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Amygdala to nucleus accumbens excitatory transmission facilitates reward seeking

The basolateral amygdala (BLA) plays a crucial role in emotional learning irrespective of valence(1–5). While the BLA projection to the nucleus accumbens (NAc) is hypothesized to modulate cue-triggered motivated behaviors(4, 6, 7,), our understanding of the interaction between these two brain region...

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Autores principales: Stuber, Garret D., Sparta, Dennis R., Stamatakis, Alice M., van Leeuwen, Wieke A., Hardjoprajitno, Juanita E., Cho, Saemi, Tye, Kay M., Kempadoo, Kimberly A., Zhang, Feng, Deisseroth, Karl, Bonci, Antonello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775282/
https://www.ncbi.nlm.nih.gov/pubmed/21716290
http://dx.doi.org/10.1038/nature10194
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author Stuber, Garret D.
Sparta, Dennis R.
Stamatakis, Alice M.
van Leeuwen, Wieke A.
Hardjoprajitno, Juanita E.
Cho, Saemi
Tye, Kay M.
Kempadoo, Kimberly A.
Zhang, Feng
Deisseroth, Karl
Bonci, Antonello
author_facet Stuber, Garret D.
Sparta, Dennis R.
Stamatakis, Alice M.
van Leeuwen, Wieke A.
Hardjoprajitno, Juanita E.
Cho, Saemi
Tye, Kay M.
Kempadoo, Kimberly A.
Zhang, Feng
Deisseroth, Karl
Bonci, Antonello
author_sort Stuber, Garret D.
collection PubMed
description The basolateral amygdala (BLA) plays a crucial role in emotional learning irrespective of valence(1–5). While the BLA projection to the nucleus accumbens (NAc) is hypothesized to modulate cue-triggered motivated behaviors(4, 6, 7,), our understanding of the interaction between these two brain regions has been limited by the inability to manipulate neural circuit elements of this pathway selectively during behavior. To circumvent this limitation, we used in vivo optogenetic stimulation or inhibition of glutamatergic fibers from the BLA to the NAc, coupled with intracranial pharmacology and ex vivo electrophysiology. We show that optical stimulation of the BLA-to-NAc pathway in mice reinforces behavioral responding to earn additional optical stimulations of these synaptic inputs. Optical stimulation of BLA-to-NAc glutamatergic fibers required intra-NAc dopamine D1-type, but not D2-type, receptor signaling. Brief optical inhibition of BLA-to-NAc fibers reduced cue-evoked intake of sucrose, demonstrating an important role of this specific pathway in controlling naturally occurring reward-related behavior. Moreover, while optical stimulation of medial prefrontal cortex (mPFC) to NAc glutamatergic fibers also elicited reliable excitatory synaptic responses, optical self-stimulation behavior was not observed by activation of this pathway. These data suggest that while the BLA is important for processing both positive and negative affect, the BLA-to-NAc glutamatergic pathway in conjunction with dopamine signaling in the NAc promotes motivated behavioral responding.
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spelling pubmed-37752822013-09-17 Amygdala to nucleus accumbens excitatory transmission facilitates reward seeking Stuber, Garret D. Sparta, Dennis R. Stamatakis, Alice M. van Leeuwen, Wieke A. Hardjoprajitno, Juanita E. Cho, Saemi Tye, Kay M. Kempadoo, Kimberly A. Zhang, Feng Deisseroth, Karl Bonci, Antonello Nature Article The basolateral amygdala (BLA) plays a crucial role in emotional learning irrespective of valence(1–5). While the BLA projection to the nucleus accumbens (NAc) is hypothesized to modulate cue-triggered motivated behaviors(4, 6, 7,), our understanding of the interaction between these two brain regions has been limited by the inability to manipulate neural circuit elements of this pathway selectively during behavior. To circumvent this limitation, we used in vivo optogenetic stimulation or inhibition of glutamatergic fibers from the BLA to the NAc, coupled with intracranial pharmacology and ex vivo electrophysiology. We show that optical stimulation of the BLA-to-NAc pathway in mice reinforces behavioral responding to earn additional optical stimulations of these synaptic inputs. Optical stimulation of BLA-to-NAc glutamatergic fibers required intra-NAc dopamine D1-type, but not D2-type, receptor signaling. Brief optical inhibition of BLA-to-NAc fibers reduced cue-evoked intake of sucrose, demonstrating an important role of this specific pathway in controlling naturally occurring reward-related behavior. Moreover, while optical stimulation of medial prefrontal cortex (mPFC) to NAc glutamatergic fibers also elicited reliable excitatory synaptic responses, optical self-stimulation behavior was not observed by activation of this pathway. These data suggest that while the BLA is important for processing both positive and negative affect, the BLA-to-NAc glutamatergic pathway in conjunction with dopamine signaling in the NAc promotes motivated behavioral responding. 2011-06-29 /pmc/articles/PMC3775282/ /pubmed/21716290 http://dx.doi.org/10.1038/nature10194 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Stuber, Garret D.
Sparta, Dennis R.
Stamatakis, Alice M.
van Leeuwen, Wieke A.
Hardjoprajitno, Juanita E.
Cho, Saemi
Tye, Kay M.
Kempadoo, Kimberly A.
Zhang, Feng
Deisseroth, Karl
Bonci, Antonello
Amygdala to nucleus accumbens excitatory transmission facilitates reward seeking
title Amygdala to nucleus accumbens excitatory transmission facilitates reward seeking
title_full Amygdala to nucleus accumbens excitatory transmission facilitates reward seeking
title_fullStr Amygdala to nucleus accumbens excitatory transmission facilitates reward seeking
title_full_unstemmed Amygdala to nucleus accumbens excitatory transmission facilitates reward seeking
title_short Amygdala to nucleus accumbens excitatory transmission facilitates reward seeking
title_sort amygdala to nucleus accumbens excitatory transmission facilitates reward seeking
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775282/
https://www.ncbi.nlm.nih.gov/pubmed/21716290
http://dx.doi.org/10.1038/nature10194
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