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Sex differences in psychotomimetic-induced behaviours in rats.

Andrea Gogos, Snezana Kusljic, Shane J Thwaites, Maarten Van den Buuse

Behavioural brain research March 30, 2017 DOI: 10.1016/j.bbr.2017.01.028 via PubMed

Summary

AI-generated from the abstract

Acute amphetamine caused greater distance traveled (locomotor hyperactivity) in female rats than in male rats, while phencyclidine-induced locomotor hyperactivity was similar in both sexes. No sex differences were observed in amphetamine- or phencyclidine-induced disruption of prepulse inhibition. Male rats showed an increased startle response after amphetamine. These findings suggest that sensitivity to amphetamine, but not phencyclidine, differs between male and female rats, and this sex difference is selective to locomotor hyperactivity and startle, not prepulse inhibition.

Study at a glance

Characteristics Animal model study Peer reviewed
Population Adult male and female Sprague-Dawley rats
Interventions Amphetamine Phencyclidine
Duration Acute
Keywords Amphetamine Female Locomotor hyperactivity Phencyclidine Prepulse inhibition
Key finding Sensitivity to amphetamine, but not phencyclidine, differs between male and female rats, and this sex difference is selective to locomotor hyperactivity and startle, but not prepulse inhibition.

Abstract

Animal model studies using equal numbers of males and females are sparse in psychiatry research. Given the marked sex differences observed in psychiatric disorders, such as schizophrenia, using both males and females in research studies is an important requirement. Thus the aim of this study was to examine sex differences in psychotomimetic-induced behavioural deficits relevant to psychosis. We therefore compared the acute effect of amphetamine or phencyclidine on locomotor activity and prepulse inhibition in adult male and female Sprague-Dawley rats. The results of this study were that: (1) amphetamine-induced distance travelled was greater in female rats than in male rats, (2) phencyclidine-induced locomotor hyperactivity was similar in male and female rats; (3) there were no sex differences in amphetamine- or phencyclidine-induced disruption of prepulse inhibition; (4) male rats had an increased startle response after amphetamine. These findings suggest that sensitivity to amphetamine, but not phencyclidine, differs between male and female rats, and that this sex difference is selective to locomotor hyperactivity and startle, but not prepulse inhibition. This study used two widely-used, validated preclinical assays relevant to psychosis; the results of this study have implications for psychiatry research, particularly for disorders where marked sex differences in onset and symptomology are observed.

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