Effects of chronic Porphyromonas gingivalis lipopolysaccharide infusion on skeletal muscles in mice.
Animals
Apoptosis
/ drug effects
Fibrosis
/ drug therapy
Lipopolysaccharides
/ pharmacology
Male
Mice
Mice, Inbred C57BL
Muscle Cells
/ drug effects
Muscle Fibers, Fast-Twitch
/ drug effects
Muscle Fibers, Slow-Twitch
/ drug effects
Muscular Diseases
/ drug therapy
Periodontitis
/ drug therapy
Porphyromonas gingivalis
/ metabolism
Sarcopenia
/ prevention & control
Apoptosis
Fibrosis
Lipopolysaccharide
Periodontitis
Sarcopenia
Signal transduction
Journal
The journal of physiological sciences : JPS
ISSN: 1880-6562
Titre abrégé: J Physiol Sci
Pays: Japan
ID NLM: 101262417
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
received:
30
12
2018
accepted:
23
02
2019
pubmed:
9
3
2019
medline:
10
8
2019
entrez:
9
3
2019
Statut:
ppublish
Résumé
Periodontitis, which is caused by various oral organisms, predominantly affects adults, and is one of the main causes of tooth loss, as well as leading to progression of numerous systemic diseases. However, its relationship to sarcopenia (aging-associated degenerative loss of skeletal muscle mass and function) remains unclear. The aim of this study was to investigate the effects of Porphyromonas gingivalis lipopolysaccharide (PG-LPS) on skeletal muscle in mice, and to establish the underlying mechanisms. Mice (C57BL/6) were injected with PG-LPS (0.8 mg/kg/day) for 4 weeks. This treatment significantly decreased the weight of fast-twitch skeletal muscles (masseter and tibialis anterior muscles), but not that of slow-twitch skeletal muscle (soleus muscle). The area of fibrosis was significantly increased in masseter muscle, but remained unchanged in the other two muscles. The number of apoptotic myocytes was significantly increased (approximately eightfold) in masseter muscle. These data suggest that persistent subclinical exposure to PG-LPS might reduce the size of fast-twitch skeletal muscle, but not slow-twitch skeletal muscle. Masseter muscle appears to be especially susceptible to the adverse effects of PG-LPS, because muscle remodeling (muscle fibrosis and myocyte apoptosis) was induced solely in masseter muscle. Thus, periodontitis might be one of the major causes of oral sarcopenia.
Identifiants
pubmed: 30848475
doi: 10.1007/s12576-019-00670-z
pii: 10.1007/s12576-019-00670-z
pmc: PMC10717087
doi:
Substances chimiques
Lipopolysaccharides
0
Types de publication
Journal Article
Langues
eng
Pagination
503-511Subventions
Organisme : KAKENHI
ID : 17K12067
Organisme : KAKENHI
ID : 15K18973
Organisme : KAKENHI
ID : 17K11977
Organisme : KAKENHI
ID : 17K17342
Organisme : KAKENHI
ID : 18K06862
Organisme : KAKENHI
ID : 16H05300
Organisme : MEXT-Supported Program for the Strategic Research Foundation at Private Universities
ID : S1511018
Organisme : Academic Contribution from Pfizer Japan
ID : AC160910
Organisme : Academic Contribution from Pfizer Japan
ID : AC1500818
Organisme : Academic Contribution from Pfizer Japan
ID : AC170780
Organisme : Mitsui Life Social Welfare Foundation
ID : N/A
Organisme : Research Promotion Grants from the Society for Tsurumi University
ID : 29002
Organisme : Research Promotion Grants from the Society for Tsurumi University
ID : 27010
Organisme : Research Promotion Grants from the Society for Tsurumi University
ID : 28006
Organisme : Research Promotion Grants from the Society for Tsurumi University
ID : 29007
Organisme : Reserach Promotion Grants from the Society for Tsurumi University
ID : 28006
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