Huperzine A: Behavioral and Pharmacological Evaluation in Rhesus Monkeys

Abstract

Huperzine A is potentially superior to pyridostigmine bromide as a pretreatment for nerve agent intoxication because it inhibits acetylcholinesterase both peripherally and centrally, unlike pyridostigmine, which acts only peripherally. Using rhesus monkeys, we evaluated the time course of acetylcholinesterase and butyrylcholinesterase inhibition following four different doses of -(-)huperzine A: 5, 10, 20, and 40 ug/kg. Acetylcholinesterase inhibition peaked 30 minutes after intramuscular injection and varied dose dependently, ranging from about 30% to 75%. Subsequently, cognitive-behavioral functioning was also evaluated at each dose of huperzine A using a six-item serial-probe recognition task that assessed attention, motivation, and working memory. The results demonstrate that huperzine A can selectively and reversibly inhibit acetylcholinesterase without cognitive-behavioral side effects, thus warranting further study.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 2008
Accession Number
ADA501469

Entities

People

  • Andrew J. Bonvillain
  • Ashima Saxena
  • Bhupendra P. Doctor
  • Matthew G. Clark
  • Todd M. Myers
  • Wei Sun

Organizations

  • United States Army Medical Research Institute of Chemical Defense

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Acetylcholinesterases
  • Alzheimer Disease
  • Animals
  • Basic Programming Language
  • Biomedical Research
  • Blood
  • Central Nervous System
  • Enzyme Inhibitors
  • Inhibition
  • Monkeys
  • Nerve Agents
  • Primates
  • Reaction Time
  • Rhesus Monkeys
  • Rodents
  • Side Effects
  • Test And Evaluation

Fields of Study

  • Biology

Readers

  • Neurotoxicology
  • Psychological Intervention/Treatment for Stress, Anxiety, PTSD, and Related Emotional and Cognitive Health Symptoms.
  • Toxicology/Environmental Toxicology