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Co-activation of glutamate and dopamine receptors within the nucleus accumbens is required for spatial memory consolidation in mice

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Abstract

Rationale

The nucleus accumbens receives glutamatergic and dopaminergic inputs converging onto common dendrites. Recent behavioral data demonstrated that intra-accumbens administrations of either glutamate or dopamine (DA) antagonist impair spatial memory consolidation. Thus, also based on the biochemical and molecular findings demonstrating interactions among the different receptors subtypes for glutamate and dopamine, it is conceivable that memory consolidation within this structure might be modulated by glutamate–dopamine receptor interactions.

Objectives

The purpose of this study was to examine the effects of intra-accumbens co-administrations of glutamate and DA antagonists on the consolidation of spatial information.

Methods

On day 1, CD1 male mice were placed in an open field containing five different objects and immediately after three sessions of habituation the animals were injected intra-accumbens with either vehicle or low doses of the N-methyl-d-aspartate (NMDA; AP-5 50 ng/side), the alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA; DNQX 5 ng/side), the D1 (SCH23390 12.5 ng/side) and the D2 (sulpiride 25 ng/side) antagonists that were ineffective alone in disrupting object displacement. Separate groups were then focally injected with a combination of one of the glutamate antagonists with one of the dopamine antagonists. Twenty-four hours later, the ability of mice to discriminate object displacement was assessed.

Results

Controls and mice injected with ineffective doses of the NMDA, the AMPA, the D1 or the D2 antagonists were always able to react to the object displacement. On the contrary, the groups administered with the different combinations (AP-5 and SCH23390, AP-5 and sulpiride, DNQX and SCH23390, DNQX and sulpiride) of glutamate and dopamine antagonists did not discriminate the spatial change.

Conclusions

These results demonstrate that glutamate–dopamine receptor interactions within the accumbens are essential for the consolidation process of spatial information.

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References

  • Ariano MA, Larson ER, Noblett KL, Sibley DR, Levine MS (1997) Coexpression of striatal dopamine receptor subtypes and excitatory amino acid subunits. Synapse 26:400–414

    Google Scholar 

  • Bardgett ME, Henry JD (1999) Locomotor activity and accumbens Fos expression driven by ventral hippocampal stimulation require D1 and D2 receptors. Neuroscience 94:59–70

    Google Scholar 

  • Bourtchouladze R, Abel T, Berman N, Gordon R, Lapidus K, Kandel ER (1998) Different training procedures recruit either one or two critical periods for contextual memory consolidation, each of which requires protein synthesis and PKA. Learn Mem 5:365–374

    Google Scholar 

  • Cepeda C, Levine MS (1998) Dopamine and N-methyl-d-aspartate receptor interactions in the neostriatum. Dev Neurosci 20:1–18

    Google Scholar 

  • Cepeda C, Buchwald NA, Levine MS (1993) Neuromodulatory actions of dopamine in the neostriatum are dependent upon the excitatory amino acid receptor subtypes activated. Proc Natl Acad Sci U S A 90:9576–9580

    Google Scholar 

  • Chao SZ, Lu W, Lee HK, Huganir RL, Wolf ME (2002) D(1) dopamine receptor stimulation increases GluR1 phosphorylation in postnatal nucleus accumbens cultures. J Neurochem 81:984–992

    Google Scholar 

  • Coccurello R, Adriani W, Oliverio A, Mele A (2000) Effect of intra-accumbens dopamine receptor agents on reactivity to spatial and non-spatial changes in mice. Psychopharmacology 152:189–199

    Google Scholar 

  • Das S, Grunert M, Williams L, Vincent SR (1997) NMDA and D1 receptors regulate the phosphorylation of CREB and the induction of c-fos in striatal neurons in primary culture. Synapse 25:227–233

    Google Scholar 

  • De Leonibus E, Costantini VJA, Castellano C, Ferretti V, Oliverio A, Mele A (2003) Distinct roles of the different ionotropic glutamate receptors within the nucleus accumbens in passive-avoidance learning and memory in mice. Eur J Neurosci 18:2365–2373

    Google Scholar 

  • Dudman JT, Eaton ME, Rajadhyaksha A, Macias W, Taher M, Barczak A, Kameyama K, Huganir R, Konradi C (2003) Dopamine D1 receptors mediate CREB phosphorylation via phosphorylation of the NMDA receptor at Ser897-NR1. J Neurochem 87:922–934

    Google Scholar 

  • Floresco SB, Blaha CD, Yang CR, Phillips AG (2001) Modulation of hippocampal and amygdala-evoked activity of nucleus accumbens neurons by dopamine: cellular mechanisms of input selection. J Neurosci 21:2851–2860

    CAS  PubMed  Google Scholar 

  • Franklin BJ, Paxinos G (1997) The mouse brain in stereotaxic coordinates. Academic Press, San Diego

    Google Scholar 

  • Gal G, Joel D, Gusak O, Feldon J, Weiner I (1997) The effects of electrolytic lesion to the shell subterritory of the nucleus accumbens on delayed non-matching-to-sample and four-arm baited eight-arm radial-maze tasks. Behav Neurosci 111:92–103

    Google Scholar 

  • Greengard P, Allen PB, Nairn AC (1999) Beyond the dopamine receptor: the DARPP-32/protein phosphatase-1 cascade. Neuron 23:435–447

    Google Scholar 

  • Groenewegen HJ, Wright CI, Beijer AV, Voorn P (1999) Convergence and segregation of ventral striatal inputs and outputs. Ann NY Acad Sci 877:49–63

    Google Scholar 

  • Hernandez PJ, Sadeghian K, Kelley AE (2002) Early consolidation of instrumental learning requires protein synthesis in the nucleus accumbens. Nat Neurosci 5:1327–1331

    Google Scholar 

  • Maldonado-Irizarry CS, Kelley AE (1995) Excitatory amino acid receptors within nucleus accumbens subregions differentially mediate spatial learning in the rat. Behav Pharmacol 6:527–539

    Google Scholar 

  • McGaugh JL (2000) Memory—a century of consolidation. Science 287:248–251

    Google Scholar 

  • Mele A, Avena M, Roullet P, De Leonibus E, Mandillo S, Sargolini F, Coccurello R, Oliverio A (2004) Nucleus accumbens and dopamine receptors in the consolidation of spatial memory. Behav Pharmacol 15:423–431

    Google Scholar 

  • Mulder AB, Manshanden I, Vos PE, Wolterink G, van Ree JM, Lopes da Silva FH (1996) Modifications in glutamatergic transmission after dopamine depletion of the nucleus accumbens. A combined in vivo/in vitro electrophysiological study in the rat. Neuroscience 72:1009–1021

    Google Scholar 

  • Pennartz CMA, Groenewegen HJ, Lopes de Silva FH (1994) The nucleus accumbens as a complex of functionally distinct neuronal ensembles: an integration of behavioral, elettrophysiological and anatomical data. Prog Neurobiol 42:719–761

    CAS  PubMed  Google Scholar 

  • Poucet B (1989) Object exploration, habituation, and response to spatial change in rats following septal or medial frontal cortical damage. Behav Neurosci 103:1009–1016

    Article  CAS  PubMed  Google Scholar 

  • Roullet P, Sargolini F, Oliverio A, Mele A (2001) NMDA and AMPA antagonist infusions into the ventral striatum impair different steps of spatial information processing in a non associative task in mice. J Neurosci 21:2143–2149

    Google Scholar 

  • Sargolini F, Roullet P, Oliverio A, Mele A (1999) Effects of lesions to the glutamatergic afferents to the nucleus accumbens in the modulation of reactivity to spatial and non-spatial novelty in mice. Neuroscience 93:855–867

    Google Scholar 

  • Sargolini F, Florian C, Oliverio A, Mele A, Roullet P (2003a) Differential involvement of NMDA and AMPA receptors within the nucleus accumbens in consolidation of information necessary for place navigation and guidance strategy of mice. Learn Mem 10:285–292

    Google Scholar 

  • Sargolini F, Roullet P, Oliverio A, Mele A (2003b) Effects of intra-accumbens focal administrations of glutamate antagonists on object recognition memory in mice. Behav Brain Res 138:153–163

    Google Scholar 

  • Schacter GB, Yang CR, Innis NK, Mogenson GJ (1989) The role of the hippocampal–nucleus accumbens pathway in radial-arm maze performance. Brain Res 494:339–349

    Google Scholar 

  • Sesack SR, Pickel VM (1990) In the rat medial nucleus accumbens, hippocampal and catecholaminergic terminals converge on spiny neurons and are in apposition to each other. Brain Res 527:266–279

    Article  CAS  PubMed  Google Scholar 

  • Sesack SR, Carr DB, Omelchenko N, Pinto A (2003) Anatomical substrate for glutamate–dopamine interactions—evidence for specificity of connections and extrasynaptic actions. Ann NY Acad Sci 1003:36–52

    Google Scholar 

  • Setlow B (1997) The nucleus accumbens and learning and memory. J Neurosci Res 49:515–521

    Google Scholar 

  • Setlow B, McGaugh JL (1998) Sulpiride infused into the nucleus accumbens posttraining impairs memory of spatial water maze training. Behav Neurosci 112:603–610

    Google Scholar 

  • Smith AD, Bolam JP (1990) The neural network of the basal ganglia as revealed by the study of synaptic connections of identified neurones. Trends Neurosci 13:259–265

    Google Scholar 

  • Smith-Roe SL, Kelley AE (2000) Coincident activation of NMDA and dopamine D1 receptors within the nucleus accumbens core is required for appetitive instrumental learning. J Neurosci 22:1063–1071

    Google Scholar 

  • Smith-Roe SL, Sadeghian K, Kelley AE (1999) Spatial learning and performance in the radial arm maze is impaired after N-methyl-d-aspartate (NMDA) receptor blockade in striatal subregions. Behav Neurosci 113:703–717

    Google Scholar 

  • Thinus-Blanc C, Durup M, Poucet B (1992) The spatial parameters encoded by hamsters during exploration: a further study. Behav Processes 26:43–57

    Google Scholar 

  • Usiello A, Sargolini F, Roullet P, Ammassari-Teule M, Passino E, Oliverio A, Mele A (1998) N-Methyl-d-aspartate receptors in the nucleus accumbens are involved in detection of spatial novelty in mice. Psychopharmacology 137:175–183

    Google Scholar 

  • Wang LY, Salter MW, MacDonald JF (1991) Regulation of kainate receptors by cAMP-dependent protein kinase and phosphatases. Science 253:1132–1135

    Google Scholar 

  • Wolf ME, Sun X, Mangiavacchi S, Chao SZ (2004) Psychomotor stimulants and neuronal plasticity. Neuropharmacology 47:61–79

    Google Scholar 

  • Zham DS (1989) The ventral striatopallidal parts of the basal ganglia in the rat: compartimentation of the ventral pallidal efferents. Neuroscience 30:33–50

    Google Scholar 

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Acknowledgements

This study was supported by Cofin grants to A.O. and A.M. and an F.I.R.B. grant to A.O. and A.M. The authors would like to thank Mr. Tullio Riosa and Mr. Genesio Ricci for their technical assistance and Dr. Agu Pert and Dr. Claudio Castellano for their useful suggestions on a previous version of the manuscript.

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Correspondence to Andrea Mele.

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Ferretti, V., Florian, C., Costantini, V.J.A. et al. Co-activation of glutamate and dopamine receptors within the nucleus accumbens is required for spatial memory consolidation in mice. Psychopharmacology 179, 108–116 (2005). https://doi.org/10.1007/s00213-005-2144-3

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  • DOI: https://doi.org/10.1007/s00213-005-2144-3

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