Effects of resveratrol on laminar shear stress-induced mitochondrial biogenesis in human vascular endothelial cellsEffects of resveratrol on laminar shear stress-induced mitochondrial biogenesis in human vascular endothelial cells
- Other Titles
- Effects of resveratrol on laminar shear stress-induced mitochondrial biogenesis in human vascular endothelial cells
- Authors
- 김지석; 박준영
- Issue Date
- 2019
- Publisher
- 한국운동영양학회
- Keywords
- Resveratrol; Laminar shear stress; SIRT1; Mitochondrial biogenesis
- Citation
- Physical Activity and Nutrition, v.23, no.1, pp 7 - 12
- Pages
- 6
- Indexed
- KCI
- Journal Title
- Physical Activity and Nutrition
- Volume
- 23
- Number
- 1
- Start Page
- 7
- End Page
- 12
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/10487
- DOI
- 10.20463/jenb.2019.0002
- ISSN
- 2733-7545
- Abstract
- [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.
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