POSSIBLE STRATEGIES FOR TREATMENT OF SMA PATIENTS - A NEUROBIOLOGISTS VIEW

被引:17
作者
GREENSMITH, L [1 ]
VRBOVA, G [1 ]
机构
[1] UNIV LONDON UNIV COLL, CTR NEUROSCI, DEPT ANAT & DEV BIOL, LONDON WC1E 6BT, ENGLAND
关键词
SMA; MOTONEURON DEATH; NEUROTROPHIC FACTORS; EXCITOTOXICITY; EMBRYONIC GRAFTS; MOTOR UNIT TERRITORY;
D O I
10.1016/0960-8966(94)00090-V
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This paper discusses possible strategies that might prevent or alleviate muscle weakness of SMA patients and hence improve their condition. The strategies discussed are as follows. (1) Prevention of motoneurone death. To achieve this two main approaches have been applied. Firstly, trophic factors have been used to prevent motoneurone death after nerve injury and clinically in diseases such as motoneurone disease. The results of these attempts will be described. Secondly, the possibility that injured motoneurones die as a result of the excitotoxic effects of the excitatory transmitter glutamate will be explored. Evidence will be presented which indicates that blocking glutamate receptors can rescue injured motoneurones from death. (2) Replacement of lost motoneurones by embryonic grafts. Motoneurones from grafts of embryonic spinal cord have been shown to survive in the adult spinal cord and are able to reinnervate skeletal muscles. The potential and practical problems of this approach will be discussed. (3) Expansion or motor unit territory of surviving motoneurones. Such an expansion of the territory occupied by individual motor units can be achieved by encouraging sprouting and ensuring that the newly formed connections between the motoneurone and muscle fibres are maintained, so that individual motor units are capable of developing more force. Strategies to achieve such an expansion of motor unit territory will be described. Finally, combinations of some of these approaches are considered.
引用
收藏
页码:359 / 369
页数:11
相关论文
共 85 条
[31]   TARGETED DISRUPTION OF THE BDNF GENE PERTURBS BRAIN AND SENSORY NEURON DEVELOPMENT BUT NOT MOTOR-NEURON DEVELOPMENT [J].
JONES, KR ;
FARINAS, I ;
BACKUS, C ;
REICHARDT, LF .
CELL, 1994, 76 (06) :989-999
[32]   N-METHYL-D-ASPARTATE RECEPTORS ARE TRANSIENTLY EXPRESSED IN THE DEVELOPING SPINAL-CORD VENTRAL HORN [J].
KALB, RG ;
LIDOW, MS ;
HALSTED, MJ ;
HOCKFIELD, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (18) :8502-8506
[33]   CELL-DEATH OF AXOTOMIZED MOTONEURONS IN NEONATAL RATS, AND ITS PREVENTION BY PERIPHERAL REINNERVATION [J].
KASHIHARA, Y ;
KUNO, M ;
MIYATA, Y .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 386 :135-148
[34]   DISRUPTION OF THE NEURATROPHIN-3 RECEPTOR GENE TRKC ELIMINATES LA MUSCLE AFFERENTS AND RESULTS IN ABNORMAL MOVEMENTS [J].
KLEIN, R ;
SILOSSANTIAGO, I ;
SMEYNE, RJ ;
LIRA, SA ;
BRAMBILLA, R ;
BRYANT, S ;
ZHANG, L ;
SNIDER, WD ;
BARBACID, M .
NATURE, 1994, 368 (6468) :249-251
[35]   TARGETED DISRUPTION OF THE TRKB NEUROTROPHIN RECEPTOR GENE RESULTS IN NERVOUS-SYSTEM LESIONS AND NEONATAL DEATH [J].
KLEIN, R ;
SMEYNE, RJ ;
WURST, W ;
LONG, LK ;
AUERBACH, BA ;
JOYNER, AL ;
BARBACID, M .
CELL, 1993, 75 (01) :113-122
[36]  
KORSCHING S, 1993, J NEUROSCI, V13, P2739
[37]  
KREUTZBERG GW, 1975, ADV NEUROL, V12, P269
[38]   THE EFFECT OF REDUCING THE PERIPHERAL FIELD ON MOTONEURON DEVELOPMENT IN THE RAT [J].
KRISHNAN, S ;
LOWRIE, MB ;
VRBOVA, G .
DEVELOPMENTAL BRAIN RESEARCH, 1985, 19 (01) :11-20
[39]  
LAMB AH, 1984, CRC CR REV CL NEUROB, V1, P141
[40]   TRKC, A NEW MEMBER OF THE TRK FAMILY OF TYROSINE PROTEIN-KINASES, IS A RECEPTOR FOR NEUROTROPHIN-3 [J].
LAMBALLE, F ;
KLEIN, R ;
BARBACID, M .
CELL, 1991, 66 (05) :967-979