Literature DB >> 16226842

Anatomical evidence for direct connections between the shell and core subregions of the rat nucleus accumbens.

Y C van Dongen1, J-M Deniau, C M A Pennartz, Y Galis-de Graaf, P Voorn, A-M Thierry, H J Groenewegen.   

Abstract

The nucleus accumbens is thought to subserve different aspects of adaptive and emotional behaviors. The anatomical substrates for such actions are multiple, parallel ventral striatopallidal output circuits originating in the nucleus accumbens shell and core subregions. Several indirect ways of interaction between the two subregions and their associated circuitry have been proposed, in particular through striato-pallido-thalamic and dopaminergic pathways. In this study, using anterograde neuroanatomical tracing with Phaseolus vulgaris-leucoagglutinin and biotinylated dextran amine as well as single-cell juxtacellular filling with neurobiotin, we investigated the intra-accumbens distribution of local axon collaterals for the identification of possible direct connections between the shell and core subregions. Our results show widespread intra-accumbens projection patterns, including reciprocal projections between specific parts of the shell and core. However, fibers originating in the core reach more distant areas of the shell, including the rostral pole (i.e. the calbindin-poor part of the shell anterior to the core) and striatal parts of the olfactory tubercle, than those arising in the shell and projecting to the core. The latter projections are more restricted to the border region between the shell and core. The density of the fiber labeling within both the shell and core was very similar. Moreover, specific intrinsic projections within shell and core were identified, including a relatively strong projection from the rostral pole to the rostral shell, reciprocal projections between the rostral and caudal shell, as well as projections within the core that have a caudal-to-rostral predominance. The results of the juxtacellular filling experiments show that medium-sized spiny projection neurons and medium-sized aspiny neurons (most likely fast-spiking) contribute to these intra-accumbens projections. While such neurons are GABAergic, the intrastriatal projection patterns indicate the existence of lateral inhibitory interactions within, as well as between, shell and core subregions of the nucleus accumbens.

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Year:  2005        PMID: 16226842     DOI: 10.1016/j.neuroscience.2005.08.050

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  51 in total

1.  On lateral septum-like characteristics of outputs from the accumbal hedonic "hotspot" of Peciña and Berridge with commentary on the transitional nature of basal forebrain "boundaries".

Authors:  Daniel S Zahm; Kenneth P Parsley; Zachary M Schwartz; Anita Y Cheng
Journal:  J Comp Neurol       Date:  2013-01-01       Impact factor: 3.215

Review 2.  Architectural Representation of Valence in the Limbic System.

Authors:  Praneeth Namburi; Ream Al-Hasani; Gwendolyn G Calhoon; Michael R Bruchas; Kay M Tye
Journal:  Neuropsychopharmacology       Date:  2015-12-09       Impact factor: 7.853

3.  Distinct prefrontal cortical regions negatively regulate evoked activity in nucleus accumbens subregions.

Authors:  Amber Asher; Daniel J Lodge
Journal:  Int J Neuropsychopharmacol       Date:  2011-10-19       Impact factor: 5.176

4.  κ-Opioid receptors within the nucleus accumbens shell mediate pair bond maintenance.

Authors:  Shanna L Resendez; Morgan Kuhnmuench; Tarin Krzywosinski; Brandon J Aragona
Journal:  J Neurosci       Date:  2012-05-16       Impact factor: 6.167

Review 5.  The nucleus accumbens and Pavlovian reward learning.

Authors:  Jeremy J Day; Regina M Carelli
Journal:  Neuroscientist       Date:  2007-04       Impact factor: 7.519

6.  Tonic inhibition of accumbal spiny neurons by extrasynaptic α4βδ GABAA receptors modulates the actions of psychostimulants.

Authors:  Edward P Maguire; Tom Macpherson; Jerome D Swinny; Claire I Dixon; Murray B Herd; Delia Belelli; David N Stephens; Sarah L King; Jeremy J Lambert
Journal:  J Neurosci       Date:  2014-01-15       Impact factor: 6.167

Review 7.  A role for phasic dopamine release within the nucleus accumbens in encoding aversion: a review of the neurochemical literature.

Authors:  Jennifer M Wenzel; Noah A Rauscher; Joseph F Cheer; Erik B Oleson
Journal:  ACS Chem Neurosci       Date:  2014-12-24       Impact factor: 4.418

8.  Enkephalin downregulation in the nucleus accumbens underlies chronic stress-induced anhedonia.

Authors:  Jean-François Poulin; Sylvie Laforest; Guy Drolet
Journal:  Stress       Date:  2013-10-31       Impact factor: 3.493

9.  Inputs to the ventrolateral bed nucleus of the stria terminalis.

Authors:  Jung-Won Shin; Joel C Geerling; Arthur D Loewy
Journal:  J Comp Neurol       Date:  2008-12-10       Impact factor: 3.215

10.  Amelioration of binge eating by nucleus accumbens shell deep brain stimulation in mice involves D2 receptor modulation.

Authors:  Casey H Halpern; Anand Tekriwal; Jessica Santollo; Jeffrey G Keating; John A Wolf; Derek Daniels; Tracy L Bale
Journal:  J Neurosci       Date:  2013-04-24       Impact factor: 6.167

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