TY - JOUR
T1 - Bombesin-induced behavioural changes
T2 - Antagonism by neuroleptics
AU - Merali, Z.
AU - Johnston, S.
AU - Zalcman, S.
N1 - Funding Information:
The expert technical assistance of Mr. H. van den Bergen in the development of the computer-assisted behavioural monitoring apparatus is greatly appreciated. The authors wish to thank Dr. D. Couiombe for statistical programs and Dr. G. Fouriezos for stereotaxic assistance. This work was supported by the Ontario Mental Health Foundation and the Natural Sciences and Engineering Research Council of Canada.
PY - 1983
Y1 - 1983
N2 - Adult male Sprague-Dawley rats were administered bombesin (BN) intracerebroventricularly (ICV), at a dose of 0.001, 0.01, 0.1, or 1.0 μg, and the behavioural effects monitored longitudinally across time for up to 24 hr. Administration of BN significantly increased the locomotor, rearing and grooming activity at all doses. The time-course of behavioural activation was dose-related (lasting up to 2.5 hr). There was no significant difference in the behavioural response of rats receiving the BN doses in an ascending or descending order. To test the effects of dopamine receptor blockade on the BN-induced behavioural changes, groups of animals were treated with fluphenazine or haloperidol (0.1 to 2.5 mg/kg, IP) 30 min prior to BN (1 μg, ICV) administration. The results revealed that the neuroleptics could effectively antagonize the BN-induced activation of locomotor, rearing and grooming activity. These data are concordant with the view that centrally administered BN stimulates spontaneous exploratory and grooming behaviours in rats, in a time- and dose-related manner. Furthermore, since neuroleptics block these effects, it remains possible that the BN-induced behavioural changes may be mediated, at least in part, through the dopaminergic system(s).
AB - Adult male Sprague-Dawley rats were administered bombesin (BN) intracerebroventricularly (ICV), at a dose of 0.001, 0.01, 0.1, or 1.0 μg, and the behavioural effects monitored longitudinally across time for up to 24 hr. Administration of BN significantly increased the locomotor, rearing and grooming activity at all doses. The time-course of behavioural activation was dose-related (lasting up to 2.5 hr). There was no significant difference in the behavioural response of rats receiving the BN doses in an ascending or descending order. To test the effects of dopamine receptor blockade on the BN-induced behavioural changes, groups of animals were treated with fluphenazine or haloperidol (0.1 to 2.5 mg/kg, IP) 30 min prior to BN (1 μg, ICV) administration. The results revealed that the neuroleptics could effectively antagonize the BN-induced activation of locomotor, rearing and grooming activity. These data are concordant with the view that centrally administered BN stimulates spontaneous exploratory and grooming behaviours in rats, in a time- and dose-related manner. Furthermore, since neuroleptics block these effects, it remains possible that the BN-induced behavioural changes may be mediated, at least in part, through the dopaminergic system(s).
KW - Behaviour
KW - Behavioural antagonism by neuroleptics
KW - Bombesin
KW - Fluphenazine
KW - Haloperidol
KW - Rats
UR - https://www.scopus.com/pages/publications/0021038897
U2 - 10.1016/0196-9781(83)90020-7
DO - 10.1016/0196-9781(83)90020-7
M3 - Article
C2 - 6657513
AN - SCOPUS:0021038897
SN - 0196-9781
VL - 4
SP - 693
EP - 697
JO - Peptides
JF - Peptides
IS - 5
ER -