烟酰胺腺嘌呤二核苷酸
NAD+激酶
烟酰胺
辅因子
烟酰胺单核苷酸
计算生物学
烟酰胺磷酸核糖转移酶
乙酰化
烟酰胺腺嘌呤二核苷酸磷酸
烟酸
烟酰胺
化学
生物
生物化学
酶
氧化酶试验
基因
作者
Jianying Zhang,Heling Wang,Sofie Lautrup,Hilde Nilsen,Jonas T. Treebak,Leiv Otto Watne,Geir Selbæk,Lindsay E. Wu,Torbjørn Omland,Eija Pirinen,T. Cheung,Jun Wang,Mathias Ziegler,Ole‐Bjørn Tysnes,Rubén Zapata‐Pérez,Santina Bruzzone,Carles Cantó,Michela Deleidi,Georges E. Janssens,Riekelt H. Houtkooper
出处
期刊:Nature Aging
日期:2025-09-09
卷期号:5 (9): 1704-1731
被引量:7
标识
DOI:10.1038/s43587-025-00947-6
摘要
Beyond their classical functions as redox cofactors, recent fundamental and clinical research has expanded our understanding of the diverse roles of nicotinamide adenine dinucleotide (NAD) and nicotinamide adenine dinucleotide phosphate (NADP) in signaling pathways, epigenetic regulation and energy homeostasis. Moreover, NAD and NADP influence numerous diseases as well as the processes of aging, and are emerging as targets for clinical intervention. Here, we summarize safety, bioavailability and efficacy data from NAD+-related clinical trials, focusing on aging and neurodegenerative diseases. We discuss the established NAD+ precursors nicotinic acid and nicotinamide, newer compounds such as nicotinamide riboside and nicotinamide mononucleotide, and emerging precursors. We also discuss technological advances including in industrial-scale production and real-time detection, which are facilitating NAD+ research and clinical translation. Finally, we emphasize the need for further large-scale studies to determine optimal dose, administration routes and frequency, as well as long-term safety and interindividual variability in response.
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