,PEOPLES R CHINA
[2] OREGON HLTH SCI UNIV,DEPT PHYSIOL,PORTLAND,OR 97201
来源
MOLECULAR BRAIN RESEARCH | 1996年 / 43卷 / 1-2期
关键词
electroacupuncture; stimulation frequency; c-fos; c-jun; preproenkephalin; preprodynorphin; proopiomelanocortin;
D O I
10.1016/S0169-328X(96)00170-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Low and high frequency electroacupuncture (EA)-produced analgesia have been shown to be mediated by different brain substrates and different opioid peptides. In this study, Fos-like immunoreactivity (FLI) and in situ hybridization of the three opioid mRNAs were used to examine the effect of low (2 Hz) and high (100 Hz) frequency EA on neuronal activities and the expression of opioid genes. 2 Hz and 100 Hz EA induced a markedly different spatial patterns of Fos expression in the rat brain, suggesting there are distinct neuronal pathways underlying EA of different frequencies. Likewise, 2 Hz and 100 Hz EA exert differential effects on opioid gene expression: while 2 Hz EA induced a more extensive and intensive preproenkephalin (PPE) mRNA expression than 100 Hz EA, it had no effect on preprodynorphin (PPD) mRNA expression which was significantly increased by 100 Hz EA stimulation. In contrast, EA of both frequencies did not affect POMC mRNA expression.
引用
收藏
页码:157 / 166
页数:10
相关论文
共 43 条
[1]   INTRACEREBROVENTRICULAR TREATMENT WITH AN ANTISENSE OLIGODEOXYNUCLEOTIDE TO KAPPA-OPIOID RECEPTORS INHIBITED KAPPA-AGONIST-INDUCED ANALGESIA IN RATS [J].
ADAMS, JU ;
CHEN, XH ;
DERIEL, JK ;
ADLER, MW ;
LIUCHEN, LY .
BRAIN RESEARCH, 1994, 667 (01) :129-132
[2]  
BRONSTEIN DM, 1990, BRAIN RES, V519, P101
[3]   EXPRESSION OF C-FOS-LIKE PROTEIN AS A MARKER FOR NEURONAL-ACTIVITY FOLLOWING NOXIOUS-STIMULATION IN THE RAT [J].
BULLITT, E .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 296 (04) :517-530
[4]   ANALGESIA INDUCED BY ELECTROACUPUNCTURE OF DIFFERENT FREQUENCIES IS MEDIATED BY DIFFERENT TYPES OF OPIOID RECEPTORS - ANOTHER CROSS-TOLERANCE STUDY [J].
CHEN, XH ;
HAN, JS .
BEHAVIOURAL BRAIN RESEARCH, 1992, 47 (02) :143-149
[5]   ELECTROACUPUNCTURE ANALGESIA COULD BE MEDIATED BY AT LEAST 2 PAIN-RELIEVING MECHANISMS - ENDORPHIN AND NON-ENDORPHIN SYSTEMS [J].
CHENG, RSS ;
POMERANZ, B .
LIFE SCIENCES, 1979, 25 (23) :1957-1962
[6]   NEURONAL ADAPTATION TO AMPHETAMINE AND DOPAMINE - MOLECULAR MECHANISMS OF PRODYNORPHIN GENE-REGULATION IN RAT STRIATUM [J].
COLE, RL ;
KONRADI, C ;
DOUGLASS, J ;
HYMAN, SE .
NEURON, 1995, 14 (04) :813-823
[7]   PROTEINS BOUND AT ADJACENT DNA ELEMENTS ACT SYNERGISTICALLY TO REGULATE HUMAN PROENKEPHALIN CAMP INDUCIBLE TRANSCRIPTION [J].
COMB, M ;
MERMOD, N ;
HYMAN, SE ;
PEARLBERG, J ;
ROSS, ME ;
GOODMAN, HM .
EMBO JOURNAL, 1988, 7 (12) :3793-3805
[8]   PATTERN AND TIME-COURSE OF IMMEDIATE-EARLY GENE-EXPRESSION IN RAT-BRAIN FOLLOWING ACUTE STRESS [J].
CULLINAN, WE ;
HERMAN, JP ;
BATTAGLIA, DF ;
AKIL, H ;
WATSON, SJ .
NEUROSCIENCE, 1995, 64 (02) :477-505
[9]   FOS AND JUN - ONCOGENIC TRANSCRIPTION FACTORS [J].
CURRAN, T .
TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 168 (02) :169-174
[10]   VISCERAL PAIN EVOKED BY THALAMIC MICROSTIMULATION IN HUMANS [J].
DAVIS, KD ;
TASKER, RR ;
KISS, ZHT ;
HUTCHISON, WD ;
DOSTROVSKY, JO .
NEUROREPORT, 1995, 6 (02) :369-374