Open access · CC-BY
via OpenAlex
Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells
Jin‐A Kim, Seong Min Kim, Sang Eun Ha, Preethi Vetrivel, Venu Venkatarame Gowda Saralamma, Eun Hee Kim, Gon Sup Kim
BMC Complementary and Alternative Medicine · 2019 · ▲ 21 citations
Abstract
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.
◌ CITATION ONLY
Full text is not openly licensed for redistribution here. Read it at the source:
Provenance
- Source
- OpenAlex
- DOI
- 10.1186/s12906-019-2714-2
- Canonical
- link ↗
- Fetched
- 2026-10-17 MST
Cite this
APA
Kim, J., Kim, S.M., Ha, S.E., Vetrivel, P., Saralamma, V.V.G., Kim, E.H., & Kim, G.S. (2019). Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells. <em>BMC Complementary and Alternative Medicine</em>. https://doi.org/10.1186/s12906-019-2714-2
Vancouver
Kim J, Kim SM, Ha SE, Vetrivel P, Saralamma VVG, Kim EH, et al. Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells. BMC Complementary and Alternative Medicine. 2019. doi:10.1186/s12906-019-2714-2.
BibTeX
@article{jina2019Sinens,
title = {Sinensetin regulates age-related sarcopenia in cultured primary thigh and calf muscle cells},
author = {Jin‐A Kim and Seong Min Kim and Sang Eun Ha and Preethi Vetrivel and Venu Venkatarame Gowda Saralamma and Eun Hee Kim and Gon Sup Kim},
journal = {BMC Complementary and Alternative Medicine},
year = {2019},
doi = {10.1186/s12906-019-2714-2},
}
Research neighborhood
References, citing works, and semantically nearest findings. Click a node to open it.
Related findings
Proceedings of Annual Meeting of the Physiological Society of Japan Proceedings of Annual Meeting of the Physiological Society of Japan 2005
Citation only
Muscle satellite cells in the age-related atrophy of skeletal muscles (sarcopenia)
Frontiers in Cell and Developmental Biology 2024
Open access · CC-BY
Cellular and transcriptomic changes by the supplementation of aged rat serum in human pluripotent stem cell-derived myogenic progenitors
e-space (Manchester Metropolitan University) 2026
Preprint · OA
The effect of lymphocytes secretome on skeletal muscle stem cells regeneration with ageing
The FASEB Journal 2018
Preprint · OA
Aging of the immune system causes reductions in muscle stem cell populations, promotes their shift to a fibrogenic phenotype, and modulates sarcopenia
Cardiovascular Research 2024
Open access · OA
The role of cellular senescence in profibrillatory atrial remodelling associated with cardiac pathology
Current Biology 2018
Open access · OA