Protein Supplementation Enhances the Effects of Intermittent Loading on Skeletal Muscles by Activating the mTORC1 Signaling Pathway in a Rat Model of Disuse Atrophy

Inactivity leads to skeletal muscle atrophy, whereas intermittent loading (IL) during hind limb unloading (HU) attenuates muscle atrophy. However, the combined effects of IL and protein supplementation on disuse muscle atrophy are unclear. Therefore, we investigated the effects of IL and a high-prot...

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Main Authors: Sho Miyatake, Kazuo Hino, Yuko Natsui, Goro Ebisu, Satoshi Fujita
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/12/9/2729
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spelling doaj-d1658bc14d2945f98683b24bf1eb127d2020-11-25T03:47:07ZengMDPI AGNutrients2072-66432020-09-01122729272910.3390/nu12092729Protein Supplementation Enhances the Effects of Intermittent Loading on Skeletal Muscles by Activating the mTORC1 Signaling Pathway in a Rat Model of Disuse AtrophySho Miyatake0Kazuo Hino1Yuko Natsui2Goro Ebisu3Satoshi Fujita4OS-1 Division, Medical Foods Research Institute, Otsuka Pharmaceutical Factory, Inc. 115 Kuguhara, Tateiwa, Muya-cho, Naruto, Tokushima 772-8601, JapanOS-1 Division, Medical Foods Research Institute, Otsuka Pharmaceutical Factory, Inc. 115 Kuguhara, Tateiwa, Muya-cho, Naruto, Tokushima 772-8601, JapanOS-1 Division, Medical Foods Research Institute, Otsuka Pharmaceutical Factory, Inc. 115 Kuguhara, Tateiwa, Muya-cho, Naruto, Tokushima 772-8601, JapanOS-1 Division, Medical Foods Research Institute, Otsuka Pharmaceutical Factory, Inc. 115 Kuguhara, Tateiwa, Muya-cho, Naruto, Tokushima 772-8601, JapanFaculty of Sport and Health Science, Ritsumeikan University, 1-1-1, Nojihigashi, Kusatsu, Shiga 525-8577, JapanInactivity leads to skeletal muscle atrophy, whereas intermittent loading (IL) during hind limb unloading (HU) attenuates muscle atrophy. However, the combined effects of IL and protein supplementation on disuse muscle atrophy are unclear. Therefore, we investigated the effects of IL and a high-protein oral nutritional supplement (HP) during HU on skeletal muscle mass and protein synthesis/breakdown. Male F344 rats were assigned to the control (CON), 14-day HU (HU), IL during HU (HU + IL), and IL during HU followed by HP administration (2.6 g protein/kg/day; HU + IL + HP) groups. Soleus and gastrocnemius muscles were sampled 30 min after the last IL and HP supplementation. HU decreased relative soleus and gastrocnemius muscle masses. Relative muscle masses and p70 ribosomal protein S6 kinase/ribosomal protein S6 phosphorylation in soleus and gastrocnemius muscles were higher in the HU + IL group than the HU group and further higher in the HU + IL + HP group than the HU + IL group in gastrocnemius muscle. Therefore, protein administration plus IL effectively prevented skeletal muscle atrophy induced by disuse, potentially via enhanced activation of targets downstream of mammalian target of rapamycin complex 1 (mTORC1) signaling pathway.https://www.mdpi.com/2072-6643/12/9/2729hind limb unloadingintermittent loadingproteinskeletal muscle
collection DOAJ
language English
format Article
sources DOAJ
author Sho Miyatake
Kazuo Hino
Yuko Natsui
Goro Ebisu
Satoshi Fujita
spellingShingle Sho Miyatake
Kazuo Hino
Yuko Natsui
Goro Ebisu
Satoshi Fujita
Protein Supplementation Enhances the Effects of Intermittent Loading on Skeletal Muscles by Activating the mTORC1 Signaling Pathway in a Rat Model of Disuse Atrophy
Nutrients
hind limb unloading
intermittent loading
protein
skeletal muscle
author_facet Sho Miyatake
Kazuo Hino
Yuko Natsui
Goro Ebisu
Satoshi Fujita
author_sort Sho Miyatake
title Protein Supplementation Enhances the Effects of Intermittent Loading on Skeletal Muscles by Activating the mTORC1 Signaling Pathway in a Rat Model of Disuse Atrophy
title_short Protein Supplementation Enhances the Effects of Intermittent Loading on Skeletal Muscles by Activating the mTORC1 Signaling Pathway in a Rat Model of Disuse Atrophy
title_full Protein Supplementation Enhances the Effects of Intermittent Loading on Skeletal Muscles by Activating the mTORC1 Signaling Pathway in a Rat Model of Disuse Atrophy
title_fullStr Protein Supplementation Enhances the Effects of Intermittent Loading on Skeletal Muscles by Activating the mTORC1 Signaling Pathway in a Rat Model of Disuse Atrophy
title_full_unstemmed Protein Supplementation Enhances the Effects of Intermittent Loading on Skeletal Muscles by Activating the mTORC1 Signaling Pathway in a Rat Model of Disuse Atrophy
title_sort protein supplementation enhances the effects of intermittent loading on skeletal muscles by activating the mtorc1 signaling pathway in a rat model of disuse atrophy
publisher MDPI AG
series Nutrients
issn 2072-6643
publishDate 2020-09-01
description Inactivity leads to skeletal muscle atrophy, whereas intermittent loading (IL) during hind limb unloading (HU) attenuates muscle atrophy. However, the combined effects of IL and protein supplementation on disuse muscle atrophy are unclear. Therefore, we investigated the effects of IL and a high-protein oral nutritional supplement (HP) during HU on skeletal muscle mass and protein synthesis/breakdown. Male F344 rats were assigned to the control (CON), 14-day HU (HU), IL during HU (HU + IL), and IL during HU followed by HP administration (2.6 g protein/kg/day; HU + IL + HP) groups. Soleus and gastrocnemius muscles were sampled 30 min after the last IL and HP supplementation. HU decreased relative soleus and gastrocnemius muscle masses. Relative muscle masses and p70 ribosomal protein S6 kinase/ribosomal protein S6 phosphorylation in soleus and gastrocnemius muscles were higher in the HU + IL group than the HU group and further higher in the HU + IL + HP group than the HU + IL group in gastrocnemius muscle. Therefore, protein administration plus IL effectively prevented skeletal muscle atrophy induced by disuse, potentially via enhanced activation of targets downstream of mammalian target of rapamycin complex 1 (mTORC1) signaling pathway.
topic hind limb unloading
intermittent loading
protein
skeletal muscle
url https://www.mdpi.com/2072-6643/12/9/2729
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