Nicotinamide Protects Against Diet‐Induced Body Weight Gain, Increases Energy Expenditure, and Induces White Adipose Tissue Beiging

• Published in: Molecular nutrition & food research Vol. 65; no. 11; pp. e2100111 - n/a
• Main Authors: Méndez‐Lara, Karen Alejandra, Rodríguez‐Millán, Elisabeth, Sebastián, David, Blanco‐Soto, Rosi, Camacho, Mercedes, Nan, Madalina N., Diarte‐Añazco, Elena M. G., Mato, Eugènia, Lope‐Piedrafita, Silvia, Roglans, Núria, Laguna, Juan Carlos, Alonso, Núria, Mauricio, Dídac, Zorzano, Antonio, Villarroya, Francesc, Villena, Josep A., Blanco‐Vaca, Francisco, Julve, Josep
• Format: Journal Article
• Language: English
• Published: Germany Wiley Subscription Services, Inc 01.06.2021
• Subjects: Adenine; Adipocytes, Beige - drug effects; Adipose tissue; Adipose Tissue, Brown - drug effects; Adipose Tissue, Brown - physiology; Adipose Tissue, White - drug effects; Adipose Tissue, White - physiology; adiposity; AMP; AMP-Activated Protein Kinases - metabolism; Animals; beiging; Body weight; Body weight gain; Complications; Diet; Diet, High-Fat - adverse effects; Dietary supplements; Dosage; Drinking water; Energy expenditure; Energy Metabolism - drug effects; Fatty liver; Glucose tolerance; High fat diet; inflammation; Kinases; Male; Males; Metabolism; Mice; Mice, Inbred C57BL; Mitochondria; Morphology; NAD; Niacinamide - administration & dosage; Niacinamide - pharmacology; Nicotinamide; Nicotinamide adenine dinucleotide; Non-alcoholic Fatty Liver Disease - drug therapy; Non-alcoholic Fatty Liver Disease - etiology; Obesity; Obesity - etiology; Obesity - prevention & control; Phenotypes; Precursors; Protein kinase; Proteins; Steatosis; Uncoupling protein 1; Weight Gain - drug effects; adiposity; fatty liver; beiging; inflammation
• ISSN: 1613-4125; 1613-4133
• DOI: 10.1002/mnfr.202100111

Scope Interventions that boost NAD+ availability are of potential therapeutic interest for obesity treatment. The potential of nicotinamide (NAM), the amide form of vitamin B3 and a physiological precursor of nicotinamide adenine dinucleotide (NAD)+, in preventing weight gain has not previously been studied in vivo. Other NAD+ precursors have been shown to decrease weight gain; however, their impact on adipose tissue is not addressed. Methods and results Two doses of NAM (high dose: 1% and low dose: 0.25%) are given by drinking water to C57BL/6J male mice, starting at the same time as the high‐fat diet feeding. NAM supplementation protects against diet‐induced obesity by augmenting global body energy expenditure in C57BL/6J male mice. The manipulation markedly alters adipose morphology and metabolism, particularly in inguinal (i) white adipose tissue (iWAT). An increased number of brown and beige adipocyte clusters, protein abundance of uncoupling protein 1 (UCP1), mitochondrial activity, adipose NAD+, and phosphorylated AMP‐activated protein kinase (P‐AMPK) levels are observed in the iWAT of treated mice. Notably, a significant improvement in hepatic steatosis, inflammation, and glucose tolerance is also observed in NAM high‐dose treated mice. Conclusion NAM influences whole‐body energy expenditure by driving changes in the adipose phenotype. Thus, NAM is an attractive potential treatment for preventing obesity and associated complications. Nicotinamide (NAM) supplementation prevented weight gain by increasing the nicotinamide adenine dinucleotide (NAD)+ content and inducing white adipose tissue beiging. Uncoupling protein 1 (UCP1), mitochondrial activity, adipose NAD+ and phosphorylated AMP‐activated protein kinase (P‐AMPK) levels were elevated in white adipose tissue of treated mice. NAM manipulation also ameliorated the inflammatory phenotype in adipose tissue and hepatic steatosis in treated mice.