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Peptide Database

Adipotide
Weight Management
AOD-9604
Weight Management
BPC-157
Healing & Recovery
Cagrilintide
Weight Management
CJC-1295
Growth Hormone
DSIP
Sleep & Recovery
Epithalon
Anti-Aging
GHK-Cu
Anti-Aging
GHRP-2
Growth Hormone
HCG
Hormone Support
Hexarelin
Growth Hormone
HGH
Growth Hormone
IGF-1 LR3
Growth Hormone
Kisspeptin
Hormone Support
Melanotan-2
Cosmetic
MOTS-C
Metabolic
NAD+
Anti-Aging
Oxytocin Acetate
Hormone Support
PEG-MGF
Recovery
PT-141
Sexual Health
Retatrutide
Weight Management
Selank
Cognitive
Semaglutide
Weight Management
Semax
Cognitive
Sermorelin
Growth Hormone
Snap-8
Cosmetic
SS-31
Mitochondrial
TB-500
Healing & Recovery
Tesamorelin
Growth Hormone
Thymosin Alpha-1
Immune
Tirzepatide
Weight Management
Total Peptides: 31
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NAD+
EfficacyHigh
Studies8
Participants572
StatusAvailable

NAD+

Nicotinamide Adenine Dinucleotide

NAD+ is a vital coenzyme present in every cell that plays crucial roles in energy metabolism, DNA repair, and cellular aging processes. As NAD+ levels naturally decline with age (by ~50% by age 50), supplementation through IV therapy or injections aims to restore cellular energy production, activate longevity pathways through sirtuin proteins, and support mitochondrial health. Research demonstrates significant improvements in cognitive function, physical performance, and biomarkers of aging.

Clinical Benefits

Enhanced cellular energy production and ATP synthesis
Activation of sirtuins (SIRT1-7) for longevity pathway support
Improved mitochondrial function and biogenesis
Enhanced DNA repair through PARP enzyme activation
Cognitive function improvements (memory, focus, processing speed)
Better sleep quality and circadian rhythm regulation

Mechanism of Action

NAD+ functions as an essential coenzyme in over 400 enzymatic reactions, primarily serving as an electron carrier in cellular respiration and energy metabolism. In mitochondria, NAD+ accepts electrons from metabolic substrates and transfers them through the electron transport chain for ATP synthesis. NAD+ also serves as a substrate for three major enzyme families: sirtuins (SIRT1-7), poly(ADP-ribose) polymerases (PARPs), and CD38/CD157. Sirtuin activation by NAD+ promotes deacetylation of key proteins involved in metabolism, stress resistance, and longevity, including PGC-1α for mitochondrial biogenesis, p53 for DNA repair, and FOXO transcription factors for stress response. PARP enzymes utilize NAD+ for DNA repair processes, while CD38 represents a major NAD+ consumer that increases with age, contributing to age-related NAD+ decline.

Key Action:

Proven Results

%
Maximum Weight Loss
Clinical research data
0%
Diabetes Risk Reduction
Clinical research data
572
Total Participants
Research studies
0%
CV Risk Reduction
Clinical data

Medical Disclaimer

NAD+ therapy is currently in research phase and not FDA-approved for specific medical conditions. This information is for educational purposes and should not replace consultation with qualified healthcare providers. Individual results may vary significantly. Professional medical supervision is recommended for all NAD+ therapeutic protocols.