Effects of increased nitrate intake from beetroot juice on blood markers of oxidative stress and inflammation in older adults with hypertension

IF 7.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Free Radical Biology and Medicine Pub Date : 2024-07-05 DOI:10.1016/j.freeradbiomed.2024.07.004
Rebeka Fejes , Nina Pilat , Martin Lutnik , Stefan Weisshaar , Anna M. Weijler , Karsten Krüger , Agnes Draxler , Laura Bragagna , Jonathan M. Peake , Richard J. Woodman , Kevin D. Croft , Catherine P. Bondonno , Jonathan M. Hodgson , Karl-Heinz Wagner , Michael Wolzt , Oliver Neubauer
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Abstract

Background

Vascular oxidative stress and low-grade inflammation are important in the pathology of cardiovascular disorders, including hypertension. Cell culture and animal studies suggest that inorganic dietary nitrate may attenuate oxidative stress and inflammation through nitric oxide (NO), and there is a need to investigate whether this translates to humans.

Aim

In this randomised, placebo-controlled crossover study, by measuring a combination of multiple blood biomarkers, we evaluated whether previously reported benefits of dietary nitrate translate to a reduced oxidative stress and an improved inflammation status in 15 men and women (age range: 56–71 years) with treated hypertension.

Methods

We investigated the effects of a single ∼400 mg-dose of nitrate at 3 h post-ingestion (3H POST) and the daily consumption of 2 × ∼400 mg of nitrate over 4 weeks (4WK POST), through nitrate-rich versus nitrate-depleted (placebo) beetroot juice. Measurements included plasma nitrate and nitrite (NOx), oxidised low-density lipoprotein (oxLDL), F2-isoprostanes, protein carbonyls, oxidised (GSSG) and reduced glutathione (GSH); and serum high-sensitive C-reactive protein (hsCRP), chemokines, cytokines, and adhesion molecules. Flow cytometry was used to assess the relative proportion of blood monocyte subsets.

Results

At 4WK POST nitrate intervention, the oxLDL/NOx ratio decreased (mainly due to increases in plasma nitrate and nitrite) and the GSH/GSSG ratio (a sensitive biomarker for alterations in the redox status) increased, compared with placebo (for both ratios P < 0.01). The relative proportion of classical (CD14+CD16) monocytes decreased at 4WK POST for placebo compared to nitrate intervention (P < 0.05). Other oxidative stress and inflammatory markers were not altered by increased nitrate intake relative to placebo.

Conclusions

The data from this study point toward a subtle alteration in the redox balance toward a less pro-oxidative profile by a regular intake of inorganic nitrate from plant foods.

Clinical trial registry number

NCT04584372 (ClinicialTrials.gov).

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从甜菜根汁中摄入更多硝酸盐对患有高血压的老年人血液中氧化应激和炎症指标的影响。
背景:血管氧化应激和低度炎症是包括高血压在内的心血管疾病的重要病理因素。目的:在这项随机、安慰剂对照交叉研究中,通过测量多种血液生物标志物,我们评估了之前报道的膳食硝酸盐对 15 名男性和女性高血压患者(年龄范围:56-71 岁)的氧化应激减少和炎症改善的益处:方法:我们通过富含硝酸盐的甜菜根汁与缺乏硝酸盐的甜菜根汁(安慰剂),研究了在进食后 3 小时(3H POST)单次摄入 400 毫克硝酸盐以及在 4 周内每天摄入 2×400 毫克硝酸盐(4WK POST)的效果。测量项目包括血浆硝酸盐和亚硝酸盐(NOx)、氧化低密度脂蛋白(oxLDL)、F2-异前列腺素、蛋白质羰基、氧化谷胱甘肽(GSSG)和还原谷胱甘肽(GSH);以及血清高敏C反应蛋白(hsCRP)、趋化因子、细胞因子和粘附分子。流式细胞术用于评估血液中单核细胞亚群的相对比例:与安慰剂相比,在硝酸盐干预后4周,oxLDL/NOx比率下降(主要是由于血浆硝酸盐和亚硝酸盐的增加),GSH/GSSG比率(氧化还原状态改变的敏感生物标志物)上升(两个比率的P < 0.01)。与硝酸盐干预相比,安慰剂干预 4WK 后,经典(CD14+CD16-)单核细胞的相对比例有所下降(P < 0.05)。与安慰剂相比,其他氧化应激和炎症指标并未因硝酸盐摄入量的增加而改变:这项研究的数据表明,通过定期从植物性食品中摄入无机硝酸盐,氧化还原平衡会发生微妙的变化,使其具有较低的促氧化性:临床试验登记号:NCT04584372(ClinicialTrials.gov)。
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来源期刊
Free Radical Biology and Medicine
Free Radical Biology and Medicine 医学-内分泌学与代谢
CiteScore
14.00
自引率
4.10%
发文量
850
审稿时长
22 days
期刊介绍: Free Radical Biology and Medicine is a leading journal in the field of redox biology, which is the study of the role of reactive oxygen species (ROS) and other oxidizing agents in biological systems. The journal serves as a premier forum for publishing innovative and groundbreaking research that explores the redox biology of health and disease, covering a wide range of topics and disciplines. Free Radical Biology and Medicine also commissions Special Issues that highlight recent advances in both basic and clinical research, with a particular emphasis on the mechanisms underlying altered metabolism and redox signaling. These Special Issues aim to provide a focused platform for the latest research in the field, fostering collaboration and knowledge exchange among researchers and clinicians.
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