Dissociable effects of histamine H1 antagonists on reaction-time performance in rats

Citation
Aa. Blokland et al., Dissociable effects of histamine H1 antagonists on reaction-time performance in rats, PHARM BIO B, 70(2-3), 2001, pp. 427-436
Citations number
24
Categorie Soggetti
Neurosciences & Behavoir
Journal title
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
ISSN journal
00913057 → ACNP
Volume
70
Issue
2-3
Year of publication
2001
Pages
427 - 436
Database
ISI
SICI code
0091-3057(200110/11)70:2-3<427:DEOHHA>2.0.ZU;2-2
Abstract
The most pronounced side effect of antiallergic histaminergic drugs (H1 ant agonists) is sedation. These effects have been linked with the effects of h istaminergic drugs on central H1 receptors. In the present study, we invest igated the dose-response relationship of different antihistamines on the pe rformance in a reaction-time task that has been developed for rats. The dos e-response relationship of diphenhydramine, cetirizine and terfenadine were examined for the various behavioural measures in this task (i.e., reaction time, motor time, premature responses and number of trials completed). In addition, the effects of scopolamine were assessed to evaluate the choliner gic profile in this task. Diphenhydramine did not reliably affect the react ion time, but increased the motor time and the proportion of premature resp onses, and decreased the number of trials completed in a session. A low dos e of cetirizine decreased the reaction time, whereas an increase in reactio n time was found for the high dose. The motor time was increased after both doses of cetirizine. Terfenadine did not affect the responding of rats in the reaction-time task at the doses tested. The effects of scopolamine were very similar to those of diphenhydramine. The reaction-time task used in t his study was able to dissociate different types of antihistamines on aspec ts of psychomotor function, which were likely to be related to central musc arinic or H1 antagonism. These findings suggest that the reaction-time task may be a sensitive tool for assessing effects of drugs on psychomotor func tion. (C) 2001 Elsevier Science Inc. All rights reserved.