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The Retrograde Connections and Anatomical Segregation of the Göttingen Minipig Nucleus Accumbens

Nucleus accumbens (NAcc) has been implicated in several psychiatric disorders such as treatment resistant depression (TRD), and obsessive-compulsive disorder (OCD), and has been an ongoing experimental target for deep brain stimulation (DBS) in both rats and humans. In order to translate basic scien...

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Autores principales: Meidahl, Anders C., Orlowski, Dariusz, Sørensen, Jens C. H., Bjarkam, Carsten R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5136552/
https://www.ncbi.nlm.nih.gov/pubmed/27994542
http://dx.doi.org/10.3389/fnana.2016.00117
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author Meidahl, Anders C.
Orlowski, Dariusz
Sørensen, Jens C. H.
Bjarkam, Carsten R.
author_facet Meidahl, Anders C.
Orlowski, Dariusz
Sørensen, Jens C. H.
Bjarkam, Carsten R.
author_sort Meidahl, Anders C.
collection PubMed
description Nucleus accumbens (NAcc) has been implicated in several psychiatric disorders such as treatment resistant depression (TRD), and obsessive-compulsive disorder (OCD), and has been an ongoing experimental target for deep brain stimulation (DBS) in both rats and humans. In order to translate basic scientific results from rodents to the human setting a large animal model is needed to thoroughly study the effect of such therapeutic interventions. The aim of the study was, accordingly, to describe the basic anatomy of the Göttingen minipig NAcc and its retrograde connections. Tracing was carried out by MRI-guided stereotactic unilateral fluorogold injections in the NAcc of Göttingen minipigs. After 2 weeks the brains were sectioned and subsequently stained with Nissl-, autometallographic (AMG) development of myelin, and DARPP-32 and calbindin immunohistochemistry. The minipig NAcc was divided in a central core and an outer medial, ventral and lateral shell. We confirmed the NAcc to be a large and well-segregated structure toward its medial, ventral and lateral borders. The fluorogold tracing revealed inputs to NAcc from the medial parts of the prefrontal cortex, BA 25 (subgenual cortex), insula bilaterally, amygdala, the CA1-region of hippocampus, entorhinal cortex, subiculum, paraventricular and anterior parts of thalamus, dorsomedial parts of hypothalamus, substantia nigra, ventral tegmental area (VTA), the retrorubral field and the dorsal and median raphe nuclei. In conclusion the Göttingen minipig NAcc is a large ventral striatal structure that can be divided into a core and shell with prominent afferent connections from several subrhinal and infra-/prelimbic brain areas.
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spelling pubmed-51365522016-12-19 The Retrograde Connections and Anatomical Segregation of the Göttingen Minipig Nucleus Accumbens Meidahl, Anders C. Orlowski, Dariusz Sørensen, Jens C. H. Bjarkam, Carsten R. Front Neuroanat Neuroscience Nucleus accumbens (NAcc) has been implicated in several psychiatric disorders such as treatment resistant depression (TRD), and obsessive-compulsive disorder (OCD), and has been an ongoing experimental target for deep brain stimulation (DBS) in both rats and humans. In order to translate basic scientific results from rodents to the human setting a large animal model is needed to thoroughly study the effect of such therapeutic interventions. The aim of the study was, accordingly, to describe the basic anatomy of the Göttingen minipig NAcc and its retrograde connections. Tracing was carried out by MRI-guided stereotactic unilateral fluorogold injections in the NAcc of Göttingen minipigs. After 2 weeks the brains were sectioned and subsequently stained with Nissl-, autometallographic (AMG) development of myelin, and DARPP-32 and calbindin immunohistochemistry. The minipig NAcc was divided in a central core and an outer medial, ventral and lateral shell. We confirmed the NAcc to be a large and well-segregated structure toward its medial, ventral and lateral borders. The fluorogold tracing revealed inputs to NAcc from the medial parts of the prefrontal cortex, BA 25 (subgenual cortex), insula bilaterally, amygdala, the CA1-region of hippocampus, entorhinal cortex, subiculum, paraventricular and anterior parts of thalamus, dorsomedial parts of hypothalamus, substantia nigra, ventral tegmental area (VTA), the retrorubral field and the dorsal and median raphe nuclei. In conclusion the Göttingen minipig NAcc is a large ventral striatal structure that can be divided into a core and shell with prominent afferent connections from several subrhinal and infra-/prelimbic brain areas. Frontiers Media S.A. 2016-12-05 /pmc/articles/PMC5136552/ /pubmed/27994542 http://dx.doi.org/10.3389/fnana.2016.00117 Text en Copyright © 2016 Meidahl, Orlowski, Sørensen and Bjarkam. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Meidahl, Anders C.
Orlowski, Dariusz
Sørensen, Jens C. H.
Bjarkam, Carsten R.
The Retrograde Connections and Anatomical Segregation of the Göttingen Minipig Nucleus Accumbens
title The Retrograde Connections and Anatomical Segregation of the Göttingen Minipig Nucleus Accumbens
title_full The Retrograde Connections and Anatomical Segregation of the Göttingen Minipig Nucleus Accumbens
title_fullStr The Retrograde Connections and Anatomical Segregation of the Göttingen Minipig Nucleus Accumbens
title_full_unstemmed The Retrograde Connections and Anatomical Segregation of the Göttingen Minipig Nucleus Accumbens
title_short The Retrograde Connections and Anatomical Segregation of the Göttingen Minipig Nucleus Accumbens
title_sort retrograde connections and anatomical segregation of the göttingen minipig nucleus accumbens
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5136552/
https://www.ncbi.nlm.nih.gov/pubmed/27994542
http://dx.doi.org/10.3389/fnana.2016.00117
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