High Dose of Dietary Nicotinamide Riboside Induces Glucose Intolerance and White Adipose Tissue Dysfunction in Mice Fed a Mildly Obesogenic Diet.
Wenbiao ShiMaria A HegemanAtanaska DonchevaMelissa Bekkenkamp-GrovensteinVincent C J de BoerJaap KeijerPublished in: Nutrients (2019)
Nicotinamide riboside (NR) is a nicotinamide adenine dinucleotide (NAD+) precursor vitamin. The scarce reports on the adverse effects on metabolic health of supplementation with high-dose NR warrant substantiation. Here, we aimed to examine the physiological responses to high-dose NR supplementation in the context of a mildly obesogenic diet and to substantiate this with molecular data. An 18-week dietary intervention was conducted in male C57BL/6JRccHsd mice, in which a diet with 9000 mg NR per kg diet (high NR) was compared to a diet with NR at the recommended vitamin B3 level (control NR). Both diets were mildly obesogenic (40 en% fat). Metabolic flexibility and glucose tolerance were analyzed and immunoblotting, qRT-PCR and histology of epididymal white adipose tissue (eWAT) were performed. Mice fed with high NR showed a reduced metabolic flexibility, a lower glucose clearance rate and aggravated systemic insulin resistance. This was consistent with molecular and morphological changes in eWAT, including sirtuin 1 (SIRT1)-mediated PPARγ (proliferator-activated receptor γ) repression, downregulated AKT/glucose transporter type 4 (GLUT4) signaling, an increased number of crown-like structures and macrophages, and an upregulation of pro-inflammatory gene markers. In conclusion, high-dose NR induces the onset of WAT dysfunction, which may in part explain the deterioration of metabolic health.
Keyphrases
- high dose
- adipose tissue
- insulin resistance
- weight loss
- physical activity
- low dose
- high fat diet induced
- stem cell transplantation
- healthcare
- public health
- randomized controlled trial
- high fat diet
- metabolic syndrome
- blood glucose
- mental health
- type diabetes
- emergency department
- cell proliferation
- gene expression
- signaling pathway
- genome wide
- single molecule
- health information
- fatty acid
- clinical trial
- poor prognosis
- electronic health record
- adverse drug
- ischemia reperfusion injury
- social media
- polycystic ovary syndrome
- human health
- binding protein
- double blind