1. Glutamatergic ionotropic blockade within accumbens disrupts working memory and might alter the endocytic machinery in rat accumbens and prefrontal cortex.
- Author
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Baiardi G, Ruiz AM, Beling A, Borgonovo J, Martínez G, Landa AI, Sosa MA, and Gargiulo PA
- Subjects
- 2-Amino-5-phosphonovalerate analogs & derivatives, 2-Amino-5-phosphonovalerate pharmacology, Adaptor Protein Complex 2 drug effects, Adaptor Protein Complex 2 metabolism, Animals, Behavior, Animal drug effects, Behavior, Animal physiology, Endocytosis drug effects, Glutamine metabolism, Immunoblotting, Male, Motor Activity drug effects, Motor Activity physiology, Nucleus Accumbens drug effects, Prefrontal Cortex drug effects, Quinoxalines pharmacology, Rats, Receptors, N-Methyl-D-Aspartate antagonists & inhibitors, Endocytosis physiology, Excitatory Amino Acid Antagonists pharmacology, Nucleus Accumbens metabolism, Prefrontal Cortex metabolism
- Abstract
Effects of blocking N-methyl-D-aspartic acid (NMDA) and non-NMDA glutamatergic receptors on performance in the hole board test was studied in male rats bilaterally cannulated into the nucleus accumbens (Acc). Rats, divided into 5 groups, received either 1 microl injections of saline, (+/-) 2-amino-7-phosphonoheptanoic acid (AP-7) (0.5 or 1 microg) or 2,3-dioxo-6-nitro-1,2,3,4,tetrahydrobenzo-(f)quinoxaline-7-sulphonamide disodium (NBQX, 0.5 or 1 microg) 10 min before testing. An increase by AP-7 was observed in ambulatory movements (0.5 microg; p < 0.05), non-ambulatory movements and number of movements (1 microg; p < 0.05); sniffing and total exploration (1 microg; p < 0.01). When holes were considered in order from the first to the fifth by the number of explorations, the most visited holes (first and second) of the AP-7 group were significantly higher than the corresponding holes of saline group (p < 0.05 for 0.5 microg and p < 0.001 for 1 microg). When the second hole was compared with the first of his group, a difference was only observed in the AP-7 1 microg group (p < 0.001). Increasing differences between the other holes and the first were observed by drug treatment. At molecular level, it was observed that AP-7 induced an increase of the coat protein AP-2 expression in Acc, but not AP-180 neither the synaptic protein synaptophysin. The increase of AP-2 was also observed in the medial prefrontal cortex by the action of AP-7 but not NBQX. We conclude that NMDA glutamatergic blockade might induce an activation of the endocytic machinery into the Acc, leading to stereotypies and perseverations, lacking cortical intentional direction.
- Published
- 2007
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