Smoking exacerbates amyloid pathology in a mouse model of Alzheimer's disease

Nat Commun. 2013;4:1495. doi: 10.1038/ncomms2494.

Abstract

Several epidemiological studies have shown that cigarette smoking might alter the incidence of Alzheimer's disease. However, inconsistent results have been reported regarding the risk of Alzheimer's disease among smokers. Previous studies in experimental animal models have reported that administration of some cigarette components (for example, nicotine) alters amyloid-β aggregation, providing a possible link. However, extrapolation of these findings towards the in vivo scenario is not straightforward as smoke inhalation involves a number of other components. Here, we analysed the effect of smoking under more relevant conditions. We exposed transgenic mouse models of Alzheimer's disease to cigarette smoke and analysed the neuropathological alterations in comparison with animals not subjected to smoke inhalation. Our results showed that smoking increases the severity of some abnormalities typical of Alzheimer's disease, including amyloidogenesis, neuroinflammation and tau phosphorylation. Our findings suggest that cigarette smoking may increase Alzheimer's disease onset and exacerbate its features and thus, may constitute an important environmental risk factor for Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / blood
  • Alzheimer Disease / metabolism*
  • Alzheimer Disease / pathology*
  • Amyloid / metabolism*
  • Amyloid beta-Peptides / metabolism
  • Animals
  • Cotinine / blood
  • Disease Models, Animal
  • Glial Fibrillary Acidic Protein / metabolism
  • Gliosis / metabolism
  • Gliosis / pathology
  • Humans
  • Mice
  • Mice, Transgenic
  • Microglia / metabolism
  • Microglia / pathology
  • Nerve Degeneration / metabolism
  • Nerve Degeneration / pathology
  • Phosphorylation
  • Presenilin-1 / metabolism
  • Smoking / metabolism
  • Smoking / pathology*
  • tau Proteins / metabolism

Substances

  • Amyloid
  • Amyloid beta-Peptides
  • Glial Fibrillary Acidic Protein
  • Presenilin-1
  • tau Proteins
  • Cotinine