Nieman David C, Valacchi Giuseppe, Wentz Laurel M, Ferrara Francesca, Pecorelli Alessandra, Woodby Brittany, Sakaguchi Camila A, Simonson Andrew
Appalachian State University.
NC State University.
Int J Sport Nutr Exerc Metab. 2020 Mar 1;30(2):112–119. doi: 10.1123/ijsnem.2019-0171. Epub 2019 Nov 21.
This double-blinded, placebo controlled, randomized crossover trial investigated the influence of 2-week mixed flavonoid versus placebo supplementation on oxinflammation markers after a 75-km cycling time trial in 22 cyclists (42.3 ± 1.7 years). Blood samples were collected before and after the 2-week supplementation, and then 0 hr, 1.5 hr, and 21 hr post 75-km cycling (176 ± 5.4 min, 73.4 ±2.0% maximal oxygen consumption). The supplement provided 678-mg flavonoids with quercetin (200 mg), green tea catechins (368 mg, 180-mg epigallocatechin gallate), and anthocyanins (128 mg) from bilberry extract, with caffeine, vitamin C, and omega-3 fatty acids added as adjuvants. Blood samples were analyzed for blood leukocyte counts, oxinflammation biomarkers, including 4-hydroxynonenal, protein carbonyls, and peripheral blood mononuclear mRNA expression for cyclooxygenease-2 and glutathione peroxidase. Each of the blood biomarkers was elevated postexercise (time effects, all ps < .01), with lower plasma levels for 4-hydroxynonenal (at 21-hr postexercise) in flavonoid versus placebo (interaction effect, p = .008). Although elevated postexercise, no trial differences for the neutrophil/lymphocyte ratio (p = .539) or peripheral blood mononuclear mRNA expression for cyclooxygenease-2 (p = .322) or glutathione peroxidase (p = .839) were shown. Flavonoid supplementation prior to intensive exercise decreased plasma peroxidation and oxidative damage, as determined by 4-hydroxynonenal. Postexercise increases were similar between the flavonoid and placebo trials for peripheral blood mononuclear mRNA expression for cyclooxygenease-2 and the nuclear factor erythroid 2-related factor 2 related gene glutathione peroxidase (NFE2L2). The data support the strategy of flavonoid supplementation to mitigate postexercise oxidative stress in endurance athletes.
这项双盲、安慰剂对照、随机交叉试验研究了在22名自行车运动员(42.3±1.7岁)完成75公里骑行计时赛后,为期2周的混合类黄酮与安慰剂补充剂对氧化炎症标志物的影响。在为期2周的补充前后采集血样,然后在75公里骑行后0小时、1.5小时和21小时(176±5.4分钟,最大耗氧量的73.4±2.0%)采集血样。补充剂提供了678毫克类黄酮,其中包括槲皮素(200毫克)、绿茶儿茶素(368毫克,180毫克表没食子儿茶素没食子酸酯)以及来自越橘提取物的花青素(128毫克),并添加了咖啡因、维生素C和ω-3脂肪酸作为佐剂。对血样进行分析,检测血液白细胞计数、氧化炎症生物标志物,包括4-羟基壬烯醛、蛋白质羰基,以及环氧化酶-2和谷胱甘肽过氧化物酶的外周血单核细胞mRNA表达。每项血液生物标志物在运动后均升高(时间效应,所有p值均<0.01),类黄酮组与安慰剂组相比,4-羟基壬烯醛的血浆水平在运动后21小时较低(交互作用效应,p = 0.008)。尽管运动后升高,但中性粒细胞/淋巴细胞比率(p = 0.539)、环氧化酶-2(p = 0.322)或谷胱甘肽过氧化物酶(p = 0.839)的外周血单核细胞mRNA表达在试验中没有差异。高强度运动前补充类黄酮可降低血浆过氧化和氧化损伤,这由4-羟基壬烯醛测定得出。类黄酮组和安慰剂组在运动后外周血单核细胞中环氧化酶-2和核因子红细胞2相关因子2相关基因谷胱甘肽过氧化物酶(NFE2L2)的mRNA表达增加情况相似。数据支持在耐力运动员中补充类黄酮以减轻运动后氧化应激的策略。