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Lespedeza cuneata protects the endothelial dysfunction via eNOS phosphorylation of PI3K/Akt signaling pathway in HUVECs

Authors
Lee, Jae HyukParveen, AmnaDo, Moon HoLim, YunsookShim, Sang HeeKim, Sun Yeou
Issue Date
15-Sep-2018
Publisher
ELSEVIER GMBH, URBAN & FISCHER VERLAG
Keywords
Lespedeza cuneata G.Don; Nitric oxide; Endothelial nitric oxide synthase; Endothelial dysfunction; PI3K/Akt signaling; Human umbilical vein endothelial cells
Citation
PHYTOMEDICINE, v.48, pp.1 - 9
Journal Title
PHYTOMEDICINE
Volume
48
Start Page
1
End Page
9
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/3341
DOI
10.1016/j.phymed.2018.05.005
ISSN
0944-7113
Abstract
Background: Lespedeza cuneata G.Don (LCE), which belongs to the genus Lespedeza (Leguminosae), is a traditional oriental medicine known to prevent diabetes and cardiovascular diseases. However, no scientific studies about the effectiveness of LCE, their responsible bioactive constituents, and its mechanisms against endothelial dysfunction have been performed. Purpose: This study was performed to investigate the role of LCE and its chemical components in ameliorating endothelial dysfunction. Methods: The production of nitric oxide (NO) was evaluated after LCE treatment in HUVECs. Cell viability was measured using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reagent. Western blot analysis was performed to determine the protein expression of endothelial nitric oxide synthase (eNOS) and protein kinase B (PKB, also known as Akt) in human umbilical vein endothelial cells (HUVECs). Results: Pretreatment with L-NAME and LY294002 significantly decreased the LCE-induced NO production, as well as eNOS and Akt phosphorylation. beta-Sitosterol and beta-Sitosterol 6'-linolenoyl-3-O-beta-D glucopyranoside are the bioactive constituents increase NO production as well as eNOS phosphorylation. Conclusion: Our findings suggest that LCE increase NO production via eNOS phosphorylation of PI3K/Akt signaling pathway.
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