Evidence of neuronal oxidative damage in Alzheimer's disease

Am J Pathol. 1996 Jul;149(1):21-8.


Oxidative stress has been proposed as a pathogenetic mechanism in Alzheimer's disease. One mechanism of oxidative damage is the nitration of tyrosine residues in proteins, mediated by peroxynitrite breakdown. Peroxynitrite, a reaction product of nitric oxide and superoxide radicals, has been implicated in N-methyl-D-aspartate receptor-mediated excitotoxic damage. Reported evidence of oxidative stress in Alzheimer's disease includes increased iron, alterations in protective enzymes, and markers of oxidative damage to proteins and lipids. In this report, we demonstrate the presence of nitrotyrosine in neurofibrillary tangles of Alzheimer's disease. Nitrotyrosine was not detected in controls lacking neurofibrillary tangles. Immunolabeling was demonstrated to be specific nitrotyrosine in a series of control experiments. These observations link oxidative stress with a key pathological lesion of Alzheimer's disease, the neurofibrillary tangle, and demonstrate a pathogenetic mechanism in common with the other major neurodegenerative diseases of aging, Parkinson's disease and amyotrophic lateral sclerosis. These findings further implicate nitric oxide expression and excitotoxicity in the pathogenesis of cell death in Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / etiology
  • Alzheimer Disease / pathology*
  • Alzheimer Disease / physiopathology
  • Antibodies, Monoclonal
  • Cerebral Cortex / pathology
  • Child, Preschool
  • Hippocampus / pathology
  • Humans
  • Immunohistochemistry
  • Infant, Newborn
  • Middle Aged
  • Neurofibrillary Tangles / pathology
  • Neurons / pathology*
  • Neurons / physiology
  • Oxidative Stress / physiology*
  • Tyrosine / analogs & derivatives*
  • Tyrosine / analysis


  • Antibodies, Monoclonal
  • Tyrosine