Fructose-rich diet and walnut supplementation differently regulate rat hypothalamic and hippocampal glucose transporters expression

J Sci Food Agric. 2021 Nov;101(14):5984-5991. doi: 10.1002/jsfa.11252. Epub 2021 Apr 28.

Abstract

Background: Nutritional modulations may be considered a strategy to protect mental health. Neuronal homeostasis is highly dependent on the availability of glucose, which represents the primary energy source for the brain. In this study, we evaluated the effects of walnut intake and fructose-rich diet on the expression of glucose transporters (GLUTs) in two rat brain regions: hypothalamus and hippocampus.

Results: Our results show that walnut supplementation of fructose-fed animals restored the hypothalamic content of GLUT1 and GLUT3 protein. Furthermore, walnut intake did not affect increased hypothalamic GLUT2 content upon fructose consumption. These effects were accompanied by distinctive alterations of hippocampal GLUTs levels. Specifically, walnut intake increased GLUT1 content, whereas GLUT2 protein was decreased within the rat hippocampus after both individual and combined treatments.

Conclusion: Overall, our study suggests that walnut supplementation exerted modulatory effects on the glucose transporters within specific brain regions in the presence of developed metabolic disorder. © 2021 Society of Chemical Industry.

Keywords: fructose; glucose transporters; hippocampus; hypothalamus; walnut.

MeSH terms

  • Animals
  • Fructose / metabolism
  • Glucose / metabolism
  • Glucose Transporter Type 1 / genetics
  • Glucose Transporter Type 1 / metabolism*
  • Glucose Transporter Type 2 / genetics
  • Glucose Transporter Type 2 / metabolism*
  • Glucose Transporter Type 3 / genetics
  • Glucose Transporter Type 3 / metabolism*
  • Hippocampus / metabolism*
  • Hypothalamus / metabolism*
  • Juglans / metabolism*
  • Male
  • Nuts / metabolism
  • Rats
  • Rats, Wistar

Substances

  • Glucose Transporter Type 1
  • Glucose Transporter Type 2
  • Glucose Transporter Type 3
  • Slc2a1 protein, rat
  • Slc2a2 protein, rat
  • Slc2a3 protein, rat
  • Fructose
  • Glucose