RECOVERY FROM SPINAL-CORD INJURY MEDIATED BY ANTIBODIES TO NEURITE GROWTH-INHIBITORS

被引:592
作者
BREGMAN, BS [1 ]
KUNKELBAGDEN, E [1 ]
SCHNELL, L [1 ]
DAI, HN [1 ]
GAO, D [1 ]
SCHWAB, ME [1 ]
机构
[1] UNIV ZURICH,BRAIN RES INST,CH-8029 ZURICH,SWITZERLAND
关键词
D O I
10.1038/378498a0
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
THERE is little axonal growth after central nervous system (CNS) injury in adult mammals. The administration of antibodies (IN-1) to neutralize the myelin-associated neurite growth inhibitory proteins leads to long-distance regrowth of a proportion of CNS axons after injury(1-5). Our aim was: to determine if spinal cord lesion in adult rats, followed by treatment with antibodies to neurite growth inhibitors, can lead to regeneration and anatomical plasticity of other spinally projecting pathways; to determine if the anatomical projections persist at long survival intervals; and to determine whether this fibre growth is associated with recovery of function. We report here that brain stem-spinal as well as corticospinal axons undergo regeneration and anatomical plasticity after application of IN-1 antibodies. There is a recovery of specific reflex and locomotor functions after spinal cord injury in these adult rats. Removal of the sensorimotor cortex in IN-1-treated rats 2-3 months later abolished the recovered contact-placing responses, suggesting that the recovery was dependent upon the regrowth of these pathways.
引用
收藏
页码:498 / 501
页数:4
相关论文
共 25 条
[1]  
ALSTERMARK B, 1987, NEUROSCI RES, V5, P66
[2]  
AMASSIAN VE, 1978, J PHYSIOL-PARIS, V74, P165
[3]   INITIATION AND MODULATION OF THE LOCOMOTOR PATTERN IN THE ADULT CHRONIC SPINAL CAT BY NORADRENERGIC, SEROTONERGIC AND DOPAMINERGIC DRUGS [J].
BARBEAU, H ;
ROSSIGNOL, S .
BRAIN RESEARCH, 1991, 546 (02) :250-260
[4]   INFANT LESION EFFECT .3. ANATOMICAL CORRELATES OF SPARING AND RECOVERY OF FUNCTION AFTER SPINAL-CORD DAMAGE IN NEWBORN AND ADULT CATS [J].
BREGMAN, BS ;
GOLDBERGER, ME .
DEVELOPMENTAL BRAIN RESEARCH, 1983, 9 (02) :137-154
[5]   EXTENSION OF THE CRITICAL PERIOD FOR DEVELOPMENTAL PLASTICITY OF THE CORTICOSPINAL PATHWAY [J].
BREGMAN, BS ;
KUNKELBAGDEN, E ;
MCATEE, M ;
ONEILL, A .
JOURNAL OF COMPARATIVE NEUROLOGY, 1989, 282 (03) :355-370
[6]   RECOVERY OF FUNCTION AFTER SPINAL-CORD INJURY - MECHANISMS UNDERLYING TRANSPLANT-MEDIATED RECOVERY OF FUNCTION DIFFER AFTER SPINAL-CORD INJURY IN NEWBORN AND ADULT-RATS [J].
BREGMAN, BS ;
KUNKELBAGDEN, E ;
REIER, PJ ;
DAI, HN ;
MCATEE, M ;
GAO, D .
EXPERIMENTAL NEUROLOGY, 1993, 123 (01) :3-16
[7]   NEURAL TISSUE-TRANSPLANTS RESCUE AXOTOMIZED RUBROSPINAL CELLS FROM RETROGRADE DEATH [J].
BREGMAN, BS ;
REIER, PJ .
JOURNAL OF COMPARATIVE NEUROLOGY, 1986, 244 (01) :86-95
[8]   INFANT LESION EFFECT .2. SPARING AND RECOVERY OF FUNCTION AFTER SPINAL-CORD DAMAGE IN NEWBORN AND ADULT CATS [J].
BREGMAN, BS ;
GOLDBERGER, ME .
DEVELOPMENTAL BRAIN RESEARCH, 1983, 9 (02) :119-135
[9]   ANATOMICAL PLASTICITY AND SPARING OF FUNCTION AFTER SPINAL-CORD DAMAGE IN NEONATAL CATS [J].
BREGMAN, BS ;
GOLDBERGER, ME .
SCIENCE, 1982, 217 (4559) :553-555
[10]   DEVELOPMENT OF SEROTONIN IMMUNOREACTIVITY IN THE RAT SPINAL-CORD AND ITS PLASTICITY AFTER NEONATAL SPINAL-CORD LESIONS [J].
BREGMAN, BS .
DEVELOPMENTAL BRAIN RESEARCH, 1987, 34 (02) :245-263