Imai Shin-Ichiro
Department of Developmental Biology, Department of Medicine (Joint), Washington University School of Medicine, St. Louis, Missouri, USA.
Institute for Research on Productive Aging (IRPA), Tokyo, Japan.
NPJ Aging. 2025 Jan 27;11(1):4. doi: 10.1038/s41514-025-00192-6.
Over the past five years, systemic NAD (nicotinamide adenine dinucleotide) decline has been accepted to be a key driving force of aging in the field of aging research. The original version of the NAD World concept was proposed in 2009, providing an integrated view of the NAD-centric, systemic regulatory network for mammalian aging and longevity control. The reformulated version of the concept, the NAD World 2.0, was then proposed in 2016, emphasizing the importance of the inter-tissue communications between the hypothalamus and peripheral tissues including adipose tissue and skeletal muscle. There has been significant progress in our understanding of the importance of nicotinamide mononucleotide (NMN), a key NAD intermediate, and nicotinamide phosphoribosyltransferase (NAMPT), particularly extracellular NAMPT (eNAMPT). With these exciting developments, the further reformulated version of the concept, the NAD World 3.0, is now proposed, featuring multi-layered feedback loops mediated by NMN and eNAMPT for mammalian aging and longevity control.
在过去五年中,全身烟酰胺腺嘌呤二核苷酸(NAD)水平下降已被公认为衰老研究领域中衰老的关键驱动力。NAD世界概念的最初版本于2009年提出,为以NAD为中心的哺乳动物衰老和寿命控制的全身调节网络提供了一个综合观点。随后在2016年提出了该概念的重新表述版本,即NAD世界2.0,强调了下丘脑与包括脂肪组织和骨骼肌在内的外周组织之间组织间通讯的重要性。我们对关键NAD中间体烟酰胺单核苷酸(NMN)和烟酰胺磷酸核糖转移酶(NAMPT),特别是细胞外NAMPT(eNAMPT)的重要性有了重大进展。随着这些令人兴奋的进展,现在提出了该概念的进一步重新表述版本,即NAD世界3.0,其特点是由NMN和eNAMPT介导的多层反馈回路用于哺乳动物衰老和寿命控制。