Detrimental effects of diet-induced obesity on τ pathology are independent of insulin resistance in τ transgenic mice

Diabetes. 2013 May;62(5):1681-8. doi: 10.2337/db12-0866. Epub 2012 Dec 18.

Abstract

The τ pathology found in Alzheimer disease (AD) is crucial in cognitive decline. Midlife development of obesity, a major risk factor of insulin resistance and type 2 diabetes, increases the risk of dementia and AD later in life. The impact of obesity on AD risk has been suggested to be related to central insulin resistance, secondary to peripheral insulin resistance. The effects of diet-induced obesity (DIO) on τ pathology remain unknown. In this study, we evaluated effects of a high-fat diet, given at an early pathological stage, in the THY-Tau22 transgenic mouse model of progressive AD-like τ pathology. We found that early and progressive obesity potentiated spatial learning deficits as well as hippocampal τ pathology at a later stage. Surprisingly, THY-Tau22 mice did not exhibit peripheral insulin resistance. Further, pathological worsening occurred while hippocampal insulin signaling was upregulated. Together, our data demonstrate that DIO worsens τ phosphorylation and learning abilities in τ transgenic mice independently from peripheral/central insulin resistance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal
  • Diet, High-Fat / adverse effects*
  • Hippocampus / metabolism*
  • Hippocampus / pathology
  • Insulin Receptor Substrate Proteins / biosynthesis
  • Insulin Receptor Substrate Proteins / genetics
  • Insulin Receptor Substrate Proteins / metabolism
  • Insulin Resistance*
  • Learning Disabilities / etiology
  • Male
  • Memory Disorders / etiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Nerve Tissue Proteins / biosynthesis
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Obesity / etiology
  • Obesity / metabolism*
  • Obesity / pathology
  • Obesity / physiopathology
  • Phosphorylation
  • Protein Processing, Post-Translational
  • Random Allocation
  • Signal Transduction
  • Spatial Behavior
  • Tauopathies / etiology
  • Tauopathies / metabolism*
  • Tauopathies / pathology
  • Tauopathies / physiopathology
  • Up-Regulation
  • tau Proteins / genetics
  • tau Proteins / metabolism*

Substances

  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse
  • Nerve Tissue Proteins
  • tau Proteins