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(+)-儿茶素抑制心脏线粒体复合物 I 和一氧化氮合酶:对膜电位和过氧化氢产生的功能影响。

(+)-Catechin inhibits heart mitochondrial complex I and nitric oxide synthase: functional consequences on membrane potential and hydrogen peroxide production.

机构信息

University of Buenos Aires, School of Pharmacy and Biochemistry, Physical Chemistry Division, Buenos Aires, Argentina.

出版信息

Food Funct. 2019 May 22;10(5):2528-2537. doi: 10.1039/c8fo01843j.

Abstract

In order to study the in vitro effect of flavan-3-ol (+)-catechin on the enzymatic activities of mitochondrial complex I and nitric oxide synthase (mtNOS), as well as the consequences on the membrane potential and H2O2 production rate, isolated mitochondria from rat heart were exposed to 3 nM to 100 μM (+)-catechin. NADH-Q1 reductase (complex I) and mtNOS activities were inhibited 25% and 50%, respectively, by the addition of 10 nM (+)-catechin to the reaction medium. Moreover, in the nM range, (+)-catechin decreased state 4 mitochondrial membrane potential by about 10 mV, but failed to change the membrane potential measured in the presence of ADP. (+)-Catechin (10 nM) inhibited not only complex I activity, but also the H2O2 production rate (35%) sustained by malate-glutamate, in accordance with the decrease observed in mitochondrial membrane potential. Considering (+)-catechin concentrations lower than 10 nM, linear and positive correlations were obtained between mitochondrial complex I activity and either NO (r2 = 0.973) or H2O2 production rates (r2 = 0.958), suggesting a functional association among these parameters. Altogether, the results indicate that (+)-catechin, at nM concentrations, inhibits mitochondrial complex I activity, leading to membrane potential decline and consequently to reduction in H2O2 and NO production rates. The decrease in mtNOS activity could also be a consequence of the direct action of (+)-catechin on the NOS structure, this effect being in accordance with the functional interaction between complex I and mtNOS, as previously reported.

摘要

为了研究黄烷-3-醇(+)-儿茶素对线粒体复合物 I 和一氧化氮合酶(mtNOS)的酶活性的体外影响,以及对膜电位和 H2O2 产生率的影响,从大鼠心脏中分离出线粒体,并将其暴露于 3 nM 至 100 μM 的(+)-儿茶素中。向反应介质中加入 10 nM 的(+)-儿茶素,可使 NADH-Q1 还原酶(复合物 I)和 mtNOS 活性分别抑制 25%和 50%。此外,在 nM 范围内,(+)-儿茶素使线粒体膜电位下降约 10 mV,但未能改变在 ADP 存在下测量的膜电位。(+)-儿茶素(10 nM)不仅抑制复合物 I 的活性,还抑制由苹果酸-谷氨酸维持的 H2O2 产生率(35%),这与观察到的线粒体膜电位下降一致。考虑到(+)-儿茶素浓度低于 10 nM,线粒体复合物 I 活性与 NO(r2 = 0.973)或 H2O2 产生率(r2 = 0.958)之间呈线性正相关,表明这些参数之间存在功能关联。总的来说,这些结果表明,(+)-儿茶素在 nM 浓度下抑制线粒体复合物 I 的活性,导致膜电位下降,进而降低 H2O2 和 NO 的产生率。mtNOS 活性的降低也可能是(+)-儿茶素直接作用于 NOS 结构的结果,这一效应与先前报道的复合物 I 和 mtNOS 之间的功能相互作用一致。

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