Role of Rutin on Nitric Oxide Synthesis in Human Umbilical Vein Endothelial Cells
Endothelial Dysfunction
0301 basic medicine
Technology
Physiology
Immunological Mechanisms in Atherosclerosis Development
Rutin
Biochemistry
Gene
Endocrinology
Role of Urotensin II in Cardiovascular Physiology and Disease
Endothelial dysfunction
Internal medicine
Immunology and Microbiology
T
Q
R
Life Sciences
Growth factor
Downregulation and upregulation
3. Good health
Chemistry
Medicine
Antioxidant
Research Article
Receptor
Nitric Oxide Synthase Type III
Human umbilical vein endothelial cell
Science
Role of Nitric Oxide in Health and Disease
Enos
Immunology
Nitric Oxide
Endothelial stem cell
03 medical and health sciences
In vitro
Health Sciences
Human Umbilical Vein Endothelial Cells
Humans
Umbilical vein
Endothelium
Basic fibroblast growth factor
Pharmacology
FOS: Clinical medicine
Nitric oxide synthase
Nitric oxide
Hydrogen Peroxide
Oxidative stress
FOS: Biological sciences
Surgery
DOI:
10.1155/2014/169370
Publication Date:
2014-06-24T17:18:30Z
AUTHORS (5)
ABSTRACT
Nitric oxide (NO), produced by endothelial nitric oxide synthase (eNOS), is a major antiatherogenic factor in the blood vessel. Oxidative stress plays an important role in the pathogenesis of various cardiovascular diseases, including atherosclerosis. Decreased availability of endothelial NO promotes the progression of endothelial dysfunction and atherosclerosis. Rutin is a flavonoid with multiple cardiovascular protective effects. This study aimed to investigate the effects of rutin on eNOS and NO production in cultured human umbilical vein endothelial cells (HUVEC). HUVEC were divided into four groups: control; oxidative stress induction with 180 μM H2O2; treatment with 300 μM rutin; and concomitant induction with rutin and H2O2for 24 hours. HUVEC treated with rutin produced higher amount of NO compared to control (P<0.01). In the oxidative stress-induced HUVEC, rutin successfully induced cells’ NO production (P<0.01). Rutin promoted NO production in HUVEC by inducing eNOS gene expression (P<0.05), eNOS protein synthesis (P<0.01), and eNOS activity (P<0.05). Treatment with rutin also led to increased gene and protein expression of basic fibroblast growth factor (bFGF) in HUVEC. Therefore, upregulation of eNOS expression by rutin may be mediated by bFGF. The results showed that rutin may improve endothelial function by augmenting NO production in human endothelial cells.
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