TY - JOUR
T1 - Peripheral nerve injury induced changes in the spinal cord and strategies to counteract/enhance the changes to promote nerve regeneration
AU - Liu, Yan
AU - Wang, Huan
N1 - Funding Information:
YL was supported by Chinese Scholar Council; HW was supported by Mayo Clinic Center for Regenerative Medicine and Fund for the Center for Regenerative Medicine Program Director, Neuroregenerative Medicine.
Publisher Copyright:
© 2019 Wolters Kluwer Medknow Publications. All rights reserved.
PY - 2020/2/1
Y1 - 2020/2/1
N2 - Peripheral nerve injury leads to morphological, molecular and gene expression changes in the spinal cord and dorsal root ganglia, some of which have positive impact on the survival of neurons and nerve regeneration, while the effect of others is the opposite. It is crucial to take prompt measures to capitalize on the positive effects of these reactions and counteract the negative impact after peripheral nerve injury at the level of spinal cord, especially for peripheral nerve injuries that are severe, located close to the cell body, involve long distance for axons to regrow and happen in immature individuals. Early nerve repair, exogenous supply of neurotrophic factors and Schwann cells can sustain the regeneration inductive environment and enhance the positive changes in neurons. Administration of neurotrophic factors, acetyl-L-carnitine, N-acetyl-cysteine, and N-methyl-D-aspartate receptor antagonist MK-801 can help counteract axotomy-induced neuronal loss and promote regeneration, which are all time-dependent. Sustaining and reactivation of Schwann cells after denervation provides another effective strategy. FK506 can be used to accelerate axonal regeneration of neurons, especially after chronic axotomy. Exploring the axotomy-induced changes after peripheral nerve injury and applying protective and promotional measures in the spinal cord which help to retain a positive functional status for neuron cell bodies will inevitably benefit regeneration of the peripheral nerve and improve functional outcomes.
AB - Peripheral nerve injury leads to morphological, molecular and gene expression changes in the spinal cord and dorsal root ganglia, some of which have positive impact on the survival of neurons and nerve regeneration, while the effect of others is the opposite. It is crucial to take prompt measures to capitalize on the positive effects of these reactions and counteract the negative impact after peripheral nerve injury at the level of spinal cord, especially for peripheral nerve injuries that are severe, located close to the cell body, involve long distance for axons to regrow and happen in immature individuals. Early nerve repair, exogenous supply of neurotrophic factors and Schwann cells can sustain the regeneration inductive environment and enhance the positive changes in neurons. Administration of neurotrophic factors, acetyl-L-carnitine, N-acetyl-cysteine, and N-methyl-D-aspartate receptor antagonist MK-801 can help counteract axotomy-induced neuronal loss and promote regeneration, which are all time-dependent. Sustaining and reactivation of Schwann cells after denervation provides another effective strategy. FK506 can be used to accelerate axonal regeneration of neurons, especially after chronic axotomy. Exploring the axotomy-induced changes after peripheral nerve injury and applying protective and promotional measures in the spinal cord which help to retain a positive functional status for neuron cell bodies will inevitably benefit regeneration of the peripheral nerve and improve functional outcomes.
KW - axotomy
KW - dorsal root ganglion
KW - neural regeneration
KW - neurotrophic factors
KW - outcomes
KW - peripheral nerve injury
KW - repair
KW - spinal cord
UR - http://www.scopus.com/inward/record.url?scp=85072667824&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85072667824&partnerID=8YFLogxK
U2 - 10.4103/1673-5374.265540
DO - 10.4103/1673-5374.265540
M3 - Review article
AN - SCOPUS:85072667824
SN - 1673-5374
VL - 15
SP - 189
EP - 198
JO - Neural Regeneration Research
JF - Neural Regeneration Research
IS - 2
ER -