Article Synopsis

  • Male C57BL/6J mice on a high-fat diet develop prediabetes, insulin resistance, and sensory neuropathy, becoming models for type 2 diabetes (T2D) when given low doses of streptozotocin.
  • Treatment with nicotinamide riboside (NR) improved glucose tolerance, reduced weight gain and liver damage, and protected against sensory neuropathy in prediabetic and T2D mice.
  • NR also showed protective effects on nerve structures, indicating a potential neuroprotective role independent of glycemic control, and suggests further testing in human obesity and T2D conditions.

Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Male C57BL/6J mice raised on high fat diet (HFD) become prediabetic and develop insulin resistance and sensory neuropathy. The same mice given low doses of streptozotocin are a model of type 2 diabetes (T2D), developing hyperglycemia, severe insulin resistance and diabetic peripheral neuropathy involving sensory and motor neurons. Because of suggestions that increased NAD(+) metabolism might address glycemic control and be neuroprotective, we treated prediabetic and T2D mice with nicotinamide riboside (NR) added to HFD. NR improved glucose tolerance, reduced weight gain, liver damage and the development of hepatic steatosis in prediabetic mice while protecting against sensory neuropathy. In T2D mice, NR greatly reduced non-fasting and fasting blood glucose, weight gain and hepatic steatosis while protecting against diabetic neuropathy. The neuroprotective effect of NR could not be explained by glycemic control alone. Corneal confocal microscopy was the most sensitive measure of neurodegeneration. This assay allowed detection of the protective effect of NR on small nerve structures in living mice. Quantitative metabolomics established that hepatic NADP(+) and NADPH levels were significantly degraded in prediabetes and T2D but were largely protected when mice were supplemented with NR. The data justify testing of NR in human models of obesity, T2D and associated neuropathies.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882590PMC
http://dx.doi.org/10.1038/srep26933DOI Listing

Publication Analysis

Top Keywords

nicotinamide riboside
8
type diabetes
8
mice
8
neuropathy mice
8
insulin resistance
8
sensory neuropathy
8
glycemic control
8
t2d mice
8
weight gain
8
hepatic steatosis
8

Similar Publications

Homocysitaconate controls inflammation through reshaping methionine metabolism and N-homocysteinylation.

Cell Metab

August 2025

Center for Clinical Research and Translational Medicine, Yangpu Hospital, School of Medicine, Tongji University, Shanghai 200092, China. Electronic address:

Inflammation and its metabolic-network interactions generate novel regulatory molecules with translational implications. Here, we identify the immunometabolic crosstalk that generates homocysitaconate, a metabolite formed by homocysteine and itaconate adduction catalyzed by S-adenosyl-L-homocysteine hydrolase (AHCY). Homocysitaconate increases 152-fold during inflammation and exhibits anti-inflammatory effects.

View Article and Find Full Text PDF

Nicotinamide riboside kinase (NRK) is an important enzyme in the nicotinamide riboside (NR) metabolic pathway, converting NR to nicotinamide mononucleotide (NMN), which has promising industrial applications. However, structural collapse in many NRKs reduces their activity and thermal stability, limiting their industrial potential. Herein, we developed an α-helix reconstruction method on a Kag-NRK from Kluyveromyces marxianus for restore its activity and stability together.

View Article and Find Full Text PDF

NAD dyshomeostasis in RYR1-related myopathies.

Skelet Muscle

August 2025

Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.

Background: Pathogenic variants in RYR1 cause a spectrum of rare congenital myopathies associated with intracellular calcium dysregulation. Glutathione redox imbalance has been reported in several Ryr1 disease model systems and clinical studies. NAD and NADP are essential cofactors in cellular metabolism and redox homeostasis.

View Article and Find Full Text PDF

Cardiomyocyte senescence, characterized by elevated cell cycle inhibitor expression, persistent DNA damage response, and mitochondrial dysfunction, contributes to myocardial stiffness and the progression of heart failure with preserved ejection fraction (HFpEF), the most common form of heart failure affecting individuals over 65. In this study, we investigated the role of NAD⁺ metabolism in cardiomyocyte senescence and cardiac function. Aged mice exhibited reduced cardiac NAD⁺ levels, impaired NAD⁺ biosynthesis and mobilization, and increased consumption, leading to suppressed SIRT1/6 activity and accumulation of senescent cardiomyocytes.

View Article and Find Full Text PDF

Background: Phosphoribosyl pyrophosphate synthetase 1 (PRPS1) deficiency is a rare neurometabolic disorder with wide spectrum of presentation. It can present in early childhood with global developmental delay, retinal dystrophy, and hearing loss, or can present as isolated neuropathy or hearing loss in adulthood. Here we describe a patient with vision impairment, fatigue, and unilateral hearing loss caused by a somatic mosaic pathogenic variant in PRPS1 gene which encodes PRPS1.

View Article and Find Full Text PDF