EFFECTS OF VARIOUS CENTRALLY ACTING DRUGS ON FIGHTING BEHAVIOR OF MICE
Fighting episodes were produced in mice by exposing the animals to a mild footshock. This method permitted the objective measurement of the frequency of discrete fighting episodes in fighting pairs of mice. The effects of variations in stimulus intensity were studied and the optimum parameters for p...
Saved in:
Published in | The Journal of pharmacology and experimental therapeutics Vol. 125; no. 1; pp. 28 - 34 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Pharmacology and Experimental Therapeutics
01.01.1959
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Fighting episodes were produced in mice by exposing the animals to a mild footshock. This method permitted the objective measurement
of the frequency of discrete fighting episodes in fighting pairs of mice. The effects of variations in stimulus intensity
were studied and the optimum parameters for producing fighting episodes were determined. A quantal type assay procedure was
devised in an effort to study the effects of centrally active drugs on the frequency of fighting episodes. Compounds were
also studied for their effect in depressing spontaneous motor activity and protecting against maximal electroshock seizures.
Reserpine and the phenothiazines that were tested suppressed fighting episodes only in doses which produced a moderate to
marked degree of motor inactivation. Diphenylhydantoin and phenobarbital were more effective as anticonvulsants than in suppressing
fighting episodes. Of the compounds studied in this battery of tests meprobamate exhibited a particular profile of activity
which differentiated it from any of the other compounds studied. This pattern of activity was characterized by a mild degree
of anticonvulsant activity, a mild depression of spontaneous motor activity and a more pronounced suppression of fighting
episodes. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-3565 1521-0103 |