Abstract |
Forty-eight normal subjects had sleep recordings and multiple sleep latency tests (an EEG measure of sleepiness) before and after a 12-hour shift of sleep-wake schedule. After 2 baseline days, subjects postponed sleep until 12:00 noon, then for three 24-hour periods were in bed from 12:00 noon until 8:00 PM. Treatment in parallel groups were administered before shifted sleeps. Sleep disturbance was greatest in the last quarter of shifted nights (6.5 to 8.5 hours after medication). Subjects taking placebo showed significant sleep loss on shifted nights and increased sleepiness the next day. Triazolam, 0.5 mg, reversed the sleep loss and consequent daytime sleepiness associated with the shifted sleep schedule. Triazolam, 0.25 mg, was not significantly better than placebo. In a dose-related manner, flurazepam mitigated the insomnia, but carryover effects left both dose groups more sleepy than were the placebo control subjects. Whether these laboratory results are applicable to clinically occurring forms of transient insomnia remains to be seen.
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Authors | W F Seidel, S A Cohen, N G Bliwise, T Roth, W C Dement |
Journal | Clinical pharmacology and therapeutics
(Clin Pharmacol Ther)
Vol. 40
Issue 3
Pg. 314-20
(Sep 1986)
ISSN: 0009-9236 [Print] United States |
PMID | 3742936
(Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
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Topics |
- Adult
- Circadian Rhythm
(drug effects)
- Dose-Response Relationship, Drug
- Double-Blind Method
- Flurazepam
(therapeutic use)
- Humans
- Sleep Initiation and Maintenance Disorders
(drug therapy)
- Triazolam
(therapeutic use)
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