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Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells

BACKGROUND: Sarcopenia, the decline of skeletal muscle tissue attributed to primary aging is a major concern in older adults. Flavonoids might have potential benefits by modulating the regulation of satellite cells, thus preventing muscle loss. Sinensetin (SIN), a citrus methylated flavone with anti...

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Autores principales: Kim, Jin-A, Kim, Seong Min, Ha, Sang Eun, Vetrivel, Preethi, Saralamma, Venu Venkatarame Gowda, Kim, Eun Hee, Kim, Gon Sup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819389/
https://www.ncbi.nlm.nih.gov/pubmed/31660942
http://dx.doi.org/10.1186/s12906-019-2714-2
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author Kim, Jin-A
Kim, Seong Min
Ha, Sang Eun
Vetrivel, Preethi
Saralamma, Venu Venkatarame Gowda
Kim, Eun Hee
Kim, Gon Sup
author_facet Kim, Jin-A
Kim, Seong Min
Ha, Sang Eun
Vetrivel, Preethi
Saralamma, Venu Venkatarame Gowda
Kim, Eun Hee
Kim, Gon Sup
author_sort Kim, Jin-A
collection PubMed
description BACKGROUND: Sarcopenia, the decline of skeletal muscle tissue attributed to primary aging is a major concern in older adults. Flavonoids might have potential benefits by modulating the regulation of satellite cells, thus preventing muscle loss. Sinensetin (SIN), a citrus methylated flavone with anti-inflammatory and anti-proliferative activity, can enhance lipolysis. The objective of the present study was to investigate whether SIN might have sarcopenia-suppressing effect on satellite cells from thigh and calf muscle tissues of young and old rats. METHODS: Primary muscle cells were obtained from thigh and calf tissues of young and old group rats by dissection. Obtained satellite cells were incubated with indicated concentrations of SIN (50 and 100 μM) treated and untreated condition in differentiation medium. Morphological changes of cells were examined using a phase-contrast microscope. Protein expression levels of myoD and myogenin were analyzed by Western blot. Cells treated with or without SIN under differentiation condition were also immunocytochemically stained for myogenin and 4′,6-diamidino-2-phenylindole (DAPI). RESULTS: Morphologically, the differentiation extracted satellite cells was found to be more evident in SIN treated group of aged rat′s cells than that in SIN untreated group. Expression levels of myoD and myogenin proteins involved in myogenesis were increased upon treatment with SIN. CONCLUSIONS: Collectively, our results indicate that SIN can alleviate age-related sarcopenia by increasing differentiation rate and protein levels of myoD and myogenin.
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spelling pubmed-68193892019-10-31 Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells Kim, Jin-A Kim, Seong Min Ha, Sang Eun Vetrivel, Preethi Saralamma, Venu Venkatarame Gowda Kim, Eun Hee Kim, Gon Sup BMC Complement Altern Med Research Article BACKGROUND: Sarcopenia, the decline of skeletal muscle tissue attributed to primary aging is a major concern in older adults. Flavonoids might have potential benefits by modulating the regulation of satellite cells, thus preventing muscle loss. Sinensetin (SIN), a citrus methylated flavone with anti-inflammatory and anti-proliferative activity, can enhance lipolysis. The objective of the present study was to investigate whether SIN might have sarcopenia-suppressing effect on satellite cells from thigh and calf muscle tissues of young and old rats. METHODS: Primary muscle cells were obtained from thigh and calf tissues of young and old group rats by dissection. Obtained satellite cells were incubated with indicated concentrations of SIN (50 and 100 μM) treated and untreated condition in differentiation medium. Morphological changes of cells were examined using a phase-contrast microscope. Protein expression levels of myoD and myogenin were analyzed by Western blot. Cells treated with or without SIN under differentiation condition were also immunocytochemically stained for myogenin and 4′,6-diamidino-2-phenylindole (DAPI). RESULTS: Morphologically, the differentiation extracted satellite cells was found to be more evident in SIN treated group of aged rat′s cells than that in SIN untreated group. Expression levels of myoD and myogenin proteins involved in myogenesis were increased upon treatment with SIN. CONCLUSIONS: Collectively, our results indicate that SIN can alleviate age-related sarcopenia by increasing differentiation rate and protein levels of myoD and myogenin. BioMed Central 2019-10-28 /pmc/articles/PMC6819389/ /pubmed/31660942 http://dx.doi.org/10.1186/s12906-019-2714-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kim, Jin-A
Kim, Seong Min
Ha, Sang Eun
Vetrivel, Preethi
Saralamma, Venu Venkatarame Gowda
Kim, Eun Hee
Kim, Gon Sup
Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells
title Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells
title_full Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells
title_fullStr Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells
title_full_unstemmed Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells
title_short Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells
title_sort sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819389/
https://www.ncbi.nlm.nih.gov/pubmed/31660942
http://dx.doi.org/10.1186/s12906-019-2714-2
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