Proteomic analysis of differential protein expression in neuropathic pain and electroacupuncture treatment models

被引:34
作者
Sung, HJ
Kim, YS
Kim, IS
Jang, SW
Kim, YR
Na, DS
Han, KH
Hwang, BG
Park, DS
Ko, JS
机构
[1] Univ Ulsan, Coll Med, Asan Inst Life Sci, Seoul 138736, South Korea
[2] Univ Ulsan, Coll Med, Dept Biochem & Mol Biol, Seoul 138736, South Korea
[3] Univ Ulsan, Coll Med, Dept Internal Med, Seoul 138736, South Korea
[4] Univ Ulsan, Coll Med, Dept Internal Med, Asan Med Ctr, Seoul, South Korea
[5] Kyung Hee Univ, Coll Oriental Med, Grad Sch, Dept EW Med, Seoul, South Korea
[6] Kyung Hee Univ, Coll Oriental Med, Dept Acupuncture & Moxibust, Seoul, South Korea
关键词
analgesia; electroacupuncture; hypothalamus; neuropathic pain;
D O I
10.1002/pmic.200300821
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Acupuncture has long been used for pain relief. Although recent studies have shown that acupuncture can reduce neuropathic pain, the mechanism of this effect is not clear and little information is available regarding proteins that are involved in the development of neuropathic pain and the effects of acupuncture. We have developed an animal model for neuropathic pain using young adult male Sprague-Dawley rats. The model was confirmed by behavioral tests. Electroacupuncture (EA) treatment was applied to Zusanli (ST36) of neuropathic pain model to examine the analgesic effect of EA. The protein expression profile of the hypothalamus in both neuropathic pain and EA treatment models was analyzed using two-dimensional electrophoresis-based proteomics. We detected thirty-six proteins that were differentially expressed in the neuropathic pain model compared with normal rats and that restored to normal expression levels after EA treatment. Twenty-one of these proteins were identified in the MS-FiT database and are involved in a number of biological processes, including inflammation, enzyme metabolism and signal transduction. Potential applications of our results include the identification and characterization of signaling pathways involved in EA treatment and further exploration of the role of selected identified proteins in the animal model.
引用
收藏
页码:2805 / 2813
页数:9
相关论文
共 41 条
[1]   Nociceptor sensitization by extracellular signal-regulated kinases [J].
Aley, KO ;
Martin, A ;
McMahon, T ;
Mok, J ;
Levine, JD ;
Messing, RO .
JOURNAL OF NEUROSCIENCE, 2001, 21 (17) :6933-6939
[2]  
ANNIKA P, 2002, CLIN EXP, V17, P345
[3]   ACUPUNCTURE-EVOKED RESPONSES OF SUBNUCLEUS RETICULARIS DORSALIS NEURONS IN THE RAT MEDULLA [J].
BING, Z ;
VILLANUEVA, L ;
LEBARS, D .
NEUROSCIENCE, 1991, 44 (03) :693-703
[4]  
CHAODONG W, 2002, AM J PHYSIOL-ENDOC M, V282, P38
[5]   Identification of MEK1 as a novel target for the treatment of neuropathic pain [J].
Ciruela, A ;
Dixon, AK ;
Bramwell, S ;
Gonzalez, MI ;
Pinnock, RD ;
Lee, K .
BRITISH JOURNAL OF PHARMACOLOGY, 2003, 138 (05) :751-756
[6]  
COLOSIA AD, 1988, J BIOL CHEM, V263, P18669
[7]   Interleukin-18 and host defense against infection [J].
Dinarello, CA ;
Fantuzzi, G .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 :S370-S384
[8]  
DOUCET SP, 1990, MOL NEUROBIOL, P27
[9]  
EARLY RJ, 1990, J ANIM SCI, V68, P4153
[10]   Elevated 14-3-3 protein and axonal loss in immunoglobulin-responsive, idiopathic acute transverse myelitis [J].
Finsterer, J ;
Voigtländer, T .
CLINICAL NEUROLOGY AND NEUROSURGERY, 2002, 105 (01) :18-22