The acute effects of dietary nitrate supplementation on postmenopausal endothelial resistance to ischemia reperfusion injury: a randomized, placebo-controlled, double blind, crossover clinical trial

交叉研究 医学 随机对照试验 安慰剂 再灌注损伤 双盲 缺血 临床试验 内科学 麻醉 病理 替代医学
作者
Jocelyn M. Delgado Spicuzza,Jigar Gosalia,Matthew Studinski,Chenée Armando,Elmira Alipour,Daniel B. Kim‐Shapiro,Michael Flanagan,Yasina B. Somani,David N. Proctor
出处
期刊:Canadian Journal of Physiology and Pharmacology [NRC Research Press]
卷期号:102 (11): 634-647 被引量:2
标识
DOI:10.1139/cjpp-2024-0061
摘要

Postmenopausal cardiovascular health is a critical determinant of longevity. Consumption of beetroot juice (BR) and other nitrate-rich foods is a safe, effective non-pharmaceutical intervention to increase systemic bioavailability of the vasoprotective molecule, nitric oxide, through the exogenous nitrate (NO 3 − )–nitrite (NO 2 − )–nitric oxide (NO) pathway. We hypothesized that a single dose of nitrate-rich beetroot juice (BR nitrate 600 mg NO 3 − /140 mL, BR placebo ∼ 0 mg/140 mL) would improve resting endothelial function and resistance to ischemia–reperfusion (IR) injury to a greater extent in early-postmenopausal (1–6 years following their final menstrual period (FMP), n = 12) compared to late-postmenopausal (6+ years after FMP, n = 12) women. Analyses with general linear models revealed a significant ( p < 0.05) time * treatment interaction effect for brachial artery adjusted flow-mediated dilation (FMD). Pairwise comparisons revealed that adjusted FMD was significantly lower following IR-injury in comparison to all other time points with BR placebo (early FMD 2.51 ± 1.18%, late FMD 1.30 ± 1.10, p < 0.001) and was lower than post-IR with BR nitrate (early FMD 3.84 ± 1.21%, late FMD 3.21 ± 1.13%, p = 0.014). A single dose of BR nitrate significantly increased resting macrovascular function in the late postmenopausal group only ( p = 0.005). Considering the postmenopausal stage-dependent variations in endothelial responsiveness to dietary nitrate, we predict differing mechanisms underpin macrovascular protection against IR injury.
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