Ishige okamurae and diphloroethohydoxycarmalol inhibit palmitic acid-impaired skeletal myogenesis and improve muscle regenerative potential

Obese sarcopenia is associated with palmitic acid (PA), an abundant circulating saturated fatty acid. This study examined a non-cytotoxic concentration of PA to provide mechanistic insights into PA-impaired skeletal myogenesis and potential medicinal and dietary interventions through edible brown se...

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Autores principales: Thilina U. Jayawardena, D.P. Nagahawatta, Yu-An Lu, Hye-Won Yang, Jun-Geon Je, Seo-Young Kim, You-Jin Jeon
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/96850050689a4790b35615036d0e73fb
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spelling oai:doaj.org-article:96850050689a4790b35615036d0e73fb2021-11-14T04:31:22ZIshige okamurae and diphloroethohydoxycarmalol inhibit palmitic acid-impaired skeletal myogenesis and improve muscle regenerative potential1756-464610.1016/j.jff.2021.104832https://doaj.org/article/96850050689a4790b35615036d0e73fb2021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S1756464621004813https://doaj.org/toc/1756-4646Obese sarcopenia is associated with palmitic acid (PA), an abundant circulating saturated fatty acid. This study examined a non-cytotoxic concentration of PA to provide mechanistic insights into PA-impaired skeletal myogenesis and potential medicinal and dietary interventions through edible brown seaweed, Ishige okamurae (IO). C2C12 cells were examined for myogenic markers, adipogenic factors, and regenerative capacity through growth regulators against PA interference to assess IO and purified diphloroethohydoxycarmalol (DPHC) as potential treatments. Both IO and DPHC improved myogenic marker (myogenin, MyoD, and MyHC) levels. PA down-regulated myogenic markers while improving adipogenic factors (PPARγ, c/EBPα, A-FABP), DPHC significantly arbitrated the negative effects. DPHC treatment also improved phosphorylation of the growth regulatory PI3K/Akt/mTOR axis over the adverse effects of PA. The results of this study suggested regulatory mechanisms through which the bioactive components IO and DPHC based on the sustainable utilization of I. okamurae inhibited the PA-induced impairment of skeletal myogenesis.Thilina U. JayawardenaD.P. NagahawattaYu-An LuHye-Won YangJun-Geon JeSeo-Young KimYou-Jin JeonElsevierarticlePalmitic acidSkeletal myogenesisMyogenic markersAdipogenic markersGrowth regulatorsIshige okamuraeNutrition. Foods and food supplyTX341-641ENJournal of Functional Foods, Vol 87, Iss , Pp 104832- (2021)
institution DOAJ
collection DOAJ
language EN
topic Palmitic acid
Skeletal myogenesis
Myogenic markers
Adipogenic markers
Growth regulators
Ishige okamurae
Nutrition. Foods and food supply
TX341-641
spellingShingle Palmitic acid
Skeletal myogenesis
Myogenic markers
Adipogenic markers
Growth regulators
Ishige okamurae
Nutrition. Foods and food supply
TX341-641
Thilina U. Jayawardena
D.P. Nagahawatta
Yu-An Lu
Hye-Won Yang
Jun-Geon Je
Seo-Young Kim
You-Jin Jeon
Ishige okamurae and diphloroethohydoxycarmalol inhibit palmitic acid-impaired skeletal myogenesis and improve muscle regenerative potential
description Obese sarcopenia is associated with palmitic acid (PA), an abundant circulating saturated fatty acid. This study examined a non-cytotoxic concentration of PA to provide mechanistic insights into PA-impaired skeletal myogenesis and potential medicinal and dietary interventions through edible brown seaweed, Ishige okamurae (IO). C2C12 cells were examined for myogenic markers, adipogenic factors, and regenerative capacity through growth regulators against PA interference to assess IO and purified diphloroethohydoxycarmalol (DPHC) as potential treatments. Both IO and DPHC improved myogenic marker (myogenin, MyoD, and MyHC) levels. PA down-regulated myogenic markers while improving adipogenic factors (PPARγ, c/EBPα, A-FABP), DPHC significantly arbitrated the negative effects. DPHC treatment also improved phosphorylation of the growth regulatory PI3K/Akt/mTOR axis over the adverse effects of PA. The results of this study suggested regulatory mechanisms through which the bioactive components IO and DPHC based on the sustainable utilization of I. okamurae inhibited the PA-induced impairment of skeletal myogenesis.
format article
author Thilina U. Jayawardena
D.P. Nagahawatta
Yu-An Lu
Hye-Won Yang
Jun-Geon Je
Seo-Young Kim
You-Jin Jeon
author_facet Thilina U. Jayawardena
D.P. Nagahawatta
Yu-An Lu
Hye-Won Yang
Jun-Geon Je
Seo-Young Kim
You-Jin Jeon
author_sort Thilina U. Jayawardena
title Ishige okamurae and diphloroethohydoxycarmalol inhibit palmitic acid-impaired skeletal myogenesis and improve muscle regenerative potential
title_short Ishige okamurae and diphloroethohydoxycarmalol inhibit palmitic acid-impaired skeletal myogenesis and improve muscle regenerative potential
title_full Ishige okamurae and diphloroethohydoxycarmalol inhibit palmitic acid-impaired skeletal myogenesis and improve muscle regenerative potential
title_fullStr Ishige okamurae and diphloroethohydoxycarmalol inhibit palmitic acid-impaired skeletal myogenesis and improve muscle regenerative potential
title_full_unstemmed Ishige okamurae and diphloroethohydoxycarmalol inhibit palmitic acid-impaired skeletal myogenesis and improve muscle regenerative potential
title_sort ishige okamurae and diphloroethohydoxycarmalol inhibit palmitic acid-impaired skeletal myogenesis and improve muscle regenerative potential
publisher Elsevier
publishDate 2021
url https://doaj.org/article/96850050689a4790b35615036d0e73fb
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