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These studies suggest that oral and intravenous administration of nicotinamide mononucleotide (NMN) is generally safe and effective in boosting NAD+ levels without significant adverse effects.
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Nicotinamide mononucleotide (NMN) is a precursor to nicotinamide adenine dinucleotide (NAD+), a crucial molecule involved in various metabolic processes, including energy production, DNA repair, and stress responses. NMN has gained attention for its potential anti-aging benefits and its ability to ameliorate age-related diseases .
Several clinical trials have investigated the safety of NMN when administered orally. A placebo-controlled, randomized, double-blind study involving 30 healthy subjects demonstrated that a daily dose of 250 mg of NMN for 12 weeks did not cause any adverse effects. The study also showed a significant increase in NAD+ levels in the blood, suggesting that NMN is a safe and effective way to boost NAD+ levels in humans.
Another study involving 10 healthy Japanese men tested single doses of 100, 250, and 500 mg of NMN. The results indicated no significant clinical symptoms or changes in vital signs, except for minor fluctuations in serum bilirubin, creatinine, chloride, and blood glucose levels, all within normal ranges. This study further confirmed the safety of NMN in humans.
A larger study with 66 middle-aged and older adults also supported these findings. Participants who took 300 mg of NMN daily for 60 days showed increased NAD+ levels without any significant adverse effects, reinforcing the safety profile of NMN.
In addition to oral administration, the safety of intravenous NMN has also been evaluated. A study involving 10 healthy volunteers found that intravenous NMN administration did not affect electrocardiograms, pulse, blood pressure, or metabolic markers in vital organs. The study also noted significant increases in blood NAD+ levels, indicating that intravenous NMN is safe and beneficial .
Preclinical studies in animals have provided additional safety data. In Sprague-Dawley rats, high doses of NMN (up to 2666 mg/kg) did not result in any mortality or adverse effects. A 90-day sub-chronic study with doses up to 1500 mg/kg/day also showed no toxic effects, establishing a No-Observable Adverse Effect Level (NOAEL) for NMN.
Similarly, studies in mice and beagle dogs demonstrated that NMN is well-tolerated even at high doses, with only minor increases in certain biomarkers, which were not clinically significant.
The collective evidence from human clinical trials and preclinical animal studies strongly suggests that NMN is safe for both oral and intravenous administration. NMN supplementation effectively increases NAD+ levels without causing significant adverse effects, making it a promising candidate for mitigating age-related disorders and promoting overall health. However, ongoing and future clinical trials are essential to further validate these findings and establish long-term safety profiles.
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