Reactions of Methamidophos with Mammalian Cholinesterase,

Abstract

The lethality of methamidophos, a phosphoramidothioate, to rats (i.p. LD50, 15 mg/kg), is similar to that of such potent organophosphate compounds as parathion and paraoxon. Certain distinctive features of its chemical structure, and reported failure of cholinesterase inhibited with methamiodophos to reactivate spontaneously in insects, prompted this study of its reactions with mammalian cholinesterase to determine if the treatment of poisoning requires modification. Atropine (10 mg/kg) or pralidoxime (60 mg/kg) afforded significant protection against lethality from methamidophos (LD50's, 60 + or - 0.4 and 52 + or - 4.9 mg/kg, respectively). Partial spontaneous recovery of inhibited cholinesterase activity was observed. However, a single dose of pralidoxime, given essentially simultaneously with methamidophos, did not hasten the recovery of cholinesterase activity. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 1978
Accession Number
ADA058683

Entities

People

  • Casey P. Robinson
  • Charles R. Crane
  • Donald Beiergrohslein
  • Paul W. Smith

Organizations

  • Federal Aviation Administration

Tags

Communities of Interest

  • Human Systems

DTIC Thesaurus Topics

  • Acetylcholinesterases
  • Atropine
  • Aviation Medicine
  • Blood
  • Central Nervous System
  • Enzymes
  • Health Services
  • Inhibition
  • Lethality
  • Medical Personnel
  • Nervous System
  • Parathion
  • Pesticides
  • Poisoning
  • Recovery
  • Tissues
  • Toxicity

Fields of Study

  • Chemistry

Readers

  • Neurotoxicology
  • Toxicology/Environmental Toxicology