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Toxicology study profile of Nicotinamide mononucleotide after acute and 90-day sub chronic dosing in Wistar rats and mutagenicity tests

Authors :
Jianjun Yu
Qiang Shen
Jiayan Li
Source :
Current Research in Toxicology, Vol 6, Iss , Pp 100171- (2024)
Publication Year :
2024
Publisher :
Elsevier, 2024.

Abstract

Nicotinamide mononucleotide (NMN) is an intermediate in biosynthesis pathway of Nicotinamide adenine dinucleotide (NAD+), an essential cofactor in all living cells involved in fundamental biological processes. Evidence stemming from recent studies have unveiled numerous roles of NAD+ metabolism on aging, longevity, delaying the progression of age-related diseases. A three-study genetic toxicity (genetox) battery (bacterial mutagenesis, in vitro cytogenetics, and in vivo mammalian test) is usually required to confirm safety of a new dietary ingredient and this study showed the data from in vivo mutagenicity test for the first time.The acute oral LD50 of NMN was greater than 2000 mg/kg body weight with 5000 mg/kg body weight as LD50 cut-off value and was classified under “Category 5 or Unclassified” as per Globally Harmonized System of Classification and Labelling of Chemicals (GHS). Based on 90 days repeated dose toxicity test the NOAEL was considered to be NLT 800 mg NMN/kg body weight in Wistar rats. The bacterial reverse mutation test, the in vitro and in vivo chromosomal aberration test, found NMN to be non-mutagenic. In the mammalian bone marrow chromosomal aberration test, it was concluded that NMN is non clastogenic at and up to 2,000 mg/kg body weight in all the animals tested to confirm safety of a new dietary ingredient and this study showed the data from in vivo mutagenicity test for the first time.

Details

Language :
English
ISSN :
2666027X
Volume :
6
Issue :
100171-
Database :
Directory of Open Access Journals
Journal :
Current Research in Toxicology
Publication Type :
Academic Journal
Accession number :
edsdoj.6dbf673b81bf4488a515c8d3a0a2aab0
Document Type :
article
Full Text :
https://doi.org/10.1016/j.crtox.2024.100171