Dependence potential of zopiclone studied in monkeys

Int Pharmacopsychiatry. 1982:17 Suppl 2:216-27.

Abstract

In gross behavioral observation the minimum effective dose of zopiclone was intravenously 0.06-0.25 mg/kg and intragastrically 1-4 mg/kg in rhesus monkeys. Zopiclone suppressed barbital withdrawal signs of rhesus monkeys at a single dose of 16 mg/kg or more. The suppressing effect of zopiclone 32 mg/kg i.g. was comparable to diazepam 8 mg/kg. Crab-eating monkeys treated with zopiclone at doses up to 32 mg/kg twice daily for up to 8 weeks manifested intermediate-grade signs upon withdrawal (i.e., less severe than after treatment with diazepam and similar to nitrazepam). Zopiclone was self-administered by rhesus monkeys relatively frequently by the intravenous route; the infrequent intragastric rate was similar to or slightly higher than with diazepam.

MeSH terms

  • Administration, Oral
  • Animals
  • Azabicyclo Compounds
  • Barbital / pharmacology
  • Diazepam / pharmacology
  • Female
  • Humans
  • Hypnotics and Sedatives / pharmacology*
  • Infusions, Parenteral
  • Macaca fascicularis
  • Macaca mulatta
  • Male
  • Nitrazepam / pharmacology
  • Piperazines / pharmacology*
  • Self Administration
  • Substance Withdrawal Syndrome / etiology
  • Substance-Related Disorders / etiology*

Substances

  • Azabicyclo Compounds
  • Hypnotics and Sedatives
  • Piperazines
  • zopiclone
  • Barbital
  • Nitrazepam
  • Diazepam