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原花青素 C1 通过 Ca(2+) 依赖途径对内皮细胞一氧化氮产生和超极化的影响。

Effect of procyanidin C1 on nitric oxide production and hyperpolarization through Ca(2+)-dependent pathway in endothelial cells.

机构信息

Department of Food Science and Biotechnology, Woosong University, Daejeon, Korea.

出版信息

J Med Food. 2012 Nov;15(11):1032-7. doi: 10.1089/jmf.2012.2297. Epub 2012 Oct 11.

Abstract

Polyphenol-rich foods, such as fruits and vegetables, are protective against cardiovascular diseases, but the mechanisms of the beneficial effects are still unknown. The goal of this research was to clarify actions of procyanidin trimer (C1) in rat aortic endothelial cells (RAECs). Procyanidin C1 at concentrations up to 50 μM was not cytotoxic to the RAECs. The addition of procyanidin C1 to RAECs exerted a time-dependent hyperpolarization measured using a membrane potential-dependent fluorescent probe, bis-(1,3-dibutylbarbituric acid) trimethine oxonol, whereas the hyperpolarization was significantly inhibited by the nonspecific K(+) channel inhibitor tetraethylammonium chloride (TEA). Moreover, procyanidin C1 elevated intracellular Ca(2+) influx, which was totally abolished in the presence of Ca(2+)-free solution with EGTA. Procyanidin C1 caused a significant increase in nitric oxide (NO) production. The effect was significantly inhibited by an NO synthase inhibitor, N(G)-monomethyl-l-arginine, or TEA. In conclusion, we demonstrated for the first time that procyanidin C1 plays a potent role in promoting Ca(2+)-mediated signals such as the hyperpolarization via multiple K(+) channel activations and the NO release in RAECs, suggesting that procyanidin C1 may represent novel and effective therapy for the treatment of cardiovascular diseases.

摘要

富含多酚的食物,如水果和蔬菜,可预防心血管疾病,但有益作用的机制尚不清楚。本研究的目的是阐明原花青素三聚体(C1)在大鼠主动脉内皮细胞(RAECs)中的作用。原花青素 C1 的浓度高达 50 μM 时对 RAECs 没有细胞毒性。用膜电位依赖性荧光探针双(1,3-二丁基巴比妥酸)三嗪氧鎓测量时,向 RAECs 中添加原花青素 C1 可发挥时间依赖性超极化作用,而超极化作用可被非特异性 K(+)通道抑制剂四乙铵(TEA)显著抑制。此外,原花青素 C1 可增加细胞内 Ca2+内流,而在含有 EGTA 的无 Ca2+溶液中,Ca2+内流则完全被阻断。原花青素 C1 可显著增加一氧化氮(NO)的产生。该作用可被一氧化氮合酶抑制剂 N(G)-单甲基-L-精氨酸或 TEA 显著抑制。综上所述,我们首次证明原花青素 C1 在促进 RAECs 中 Ca2+介导的信号(如通过多种 K+通道激活和 NO 释放实现的超极化)中发挥强大作用,提示原花青素 C1 可能为心血管疾病的治疗提供新的有效治疗方法。

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