Omega-3 Supplementation Improves Isometric Strength But Not Muscle Anabolic and Catabolic Signaling in Response to Resistance Exercise in Healthy Older Adults

Author:

Dalle Sebastiaan1ORCID,Van Roie Evelien2,Hiroux Charlotte1,Vanmunster Mathias1,Coudyzer Walter3,Suhr Frank1,Bogaerts Stijn4,Van Thienen Ruud5,Koppo Katrien1

Affiliation:

1. Exercise Physiology Research Group, Department of Movement Sciences, KU Leuven, Belgium

2. Physical Activity, Sports and Health Research Group, Department of Movement Sciences, KU Leuven, Belgium

3. Department of Morphology and Medical Imaging, Faculty of Medicine, Radiology Section, KU Leuven, Belgium

4. Locomotor and Neurological Disorders, Department of Development and Regeneration, KU Leuven, Belgium

5. Research Group for Neurorehabilitation, Department of Rehabilitation Sciences, KU Leuven, Belgium

Abstract

Abstract Old skeletal muscle exhibits decreased anabolic sensitivity, eventually contributing to muscle wasting. Besides anabolism, also muscle inflammation and catabolism are critical players in regulating the old skeletal muscle’s sensitivity. Omega-3 fatty acids (ω-3) are an interesting candidate to reverse anabolic insensitivity via anabolic actions. Yet, it remains unknown whether ω-3 also attenuates muscle inflammation and catabolism. The present study investigates the effect of ω-3 supplementation on muscle inflammation and metabolism (anabolism/catabolism) upon resistance exercise (RE). Twenty-three older adults (65–84 years; 8♀) were randomized to receive ω-3 (~3 g/d) or corn oil (placebo [PLAC]) and engaged in a 12-week RE program (3×/wk). Before and after intervention, muscle volume, strength, and systemic inflammation were assessed, and muscle biopsies were analyzed for markers of anabolism, catabolism, and inflammation. Isometric knee-extensor strength increased in ω-3 (+12.2%), but not in PLAC (−1.4%; pinteraction = .015), whereas leg press strength improved in both conditions (+27.1%; ptime < .001). RE, but not ω-3, decreased inflammatory (p65NF-κB) and catabolic (FOXO1, LC3b) markers, and improved muscle quality. Yet, muscle volume remained unaffected by RE and ω-3. Accordingly, muscle anabolism (mTORC1) and plasma C-reactive protein remained unchanged by RE and ω-3, whereas serum IL-6 tended to decrease in ω-3 (pinteraction = .07). These results show that, despite no changes in muscle volume, RE-induced gains in isometric strength can be further enhanced by ω-3. However, ω-3 did not improve RE-induced beneficial catabolic or inflammatory adaptations. Irrespective of muscle volume, gains in strength (primary criterion for sarcopenia) might be explained by changes in muscle quality due to muscle inflammatory or catabolic signaling.

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Ageing

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