Improved skeletal muscle fatigue resistance in experimental autoimmune myositis mice following high-intensity interval training.


Journal

Arthritis research & therapy
ISSN: 1478-6362
Titre abrégé: Arthritis Res Ther
Pays: England
ID NLM: 101154438

Informations de publication

Date de publication:
27 06 2022
Historique:
received: 27 04 2022
accepted: 18 06 2022
entrez: 27 6 2022
pubmed: 28 6 2022
medline: 30 6 2022
Statut: epublish

Résumé

Muscle weakness and decreased fatigue resistance are key manifestations of systemic autoimmune myopathies (SAMs). We here examined whether high-intensity interval training (HIIT) improves fatigue resistance in the skeletal muscle of experimental autoimmune myositis (EAM) mice, a widely used animal model for SAM. Female BALB/c mice were randomly assigned to control (CNT) or EAM groups (n = 28 in each group). EAM was induced by immunization with three injections of myosin emulsified in complete Freund's adjuvant. The plantar flexor (PF) muscles of mice with EAM were exposed to either an acute bout or 4 weeks of HIIT (a total of 14 sessions). The fatigue resistance of PF muscles was lower in the EAM than in the CNT group (P < 0.05). These changes were associated with decreased activities of citrate synthase and cytochrome c oxidase and increased expression levels of the endoplasmic reticulum stress proteins (glucose-regulated protein 78 and 94, and PKR-like ER kinase) (P < 0.05). HIIT restored all these alterations and increased the peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α) and the mitochondrial electron transport chain complexes (I, III, and IV) in the muscles of EAM mice (P < 0.05). HIIT improves fatigue resistance in a SAM mouse model, and this can be explained by the restoration of mitochondria oxidative capacity via inhibition of the ER stress pathway and PGC-1α-mediated mitochondrial biogenesis.

Sections du résumé

BACKGROUND
Muscle weakness and decreased fatigue resistance are key manifestations of systemic autoimmune myopathies (SAMs). We here examined whether high-intensity interval training (HIIT) improves fatigue resistance in the skeletal muscle of experimental autoimmune myositis (EAM) mice, a widely used animal model for SAM.
METHODS
Female BALB/c mice were randomly assigned to control (CNT) or EAM groups (n = 28 in each group). EAM was induced by immunization with three injections of myosin emulsified in complete Freund's adjuvant. The plantar flexor (PF) muscles of mice with EAM were exposed to either an acute bout or 4 weeks of HIIT (a total of 14 sessions).
RESULTS
The fatigue resistance of PF muscles was lower in the EAM than in the CNT group (P < 0.05). These changes were associated with decreased activities of citrate synthase and cytochrome c oxidase and increased expression levels of the endoplasmic reticulum stress proteins (glucose-regulated protein 78 and 94, and PKR-like ER kinase) (P < 0.05). HIIT restored all these alterations and increased the peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α) and the mitochondrial electron transport chain complexes (I, III, and IV) in the muscles of EAM mice (P < 0.05).
CONCLUSIONS
HIIT improves fatigue resistance in a SAM mouse model, and this can be explained by the restoration of mitochondria oxidative capacity via inhibition of the ER stress pathway and PGC-1α-mediated mitochondrial biogenesis.

Identifiants

pubmed: 35761371
doi: 10.1186/s13075-022-02846-2
pii: 10.1186/s13075-022-02846-2
pmc: PMC9235155
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

156

Informations de copyright

© 2022. The Author(s).

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Auteurs

Takashi Yamada (T)

Graduate School of Health Sciences, Sapporo Medical University, Sapporo, 060-8556, Japan. takashi.yamada1976@sapmed.ac.jp.

Yuki Ashida (Y)

Graduate School of Health Sciences, Sapporo Medical University, Sapporo, 060-8556, Japan.
Research fellow of Japan Society for Promotion of Science, Tokyo, Japan.

Katsuyuki Tamai (K)

Graduate School of Health Sciences, Sapporo Medical University, Sapporo, 060-8556, Japan.

Iori Kimura (I)

Graduate School of Health Sciences, Sapporo Medical University, Sapporo, 060-8556, Japan.

Nao Yamauchi (N)

Graduate School of Health Sciences, Sapporo Medical University, Sapporo, 060-8556, Japan.

Azuma Naito (A)

Graduate School of Health Sciences, Sapporo Medical University, Sapporo, 060-8556, Japan.

Nao Tokuda (N)

Graduate School of Health Sciences, Sapporo Medical University, Sapporo, 060-8556, Japan.

Håkan Westerblad (H)

Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.

Daniel C Andersson (DC)

Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Heart, Vascular and Neurology Theme, Cardiology Unit, Karolinska University Hospital, Stockholm, Sweden.

Koichi Himori (K)

Graduate School of Health Sciences, Sapporo Medical University, Sapporo, 060-8556, Japan.
Research fellow of Japan Society for Promotion of Science, Tokyo, Japan.

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