Abstract

Green tea consumption is associated with reduced cardiovascular mortality in some epidemiological studies. Epigallocatechin gallate (EGCG), a bioactive polyphenol in green tea, mimics metabolic actions of insulin to inhibit gluconeogenesis in hepatocytes. Because signaling pathways regulating metabolic and vasodilator actions of insulin are shared in common, we hypothesized that EGCG may also have vasodilator actions to stimulate production of nitric oxide (NO) from endothelial cells. Acute intra-arterial administration of EGCG to mesenteric vascular beds isolated ex vivo from WKY rats caused dose-dependent vasorelaxation. This was inhibitable by L-NAME (NO synthase inhibitor), wortmannin (phosphatidylinositol 3-kinase inhibitor), or PP2 (Src family kinase inhibitor). Treatment of bovine aortic endothelial cells (BAEC) with EGCG (50 microm) acutely stimulated production of NO (assessed with NO-specific fluorescent dye DAF-2) that was inhibitable by l-NAME, wortmannin, or PP2. Stimulation of BAEC with EGCG also resulted in dose- and time-dependent phosphorylation of eNOS that was inhibitable by wortmannin or PP2 (but not by MEK inhibitor PD98059). Specific knockdown of Fyn (but not Src) with small interfering RNA inhibited both EGCG-stimulated phosphorylation of Akt and eNOS as well as production of NO in BAEC. Treatment of BAEC with EGCG generated intracellular H(2)O(2) (assessed with H(2)O(2)-specific fluorescent dye CM-H(2)DCF-DA), whereas treatment with N-acetylcysteine inhibited EGCG-stimulated phosphorylation of Fyn, Akt, and eNOS. We conclude that EGCG has endothelial-dependent vasodilator actions mediated by intracellular signaling pathways requiring reactive oxygen species and Fyn that lead to activation of phosphatidylinositol 3-kinase, Akt, and eNOS. This mechanism may explain, in part, beneficial vascular and metabolic health effects of green tea consumption.

Highlights

  • Reciprocal relationships between insulin resistance and endothelial dysfunction contribute importantly to the pathophysiology of diabetes and its cardiovascular complications [1]

  • We demonstrate novel contributions of reactive oxygen species and Fyn in the vasodilator actions of Epigallocatechin gallate (EGCG) resulting from activation of eNOS in endothelium that are distinct from insulin signaling

  • Elucidating molecular mechanisms underlying vascular actions of EGCG is important for understanding potential health benefits of green tea consumption in patients with diabetes and related cardiovascular diseases that are characterized by both insulin resistance and endothelial dysfunction

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Summary

Introduction

Reciprocal relationships between insulin resistance and endothelial dysfunction contribute importantly to the pathophysiology of diabetes and its cardiovascular complications [1]. Vascular actions of insulin to stimulate production of nitric oxide (NO) enhance capillary recruitment and vasodilation This leads to increased blood flow to skeletal muscle resulting in increased delivery of glucose and insulin to metabolic targets of insulin action [2]. We demonstrate novel contributions of reactive oxygen species and Fyn in the vasodilator actions of EGCG resulting from activation of eNOS in endothelium that are distinct from insulin signaling. Elucidating molecular mechanisms underlying vascular actions of EGCG is important for understanding potential health benefits of green tea consumption in patients with diabetes and related cardiovascular diseases that are characterized by both insulin resistance and endothelial dysfunction

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