Chronic repetitive cooling and caffeine-induced intracellular Ca2+ elevation differentially impact adaptations in slow- and fast-twitch rat skeletal muscles

Author:

Takagi Ryo1ORCID,Tabuchi Ayaka2,Hayakawa Kosei2,Osana Shion23,Yabuta Hiroya2,Hoshino Daisuke2ORCID,Poole David C.45ORCID,Kano Yutaka26ORCID

Affiliation:

1. Ritsumeikan Global Innovation Research Organization, Ritsumeikan University, Shiga, Japan

2. Graduate School of Informatics and Engineering, University of Electro-Communications, Tokyo, Japan

3. Department of Sport and Medical Science, Kokushikan University, Tokyo, Japan

4. Department of Anatomy and Physiology, Kansas State University, Manhattan, Kansas, United States

5. Department of Kinesiology, Kansas State University, Manhattan, Kansas, United States

6. Center for Neuroscience and Biomedical Engineering, University of Electro-Communications, Tokyo, Japan

Abstract

Intracellular Ca2+ concentration ([Ca2+]i) is considered important in the regulation of skeletal muscle mass. This study tested the hypothesis that chronic repeated cooling and/or caffeine ingestion would acutely increase [Ca2+]i and hypertrophy muscles potentially in a fiber-type-dependent manner. Control rats and those fed caffeine were subjected to repeated bidiurnal treatments of percutaneous icing, under anesthesia, to reduce the muscle temperature below ∼5°C. The predominantly fast-twitch tibialis anterior (TA) and slow-twitch soleus (SOL) muscles were evaluated after 28 days of intervention. The [Ca2+]i elevating response to icing was enhanced by caffeine loading only in the SOL muscle, with the response present across a significantly higher temperature range than in the TA muscle under caffeine-loading conditions. In both the TA and SOL muscles, myofiber cross-sectional area (CSA) was decreased by chronic caffeine treatment (mean reductions of 10.5% and 20.4%, respectively). However, in the TA, but not the SOL, CSA was restored by icing (+15.4 ± 4.3% vs. noniced, P < 0.01). In the SOL, but not TA, icing + caffeine increased myofiber number (20.5 ± 6.7%, P < 0.05) and satellite cell density (2.5 ± 0.3-fold) in cross sections. These contrasting muscle responses to cooling and caffeine may reflect fiber-type-specific [Ca2+]i responses and/or differential responses to elevated [Ca2+]i.

Funder

MEXT | Japan Society for the Promotion of Science

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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