Diet-induced vitamin D deficiency reduces skeletal muscle mitochondrial respiration

Author:

Ashcroft Stephen P123,Fletcher Gareth3,Philp Ashleigh M34,Jenkinson Carl56,Das Shatarupa78,Hansbro Philip M78,Atherton Philip J2,Philp Andrew34

Affiliation:

1. 1School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, UK

2. 2MRC-Versus Arthritis Centre for Musculoskeletal Ageing Research, Clinical, Metabolic and Molecular Physiology, University of Nottingham, Royal Derby Hospital Centre, Derby, UK

3. 3Mitochondrial Metabolism and Ageing Laboratory, Garvan Institute of Medical Research, Sydney, New South Wales, Australia

4. 4St Vincent’s Clinical School, UNSW Medicine, UNSW Sydney, New South Wales, Australia

5. 5Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK

6. 6ANZAC Research Institute, University of Sydney, Sydney, New South Wales, Australia

7. 7Centenary Institute, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia

8. 8UTS Centenary Centre for Inflammation, University Technology Sydney, New South Wales, Australia

Abstract

Vitamin D deficiency is associated with symptoms of skeletal muscle myopathy including muscle weakness and fatigue. Recently, vitamin D-related metabolites have been linked to the maintenance of mitochondrial function within skeletal muscle. However, current evidence is limited to in vitro models and the effects of diet-induced vitamin D deficiency upon skeletal muscle mitochondrial function in vivo have received little attention. In order to examine the role of vitamin D in the maintenance of mitochondrial function in vivo, we utilised an established model of diet-induced vitamin D deficiency in C57BL/6J mice. Mice were either fed a control diet (2200 IU/kg i.e. vitamin D replete) or a vitamin D-deplete (0 IU/kg) diet for periods of 1, 2 and 3 months. Gastrocnemius muscle mitochondrial function and ADP sensitivity were assessed via high-resolution respirometry and mitochondrial protein content via immunoblotting. As a result of 3 months of diet-induced vitamin D deficiency, respiration supported via complex I + II (CI + IIP) and the electron transport chain (ETC) were 35 and 37% lower when compared to vitamin D-replete mice (P < 0.05). Despite functional alterations, citrate synthase activity, AMPK phosphorylation, mitofilin, OPA1 and ETC subunit protein content remained unchanged in response to dietary intervention (P > 0.05). In conclusion, we report that 3 months of diet-induced vitamin D deficiency reduced skeletal muscle mitochondrial respiration in C57BL/6J mice. Our data, when combined with previous in vitro observations, suggest that vitamin D-mediated regulation of mitochondrial function may underlie the exacerbated muscle fatigue and performance deficits observed during vitamin D deficiency.

Publisher

Bioscientifica

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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