School of Cardiovascular Medicine and Sciences, Department of Clinical Pharmacology, King's College London British Heart Foundation Centre, London, UK.
Biomedical Research Centre, Clinical Research Facility, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Br J Clin Pharmacol. 2019 Jul;85(7):1443-1453. doi: 10.1111/bcp.13913. Epub 2019 May 9.
Dietary inorganic nitrate (NO ) lowers peripheral blood pressure (BP) in healthy volunteers, but lacks such effect in individuals with, or at risk of, type 2 diabetes mellitus (T2DM). Whilst this is commonly assumed to be a consequence of chronic hyperglycaemia/hyperinsulinaemia, we hypothesized that acute physiological elevations in plasma [glucose]/[insulin] blunt the haemodynamic responses to NO , a pertinent question for carbohydrate-rich Western diets.
We conducted an acute, randomized, placebo-controlled, double-blind, crossover study on the haemodynamic and metabolic effects of potassium nitrate (8 or 24 mmol KNO ) vs. potassium chloride (KCl; placebo) administered 1 hour prior to an oral glucose tolerance test in 33 healthy volunteers.
Compared to placebo, there were no significant differences in systolic or diastolic BP (P = 0.27 and P = 0.30 on ANOVA, respectively) with KNO , nor in pulse wave velocity or central systolic BP (P = 0.99 and P = 0.54 on ANOVA, respectively). Whilst there were significant elevations from baseline for plasma [glucose] and [C-peptide], no differences between interventions were observed. A significant increase in plasma [insulin] was observed with KNO vs. KCl (n = 33; P = 0.014 on ANOVA) with the effect driven by the high-dose cohort (24 mmol, n = 13; P < 0.001 on ANOVA; at T = 0.75 h mean difference 210.4 pmol/L (95% CI 28.5 to 392.3), P = 0.012).
In healthy adults, acute physiological elevations of plasma [glucose] and [insulin] result in a lack of BP-lowering with dietary nitrate. The increase in plasma [insulin] without a corresponding change in [C-peptide] or [glucose] suggests that high-dose NO decreases insulin clearance. A likely mechanism is via NO-dependent inhibition of insulin-degrading enzyme.
膳食无机硝酸盐(NO )可降低健康志愿者的外周血压(BP),但在 2 型糖尿病(T2DM)患者或有此风险的个体中缺乏这种作用。虽然这通常被认为是慢性高血糖/高胰岛素血症的结果,但我们假设急性生理升高的血浆[葡萄糖]/[胰岛素]会使硝酸盐引起的血液动力学反应迟钝,这是富含碳水化合物的西方饮食的一个相关问题。
我们对 33 名健康志愿者进行了一项急性、随机、安慰剂对照、双盲、交叉研究,比较了钾硝酸盐(8 或 24mmol KNO )与钾氯(KCl;安慰剂)对口服葡萄糖耐量试验前 1 小时给药对血流动力学和代谢的影响。
与安慰剂相比,KNO 对收缩压或舒张压均无显著差异(ANOVA 分析时 P=0.27 和 P=0.30),也无脉搏波速度或中心收缩压的差异(ANOVA 分析时 P=0.99 和 P=0.54)。尽管基线时血浆[葡萄糖]和[C 肽]有显著升高,但干预组之间没有差异。与 KCl 相比,KNO 可显著升高血浆[胰岛素](n=33;ANOVA 分析时 P=0.014),这种作用是由高剂量组(24mmol,n=13;ANOVA 分析时 P<0.001;在 T=0.75h 时平均差值 210.4pmol/L(95%CI 28.5 至 392.3),P=0.012)驱动的。
在健康成年人中,血浆[葡萄糖]和[胰岛素]的急性生理升高导致饮食硝酸盐降低血压。血浆[胰岛素]升高而[C 肽]或[葡萄糖]无相应变化表明,高剂量 NO 可降低胰岛素清除率。一种可能的机制是通过 NO 依赖性抑制胰岛素降解酶。