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Increase in muscle endurance in mice by dietary Yamabushitake mushroom (Hericium erinaceus) possibly via activation of PPARδ
Skeletal muscle fiber is largely classified into two types: type 1 (slow‐twitch) and type 2 (fast‐twitch) fibers. Meat quality and composition of fiber types are thought to be closely related. Previous research showed that overexpression of constitutively active peroxisome proliferator‐activated rec...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594082/ https://www.ncbi.nlm.nih.gov/pubmed/30938015 http://dx.doi.org/10.1111/asj.13199 |
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author | Komiya, Yusuke Nakamura, Toshiya Ishii, Momoko Shimizu, Kuniyoshi Hiraki, Eri Kawabata, Fuminori Nakamura, Mako Tatsumi, Ryuichi Ikeuchi, Yoshihide Mizunoya, Wataru |
author_facet | Komiya, Yusuke Nakamura, Toshiya Ishii, Momoko Shimizu, Kuniyoshi Hiraki, Eri Kawabata, Fuminori Nakamura, Mako Tatsumi, Ryuichi Ikeuchi, Yoshihide Mizunoya, Wataru |
author_sort | Komiya, Yusuke |
collection | PubMed |
description | Skeletal muscle fiber is largely classified into two types: type 1 (slow‐twitch) and type 2 (fast‐twitch) fibers. Meat quality and composition of fiber types are thought to be closely related. Previous research showed that overexpression of constitutively active peroxisome proliferator‐activated receptor (PPAR)δ, a nuclear receptor present in skeletal muscle, increased type 1 fibers in mice. In this study, we found that hexane extracts of Yamabushitake mushroom (Hericium erinaceus) showed PPARδ agonistic activity in vitro. Eight‐week‐old C57BL/6J mice were fed a diet supplemented with 5% (w/w) freeze‐dried Yamabushitake mushroom for 24 hr. After the treatment period, the extensor digitorum longus (EDL) muscles were excised. The Yamabushitake‐supplemented diet up‐regulated the PPARδ target genes Pdk4 and Ucp3 in mouse skeletal muscles in vivo. Furthermore, feeding the Yamabushitake‐supplemented diet to mice for 8 weeks resulted in a significant increase in muscle endurance. These results indicate that Yamabushitake mushroom contains PPARδ agonistic ligands and that dietary intake of Yamabushitake mushroom could activate PPARδ in skeletal muscle of mice. Unexpectedly, we observed no significant alterations in composition of muscle fiber types between the mice fed control and Yamabushitake‐supplemented diets. |
format | Online Article Text |
id | pubmed-6594082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65940822019-07-10 Increase in muscle endurance in mice by dietary Yamabushitake mushroom (Hericium erinaceus) possibly via activation of PPARδ Komiya, Yusuke Nakamura, Toshiya Ishii, Momoko Shimizu, Kuniyoshi Hiraki, Eri Kawabata, Fuminori Nakamura, Mako Tatsumi, Ryuichi Ikeuchi, Yoshihide Mizunoya, Wataru Anim Sci J Original Articles Skeletal muscle fiber is largely classified into two types: type 1 (slow‐twitch) and type 2 (fast‐twitch) fibers. Meat quality and composition of fiber types are thought to be closely related. Previous research showed that overexpression of constitutively active peroxisome proliferator‐activated receptor (PPAR)δ, a nuclear receptor present in skeletal muscle, increased type 1 fibers in mice. In this study, we found that hexane extracts of Yamabushitake mushroom (Hericium erinaceus) showed PPARδ agonistic activity in vitro. Eight‐week‐old C57BL/6J mice were fed a diet supplemented with 5% (w/w) freeze‐dried Yamabushitake mushroom for 24 hr. After the treatment period, the extensor digitorum longus (EDL) muscles were excised. The Yamabushitake‐supplemented diet up‐regulated the PPARδ target genes Pdk4 and Ucp3 in mouse skeletal muscles in vivo. Furthermore, feeding the Yamabushitake‐supplemented diet to mice for 8 weeks resulted in a significant increase in muscle endurance. These results indicate that Yamabushitake mushroom contains PPARδ agonistic ligands and that dietary intake of Yamabushitake mushroom could activate PPARδ in skeletal muscle of mice. Unexpectedly, we observed no significant alterations in composition of muscle fiber types between the mice fed control and Yamabushitake‐supplemented diets. John Wiley and Sons Inc. 2019-04-01 2019-06 /pmc/articles/PMC6594082/ /pubmed/30938015 http://dx.doi.org/10.1111/asj.13199 Text en © 2019 The Authors. Animal Science Journal published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Animal Science. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Komiya, Yusuke Nakamura, Toshiya Ishii, Momoko Shimizu, Kuniyoshi Hiraki, Eri Kawabata, Fuminori Nakamura, Mako Tatsumi, Ryuichi Ikeuchi, Yoshihide Mizunoya, Wataru Increase in muscle endurance in mice by dietary Yamabushitake mushroom (Hericium erinaceus) possibly via activation of PPARδ |
title | Increase in muscle endurance in mice by dietary Yamabushitake mushroom (Hericium erinaceus) possibly via activation of PPARδ |
title_full | Increase in muscle endurance in mice by dietary Yamabushitake mushroom (Hericium erinaceus) possibly via activation of PPARδ |
title_fullStr | Increase in muscle endurance in mice by dietary Yamabushitake mushroom (Hericium erinaceus) possibly via activation of PPARδ |
title_full_unstemmed | Increase in muscle endurance in mice by dietary Yamabushitake mushroom (Hericium erinaceus) possibly via activation of PPARδ |
title_short | Increase in muscle endurance in mice by dietary Yamabushitake mushroom (Hericium erinaceus) possibly via activation of PPARδ |
title_sort | increase in muscle endurance in mice by dietary yamabushitake mushroom (hericium erinaceus) possibly via activation of pparδ |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594082/ https://www.ncbi.nlm.nih.gov/pubmed/30938015 http://dx.doi.org/10.1111/asj.13199 |
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