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
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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