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Recognition memory, chlordiazepoxide and rhesus monkeys: some problems and results
Behavioural Brain Research
|June 1, 1980
Summary
Chlordiazepoxide (CDP) did not impair monkeys' performance on a pair comparison task, even at high doses. However, the drug did increase response latencies, suggesting potential effects on mnemonic processing.
Area of Science:
- Neuroscience
- Cognitive Psychology
- Pharmacology
Background:
- The Konorski pair comparison task is a standard method for assessing mnemonic processing in animals.
- Chlordiazepoxide (CDP) is a benzodiazepine anxiolytic with known effects on cognitive function.
- Previous studies have shown CDP impairs performance in pigeons on similar tasks.
Purpose of the Study:
- To investigate the effects of chlordiazepoxide (CDP) on mnemonic processing in monkeys using a pair comparison task.
- To determine if stimulus presentation duration influences CDP's effects on cognitive performance.
- To assess CDP's impact on signal detection performance.
Main Methods:
- Monkeys were trained on a simultaneous pair comparison task involving same/different color stimuli.
- Delays were introduced between stimuli to assess forgetting curves.
- Chlordiazepoxide (CDP) was administered at various doses (up to 80 mg/kg) to evaluate its effects.
- Stimulus presentation times were shortened, and signal detection was assessed in subsequent experiments.
Main Results:
- High doses of chlordiazepoxide (CDP) did not significantly impair percent correct performance on the pair comparison task.
- Response latencies increased with CDP administration, occasionally leading to missed responses.
- No significant disruption in mnemonic processing was observed in monkeys, contrasting with previous findings in pigeons.
Conclusions:
- Chlordiazepoxide (CDP) does not appear to significantly disrupt mnemonic processing in monkeys on this specific pair comparison task.
- Increased response latencies suggest a potential, albeit subtle, effect of CDP on cognitive processing speed or response initiation.
- Further research may be needed to elucidate the precise mechanisms and dose-dependency of CDP's effects on primate cognition.