Magnetic Resonance Imaging as a Biomarker in Rodent Peripheral Nerve Injury Models Reveals an Age-Related Impairment of Nerve Regeneration.
Age Factors
Animals
Axons
/ pathology
Biomarkers
/ metabolism
Disease Models, Animal
Magnetic Resonance Imaging
Male
Mice
Mice, Inbred C57BL
Myelin Sheath
/ metabolism
Nerve Regeneration
/ drug effects
Peripheral Nerve Injuries
/ diagnostic imaging
Rats
Recovery of Function
/ drug effects
Sciatic Nerve
/ injuries
Sciatic Neuropathy
/ metabolism
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
18 09 2019
18 09 2019
Historique:
received:
29
05
2019
accepted:
24
08
2019
entrez:
20
9
2019
pubmed:
20
9
2019
medline:
24
11
2020
Statut:
epublish
Résumé
Assessment of myelin integrity in peripheral nerve injuries and pathologies has largely been limited to post-mortem analysis owing to the difficulty in obtaining biopsies without affecting nerve function. This is further encumbered by the small size of the tissue and its location. Therefore, the development of robust, non-invasive methods is highly attractive. In this study, we used magnetic resonance imaging (MRI) techniques, including magnetization transfer ratio (MTR), to longitudinally and non-invasively characterize both the sciatic nerve crush and lysolecithin (LCP) demyelination models of peripheral nerve injury in rodents. Electrophysiological, gene expression and histological assessments complemented the extensive MRI analyses in young and aged animals. In the nerve crush model, MTR analysis indicated a slower recovery in regions distal to the site of injury in aged animals, as well as incomplete recovery at six weeks post-crush when analyzing across the entire nerve surface. Similar regional impairments were also found in the LCP demyelination model. This research underlines the power of MTR for the study of peripheral nerve injury in small tissues such as the sciatic nerve of rodents and contributes new knowledge to the effect of aging on recovery after injury. A particular advantage of the approach is the translational potential to human neuropathies.
Identifiants
pubmed: 31534149
doi: 10.1038/s41598-019-49850-2
pii: 10.1038/s41598-019-49850-2
pmc: PMC6751200
doi:
Substances chimiques
Biomarkers
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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