» Articles » PMID: 29514713

A Need for NAD+ in Muscle Development, Homeostasis, and Aging

Overview
Journal Skelet Muscle
Specialty Physiology
Date 2018 Mar 9
PMID 29514713
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

Skeletal muscle enables posture, breathing, and locomotion. Skeletal muscle also impacts systemic processes such as metabolism, thermoregulation, and immunity. Skeletal muscle is energetically expensive and is a major consumer of glucose and fatty acids. Metabolism of fatty acids and glucose requires NAD+ function as a hydrogen/electron transfer molecule. Therefore, NAD+ plays a vital role in energy production. In addition, NAD+ also functions as a cosubstrate for post-translational modifications such as deacetylation and ADP-ribosylation. Therefore, NAD+ levels influence a myriad of cellular processes including mitochondrial biogenesis, transcription, and organization of the extracellular matrix. Clearly, NAD+ is a major player in skeletal muscle development, regeneration, aging, and disease. The vast majority of studies indicate that lower NAD+ levels are deleterious for muscle health and higher NAD+ levels augment muscle health. However, the downstream mechanisms of NAD+ function throughout different cellular compartments are not well understood. The purpose of this review is to highlight recent studies investigating NAD+ function in muscle development, homeostasis, disease, and regeneration. Emerging research areas include elucidating roles for NAD+ in muscle lysosome function and calcium mobilization, mechanisms controlling fluctuations in NAD+ levels during muscle development and regeneration, and interactions between targets of NAD+ signaling (especially mitochondria and the extracellular matrix). This knowledge should facilitate identification of more precise pharmacological and activity-based interventions to raise NAD+ levels in skeletal muscle, thereby promoting human health and function in normal and disease states.

Citing Articles

Transcriptome Analysis of Muscle Growth-Related circRNA in the Pacific Abalone .

Huang J, He J, She Z, Zhou M, Li D, Chen J Genes (Basel). 2025; 16(1).

PMID: 39858612 PMC: 11764893. DOI: 10.3390/genes16010065.


Nicotinic acid improves mitochondrial function and associated transcriptional pathways in older inactive males.

Deane C, Willis C, Gallagher I, Brook M, Gharahdaghi N, Wylie L Transl Exerc Biomed. 2024; 1(3-4):277-294.

PMID: 39703532 PMC: 11653476. DOI: 10.1515/teb-2024-0030.


Mechanisms of the NAD salvage pathway in enhancing skeletal muscle function.

Su M, Qiu F, Li Y, Che T, Li N, Zhang S Front Cell Dev Biol. 2024; 12:1464815.

PMID: 39372950 PMC: 11450036. DOI: 10.3389/fcell.2024.1464815.


Protective Effect of Nicotinamide Riboside on Glucocorticoid-Induced Glaucoma: Mitigating Mitochondrial Damage and Extracellular Matrix Deposition.

Zhang N, Zhang P, Deng X, Zhu M, Hu Y, Ji D Invest Ophthalmol Vis Sci. 2024; 65(8):1.

PMID: 38949632 PMC: 11221610. DOI: 10.1167/iovs.65.8.1.


Nicotinamide N-Methyltransferase (NNMT): A New Hope for Treating Aging and Age-Related Conditions.

Li J, Sun W, Zhu X, Mei Y, Li W, Li J Metabolites. 2024; 14(6).

PMID: 38921477 PMC: 11205546. DOI: 10.3390/metabo14060343.


References
1.
Snow C, Goody M, Kelly M, Oster E, Jones R, Khalil A . Time-lapse analysis and mathematical characterization elucidate novel mechanisms underlying muscle morphogenesis. PLoS Genet. 2008; 4(10):e1000219. PMC: 2543113. DOI: 10.1371/journal.pgen.1000219. View

2.
Howitz K, Bitterman K, Cohen H, Lamming D, Lavu S, Wood J . Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan. Nature. 2003; 425(6954):191-6. DOI: 10.1038/nature01960. View

3.
Fulco M, Schiltz R, Iezzi S, King M, Zhao P, Kashiwaya Y . Sir2 regulates skeletal muscle differentiation as a potential sensor of the redox state. Mol Cell. 2003; 12(1):51-62. DOI: 10.1016/s1097-2765(03)00226-0. View

4.
Mills K, Yoshida S, Stein L, Grozio A, Kubota S, Sasaki Y . Long-Term Administration of Nicotinamide Mononucleotide Mitigates Age-Associated Physiological Decline in Mice. Cell Metab. 2017; 24(6):795-806. PMC: 5668137. DOI: 10.1016/j.cmet.2016.09.013. View

5.
Vrablik T, Wang W, Upadhyay A, Hanna-Rose W . Muscle type-specific responses to NAD+ salvage biosynthesis promote muscle function in Caenorhabditis elegans. Dev Biol. 2010; 349(2):387-94. PMC: 3019288. DOI: 10.1016/j.ydbio.2010.11.014. View