Literature DB >> 8550887

Patterns of convergence and segregation in the medial nucleus accumbens of the rat: relationships of prefrontal cortical, midline thalamic, and basal amygdaloid afferents.

C I Wright1, H J Groenewegen.   

Abstract

In the rat, fibers from the prelimbic cortex terminate in the medial nucleus accumbens. Anterior paraventricular thalamic and parvicellular basal amygdaloid fibers reached both the prelimbic cortex and the medial nucleus accumbens. All three afferent systems have an inhomogenous distribution within the nucleus accumbens, and whether or not these projections actually reach the same areas is unknown. Our aim was to evaluate the relationships of the three afferents with respect to the shell, the core, and the cell clusters of the nucleus accumbens. Double anterograde tracing and single anterograde tracing combined with immunohistochemistry for calbindin (D28k) or Nissl stain was used. Following tracer injections in the prelimbic cortex and the anterior paraventricular thalamus, a complementary (i.e., nonoverlapping) pattern of fibers was found in the shell. Thus, afferents from the prelimbic cortex are associated with cell clusters, whereas those from the anterior paraventricular thalamus avoid these cells but are affiliated with regions exhibiting weak homogeneous calbindin immunoreactivity. In the calbindin-poor patches of the core, the situation is reversed as both sets of fibers overlap. In cases with injections in the prelimbic cortex and the parvicellular basal amygdala, a pattern of overlap was seen in the shell and core. Thus, the fibers in the shell were found together in association with cell clusters, whereas regions of weak homogeneous calbindin immunoreactivity were avoided. In the core, overlap was seen in the patch compartment. Finally, with parvicellular basal amygdala/paraventricular thalamus injections, a complementary fiber organization was present in the shell, but overlap was prominent in the patches of the core. The results demonstrate that the relationships of prelimbic cortical, paraventricular thalamic, and parvicellular basal amygdaloid afferents in the nucleus accumbens vary according to their compartmental (immunohistochemical and cellular) affiliation. Compartmentalization is therefore a possible anatomical substrate for condensation or segregation of neuronal signals passing through the nucleus accumbens.

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Year:  1995        PMID: 8550887     DOI: 10.1002/cne.903610304

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  51 in total

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2.  The spatial organization of the cortical projection system of the nucleus accumbens of the dog brain.

Authors:  O G Chivileva
Journal:  Neurosci Behav Physiol       Date:  1999 Jan-Feb

3.  Disrupted activity in the hippocampal-accumbens circuit of type III neuregulin 1 mutant mice.

Authors:  Malcolm W Nason; Avishek Adhikari; Marjan Bozinoski; Joshua A Gordon; Lorna W Role
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4.  Chronic administration of the neurotrophic agent cerebrolysin ameliorates the behavioral and morphological changes induced by neonatal ventral hippocampus lesion in a rat model of schizophrenia.

Authors:  Rubén Antonio Vázquez-Roque; Brenda Ramos; Carolina Tecuatl; Ismael Juárez; Anthony Adame; Fidel de la Cruz; Sergio Zamudio; Raúl Mena; Edward Rockenstein; Eliezer Masliah; Gonzalo Flores
Journal:  J Neurosci Res       Date:  2011-09-19       Impact factor: 4.164

5.  Selective activation of medial prefrontal-to-accumbens projection neurons by amygdala stimulation and Pavlovian conditioned stimuli.

Authors:  Vincent B McGinty; Anthony A Grace
Journal:  Cereb Cortex       Date:  2007-12-07       Impact factor: 5.357

6.  When administered into the nucleus accumbens core or shell, the NMDA receptor antagonist AP-5 reinstates cocaine-seeking behavior in the rat.

Authors:  Katie R Famous; Heath D Schmidt; R Christopher Pierce
Journal:  Neurosci Lett       Date:  2007-05-03       Impact factor: 3.046

7.  Fos and glutamate AMPA receptor subunit coexpression associated with cue-elicited cocaine-seeking behavior in abstinent rats.

Authors:  A R Zavala; S Biswas; R E Harlan; J L Neisewander
Journal:  Neuroscience       Date:  2007-02-01       Impact factor: 3.590

8.  Assessing contributions of nucleus accumbens shell subregions to reward-seeking behavior.

Authors:  Michael D Reed; David G C Hildebrand; Gabrielle Santangelo; Anthony Moffa; Ashley S Pira; Lisa Rycyna; Mia Radic; Katherine Price; Jonathan Archbold; Kristi McConnell; Lauren Girard; Kristen Morin; Anna Tang; Marcelo Febo; James R Stellar
Journal:  Drug Alcohol Depend       Date:  2015-05-12       Impact factor: 4.492

9.  Cue-evoked encoding of movement planning and execution in the rat nucleus accumbens.

Authors:  Sharif A Taha; Saleem M Nicola; Howard L Fields
Journal:  J Physiol       Date:  2007-08-30       Impact factor: 5.182

Review 10.  Amygdalostriatal projections in the neurocircuitry for motivation: a neuroanatomical thread through the career of Ann Kelley.

Authors:  Eric P Zorrilla; George F Koob
Journal:  Neurosci Biobehav Rev       Date:  2012-12-07       Impact factor: 8.989

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