2-deoxyglucose induces beta-APP overexpression, tau hyperphosphorylation and expansion of the trans-part of the Golgi complex in rat cerebral cortex

Acta Neurobiol Exp (Wars). 2004;64(4):491-502. doi: 10.55782/ane-2004-1533.

Abstract

The effects of a single intraperitoneal injection of a non-metabolizable glucose analog 2-deoxyglucose (2-DG, 500 mg/kg) on the levels of beta-APP expression, and phosphorylated and unphosphorylated tau protein in the rat cerebral cortex were investigated. The effects of 2-DG on the ultrastructure of cortical neurons with particular emphasis on the morphology of the Golgi apparatus, and on brain bioenergetics assessed by in vivo 31P-MRS technique were also evaluated. Seven and a half hours after injection of 2-deoxyglucose a significant increase in brain cortex beta-APP expression, increased tau phosphorylation, and a marked relative expansion of the trans- part of the Golgi intracellular secretory pathway in cortical neurons has been found. The changes of beta-APP expression and tau phosphorylation appeared within 1 h after 2-DG application and continued for at least 24 h. However, brain 31P resonance spectra remained unchanged for up to 7.5 h after 2-DG. It is suggested that the increase of beta-APP expression represents a response of brain tissues to 2-DG-evoked biochemical stress, while tau hyperphosphorylation and the change in Golgi morphology may be secondary phenomena.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Protein Precursor / metabolism*
  • Analysis of Variance
  • Animals
  • Antimetabolites / toxicity
  • Cell Count / methods
  • Cerebral Cortex / cytology
  • Cerebral Cortex / drug effects*
  • Deoxyglucose / toxicity*
  • Golgi Apparatus / drug effects*
  • Golgi Apparatus / metabolism
  • Golgi Apparatus / ultrastructure
  • Immunohistochemistry / methods
  • Magnetic Resonance Spectroscopy / methods
  • Male
  • Microscopy, Electron, Transmission / methods
  • Neurons / metabolism
  • Neurons / ultrastructure
  • Phosphorylation / drug effects
  • Rats
  • Rats, Wistar
  • Time Factors
  • tau Proteins / metabolism*

Substances

  • Amyloid beta-Protein Precursor
  • Antimetabolites
  • tau Proteins
  • Deoxyglucose