Literature DB >> 7862837

Development of acute tolerance after oral doses of diazepam and flunitrazepam.

J Ingum1, R Bjørklund, R Volden, J Mørland.   

Abstract

Flunitrazepam (1 and 2 mg), diazepam (10 and 20 mg) or placebo was administered to healthy, male volunteers, and the time course of psychomotor impairment, as indicated by simple and complex choice reaction time and movement time, was studied during a period of 6 h after drug intake. To examine whether acute tolerance developed, the observed performance during decreasing drug plasma concentration was compared to the predicted performance based on kinetic-dynamic modelling of the observed performance during the first 1.5 h after intake when the drug plasma concentrations were increasing or at peak level. Placebo corrections of the test scores were accomplished to adjust for diurnal variation and the possible influence of learning during the test day. After the flunitrazepam treatments, the predictions overestimated the actual performance significantly with respect to simple and choice reaction time at the 6-h session after intake. After the diazepam treatments, however, no significant deviation was detected between predicted and observed performance. The results indicate that acute tolerance develops with respect to impairment of attention demanding performance after medium to large doses of flunitrazepam, and that tolerance is expressed after approximately 4-6 h following intake.

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Year:  1994        PMID: 7862837     DOI: 10.1007/bf02245201

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  22 in total

1.  Pharmacokinetics and pharmacodynamics of oral diazepam: effect of dose, plasma concentration, and time.

Authors:  H Friedman; D J Greenblatt; G R Peters; C M Metzler; M D Charlton; J S Harmatz; E J Antal; E C Sanborn; S F Francom
Journal:  Clin Pharmacol Ther       Date:  1992-08       Impact factor: 6.875

2.  Relationship between drug plasma concentrations and psychomotor performance after single doses of ethanol and benzodiazepines.

Authors:  J Ingum; R Bjørklund; A Bjørneboe; A S Christophersen; E Dahlin; J Mørland
Journal:  Psychopharmacology (Berl)       Date:  1992       Impact factor: 4.530

3.  Acute tolerance to diazepam induced by benzodiazepines.

Authors:  P T Wong; Y L Yoong; M C Gwee
Journal:  Clin Exp Pharmacol Physiol       Date:  1986-01       Impact factor: 2.557

4.  Routes to action in reaction time tasks.

Authors:  C D Frith; D J Done
Journal:  Psychol Res       Date:  1986

5.  Profile of acute tolerance to three sedative anxiolytics.

Authors:  E H Ellinwood; M Linnoila; M E Easler; D W Molter
Journal:  Psychopharmacology (Berl)       Date:  1983       Impact factor: 4.530

Review 6.  Understanding the dose-effect relationship: clinical application of pharmacokinetic-pharmacodynamic models.

Authors:  N H Holford; L B Sheiner
Journal:  Clin Pharmacokinet       Date:  1981 Nov-Dec       Impact factor: 6.447

7.  Thyrotropin-releasing hormone antagonism of ethanol inebriation.

Authors:  H Knutsen; L O Dolva; S Skrede; R Bjørklund; J Mørland
Journal:  Alcohol Clin Exp Res       Date:  1989-06       Impact factor: 3.455

8.  Relative amnesic actions of diazepam, flunitrazepam and lorazepam in man.

Authors:  K A George; J W Dundee
Journal:  Br J Clin Pharmacol       Date:  1977-02       Impact factor: 4.335

9.  Benzodiazepine pharmacodynamics: evidence for biophase rate limiting mechanisms.

Authors:  E H Ellinwood; A M Nikaido; D G Heatherly; T D Bjornsson
Journal:  Psychopharmacology (Berl)       Date:  1987       Impact factor: 4.530

10.  Benzodiazepine concentrations in brain directly reflect receptor occupancy: studies of diazepam, lorazepam, and oxazepam.

Authors:  D J Greenblatt; V H Sethy
Journal:  Psychopharmacology (Berl)       Date:  1990       Impact factor: 4.530

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Authors:  Jørgen G Bramness; Svetlana Skurtveit; Jørg Mørland
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  4 in total

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