Mitochondrial Abnormalities and Synaptic Loss Underlie Memory Deficits Seen in Mouse Models of Obesity and Alzheimer's Disease

J Alzheimers Dis. 2017;55(3):915-932. doi: 10.3233/JAD-160640.

Abstract

Obesity is associated with impaired memory in humans, and obesity induced by high-fat diets leads to cognitive deficits in rodents and in mouse models of Alzheimer's disease (AD). However, it remains unclear how high-fat diets contribute to memory impairment. Therefore, we tested the effect of a high-fat diet on memory in male and female control non-transgenic (Non-Tg) and triple-transgenic AD (3xTgAD) mice and determined if a high-fat diet caused similar ultrastructural abnormalities to those observed in AD. Behavior was assessed in mice on control or high-fat diet at 4, 8, or 14 months of age and ultrastructural analysis at 8 months of age. A high-fat diet increased body weight, fat weight, and insulin levels with some differences in these metabolic responses observed between Non-Tg and 3xTgAD mice. In both sexes, high-fat feeding caused memory impairments in Non-Tg mice and accelerated memory deficits in 3xTgAD mice. In 3xTgAD mice, changes in hippocampal mitochondrial morphology were observed in capillaries and brain neuropil that were accompanied by a reduction in synapse number. A high-fat diet also caused mitochondria abnormalities and a reduction in synapse number in Non-Tg mice, but did not exacerbate the changes seen in 3xTgAD mice. Our data demonstrate that a high-fat diet affected memory in Non-Tg mice and produced similar impairments in mitochondrial morphology and synapse number comparable to those seen in AD mice, suggesting that the detrimental effects of a high-fat diet on memory might be due to changes in mitochondrial morphology leading to a reduction in synaptic number.

Keywords: 3xTgAD; Alzheimer’s disease; Non-Tg; high-fat diet; memory; mitochondria; obesity; synapses.

MeSH terms

  • Alzheimer Disease / complications*
  • Alzheimer Disease / genetics
  • Alzheimer Disease / pathology*
  • Amyloid beta-Protein Precursor / genetics
  • Animals
  • Blood Glucose / genetics
  • Blood Pressure / genetics
  • Diet, High-Fat / methods
  • Disease Models, Animal
  • Endothelium, Vascular / pathology
  • Endothelium, Vascular / ultrastructure
  • Female
  • Hippocampus / pathology
  • Hippocampus / ultrastructure*
  • Humans
  • Insulin / blood
  • Male
  • Maze Learning / physiology
  • Memory Disorders / etiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microscopy, Electron, Transmission
  • Mitochondria / pathology*
  • Mitochondria / ultrastructure
  • Obesity / etiology
  • Obesity / pathology*
  • Presenilin-1 / genetics
  • Recognition, Psychology / physiology
  • Smell / physiology
  • Synapses / pathology*
  • Synapses / ultrastructure
  • tau Proteins / genetics

Substances

  • Amyloid beta-Protein Precursor
  • Blood Glucose
  • Insulin
  • Presenilin-1
  • tau Proteins