Effects of Fucoxanthin on the Inhibition of Dexamethasone-Induced Skeletal Muscle Loss in Mice

Fucoxanthin (Fx) has preventive effect against muscle atrophy and myotube loss in vitro, but it has not yet been examined in vivo. Therefore, we aimed to investigate the effect of Fx on dexamethasone (Dex)-induced muscle atrophy and fat mass in mice. ICR mice were fed with Fx diets from 2 weeks befo...

Full description

Bibliographic Details
Main Authors: Maki Yoshikawa, Masashi Hosokawa, Kazuo Miyashita, Hoyoku Nishino, Takeshi Hashimoto
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/13/4/1079
_version_ 1797539989513306112
author Maki Yoshikawa
Masashi Hosokawa
Kazuo Miyashita
Hoyoku Nishino
Takeshi Hashimoto
author_facet Maki Yoshikawa
Masashi Hosokawa
Kazuo Miyashita
Hoyoku Nishino
Takeshi Hashimoto
author_sort Maki Yoshikawa
collection DOAJ
description Fucoxanthin (Fx) has preventive effect against muscle atrophy and myotube loss in vitro, but it has not yet been examined in vivo. Therefore, we aimed to investigate the effect of Fx on dexamethasone (Dex)-induced muscle atrophy and fat mass in mice. ICR mice were fed with Fx diets from 2 weeks before Dex treatment to the end of the study. Muscle atrophy was induced in the mice by oral administration of Dex. Body weight was significantly lower by Dex treatment. Visceral fat mass in the Fx-treated group were significantly lower than those in the control group. The Dex-induced decrease in tibialis anterior muscle mass was ameliorated by Fx treatment. Fx treatment significantly attenuated muscle lipid peroxidation compared with the control and Dex-treated groups. The phosphorylation of AMPK was significantly higher in the Dex-treated group than in the control group. The expression of cytochrome c oxidase (COX) IV was significantly higher in the Fx-treated group than in the control group. These results suggest that Fx may be a beneficial material to prevent muscle atrophy in vivo, in addition to the effect of fat loss.
first_indexed 2024-03-10T12:53:41Z
format Article
id doaj.art-de8f5e6a4d0047ae9da90a955ec7a9fe
institution Directory Open Access Journal
issn 2072-6643
language English
last_indexed 2024-03-10T12:53:41Z
publishDate 2021-03-01
publisher MDPI AG
record_format Article
series Nutrients
spelling doaj.art-de8f5e6a4d0047ae9da90a955ec7a9fe2023-11-21T12:05:38ZengMDPI AGNutrients2072-66432021-03-01134107910.3390/nu13041079Effects of Fucoxanthin on the Inhibition of Dexamethasone-Induced Skeletal Muscle Loss in MiceMaki Yoshikawa0Masashi Hosokawa1Kazuo Miyashita2Hoyoku Nishino3Takeshi Hashimoto4Faculty of Sport and Health Sciences, Ritsumeikan University, 1-1-1 Nojihigashi, Kusatsu 525-8577, JapanFaculty of Fisheries Sciences, Hokkaido University, 3-1-1, Minato-cho, Hakodate 041-8611, JapanFaculty of Fisheries Sciences, Hokkaido University, 3-1-1, Minato-cho, Hakodate 041-8611, JapanKyoto Prefecture University of Medicine, 465 Kajii-cho, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, JapanFaculty of Sport and Health Sciences, Ritsumeikan University, 1-1-1 Nojihigashi, Kusatsu 525-8577, JapanFucoxanthin (Fx) has preventive effect against muscle atrophy and myotube loss in vitro, but it has not yet been examined in vivo. Therefore, we aimed to investigate the effect of Fx on dexamethasone (Dex)-induced muscle atrophy and fat mass in mice. ICR mice were fed with Fx diets from 2 weeks before Dex treatment to the end of the study. Muscle atrophy was induced in the mice by oral administration of Dex. Body weight was significantly lower by Dex treatment. Visceral fat mass in the Fx-treated group were significantly lower than those in the control group. The Dex-induced decrease in tibialis anterior muscle mass was ameliorated by Fx treatment. Fx treatment significantly attenuated muscle lipid peroxidation compared with the control and Dex-treated groups. The phosphorylation of AMPK was significantly higher in the Dex-treated group than in the control group. The expression of cytochrome c oxidase (COX) IV was significantly higher in the Fx-treated group than in the control group. These results suggest that Fx may be a beneficial material to prevent muscle atrophy in vivo, in addition to the effect of fat loss.https://www.mdpi.com/2072-6643/13/4/1079carotenoidantioxidantsarcopenic obesity
spellingShingle Maki Yoshikawa
Masashi Hosokawa
Kazuo Miyashita
Hoyoku Nishino
Takeshi Hashimoto
Effects of Fucoxanthin on the Inhibition of Dexamethasone-Induced Skeletal Muscle Loss in Mice
Nutrients
carotenoid
antioxidant
sarcopenic obesity
title Effects of Fucoxanthin on the Inhibition of Dexamethasone-Induced Skeletal Muscle Loss in Mice
title_full Effects of Fucoxanthin on the Inhibition of Dexamethasone-Induced Skeletal Muscle Loss in Mice
title_fullStr Effects of Fucoxanthin on the Inhibition of Dexamethasone-Induced Skeletal Muscle Loss in Mice
title_full_unstemmed Effects of Fucoxanthin on the Inhibition of Dexamethasone-Induced Skeletal Muscle Loss in Mice
title_short Effects of Fucoxanthin on the Inhibition of Dexamethasone-Induced Skeletal Muscle Loss in Mice
title_sort effects of fucoxanthin on the inhibition of dexamethasone induced skeletal muscle loss in mice
topic carotenoid
antioxidant
sarcopenic obesity
url https://www.mdpi.com/2072-6643/13/4/1079
work_keys_str_mv AT makiyoshikawa effectsoffucoxanthinontheinhibitionofdexamethasoneinducedskeletalmusclelossinmice
AT masashihosokawa effectsoffucoxanthinontheinhibitionofdexamethasoneinducedskeletalmusclelossinmice
AT kazuomiyashita effectsoffucoxanthinontheinhibitionofdexamethasoneinducedskeletalmusclelossinmice
AT hoyokunishino effectsoffucoxanthinontheinhibitionofdexamethasoneinducedskeletalmusclelossinmice
AT takeshihashimoto effectsoffucoxanthinontheinhibitionofdexamethasoneinducedskeletalmusclelossinmice