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Effects of resveratrol on laminar shear stress-induced mitochondrial biogenesis in human vascular endothelial cells

[PURPOSE]: The purpose of the study was to determine the combined effects of resveratrol supplementation with high-flow LSS on mitochondrial biogenesis in human vascular endothelial cells. [METHODS]: Cultured human umbilical vein endothelial cells were treated with 20 μM of RSV. For the shear experi...

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Detalles Bibliográficos
Autores principales: Kim, Ji-Seok, Park, Joon-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 한국운동영양학회 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477816/
https://www.ncbi.nlm.nih.gov/pubmed/31010269
http://dx.doi.org/10.20463/jenb.2019.0002
Descripción
Sumario:[PURPOSE]: The purpose of the study was to determine the combined effects of resveratrol supplementation with high-flow LSS on mitochondrial biogenesis in human vascular endothelial cells. [METHODS]: Cultured human umbilical vein endothelial cells were treated with 20 μM of RSV. For the shear experiments, cells grown to a >90% confluence were exposed to physiological levels of LSS (5 to 20 dyne/cm2) for 12 to 36 hours using a cone and plate shear apparatus. Gene expressions were analyzed by western blotting. [RESULTS]: Depletion of mitochondrial integrity was directly associated with increase in endothelial activation/dysfunction. The expressions of mitochondrial biogenesis regulator genes, such as SIRT1, PGC-1α, and TFAM, and the mitochondrial contents were significantly increased after treatment with both resveratrol and high-flow LSS for 12 hours. However, supplementation of resveratrol to high-flow LSS for a prolonged duration had no synergistic effect on the levels of mitochondrial biogenesis regulator gene expressions and mitochondrial content compared to the LSS treatment alone. [CONCLUSION]: The present study demonstrated that the supplementation of resveratrol to high-flow LSS has no synergistic effects on enhancing mitochondrial integrity in human vascular endothelial cells.