Cigarette Smoking Exacerbates Skeletal Muscle Injury without Compromising Its Regenerative Capacity.
Animals
Cigarette Smoking
/ adverse effects
Male
Mice, Inbred BALB C
Muscle Contraction
/ physiology
Muscle Fibers, Skeletal
/ metabolism
Muscle, Skeletal
/ injuries
Muscular Diseases
/ metabolism
PAX7 Transcription Factor
/ metabolism
Pulmonary Disease, Chronic Obstructive
/ metabolism
Quality of Life
Regeneration
/ physiology
Smoking
/ physiopathology
barium chloride
chronic obstructive pulmonary disease
fiber type shift
paired box 7
skeletal muscle dysfunction
Journal
American journal of respiratory cell and molecular biology
ISSN: 1535-4989
Titre abrégé: Am J Respir Cell Mol Biol
Pays: United States
ID NLM: 8917225
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
pubmed:
29
8
2019
medline:
12
5
2020
entrez:
29
8
2019
Statut:
ppublish
Résumé
Skeletal muscle dysfunction in patients with chronic obstructive pulmonary disease negatively impacts quality of life and survival. Cigarette smoking (CS) is the major risk factor for chronic obstructive pulmonary disease and skeletal muscle dysfunction; however, how CS affects skeletal muscle function remains enigmatic. To examine the impact of CS on skeletal muscle inflammation and regeneration, male BALB/c mice were exposed to CS for 8 weeks before muscle injury was induced by barium chloride injection, and were maintained on the CS protocol for up to 21 days after injury. Barium chloride injection resulted in architectural damage to the tibialis anterior muscle, resulting in a decrease contractile function, which was worsened by CS exposure. CS exposure caused muscle atrophy (reduction in gross weight and myofiber cross-sectional area) and altered fiber type composition (31% reduction of oxidative fibers). Both contractile function and loss in myofiber cross-sectional area by CS exposure gradually recovered over time. Satellite cells are muscle stem cells that confer skeletal muscle the plasticity to adapt to changing demands. CS exposure blunted Pax7
Identifiants
pubmed: 31461300
doi: 10.1165/rcmb.2019-0106OC
doi:
Substances chimiques
PAX7 Transcription Factor
0
PAX7 protein, human
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
217-230Commentaires et corrections
Type : CommentIn