亚硝酸盐
药代动力学
骨骼肌
呼吸
药效学
线粒体
医学
内科学
内分泌学
膳食硝酸盐
药理学
生理学
药品
细胞呼吸
功能(生物学)
药物反应
血小板
生物
一氧化氮
老化
血小板聚集
亚硝酸戊酯
体力活动
肌萎缩
作者
Daniel E. Forman,Subashan Perera,Sruti S. Shiva,Nancy W. Glynn,Tara S Stakich,Sofhia V Ramos,Giovanna Distéfano,Cody Wolf,Angelina Kendi,Adam J Sterczala,Ian J Sipula,FIONA BELLO,Michael J. Jurczak,Frank C Sciurba,Mark T. Gladwin,Anne B Newman,Paul M Coen
标识
DOI:10.1093/gerona/glag034
摘要
BACKGROUND: Age-associated decline in mitochondrial oxidative capacity is associated with increased risk of disease, frailty, and disability. Oral nitrite and nitrate supplementation have been demonstrated to improve mitochondrial energetics and physical function in younger adults, but effects in older adults (age ≥70 years) remain unclear. METHODS: We conducted a randomized, placebo-controlled, double-blind, two-arm trial with a parallel group design to examine the effect of 20 mg sodium nitrite supplements administered three times a day for 12 weeks versus placebo in older (age ≥70 years) sedentary adults. Change in muscle mitochondrial respiration (complex I and II supported maximal oxidative phosphorylation [CI&II MaxOXPHOS]) was the primary outcome. Platelet bioenergetics, cardiorespiratory fitness, and other physical function measures were also assessed. RESULTS: Sixty-four adults (75.7 ± 5.7 years) completed the trial. Nitrite supplementation was not associated with improvements in skeletal muscle mitochondrial respiration, nor improvements in exercise capacity and physical function. However, platelet mitochondrial respiration changed significantly following an acute dose of oral nitrite. Notably, while nitrite levels increased 16- to 30-fold in plasma following an acute dose, levels increased only 1.6-fold in skeletal muscle. CONCLUSIONS: The divergent response of skeletal muscle versus platelet mitochondrial respiration in response to nitrite supplementation suggests tissue-specific pharmacokinetics and pharmacodynamics that likely impact the efficacy of nitrite supplementation. Results also suggest there may be age-related changes in drug delivery, metabolism, and mitochondrial responsiveness compared to the effects of nitrite/nitrate previously demonstrated in younger adults. Clinical Trial Registration Number: ClinicalTrials.gov NCT04405180.
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