烟酰胺单核苷酸
NAD+激酶
烟酰胺腺嘌呤二核苷酸
烟酰胺
烟酰胺磷酸核糖转移酶
辅因子
药理学
生物化学
化学
内科学
医学
酶
内分泌学
作者
Keisuke Okabe,Keisuke Yaku,Yoshiaki Uchida,Yuichiro Fukamizu,Toshiya Sato,Takanobu Sakurai,Kazuyuki Tobe,Takashi Nakagawa
标识
DOI:10.3389/fnut.2022.868640
摘要
Nicotinamide mononucleotide (NNM) is an orally bioavailable NAD + precursor that has demonstrated beneficial effects against aging and aging-associated diseases in animal models. NMN is ultimately converted to NAD + , a redox cofactor that mediates many metabolic enzymes. NAD + also serves as the substrate for poly(ADP-ribose) polymerase (PARP) and sirtuins, and regulates various biological processes, such as metabolism, DNA repair, gene expression, and stress responses. Previous mouse models showed that NMN administration can increase NAD + in various organs and ameliorate aging-related diseases, such as obesity, diabetes, heart failure, stroke, kidney failure, and Alzheimer’s disease through NAD + -mediated pathways. However, evidence of its effect on humans is still scarce. In this study, we conducted a placebo-controlled, randomized, double blind, parallel-group trial to investigate the safety of orally administered NMN and its efficacy to increase NAD + levels in thirty healthy subjects. Healthy volunteers received 250 mg/day of NMN ( n = 15) or placebo ( n = 15) for 12 weeks, and physiological and laboratory tests were performed during this period. In addition, NAD + and its related metabolites in whole blood were examined. Oral supplementation of NMN for 12 weeks caused no abnormalities in physiological and laboratory tests, and no obvious adverse effects were observed. NAD + levels in whole blood were significantly increased after NMN administration. We also observed the significant rise in nicotinic acid mononucleotide (NAMN) levels, but not in NMN. We also found that the increased amount of NAD + was strongly correlated with pulse rate before the administration of NMN. These results suggest that oral administration of NMN is a safe and practical strategy to boost NAD + levels in humans. Clinical Trial Registration: JRCT [ https://jrct.niph.go.jp/ ], identifier: [jRCTs041200034].
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