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Nicotinamide and Pyridoxine Stimulate Muscle Stem Cell Expansion and Enhance Regenerative Capacity During Aging Publisher Pubmed



Ancel S1, 2 ; Michaud J1 ; Migliavacca E1 ; Jomard C3 ; Fessard A3 ; Garcia P1, 3 ; Karaz S1 ; Raja S1, 2 ; Jacot GE1 ; Desgeorges T1 ; Sanchezgarcia JL1 ; Tauzin L4 ; Ratinaud Y1 ; Brinon B1 Show All Authors
Authors
  1. Ancel S1, 2
  2. Michaud J1
  3. Migliavacca E1
  4. Jomard C3
  5. Fessard A3
  6. Garcia P1, 3
  7. Karaz S1
  8. Raja S1, 2
  9. Jacot GE1
  10. Desgeorges T1
  11. Sanchezgarcia JL1
  12. Tauzin L4
  13. Ratinaud Y1
  14. Brinon B1
  15. Metairon S4
  16. Pinero L1
  17. Barron D1
  18. Blum S5
  19. Karagounis LG5, 6
  20. Heshmat R7
  21. Ostovar A7
  22. Farzadfar F7
  23. Scionti I3
  24. Mounier R3
  25. Gondin J3
  26. Stuelsatz P1
  27. Feige JN1, 2
Show Affiliations
Authors Affiliations
  1. 1. Nestle Institute of Health Sciences, Nestle Research, Lausanne, Switzerland
  2. 2. School of Life Sciences, Ecole Polytechnique Federale de Lausanne, Lausanne, Switzerland
  3. 3. Institut NeuroMyoGene, Physiopathologie et Genetique du Neurone et du Muscle, Universite Claude Bernard Lyon 1, CNRS UMR5261, INSERM U1315, Lyon, France
  4. 4. Nestle Institute of Food Safety and Analytical Sciences, Nestle Research, Lausanne, Switzerland
  5. 5. Translational Research, Nestle Health Science, Lausanne, Switzerland
  6. 6. Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, Australia
  7. 7. Chronic Diseases Research Center, Endocrinology and Metabolism Population Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of Clinical Investigation Published:2024


Abstract

Skeletal muscle relies on resident muscle stem cells (MuSCs) for growth and repair. Aging and muscle diseases impair MuSC function, leading to stem cell exhaustion and regenerative decline that contribute to the progressive loss of skeletal muscle mass and strength. In the absence of clinically available nutritional solutions specifically targeting MuSCs, we used a human myogenic progenitor high-content imaging screen of natural molecules from food to identify nicotinamide (NAM) and pyridoxine (PN) as bioactive nutrients that stimulate MuSCs and have a history of safe human use. NAM and PN synergize via CK1-mediated cytoplasmic β-catenin activation and AKT signaling to promote amplification and differentiation of MuSCs. Oral treatment with a combination of NAM and PN accelerated muscle regeneration in vivo by stimulating MuSCs, increased muscle strength during recovery, and overcame MuSC dysfunction and regenerative failure during aging. Levels of NAM and bioactive PN spontaneously declined during aging in model organisms and interindependently associated with muscle mass and walking speed in a cohort of 186 aged people. Collectively, our results establish the NAM/PN combination as a nutritional intervention that stimulates MuSCs, enhances muscle regeneration, and alleviates age-related muscle decline with a direct opportunity for clinical translation. © 2024, Ancel et al.
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