The Effect of Lower Limb Combined Neuromuscular Electrical Stimulation on Skeletal Muscle Cross-Sectional Area and Inflammatory Signaling.
Humans
Male
Electric Stimulation Therapy
/ methods
Muscle, Skeletal
/ metabolism
Adult
Muscular Atrophy
/ metabolism
Spinal Cord Injuries
/ therapy
Signal Transduction
Lower Extremity
Female
Inflammation
/ metabolism
Muscle Proteins
/ metabolism
SKP Cullin F-Box Protein Ligases
/ metabolism
Middle Aged
Toll-Like Receptor 4
/ metabolism
inflammatory signaling
muscle cross-sectional area
myofiber adaptation
neuromuscular electrical stimulation
spinal cord injury
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
16 Oct 2024
16 Oct 2024
Historique:
received:
27
06
2024
revised:
07
10
2024
accepted:
09
10
2024
medline:
26
10
2024
pubmed:
26
10
2024
entrez:
26
10
2024
Statut:
epublish
Résumé
In individuals with a spinal cord injury (SCI), rapid skeletal muscle atrophy and metabolic dysfunction pose profound rehabilitation challenges, often resulting in substantial loss of muscle mass and function. This study evaluates the effect of combined neuromuscular electrical stimulation (Comb-NMES) on skeletal muscle cross-sectional area (CSA) and inflammatory signaling within the acute phase of SCI. We applied a novel Comb-NMES regimen, integrating both high-frequency resistance and low-frequency aerobic protocols on the vastus lateralis muscle, to participants early post-SCI. Muscle biopsies were analyzed for CSA and inflammatory markers pre- and post-intervention. The results suggest a potential preservation of muscle CSA in the Comb-NMES group compared to a control group. Inflammatory signaling proteins such as TLR4 and Atrogin-1 were downregulated, whereas markers associated with muscle repair and growth were modulated beneficially in the Comb-NMES group. The study's findings suggest that early application of Comb-NMES post-SCI may attenuate inflammatory pathways linked to muscle atrophy and promote muscle repair. However, the small sample size and variability in injury characteristics emphasize the need for further research to corroborate these results across a more diverse and extensive SCI population.
Identifiants
pubmed: 39456876
pii: ijms252011095
doi: 10.3390/ijms252011095
pii:
doi:
Substances chimiques
Muscle Proteins
0
SKP Cullin F-Box Protein Ligases
EC 2.3.2.27
Toll-Like Receptor 4
0
FBXO32 protein, human
EC 2.3.2.27
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Eunice Kennedy Shriver National Institute of Child Health & Human Development
ID : K01HD087463