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1.
Fundam Clin Pharmacol ; 5(9): 797-806, 1991.
Article in English | MEDLINE | ID: mdl-1794835

ABSTRACT

The purpose of this study was to investigate the interaction between 40 mg afloqualone, a new centrally acting muscle relaxant and 0.5 g/kg ethanol using a double-blind three-way cross-over trial in which subjects were each given afloqualone with ethanol, ethanol alone and afloqualone alone. We first compared the effects of 40 mg oral afloqualone and 15 mg diazepam (considered as a reference drug) on the psychomotor and cognitive performance and muscular relaxation of 12 healthy male volunteers. Performance was assessed by six objective tests and eight visual analogue self-rating scales. All the above treatments were separated by a 2-week interval. Volunteers performed the objective tests 1 h after drug ingestion, and the self-rating scale evaluations before drug intake and 1, 3.5, 6 and 8 h thereafter. Afloqualone impaired psychomotor performance less than diazepam as shown by the number of correct answers in the digit symbol cancellation test and the time needed to complete this test. However, the measurement of the frontalis muscle action potential showed that the muscle relaxant activity of 40 mg afloqualone was equivalent to that of 15 mg diazepam. Furthermore, afloqualone given at an effective relaxant dose did not enhance the effects of a single dose of ethanol which predominated on either psychomotor performance or subjective feelings.


Subject(s)
Ethanol/pharmacology , Muscle Relaxants, Central/pharmacology , Psychomotor Performance/drug effects , Quinazolines/pharmacology , Administration, Oral , Adolescent , Adult , Diazepam/pharmacology , Double-Blind Method , Drug Interactions , Ethanol/administration & dosage , Humans , Male , Muscle Relaxation/drug effects , Quinazolines/administration & dosage
2.
Int Clin Psychopharmacol ; 5(1): 57-64, 1990 Jan.
Article in English | MEDLINE | ID: mdl-2332608

ABSTRACT

A double-blind crossover design was used to evaluate the effect of two different formulations of prazepam, on motor and cognitive functions and subjective symptoms. Ten healthy male volunteers received 20 mg of prazepam both in tablet and liquid (as drops) formulation, separated by a 1 week interval. All subjects completed a battery of 9 performance tests 2.25 h and 4.75 h after drug intake (corresponding to the times of peak plasma concentration). They also rated themselves on eight visual analogue scales before, 2 h, 4.5 h and 8 h following drug intake. A significant difference between liquid drops and tablets was demonstrated in 4 of the 9 performance tests and 2 of the 8 items of the self rating scales. These results suggest that a single dose of prazepam administered in liquid drop form exhibits greater sedative properties than the same dose administered as tablets in healthy volunteers, probably as a result of more rapid absorption.


Subject(s)
Cognition/drug effects , Prazepam/pharmacology , Prodrugs/pharmacokinetics , Psychomotor Performance/drug effects , Chemistry, Pharmaceutical , Double-Blind Method , Humans , Male , Prazepam/pharmacokinetics , Reference Values
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