代谢组
NAD+激酶
烟酰胺磷酸核糖转移酶
骨骼肌
转录组
烟酰胺
糖酵解
生物化学
西妥因1
化学
烟酰胺
生物
代谢物
新陈代谢
内分泌学
基因表达
酶
基因
下调和上调
作者
Yasir Elhassan,Katarína Kľučková,Rachel S. Fletcher,Mark S. Schmidt,Antje Garten,Craig Doig,David M. Cartwright,Lucy Oakey,Claire V. Burley,Ned Jenkinson,Martin Wilson,Samuel J. E. Lucas,İldem Akerman,Alex P. Seabright,Yu‐Chiang Lai,Daniel A. Tennant,Peter Nightingale,Gareth A. Wallis,Konstantinos Manolopoulos,Charles Brenner,Andrew Philp,Gareth G. Lavery
出处
期刊:Cell Reports
[Elsevier]
日期:2019-08-01
卷期号:28 (7): 1717-1728.e6
被引量:314
标识
DOI:10.1016/j.celrep.2019.07.043
摘要
Nicotinamide adenine dinucleotide (NAD+) is modulated by conditions of metabolic stress and has been reported to decline with aging in preclinical models, but human data are sparse. Nicotinamide riboside (NR) supplementation ameliorates metabolic dysfunction in rodents. We aimed to establish whether oral NR supplementation in aged participants can increase the skeletal muscle NAD+ metabolome and if it can alter muscle mitochondrial bioenergetics. We supplemented 12 aged men with 1 g NR per day for 21 days in a placebo-controlled, randomized, double-blind, crossover trial. Targeted metabolomics showed that NR elevated the muscle NAD+ metabolome, evident by increased nicotinic acid adenine dinucleotide and nicotinamide clearance products. Muscle RNA sequencing revealed NR-mediated downregulation of energy metabolism and mitochondria pathways, without altering mitochondrial bioenergetics. NR also depressed levels of circulating inflammatory cytokines. Our data establish that oral NR is available to aged human muscle and identify anti-inflammatory effects of NR.
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