University of Buenos Aires, School of Pharmacy and Biochemistry, Physical Chemistry Division, Buenos Aires, Argentina.
Food Funct. 2019 May 22;10(5):2528-2537. doi: 10.1039/c8fo01843j.
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.
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。