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Impairments of social behavior and memory after neonatal gastrin-releasing peptide receptor blockade in rats: Implications for an animal model of neurodevelopmental disorders.

Authors: Presti-Torres, J  De Lima, MN  Scalco, FS  Caldana, F  Garcia, VA  Guimaraes, MR  Schwartsmann, G  Roesler, R  Schroder, N 
Citation: Presti-Torres J, etal., Neuropharmacology. 2007 Mar;52(3):724-32. Epub 2006 Nov 13.
Pubmed: (View Article at PubMed) PMID:17097693
DOI: Full-text: DOI:10.1016/j.neuropharm.2006.09.020

The gastrin-releasing peptide receptor (GRPR) has been implicated in central nervous system (CNS) diseases, including neurodevelopmental disorders associated with autism. In the present study we examined the effects of GRPR blockade during the neonatal period on behavioral measures relevant to animal models of neurodevelopmental disorders. Male Wistar rats were given an intraperitoneal (i.p.) injection of either saline (SAL) or the GRPR antagonist [D-Tpi(6), Leu(13) psi(CH(2)NH)-Leu(14)] bombesin (6-14) (RC-3095; 1 or 10mg/kg) twice daily for 10days from postnatal days (PN) 1 to 10. Animals treated with RC-3095 showed pronounced deficits in social interaction when tested at PN 30-35 and impaired 24-h retention of memory for both novel object recognition (NOR) and inhibitory avoidance (IA) tasks tested at PN 60-71. Neither short-term memory tested 1.5h posttraining nor open field behavior were affected by neonatal GRPR blockade. The implications of the findings for animal models of neurodevelopmental disorders are discussed.

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RGD Object Information
RGD ID: 1641840
Created: 2007-08-23
Species: All species
Last Modified: 2007-08-23
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.