ASK1 is involved in cognitive impairment caused by long-term high-fat diet feeding in mice

Sci Rep. 2015 Jun 5:5:10844. doi: 10.1038/srep10844.

Abstract

Although high-fat diet intake is known to cause obesity and diabetes, the effect of high-fat diet itself on cognitive function remains to be clarified. We have previously shown that apoptosis signal-regulating kinase 1 (ASK1) is responsible for cognitive impairment caused by chronic cerebral hypoperfusion. The present work, by using ASK1 deficient mice, was undertaken to explore the influence of chronic high-fat diet intake on cognitive function and the role of ASK1. Cognitive function in wild-type mice fed high-fat diet from 2 to 24 months of age was significantly impaired compared to those fed control diet, which was associated with the significant white matter lesions, reduction of hippocampal capillary density, and decrement of hippocampal neuronal cell. However, ASK1 deficiency abolished the development of cognitive impairment and cerebral injury caused by high-fat diet. Our results provided the evidence that high-fat diet itself causes cognitive impairment and ASK1 participates in such cognitive impairment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / blood
  • Adiponectin / genetics
  • Adiponectin / metabolism
  • Amyloid beta-Peptides / metabolism
  • Animals
  • Blood Pressure
  • Body Weight
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology
  • Cognition
  • Cognition Disorders / etiology*
  • Cognition Disorders / metabolism*
  • Cognition Disorders / pathology
  • Diet, High-Fat / adverse effects*
  • Disease Models, Animal
  • Hippocampus / metabolism
  • Hippocampus / pathology
  • MAP Kinase Kinase Kinase 5 / genetics
  • MAP Kinase Kinase Kinase 5 / metabolism*
  • Mice
  • Mice, Knockout
  • NADPH Oxidases / genetics
  • NADPH Oxidases / metabolism
  • Neurons / metabolism
  • Organ Size
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Thyroid Hormones / blood
  • Time Factors
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • White Matter / metabolism
  • White Matter / pathology

Substances

  • Adiponectin
  • Amyloid beta-Peptides
  • RNA, Messenger
  • Thyroid Hormones
  • Tumor Necrosis Factor-alpha
  • NADPH Oxidases
  • MAP Kinase Kinase Kinase 5
  • Map3k5 protein, mouse