Adipose Tissue and Brain Metabolic Responses to Western Diet-Is There a Similarity between the Two?

Int J Mol Sci. 2020 Jan 25;21(3):786. doi: 10.3390/ijms21030786.

Abstract

Dietary fats and sugars were identified as risk factors for overweight and neurodegeneration, especially in middle-age, an earlier stage of the aging process. Therefore, our aim was to study the metabolic response of both white adipose tissue and brain in middle aged rats fed a typical Western diet (high in saturated fats and fructose, HFF) and verify whether a similarity exists between the two tissues. Specific cyto/adipokines (tumor necrosis factor alpha (TNF-α), adiponectin), critical obesity-inflammatory markers (haptoglobin, lipocalin), and insulin signaling or survival protein network (insulin receptor substrate 1 (IRS), Akt, Erk) were quantified in epididymal white adipose tissue (e-WAT), hippocampus, and frontal cortex. We found a significant increase of TNF-α in both e-WAT and hippocampus of HFF rats, while the expression of haptoglobin and lipocalin was differently affected in the various tissues. Interestingly, adiponectin amount was found significantly reduced in e-WAT, hippocampus, and frontal cortex of HFF rats. Insulin signaling was impaired by HFF diet in e-WAT but not in brain. The above changes were associated with the decrease in brain derived neurotrophic factor (BDNF) and synaptotagmin I and the increase in post-synaptic protein PSD-95 in HFF rats. Overall, our investigation supports for the first time similarities in the response of adipose tissue and brain to Western diet.

Keywords: BDNF; adiponectin; adipose tissue; frontal cortex; haptoglobin; hippocampus; lipocalin; synaptic proteins..

MeSH terms

  • Adipocytes / metabolism
  • Adipose Tissue / metabolism*
  • Animals
  • Biomarkers
  • Brain / metabolism*
  • Cytokines / blood
  • Cytokines / metabolism
  • Diet, Western*
  • Energy Metabolism*
  • Inflammation Mediators / blood
  • Inflammation Mediators / metabolism
  • Insulin / metabolism
  • Male
  • Models, Biological
  • Organ Specificity
  • Rats
  • Receptor, trkB / metabolism
  • Signal Transduction

Substances

  • Biomarkers
  • Cytokines
  • Inflammation Mediators
  • Insulin
  • Ntrk2 protein, rat
  • Receptor, trkB