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Biochem Pharmacol. 2022 Apr;198:114946. doi: 10.1016/j.bcp.2022.114946. Epub 2022 Feb 5.
A decline in NAD+ is a feature of ageing and may play a causal role in the process. NAD+ plays a pivotal role in myriad processes important in cellular metabolism and is a cosubstrate for enzymes that play key roles in pathways that modify ageing. Thus, interventions that increase NAD+ may slow aspects of the ageing trajectory and there is great interest in pharmacological NAD+ restoration. Dietary supplementation with NAD+ precursors, particularly nicotinamide riboside, has increased NAD+ levels in several human intervention studies and arguably been the most robust approach to date. However, consistency and reliability of such approaches to increase NAD+, and also impact on markers of efficacy to slow or reverse features of ageing, has been inconsistent. We argue that a major element of this variability may arise from the use of single-target approaches that do not consider the underlying biological complexity leading to NAD+ decline. Thus, a systems approach - targeting multiple key nodes in the NAD+ interactome - is likely to be more efficacious and reliable.
NAD+ 的减少是衰老的一个特征,并且可能在这个过程中起因果作用。NAD+ 在细胞代谢中许多重要过程中起着关键作用,并且是修饰衰老途径中起关键作用的酶的辅助底物。因此,增加 NAD+ 的干预措施可能会减缓衰老轨迹的某些方面,并且人们对药理学 NAD+ 恢复非常感兴趣。用 NAD+ 前体(特别是烟酰胺核糖苷)进行饮食补充,已在几项人类干预研究中增加了 NAD+ 水平,并且可以说是迄今为止最有效的方法。然而,增加 NAD+ 的这种方法的一致性和可靠性,以及对减缓或逆转衰老特征的疗效标志物的影响,一直不一致。我们认为,这种可变性的一个主要因素可能源于使用不考虑导致 NAD+ 减少的潜在生物学复杂性的单一靶标方法。因此,靶向 NAD+ 相互作用组中的多个关键节点的系统方法可能更有效和可靠。