Previous studies have demonstrated that Lister hooded rats will exhibi
t characteristic bursts of locomotion when exposed to a 20-kHz acousti
c stimulus; this ultrasound-induced locomotion has been suggested as a
potential model for panic attacks. Although ultrasound presentation r
arely induces convulsions, the locomotor bursts exhibited resemble pn-
convulsant running. The present studies examined the interactions betw
een strychnine treatment and experimenter-presented ultrasounds on beh
aviour in male Lister hooded rats. Strychnine was selected because it
is a potent and effective convulsion-inducing agent which is not known
to induce anxiety in humans. Behaviour in a circular arena (75 cm dia
meter) was observed live, videotaped and traced electronically. In exp
eriments 1 and 2, moderate (60 s) or relatively brief (15 s) exposure
to an ultrasound stimulus (20 kHz, 98 dB, SPL) typically resulted in 5
- to 10-s bursts of locomotion in saline-treated subjects; strychnine
treatment (0.5, 0.7, 1.0 mg/kg, injected IP, 10 min prior to testing)
significantly increased this ultrasound-induced locomotion in a dose-d
ependent manner. Experiment 3 demonstrated that the strychnine enhance
ment of the ultrasound response was not different in naive animals whe
n compared to those subjects which had received occasional strychnine
and/or ultrasound treatment previously. Experiment 3 also demonstrated
that strychnine treatment can cause at least modest running in subjec
ts exposed to a 2 kHz tone (96 dB SPL). In experiment 4, exposure to t
he 20 kHz, 98 dB ultrasound stimulus for a much longer period, 9 min,
resulted in irregular cycles of bursts of locomotion, followed immedia
tely by periods of relative inactivity in saline-treated animals; appr
oximately 10% of these subjects exhibited tonic-clonic convulsions. No
convulsions occurred in strychnine-treated subjects during the period
10-20 min post-injection in the absence of ultrasound exposure, in co
ntrast, the frequency of occurrence of convulsions in strychnine-treat
ed subjects (10-20 min post-injection) exposed to the ultrasound stimu
lus was greater than 50%; these convulsions typically occurred at the
end of a locomotor burst. The results of the present studies suggest t
hat then may be a relationship between ultrasound-induced locomotor bu
rsts and convulsant activity.