1-MNA

1-MNA, a novel myokine, is a game-changer in cellular health by blocking the enzyme NNMT and optimizing NAD levels in the cells. 1-MNA offers a comprehensive approach to cellular health. Its anti-inflammatory, anti-thrombotic properties and positive effect on vascular endothelium and skeletal muscle energy metabolism make it a promising supplement in the medical field.
Optimized NAD Levels: 1-MNA works to restore and optimize NAD levels in cells, a crucial component for cellular health and energy production.
Anti-inflammatory and Anti-thrombotic Properties: 1-MNA possesses anti-inflammatory and anti-thrombotic characteristics, contributing to improved vascular health.
Inhibition of NNMT: 1-MNA has been shown to inhibit the enzyme NNMT, which when present in high levels, is associated with various diseases. By inhibiting this enzyme, 1-MNA can contribute to overall cellular health and disease prevention.

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Cellular Pathways 

1-MNA safely increases NAD levels and blocks NNMT, improves cell energy metabolism anti-inflammatory and anti-thrombotic properties positive effect on vascular endothelium

Why this matters:

SIRT-1 Downstream Effects
Stimulates caloric restriction and exercise pathways through these gene transcription factors:
PGC-1a
The core regulator of mitochondrial biogenesis
PPAR
Regulate fat oxidation
AMPK
Master regulator of cell energy
NF-kB
Inhibition leads to decreased inflammation and oxidative stress 

Clinical Studies

NAD(H) and NADP(H) Redox Couples and Cellular Energy Metabolism
NAD+/NADH and NADP+/NADPH redox systems are crucial for cellular redox balance and metabolism. Imbalances in these systems are linked to various diseases. Recent advances, including new biosynthetic enzymes and genetically encoded biosensors, have improved our understanding of how cells regulate NAD(H) and NADP(H) pools. Research is increasingly focused on redox stress and the role of NAD+-consuming proteins in maintaining cellular health.

Synergy with GLP-1s

Semaglutide, Tirzepatide, Liraglutide
Studies show 15% reduction in body weight when semaglutide was accompanied by caloric restriction and exercise. Using an exercise mimetic like LeuSynergy is foundational in weight loss and metabolic health outcomes.
Insulin Independent Pathways for Glucose Disposal
GLP-1
Increase in GLUT4 expression by activating AMPK
LeuSynergy
Increase in GLUT4 expression through SIRT1 deacetylation of PGC-1a
GLP-1
Direct effects on hepatocytes by activating genes involved in beta-oxidation of fatty acids
LeuSynergy
Activation of PGC-1a and PPAR resulting in an increase in fatty acid oxidation and oxidative phosphorylation
GLP-1
Reduced oxidative stress in pancreatic islets. Increases B-cell mass by regulating cell kinectics and suppressing oxidative and ER stress, and amerlioration of glucolipotoxicity.
LeuSynergy
SIRT1 deacetylation and inhibition of NF-kB protecting beta cells from oxidative stress and inflammatory cytokines.

References

  1. Xiao, Wusheng & Wang, Rui-Sheng & Handy, Diane &Loscalzo, Joseph. (2017). NAD(H) and DADP(H) Redox Couples and Cellular Endergy Metabolism. Antioxidants & Redox Signaling. 28. 10.1089/ars.
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