Neural plasticity after peripheral nerve injury and regeneration

被引:752
作者
Navarro, X. [1 ]
Vivo, Meritxell
Valero-Cabre, Antoni
机构
[1] Univ Autonoma Barcelona, Fac Med, Inst Neurosci, Grp Neuroplastic & Regenerat, E-08193 Bellaterra, Spain
[2] Univ Autonoma Barcelona, Dept Cell Biol Physiol & Immunol, E-08193 Bellaterra, Spain
[3] Inst Guttmann, Badalona, Spain
[4] Boston Univ, Sch Med, Dept Anat & Neurobiol, Boston, MA 02118 USA
[5] Fdn Ophtalmol Rothschild, Dept Neurol, CNRS, Unit 5105 ERT Treat Vis, Paris, France
关键词
axonal regeneration; peripheral nerve; nerve injury; neuroplasticity; neurorehabilitation; cortical reorganization; spinal cord; DORSAL-ROOT GANGLION; RAT SPINAL-CORD; PRIMARY MOTOR CORTEX; RETROGRADE AXONAL-TRANSPORT; CHRONIC CONSTRICTION INJURY; SODIUM-CHANNEL EXPRESSION; PHANTOM-LIMB PAIN; NEURONS FOLLOWING AXOTOMY; PRIMARY AFFERENT NEURONS; PRIMARY SENSORY NEURONS;
D O I
10.1016/j.pneurobio.2007.06.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Injuries to the peripheral nerves result in partial or total loss of motor, sensory and autonomic functions conveyed by the lesioned nerves to the denervated segments of the body, due to the interruption of axons continuity, degeneration of nerve fibers distal to the lesion and eventual death of axotornized neurons. Injuries to the peripheral nervous system may thus result in considerable disability. After axotomy, neuronal phenotype switches from a transmitter to a regenerative state, inducing the down- and up-regulation of numerous cellular components as well as the synthesis de novo of some molecules normally not expressed in adult neurons. These changes in gene expression activate and regulate the pathways responsible for neuronal survival and axonal regeneration. Functional deficits caused by nerve injuries can be compensated by three neural mechanisms: the reinnervation of denervated targets by regeneration of injured axons, the reinnervation by collateral branching of undamaged axons, and the remodeling of nervous system circuitry related to the lost functions. Plasticity of central connections may compensate functionally for the lack of specificity in target reinnervation; plasticity in human has, however, limited effects on disturbed sensory localization or fine motor control after injuries, and may even result in maladaptive changes, such as neuropathic pain, hyperreflexia and dystonia. Recent research has uncovered that peripheral nerve injuries induce a concurrent cascade of events, at the systemic, cellular and molecular levels, initiated by the nerve injury and progressing throughout plastic changes at the spinal cord, brainstem relay nuclei, thalamus and brain cortex. Mechanisms for these changes are ubiquitous in central substrates and include neurochemical changes, functional alterations of excitatory and inhibitory connections, atrophy and degeneration of normal substrates, sprouting of new connections, and reorganization of somatosensory and motor maps. An important direction for ongoing research is the development of therapeutic strategies that enhance axonal regeneration, promote selective target reinnervation, but are also able to modulate central nervous system reorganization, amplifying those positive adaptive changes that help to improve functional recovery but also diminishing undesirable consequences. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:163 / 201
页数:39
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