Moving from an averaged to specific view of spinal cord pain processing circuits

被引:85
作者
Graham, B. A.
Brichta, A. M.
Callister, R. J. [1 ]
机构
[1] Univ Newcastle, Fac Hlth, Sch Biomed Sci, Callaghan, NSW 2308, Australia
[2] Univ Newcastle, Hunter Med Res Inst, Callaghan, NSW, Australia
关键词
D O I
10.1152/jn.00581.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurons in the superficial dorsal horn (SDH) of the spinal cord play a critical role in processing potentially painful or noxious signals from skin, muscle, and viscera. Many acute pain therapies are based on the notion that altering the excitability of SDH neurons can block or gate these signals and reduce pain. This same notion also underlies treatments for certain chronic pain states. Basic scientists are now beginning to identify a number of potential molecular targets for spinal cord - based pain therapies with a focus on ion channels and receptors that can alter neuronal excitability. The current challenge in pain research is to identify which are the most promising targets and how their manipulation alters pain processing. In this review, we propose that our understanding of spinal pain processing mechanisms and translation of these discoveries into pain therapies could be improved by 1) better appreciating and understanding neuronal heterogeneity in the SDH; 2) establishing connectivity patterns among SDH neuron types; and 3) testing and extending findings made in vitro to intact (in vivo) animal models. As this information becomes available, it will be possible to determine the precise distribution of potential therapeutic targets on various SDH neuron types within specific circuits known to be functionally important in spinal pain processing.
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收藏
页码:1057 / 1063
页数:7
相关论文
共 73 条
[1]   DIFFERENT POPULATIONS OF PARVALBUMIN-D28K-IMMUNOREACTIVE AND CALBINDIN-D28K-IMMUNOREACTIVE NEURONS CONTAIN GABA AND ACCUMULATE H-3 D-ASPARTATE IN THE DORSAL HORN OF THE RAT SPINAL-CORD [J].
ANTAL, M ;
POLGAR, E ;
CHALMERS, J ;
MINSON, JB ;
LLEWELLYNSMITH, I ;
HEIZMANN, CW ;
SOMOGYI, P .
JOURNAL OF COMPARATIVE NEUROLOGY, 1991, 314 (01) :114-124
[2]   A vector for expressing foreign genes in the brains and hearts of transgenic mice [J].
Borchelt, DR ;
Davis, J ;
Fischer, M ;
Lee, MK ;
Slunt, HH ;
Ratovitsky, T ;
Regard, J ;
Copeland, NG ;
Jenkins, NA ;
Sisodia, SS ;
Price, DL .
GENETIC ANALYSIS-BIOMOLECULAR ENGINEERING, 1996, 13 (06) :159-163
[3]   SPINAL NEURONS SPECIFICALLY EXCITED BY NOXIOUS OR THERMAL STIMULI - MARGINAL ZONE OF DORSAL HORN [J].
CHRISTENSEN, BN ;
PERL, ER .
JOURNAL OF NEUROPHYSIOLOGY, 1970, 33 (02) :293-+
[4]   Pain mechanisms: Labeled lines versus convergence in central processing [J].
Craig, AD .
ANNUAL REVIEW OF NEUROSCIENCE, 2003, 26 :1-30
[5]   A new view of pain as a homeostatic emotion [J].
Craig, ADB .
TRENDS IN NEUROSCIENCES, 2003, 26 (06) :303-307
[6]  
Fields HL., 2006, Wall and Melzack's Textbook of Pain, P125
[7]   Responsiveness of rat substantia gelatinosa neurones to mechanical but not thermal stimuli revealed by in vivo patch-clamp recording [J].
Furue, H ;
Narikawa, K ;
Kumamoto, E ;
Yoshimura, M .
JOURNAL OF PHYSIOLOGY-LONDON, 1999, 521 (02) :529-535
[8]  
Galhardo V, 1999, J COMP NEUROL, V414, P315
[9]  
Gao KM, 1997, J NEUROSCI, V17, P3285
[10]   Serotonergic raphe magnus cells that respond to noxious tail heat are not ON or OFF cells [J].
Gao, KM ;
Mason, P .
JOURNAL OF NEUROPHYSIOLOGY, 2000, 84 (04) :1719-1725