NAD+激酶
烟酰胺
烟酸
烟酰胺腺嘌呤二核苷酸
化学
烟酰胺
生物化学
药理学
烟酰胺磷酸核糖转移酶
代谢途径
新陈代谢
医学
内科学
酶
作者
Xiangyü Li,Hong Yang,Han Jin,Hasan Türkez,Gürkan Öztürk,Levent Doğanay,Cheng Zhang,Jens Nielsen,Mathias Uhlén,Jan Borén,Adil Mardinoğlu
标识
DOI:10.1016/j.freeradbiomed.2023.05.032
摘要
NAD+ and glutathione precursors are currently used as metabolic modulators for improving the metabolic conditions associated with various human diseases, including non-alcoholic fatty liver disease, neurodegenerative diseases, mitochondrial myopathy, and age-induced diabetes. Here, we performed a one-day double blinded, placebo-controlled human clinical study to assess the safety and acute effects of six different Combined Metabolic Activators (CMAs) with 1 g of different NAD+ precursors based on global metabolomics analysis. Our integrative analysis showed that the NAD+ salvage pathway is the main source for boosting the NAD+ levels with the administration of CMAs without NAD+ precursors. We observed that incorporation of nicotinamide (Nam) in the CMAs can boost the NAD+ products, followed by niacin (NA), nicotinamide riboside (NR) and nicotinamide mononucleotide (NMN), but not flush free niacin (FFN). In addition, the NA administration led to a flushing reaction, accompanied by decreased phospholipids and increased bilirubin and bilirubin derivatives, which could be potentially risky. In conclusion, this study provided a plasma metabolomic landscape of different CMA formulations, and proposed that CMAs with Nam, NMN as well as NR can be administered for boosting NAD+ levels to improve altered metabolic conditions.
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