EFFECTS OF DAYTIME ADMINISTRATION OF ZOLPIDEM AND TRIAZOLAM ON PERFORMANCE

Citation
Nj. Wesensten et al., EFFECTS OF DAYTIME ADMINISTRATION OF ZOLPIDEM AND TRIAZOLAM ON PERFORMANCE, Aviation, space, and environmental medicine, 67(2), 1996, pp. 115-120
Citations number
21
Categorie Soggetti
Medicine Miscellaneus
ISSN journal
00956562
Volume
67
Issue
2
Year of publication
1996
Pages
115 - 120
Database
ISI
SICI code
0095-6562(1996)67:2<115:EODAOZ>2.0.ZU;2-J
Abstract
Background and Hypotheses: The performance-impairing effects of the sh ort,acting imidazopyridine zolpidem (Ambien) were compared to those of triazolam (Halcion) following daytime administration. Methods: There were 70 male subjects who received oral zolpidem (5, 10 or 15 mg), tri azolam (0.125, 0.25 or 0.5 mg), or placebo at 1000 hours. Performance on Logical Reasoning, Column Addition, and Repeated Acquisition (compu terized tasks of the Waiter Reed Performance Assessment Battery) was a ssessed prior to drug administration, then at 1.5 h (estimated time of peak drug effects) and 6 h post-administration. Results: Number of tr ials completed (TC) and response time (RT) for correct answers on the Logical Reasoning (LR) and Column Addition (CA) tasks (expressed as pe rcentage of pre-drug performance) were impaired by triazolam 0.5 mg (T C = 76.6 and 67.4% for LR and CA; RT = 182.1 and 127.0% for LR, CA) an d zolpidem 15 mg (TC = 87.0 and 75.8% for LR, CA; RT = 198.7 and 161.8 % for LR, CA) at 1.5 h post-administration. By 6 h post-administration , drug effects on performance had dissipated. Other doses of triazolam and zolpidem failed to impair performance significantly. Conclusions: These results indicate substantial performance impairment at estimate d peak plasma concentrations of both triazolam and zolpidem, at or nea r doses coinciding with somnogenic efficacy. Thus, the present results suggest no advantage of benzodiazepine receptor-subtype-specific drug s (e.g., zolpidem). Rather, these results suggest that the performance -impairing effects of both drugs are dose-dependent and functionally c oupled to their sleep-inducing properties.