Two Weeks of Smoking Cessation Reverse Cigarette Smoke-Induced Skeletal Muscle Atrophy and Mitochondrial Dysfunction in Mice

Author:

Ajime Tom Tanjeko123ORCID,Serré Jef1,Wüst Rob C I4,Messa Guy Anselme Mpaka3,Poffé Chiel5,Swaminathan Anandini6,Maes Karen1,Janssens Wim1,Troosters Thierry12,Degens Hans36,Gayan-Ramirez Ghislaine1

Affiliation:

1. Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU-Leuven, Leuven, Belgium

2. Research Group for Rehabilitation in Internal Disorders, Department of Rehabilitation Sciences, KU-Leuven, Leuven, Belgium

3. Department of Life Sciences, Research Center for Musculoskeletal Science and Sports Medicine, Manchester Metropolitan University, Manchester, UK

4. Laboratory of Myology, Department of Human Movement Sciences, Faculty of Behavioral and Movement Sciences, Amsterdam Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands

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

6. Lithuanian Sports University, Kaunas, Lithuania

Abstract

Abstract Introduction Apart from its adverse effects on the respiratory system, cigarette smoking also induces skeletal muscle atrophy and dysfunction. Whether short-term smoking cessation can restore muscle mass and function is unknown. We, therefore, studied the impact of 1- and 2-week smoking cessation on skeletal muscles in a mouse model. Methods Male mice were divided into four groups: Air-exposed (14 weeks); cigarette smoke (CS)-exposed (14 weeks); CS-exposed (13 weeks) followed by 1-week cessation; CS-exposed (12 weeks) followed by 2 weeks cessation to examine exercise capacity, physical activity levels, body composition, muscle function, capillarization, mitochondrial function and protein expression in the soleus, plantaris, and diaphragm muscles. Results CS-induced loss of body and muscle mass was significantly improved within 1 week of cessation due to increased lean and fat mass. Mitochondrial respiration and protein levels of the respiratory complexes in the soleus were lower in CS-exposed mice, but similar to control values after 2 weeks of cessation. Exposing isolated soleus muscles to CS extracts reduced mitochondrial respiration that was reversed after removing the extract. While physical activity was reduced in all groups, exercise capacity, limb muscle force, fatigue resistance, fiber size and capillarization, and diaphragm cytoplasmic HIF-1α were unaltered by CS-exposure. However, CS-induced diaphragm atrophy and increased capillary density were not seen after 2 weeks of smoking cessation. Conclusion In male mice, 2 weeks of smoking cessation reversed smoking-induced mitochondrial dysfunction, limb muscle mass loss, and diaphragm muscle atrophy, highlighting immediate benefits of cessation on skeletal muscles. Implications Our study demonstrates that CS-induced skeletal muscle mitochondrial dysfunction and atrophy are significantly improved by 2 weeks of cessation in male mice. We show for the first time that smoking cessation as short as 1 to 2 weeks is associated with immediate beneficial effects on skeletal muscle structure and function with the diaphragm being particularly sensitive to CS-exposure and cessation. This could help motivate smokers to quit smoking as early as possible. The knowledge that smoking cessation has potential positive extrapulmonary effects is particularly relevant for patients referred to rehabilitation programs and those admitted to hospitals suffering from acute or chronic muscle deterioration yet struggling with smoking cessation.

Funder

Directorate-General for Education and Culture

Publisher

Oxford University Press (OUP)

Subject

Public Health, Environmental and Occupational Health

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1. Sex-specific lung inflammation and mitochondrial damage in a model of electronic cigarette exposure in asthma;American Journal of Physiology-Lung Cellular and Molecular Physiology;2023-11-01

2. Tissue-specific mitochondrial toxicity of cigarette smoke concentrate: consequence to oxidative phosphorylation;American Journal of Physiology-Heart and Circulatory Physiology;2023-11-01

3. The effect of smoking on respiratory functions in athletes;Revista de Gestão e Secretariado (Management and Administrative Professional Review);2023-10-31

4. Role of nutrition in patients with coexisting chronic obstructive pulmonary disease and sarcopenia;Frontiers in Nutrition;2023-08-08

5. A modelling approach to disentangle the factors limiting muscle oxygenation in smokers;European Journal of Applied Physiology;2023-08-06

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