Pyridostigmine-Induced Neurodegeneration: Role of Neuronal Apoptosis

Abstract

Although pyridostigmine is a highly charged molecule, some reports suggest it can penetrate into the brain. To determine whether the drug can cause neurotoxic damage centrally, pyridostigmine was injected into rats, the animals were sacrificed at intervals after drug administration and brains examined histologically. Using TUNEL staining and electron microscopy, apoptotic brain cell destruction was noted in cerebral cortex and at higher doses, cell damage was also noted in striatum and hippocampus. Pretreatment with atropine prevented pyridostigmine induced brain cell apoptosis, showing the involvement of muscarinic receptors. However, antioxidants did not block pyridostigmine-induced apoptosis suggesting that oxidative mechanisms are not involved. Even up to 30 days after injection of pyridostigmine, apoptotic cell death was still evident in rat cortex. Therefore the cell death process initiated by physostigmine continues long after termination of drug treatment. These observations are important because they implicate physostigmine as a causative factor in the Gulf War Syndrome.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1998
Accession Number
ADA361278

Entities

People

  • Gary E. Isom

Organizations

  • Purdue University

Tags

DTIC Thesaurus Topics

  • Acetylcholinesterases
  • Apoptosis
  • Atropine
  • Biological Staining And Labeling
  • Blood
  • Brain
  • Brain Injuries
  • Cell Physiological Processes
  • Cerebral Cortex
  • Chemistry
  • Electron Microscopy
  • Medical Personnel
  • Microscopy
  • Neurodegeneration
  • Persian Gulf Syndrome
  • Programmed Cell Death
  • Skeletal Muscle

Fields of Study

  • Biology

Readers

  • Immunology and Pathology
  • Neuroscience
  • Toxicology/Environmental Toxicology

Technology Areas

  • Microelectronics