Early obesity leads to increases in hepatic arginase I and related systemic changes in nitric oxide and L-arginine metabolism in mice

J Physiol Biochem. 2018 Feb;74(1):9-16. doi: 10.1007/s13105-017-0597-6. Epub 2017 Nov 3.

Abstract

Obesity is a risk factor for vascular endothelial cell dysfunction characterized by low-grade, chronic inflammation. Increased levels of arginase I and concomitant decreases in L-arginine bioavailability are known to play a role in the pathogenesis of vascular endothelial cell dysfunction. In the present study, we focused on changes in the systemic expression of arginase I as well as L-arginine metabolism in the pre-disease state of early obesity prior to the onset of atherosclerosis. C57BL/6 mice were fed a control diet (CD; 10% fat) or high-fat diet (HFD; 60% fat) for 8 weeks. The mRNA expression of arginase I in the liver, adipose tissue, aorta, and muscle; protein expression of arginase I in the liver and plasma; and systemic levels of L-arginine bioavailability and NO2- were assessed. HFD-fed mice showed early obesity without severe disease symptoms. Arginase I mRNA and protein expression levels in the liver were significantly higher in HFD-fed obese mice than in CD-fed mice. Arginase I levels were slightly increased, whereas L-arginine levels were significantly reduced, and these changes were followed by reductions in NO2- levels. Furthermore, hepatic arginase I levels positively correlated with plasma arginase I levels and negatively correlated with L-arginine bioavailability in plasma. These results suggested that increases in the expression of hepatic arginase I and reductions in plasma L-arginine and NO2- levels might lead to vascular endothelial dysfunction in the pre-disease state of early obesity.

Keywords: Arginase; L-Arginine metabolism; Nitric oxide; Obesity; Pre-disease state.

MeSH terms

  • Animals
  • Aorta / enzymology
  • Aorta / metabolism
  • Arginase / blood
  • Arginase / genetics
  • Arginase / metabolism*
  • Arginine / blood*
  • Atherosclerosis / etiology
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Diet, High-Fat / adverse effects
  • Endothelium, Vascular / immunology
  • Endothelium, Vascular / metabolism*
  • Endothelium, Vascular / pathology
  • Enzyme Induction
  • Liver / immunology
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Mice, Inbred C57BL
  • Muscle, Skeletal / enzymology
  • Muscle, Skeletal / metabolism
  • Nitric Oxide / blood*
  • Obesity / etiology
  • Obesity / immunology
  • Obesity / metabolism*
  • Obesity / pathology
  • Organ Specificity
  • Severity of Illness Index
  • Systemic Vasculitis / etiology
  • Systemic Vasculitis / immunology
  • Systemic Vasculitis / metabolism*
  • Systemic Vasculitis / physiopathology
  • Weight Gain

Substances

  • Biomarkers
  • Nitric Oxide
  • Arginine
  • Arg1 protein, mouse
  • Arg2 protein, mouse
  • Arginase