首页> 外文OA文献 >EGCG, a green tea polyphenol, improves endothelial function and insulin sensitivity, reduces blood pressure, and protects against myocardial I/R injury in SHR RID B-1970-2008
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EGCG, a green tea polyphenol, improves endothelial function and insulin sensitivity, reduces blood pressure, and protects against myocardial I/R injury in SHR RID B-1970-2008

机译:EGCG是一种绿茶多酚,可改善SHR RID B-1970-2008中的内皮功能和胰岛素敏感性,降低血压并防止心肌I / R损伤

摘要

Epigallocatechin gallate (EGCG), a bioactive polyphenol in green tea, may augment metabolic and vascular actions of insulin. Therefore, we investigated effects of EGCG treatment to simultaneously improve cardiovascular and metabolic function in spontaneously hypertensive rats (SHR; model of metabolic syndrome with hypertension, insulin resistance, and overweight). In acute studies, EGCG (1-100 microM) elicited dose-dependent vasodilation in mesenteric vascular beds (MVB) isolated from SHR ex vivo that was inhibitable by N(omega)-nitro-L-arginine methyl ester (L-NAME; nitric oxide synthase antagonist) or wortmannin [phosphatidylinositol (PI) 3-kinase inhibitor]. In chronic studies, 9-wk-old SHR were treated by gavage for 3 wk with EGCG (200 mg.kg(-1).day(-1)), enalapril (30 mg.kg(-1).day(-1)), or vehicle. A separate group of SHR receiving L-NAME (80 mg/l in drinking water) was treated for 3 wk with either EGCG or vehicle. Vasodilator actions of insulin were significantly improved in MVB from EGCG- or enalapril-treated SHR (when compared with vehicle-treated SHR). Both EGCG and enalapril therapy significantly lowered systolic blood pressure (SBP) in SHR. EGCG therapy of SHR significantly reduced infarct size and improved cardiac function in Langendorff-perfused hearts exposed to ischemia-reperfusion (I/R) injury. In SHR given L-NAME, beneficial effects of EGCG on SBP and I/R were not observed. Both enalapril and EGCG treatment of SHR improved insulin sensitivity and raised plasma adiponectin levels. We conclude that acute actions of EGCG to stimulate production of nitric oxide from endothelium using PI 3-kinase-dependent pathways may explain, in part, beneficial effects of EGCG therapy to simultaneously improve metabolic and cardiovascular pathophysiology in SHR. These findings may be relevant to understanding potential benefits of green tea consumption in patients with the metabolic syndrome.
机译:没食子儿茶素没食子酸酯(EGCG)是绿茶中的一种生物活性多酚,可增强胰岛素的代谢和血管作用。因此,我们研究了EGCG治疗同时改善自发性高血压大鼠的心血管和代谢功能的作用(SHR;具有高血压,胰岛素抵抗和超重的代谢综合征模型)。在急性研究中,EGCG(1-100 microM)在离体SHR分离的肠系膜血管床(MVB)中引起剂量依赖性血管舒张,可被N(ω)-硝基-L-精氨酸甲酯(L-NAME;硝酸)抑制氧化物合酶拮抗剂)或渥曼青霉素[磷脂酰肌醇(PI)3-激酶抑制剂]。在慢性研究中,对9周龄的SHR分别用EGCG(200 mg.kg(-1).day(-1)),依那普利(30 mg.kg(-1).day(- 1))或车辆。接受L-NAME的另一组SHR(在饮用水中为80 mg / l)用EGCG或溶媒治疗3周。与EGCG或依那普利治疗的SHR相比,MVB中胰岛素的血管舒张作用显着改善(与媒介物治疗的SHR相比)。 EGCG和依那普利治疗均能显着降低SHR的收缩压(SBP)。 EGCG疗法治疗SHR可以显着减少缺血再灌注(I / R)损伤的Langendorff灌注心脏的梗塞面积并改善心脏功能。在给予L-NAME的SHR中,未观察到EGCG对SBP和I / R的有益作用。依那普利和EGCG治疗SHR均可改善胰岛素敏感性,并提高血浆脂联素水平。我们得出结论,使用PI 3激酶依赖性途径,EGCG刺激内皮细胞产生一氧化氮的急性作用可能部分解释了EGCG治疗同时改善SHR代谢和心血管病理生理的有益作用。这些发现可能与了解代谢综合征患者食用绿茶的潜在益处有关。

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