Preserved acute pain and reduced neuropathic pain in mice lacking PKC gamma

被引:548
作者
Malmberg, AB
Chen, C
Tonegawa, S
Basbaum, AI
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL, SAN FRANCISCO, CA 92143 USA
[2] UNIV CALIF SAN FRANCISCO, WM KECK FDN CTR INTEGRAT NEUROSCI, SAN FRANCISCO, CA 92143 USA
[3] MIT, CTR CANC RES, HOWARD HUGHES MED INST, CAMBRIDGE, MA 02139 USA
[4] MIT, DEPT BIOL, CAMBRIDGE, MA 02139 USA
关键词
D O I
10.1126/science.278.5336.279
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In normal animals, peripheral nerve injury produces a persistent, neuropathic pain state in which pain is exaggerated and can be produced by nonpainful stimuli. Here, mice that lack protein kinase C gamma (PKC gamma) displayed normal responses to acute pain stimuli, but they almost completely failed to develop a neuropathic pain syndrome after partial sciatic nerve section, and the neurochemical changes that occurred in the spinal cord after nerve injury were blunted. Also, PKC gamma was shown to be restricted to a small subset of dorsal horn neurons, thus identifying a potential biochemical target for the prevention and therapy of persistent pain.
引用
收藏
页码:279 / 283
页数:5
相关论文
共 39 条
[1]   Spinal cord substance P receptor immunoreactivity increases in both inflammatory and nerve injury models of persistent pain [J].
Abbadie, C ;
Brown, JL ;
Mantyh, PW ;
Basbaum, AI .
NEUROSCIENCE, 1996, 70 (01) :201-209
[2]   PKC-GAMMA MUTANT MICE EXHIBIT MILD DEFICITS IN SPATIAL AND CONTEXTUAL LEARNING [J].
ABELIOVICH, A ;
PAYLOR, R ;
CHEN, C ;
KIM, JJ ;
WEHNER, JM ;
TONEGAWA, S .
CELL, 1993, 75 (07) :1263-1271
[3]   MODIFIED HIPPOCAMPAL LONG-TERM POTENTIATION IN PKC-GAMMA-MUTANT MICE [J].
ABELIOVICH, A ;
CHEN, C ;
GODA, Y ;
SILVA, AJ ;
STEVENS, CF ;
TONEGAWA, S .
CELL, 1993, 75 (07) :1253-1262
[4]   PHYSIOLOGY AND MORPHOLOGY OF SUBSTANTIA GELATINOSA NEURONS INTRACELLULARLY STAINED WITH HORSERADISH-PEROXIDASE [J].
BENNETT, GJ ;
ABDELMOUMENE, M ;
HAYASHI, H ;
DUBNER, R .
JOURNAL OF COMPARATIVE NEUROLOGY, 1980, 194 (04) :809-&
[5]   MORPHOLOGICAL CHARACTERIZATION OF SUBSTANCE-P RECEPTOR-IMMUNOREACTIVE NEURONS IN THE RAT SPINAL-CORD AND TRIGEMINAL NUCLEUS CAUDALIS [J].
BROWN, JL ;
LIU, HT ;
MAGGIO, JE ;
VIGNA, SR ;
MANTYH, PW ;
BASBAUM, AI .
JOURNAL OF COMPARATIVE NEUROLOGY, 1995, 356 (03) :327-344
[6]   ENHANCEMENT OF THE N-METHYL-D-ASPARTATE RESPONSE IN SPINAL DORSAL HORN NEURONS BY CAMP-DEPENDENT PROTEIN-KINASE [J].
CERNE, R ;
RUSIN, KI ;
RANDIC, M .
NEUROSCIENCE LETTERS, 1993, 161 (02) :124-128
[7]   QUANTITATIVE ASSESSMENT OF TACTILE ALLODYNIA IN THE RAT PAW [J].
CHAPLAN, SR ;
BACH, FW ;
POGREL, JW ;
CHUNG, JM ;
YAKSH, TL .
JOURNAL OF NEUROSCIENCE METHODS, 1994, 53 (01) :55-63
[8]   Impaired motor coordination correlates with persistent multiple climbing fiber innervation in PKC gamma mutant mice [J].
Chen, C ;
Kano, M ;
Abeliovich, A ;
Chen, L ;
Bao, SW ;
Kim, JJ ;
Hashimoto, K ;
Thompson, RF ;
Tonegawa, S .
CELL, 1995, 83 (07) :1233-1242
[9]   A P2X PURINOCEPTOR EXPRESSED BY A SUBSET OF SENSORY NEURONS [J].
CHEN, CC ;
AKOPIAN, AN ;
SIVILOTTI, L ;
COLQUHOUN, D ;
BURNSTOCK, G ;
WOOD, JN .
NATURE, 1995, 377 (6548) :428-431
[10]   CONTRIBUTION OF PROTEIN-KINASE-C TO CENTRAL SENSITIZATION AND PERSISTENT PAIN FOLLOWING TISSUE-INJURY [J].
CODERRE, TJ .
NEUROSCIENCE LETTERS, 1992, 140 (02) :181-184