Fadda, Paola, Bedogni, Francesco, Fresu, Alessandra, Collu, Maria, Racagni, Giorgio and Riva, Marco A. 2007. Reduction of corticostriatal glutamatergic fibers in basic fibroblast growth factor deficient mice is associated with hyperactivity and enhanced dopaminergic transmission. Biological Psychiatry 62 (3) , pp. 235-242. 10.1016/j.biopsych.2006.08.003 |
Abstract
Background Basic fibroblast growth factor (FGF2) plays a crucial role during the development of the cerebral cortex. Mice with a knockout of the FGF2 gene have a reduced number of glutamatergic neurons within the deep layers of the cerebral cortex. Methods We used molecular and behavioral analyses to investigate possible alterations in corticostriatal function in FGF2 −/− mice. Results We found that FGF2 deficiency leads to decreased expression of presynaptic markers of integrity for glutamatergic fibers in the striatum, namely the membrane excitatory amino acid transporter 3 (EAAT3) and the vesicular glutamate transporter 1 (VGLUT1). The reduction of corticostriatal glutamatergic function in FGF2 −/− mice is associated with enhanced locomotor activity in a novel environment and increased responsiveness to dopaminergic drugs, such as cocaine or amphetamine. The behavioral alterations of FGF2 −/− can be normalized by injection of a low dose of the dopaminergic agonist apomorphine (.1 mg/kg) that reduces dopamine release by acting on presynaptic receptors. Conclusions Our data demonstrate that FGF2 −/− mice have an increased tone and responsiveness of the dopaminergic system and suggest that these animals might represent a model to study disorders that are characterized by an imbalance between glutamatergic and dopaminergic neurotransmission.
Item Type: | Article |
---|---|
Date Type: | Publication |
Status: | Published |
Schools: | Biosciences |
Publisher: | Elsevier |
ISSN: | 0006-3223 |
Date of Acceptance: | 9 August 2006 |
Last Modified: | 06 Jul 2020 12:02 |
URI: | https://orca.cardiff.ac.uk/id/eprint/133003 |
Citation Data
Cited 18 times in Scopus. View in Scopus. Powered By Scopus® Data
Actions (repository staff only)
Edit Item |