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Substance P enhances endogenous neurogenesis to improve functional recovery after spinal cord injury.
- Source :
-
The international journal of biochemistry & cell biology [Int J Biochem Cell Biol] 2017 Aug; Vol. 89, pp. 110-119. Date of Electronic Publication: 2017 Jun 01. - Publication Year :
- 2017
-
Abstract
- Endogenous neural stem cells (NSCs) are the most promising sources for replacing cells lost after spinal cord injury (SCI). We have previously shown that substance P (SP), a neuropeptide, improves functional recovery after SCI and increases the numbers of cells in lesion sites, but how this occurs is unclear. Here, we investigate whether SP regulates the neurogenesis of resident NSCs as well as exerting a beneficial effect on functional improvement. We found that SP (5nmol/kg) treatment markedly improved functional recovery and elicited robust activation of endogenous NSCs and boosted the number of EdU <superscript>+</superscript> proliferating cells differentiating into neurons, but it reduced astroglial differentiation in the lesion sites. Consistently, treatment with SP (10nM) in vitro significantly increased the proliferation of NSCs via activating the Erk1/2 signaling pathway and promoted neuronal differentiation but not astroglial differentiation. These results suggest that SP may represent a potential therapeutic agent for SCI via enhancing endogenous neurogenesis.<br /> (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Cell Proliferation drug effects
Male
Mice
Mice, Inbred C57BL
Motor Activity drug effects
Motor Activity physiology
Neural Stem Cells drug effects
Neural Stem Cells pathology
Neurons drug effects
Neurons pathology
Neurogenesis drug effects
Recovery of Function drug effects
Spinal Cord Injuries pathology
Spinal Cord Injuries physiopathology
Substance P pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1878-5875
- Volume :
- 89
- Database :
- MEDLINE
- Journal :
- The international journal of biochemistry & cell biology
- Publication Type :
- Academic Journal
- Accession number :
- 28579528
- Full Text :
- https://doi.org/10.1016/j.biocel.2017.05.030