Common animal models for spasticity and pain

被引:36
作者
Eaton, M [1 ]
机构
[1] VA Med Ctr, Ctr Excellence Funct Recovery Chron Spinal Cord I, Dept Vet Affairs Rehabil Res & Dev, Miami, FL USA
[2] Univ Miami, Sch Med, Miami Project Cure Paralysis, Miami, FL 33152 USA
关键词
allodynia; cell therapy; hyperalgesia; partial nerve injury; sacral transection;
D O I
10.1682/JRRD.2003.08.0041
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Animal models of spasticity and pain have allowed for the elucidation of possible mechanisms and the evaluation of potential therapeutic interventions for these serious clinical problems. Each model mirrors the clinical appearance of many features of the syndrome, but few reproduce the myriad patient reports of either intensity or relevant contributing factors, especially in models of chronic neuropathic pain. Often these models have been used to predict the potency and efficacy of pharmacologic agents that work in human pain states. Pain models have relied on measurements of the shifts in behavioral hypersensitivity. to tactile and thermal stimuli, tests that are not used quantitatively in human patients. Even with the multiple peripheral and central models of spasticity and pain used in animals, only a few actually test human conditions: namely, diabetic neuropathy, chemotherapy, and immunotherapy for tumors. However, all these models have allowed for the comparison of certain behavioral, cellular, biochemical, and molecular mechanisms with human patient populations. Here we review the few extant models of spasticity, nerve injury, and central injury models of pain, and describe their features and use.
引用
收藏
页码:41 / 54
页数:14
相关论文
共 167 条
[51]   Reduction of pathological and behavioral deficits following spinal cord contusion injury with the selective cyclooxygenase-2 inhibitor NS-398 [J].
Hains, BC ;
Yucra, JA ;
Hulsebosch, CE .
JOURNAL OF NEUROTRAUMA, 2001, 18 (04) :409-423
[52]   A NEW AND SENSITIVE METHOD FOR MEASURING THERMAL NOCICEPTION IN CUTANEOUS HYPERALGESIA [J].
HARGREAVES, K ;
DUBNER, R ;
BROWN, F ;
FLORES, C ;
JORIS, J .
PAIN, 1988, 32 (01) :77-88
[53]  
Heapy CG, 1987, BRIT J PHARMACOL, V90, P164
[54]   RECORDINGS OF ABNORMAL ACTIVITY IN PATIENTS WITH DEAFFERENTATION AND CENTRAL PAIN [J].
HIRAYAMA, T ;
DOSTROVSKY, JO ;
GORECKI, J ;
TASKER, RR ;
LENZ, FA .
STEREOTACTIC AND FUNCTIONAL NEUROSURGERY, 1989, 52 (2-4) :120-126
[55]  
Hottinger AF, 1999, ADV TECH STAND NEUR, V25, P3
[56]   Changes in neuronal receptive field characteristics in caudal brain stem following chronic spinal cord injury [J].
Hubscher, CH ;
Johnson, RD .
JOURNAL OF NEUROTRAUMA, 1999, 16 (06) :533-541
[57]   Rodent model of chronic central pain after spinal cord contusion injury and effects of gabapentin [J].
Hulsebosch, CE ;
Xu, GY ;
Perez-Polo, JR ;
Westlund, KN ;
Taylor, CP ;
McAdoo, DJ .
JOURNAL OF NEUROTRAUMA, 2000, 17 (12) :1205-1217
[58]   CHANGES IN SEGMENTAL REFLEXES FOLLOWING CHRONIC SPINAL-CORD HEMISECTION IN THE CAT .1. INCREASED MONO-SYNAPTIC AND POLYSYNAPTIC VENTRAL ROOT DISCHARGES [J].
HULTBORN, H ;
MALMSTEN, J .
ACTA PHYSIOLOGICA SCANDINAVICA, 1983, 119 (04) :405-422
[59]   FORMALIN TEST IN MICE, A USEFUL TECHNIQUE FOR EVALUATING MILD ANALGESICS [J].
HUNSKAAR, S ;
FASMER, OB ;
HOLE, K .
JOURNAL OF NEUROSCIENCE METHODS, 1985, 14 (01) :69-76
[60]  
HWANG AS, 1986, LIFE SCI, V38, P2389