首页> 外文期刊>European Journal of Pharmacology: An International Journal >Resveratrol prevents norepinephrine induced hypertrophy in adult rat cardiomyocytes, by activating NO-AMPK pathway.
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Resveratrol prevents norepinephrine induced hypertrophy in adult rat cardiomyocytes, by activating NO-AMPK pathway.

机译:白藜芦醇通过激活NO-AMPK途径,防止去甲肾上腺素引起的成年大鼠心肌肥大。

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Increased adrenergic drive is a major factor influencing the development of pathological cardiac hypertrophy, a stage which precedes overt heart failure. We examined the effect of resveratrol, a polyphenol (found predominantly in grapes), in preventing norepinephrine induced hypertrophy of adult cardiomyocyte, and the role of nitric oxide (NO) and adenosine monophosphate kinase (AMPK) in the effects of resveratrol. Cardiomyocytes isolated from adult rats were pretreated, or not, with resveratrol and then exposed to norepinephrine for 24h. In other experiments cardiomyocytes were also treated with different pharmacological inhibitors of NO synthase, AMPK and sirtuin for elucidating the signaling pathways underlying the effect of resveratrol. In order to validate the role of these signaling molecules in the in vivo settings, we also examined hearts from resveratrol treated spontaneously hypertensive rats (SHR), a genetic model of essential hypertension. Cardiomyocyte hypertrophy was determined by morphometry and (3)H-phenylalanine incorporation assay. NO levels and AMPK activity were measured using a specific assay kit and western blot analysis respectively. In vitro, resveratrol prevented the norepinephrine-induced increase in cardiomyocytes size and protein synthesis. Pharmacological inhibition of NO-AMPK signaling abolished the anti-hypertrophic action of resveratrol. Consistent with the in vitro findings, the anti-hypertrophic effect of resveratrol in the SHR model was associated with increases in NO and AMPK activity. This study demonstrates that NO-AMPK signaling is linked to the anti-hypertrophic effect of resveratrol in adult cardiomyocytes in vitro, and in the SHR model in vivo.
机译:肾上腺素驱动增加是影响病理性心脏肥大发展的主要因素,该阶段是在明显的心力衰竭之前。我们检查了白藜芦醇(一种多酚(主要存在于葡萄中))在预防去甲肾上腺素引起的成人心肌肥大中的作用,以及一氧化氮(NO)和单磷酸腺苷激酶(AMPK)在白藜芦醇中的作用。从成年大鼠分离的心肌细胞是否用白藜芦醇预处理,然后暴露于去甲肾上腺素24h。在其他实验中,还用NO合酶,AMPK和sirtuin的不同药理抑制剂处理了心肌细胞,以阐明白藜芦醇作用的信号通路。为了验证这些信号分子在体内的作用,我们还检查了白藜芦醇治疗的自发性高血压大鼠(SHR)的心脏,这是原发性高血压的遗传模型。通过形态测定法和(3)H-苯丙氨酸掺入测定法确定心肌细胞肥大。 NO水平和AMPK活性分别使用特异性测定试剂盒和western blot分析进行测量。在体外,白藜芦醇阻止了去甲肾上腺素引起的心肌细胞大小和蛋白质合成的增加。 NO-AMPK信号的药理抑制作用取消了白藜芦醇的抗肥大作用。与体外研究结果一致,白藜芦醇在SHR模型中的抗肥大作用与NO和AMPK活性增加有关。这项研究表明,NO-AMPK信号传导与白藜芦醇在成人心肌细胞和体外SHR模型中的抗肥大作用有关。

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