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Thermoneutral Housing and a Western Diet Combination Exacerbates Dysferlin-Deficient Muscular Dystrophy.
Donen, Graham S; White, Zoe; Sauge, Elodie; Ritso, Morten; Theret, Marine; Boyd, John; Devlin, Angela M; Rossi, Fabio M V; Bernatchez, Pascal.
  • Donen GS; University of British Columbia (UBC), Department of Anesthesiology, Pharmacology & Therapeutics, Vancouver, Canada.
  • White Z; UBC Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, Canada.
  • Sauge E; University of British Columbia (UBC), Department of Anesthesiology, Pharmacology & Therapeutics, Vancouver, Canada.
  • Ritso M; UBC Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, Canada.
  • Theret M; University of British Columbia (UBC), Department of Anesthesiology, Pharmacology & Therapeutics, Vancouver, Canada.
  • Boyd J; UBC Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, Canada.
  • Devlin AM; The Biomedical Research Centre, UBC, Vancouver, Canada.
  • Rossi FMV; The Biomedical Research Centre, UBC, Vancouver, Canada.
  • Bernatchez P; UBC Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, Canada.
Muscle Nerve ; 66(4): 513-522, 2022 10.
Article en En | MEDLINE | ID: mdl-35859452
ABSTRACT
INTRODUCTION/

AIMS:

Most mouse models of muscular dystrophy (MD) show mild phenotypes, which limits the translatability of experimental therapies to patients. A growing body of evidence suggests that MD is accompanied by metabolic abnormalities that could potentially exacerbate the primary muscle wasting process. Since thermoneutral (TN) housing of mice (~30°C) has been shown to affect many metabolic parameters, particularly when combined with a Western diet (WD), our aim was to determine whether the combination of TN and WD exacerbates muscle wasting in dysferlin-deficient BLAJ mice, a common model of limb-girdle MD type 2b (LGMD2b).

METHODS:

The 2-mo-old wild-type (WT) and BLAJ mice were housed at TN or room temperature (RT) and fed a WD or regular chow for 9 mo. Ambulatory function, muscle histology, and protein immunoblots of skeletal muscle were assessed.

RESULTS:

BLAJ mice at RT and fed a chow diet showed normal ambulation function similar to WT mice, whereas 90% of BLAJ mice under WD and TN combination showed ambulatory dysfunction (p < 0.001), and an up to 4.1-fold increase in quadriceps and gastrocnemius fat infiltration. Western blotting revealed decreased autophagy marker microtubules-associated protein 1 light chain 3-B (LC3BII/LC3BI) ratio and up-regulation of protein kinase B/AKT and ribosomal protein S6 phosphorylation, suggesting inefficient cellular debris and protein clearance in TN BLAJ mice fed a WD. Male and female BLAJ mice under TN and WD combination showed heterogenous fibro-fatty infiltrate composition.

DISCUSSION:

TN and WD combination exacerbates rodent LGMD2b without affecting WT mice. This improves rodent modeling of human MD and helps elucidate how metabolic abnormalities may play a causal role in muscle wasting.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Distrofia Muscular de Cinturas / Distrofias Musculares Límite: Animals / Female / Humans / Male Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Distrofia Muscular de Cinturas / Distrofias Musculares Límite: Animals / Female / Humans / Male Idioma: En Año: 2022 Tipo del documento: Article