Naringenin Supplementation to a Chow Diet Enhances Energy Expenditure and Fatty Acid Oxidation, and Reduces Adiposity in Lean, Pair-Fed Ldlr-/- Mice

Mol Nutr Food Res. 2019 Mar;63(6):e1800833. doi: 10.1002/mnfr.201800833. Epub 2019 Jan 2.

Abstract

Scope: Naringenin is a citrus-derived flavonoid that has potent lipid-lowering and insulin-sensitizing effects in obese mouse models of metabolic dysfunction. However, in these models, a significant effect of naringenin supplementation is the prevention of weight gain, which in itself can confer metabolic protection. Therefore, in the present study, the effect of naringenin supplementation in lean, chow-fed Ldlr-/- mice is investigated.

Methods and results: In Ldlr-/- mice with isocaloric food consumption, treatment with naringenin for 8 weeks reduces body weight and adiposity compared to littermate controls pair-fed the chow diet alone. Furthermore, naringenin treatment reduces plasma lipids and enhances insulin sensitivity compared to chow-fed controls. Metabolic cage studies reveal that naringenin-treated mice have elevated energy expenditure with no change in ambulatory activity. Additionally, naringenin-treated mice have an increased respiratory exchange ratio and food consumption during the dark cycle. Treatment increases the expression of fatty acid oxidation genes in liver, and increased β-hydroxybutyrate concentrations in plasma, indicating that one mechanism through which naringenin mediates metabolic improvement is enhanced hepatic fatty acid oxidation.

Conclusions: These studies highlight the potential therapeutic utility of naringenin and suggest that this flavonoid maintains potent metabolic properties in the absence of obesity or a high-fat diet.

Keywords: energy expenditure; flavonoids; lipoproteins; metabolism; pair-feeding.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiposity / drug effects*
  • Adiposity / physiology
  • Animals
  • Dietary Supplements
  • Energy Metabolism / drug effects*
  • Fatty Acids / metabolism*
  • Flavanones / pharmacology*
  • Insulin / blood
  • Lipids / blood
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • Oxidation-Reduction
  • Receptors, LDL / genetics

Substances

  • Fatty Acids
  • Flavanones
  • Insulin
  • Lipids
  • Receptors, LDL
  • naringenin

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