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Study 10 of 23NAD+ (Nicotinamide Adenine Dinucleotide) literaturebiorxiv-preprint · Observational2026

Preliminary evaluation of NMN reprotoxicity using human sperm assay

NMN does not impair human sperm motility at concentrations of 50 µM and 100 µM, but 150 µM may have harmful effects.

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Where it sits

this study against the rest of the nad+ (nicotinamide adenine dinucleotide) corpus
7
Preclinical
14
Observational · this one
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Randomised
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Summary and findings

This study evaluated the effects of nicotinamide mononucleotide (NMN) on human sperm progressive motility using a Human Sperm Assay. Seven normozoospermic semen samples were exposed to NMN at concentrations of 0, 50, 100, or 150 µM over a 24-hour period. The findings indicated that NMN at 50 µM and 100 µM did not impair motility, while 150 µM resulted in a significant reduction in motility.

How much of this paper we could read: full text read (0.70). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Not reported in abstract.2026

Abstract

The authors’ words, as biorxiv-preprint supplied them

<title>Abstract</title> <p>Human spermatozoa are highly susceptible to oxidative injury owing to their polyunsaturated fatty acid-rich plasma membrane and limited antioxidant defenses. Nicotinamide mononucleotide (NMN), a key NAD⁺ precursor, has gained attention for its roles in cellular energetics and redox balance. However, direct evidence regarding its potential reprotoxic effects on human spermatozoa is lacking. This preliminary Human Sperm Assay (HSA) evaluated the compatibility of NMN with human sperm progressive motility. Seven normozoospermic semen samples were exposed to NMN at 0 (control), 50, 100, or 150 µM. Progressive motility was assessed according to WHO 2021 criteria at baseline and after 0.5, 1, 2, 4, and 24 hours of incubation. NMN at 50 µM and 100 µM did not impair progressive motility relative to untreated controls throughout the 24-hour incubation. In contrast, exposure to 150 µM NMN resulted in a substantial reduction in progressive motility. These preliminary findings suggest that NMN does not exert reprotoxic effects on sperm progressive motility at 50 and 100 µM, whereas 150 µM induces motility impairment. Larger studies with additional sperm function parameters are warranted to confirm the short-term safety of these lower concentrations.</p>

Background

The paper addresses the potential reprotoxicity of NMN (Nicotinamide Mononucleotide) in human sperm, a topic of growing interest due to the increasing use of NAD+ precursors. Prior literature has suggested various biological roles for NAD+ in cellular metabolism, but its effects on human reproductive health remain underexplored. This study is significant as it attempts to fill a gap in understanding the safety profile of NMN in human reproductive biology.

Methods

The study utilized a human sperm assay to assess the reprotoxicity of NMN. Specific details regarding the study design, sample size (n), dose, duration, and outcome measures were not reported in the abstract, which limits the ability to evaluate the robustness of the findings.

Results

Not reported in abstract.

Interpretation

Due to the lack of reported results and specific numeric findings, it is difficult to compare this study's outcomes to existing literature or to assess the clinical significance of any observed effects. The absence of detailed data raises concerns about the reliability of the conclusions drawn from this preliminary evaluation.

Key findings

  • Not reported in abstract.

Limitations

  • Not reported in abstract.
  • Preliminary evaluation with no detailed results.
  • Lack of specified doses and outcomes.

Elsewhere in the NAD+ (Nicotinamide Adenine Dinucleotide) corpus

BMetabolite-specific Reproducibility of Cerebral <sup>31</sup> P-MRS at 3T: Recommendations for Clinical Researchbiorxiv-preprint · 2026 · Test-retest variability ranged from ∼5-25 CoV%, n=Not reported in abstract.HumanCAging disrupts cumulus-oocyte NAD homeostasisbiorxiv-preprint · 2023 · n=30 · Not reported in abstract.mixedCThe placental metabolic clock.Science (New York, N.Y.) · 2026AnimalDMitochondrial quality control in human ageing and longevity.Nature metabolism · 2026DBacteria sense virus-induced genome degradation via methylated mononucleotides.Science (New York, N.Y.) · 2026 · Not reported in abstract.CMechanisms of apoptosis in colon cancer cells induced by IDO1 inhibitor and irradiation: A metabolomic studybiorxiv-preprint · 2026 · NAD+ levels decreased by additional 1-MT in radiated Colon26 cells (452 vs. 1027 nmol/g, p = 0.0495)Animal