Cargando…
Chemogenetic suppression of anterior cingulate cortical neurons projecting to the visual cortex disrupts attentional behavior in mice
AIM: Attention is a goal‐directed cognitive process that facilitates the detection of task‐relevant sensory stimuli from dynamic environments. Anterior cingulate cortical area (ACA) is known to play a key role in attentional behavior, but the specific circuits mediating attention remain largely unkn...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340833/ https://www.ncbi.nlm.nih.gov/pubmed/33955711 http://dx.doi.org/10.1002/npr2.12176 |
_version_ | 1783733834192257024 |
---|---|
author | Norman, Kevin J. Koike, Hiroyuki McCraney, Sarah E. Garkun, Yury Bateh, Julia Falk, Elisa N. Im, Susanna Caro, Keaven Demars, Michael P. Morishita, Hirofumi |
author_facet | Norman, Kevin J. Koike, Hiroyuki McCraney, Sarah E. Garkun, Yury Bateh, Julia Falk, Elisa N. Im, Susanna Caro, Keaven Demars, Michael P. Morishita, Hirofumi |
author_sort | Norman, Kevin J. |
collection | PubMed |
description | AIM: Attention is a goal‐directed cognitive process that facilitates the detection of task‐relevant sensory stimuli from dynamic environments. Anterior cingulate cortical area (ACA) is known to play a key role in attentional behavior, but the specific circuits mediating attention remain largely unknown. As ACA modulates sensory processing in the visual cortex (VIS), we aim to test a hypothesis that frontal top‐down neurons projecting from ACA to VIS (ACA(VIS)) contributes to visual attention behavior through chemogenetic approach. METHODS: Adult, male mice were trained to perform the 5‐choice serial reaction time task (5CSRTT) using a touchscreen system. An intersectional viral approach was used to selectively express inhibitory designer receptors exclusively activated by designer drugs (iDREADD) or a static fluorophore (mCherry) in ACA(VIS) neurons. Mice received counterbalanced injections (i.p.) of the iDREADD ligand (clozapine‐N‐oxide; CNO) or vehicle (saline) prior to 5CSRTT testing. Finally, mice underwent progressive ratio testing and open field testing following CNO or saline administration. RESULTS: Chemogenetic suppression of ACA(VIS) neuron activity decreased correct task performance during the 5CSRTT mainly driven by an increase in omission and a trending decrease in accuracy with no change in behavioral outcomes associated with motivation, impulsivity, or compulsivity. Breakpoint during the progressive ratio task and distance moved in the open field test were unaffected by ACA(VIS) neuron suppression. CNO administration itself had no effect on task performance in mCherry‐expressing mice. CONCLUSION: These results identify long‐range frontal‐sensory ACA(VIS) projection neurons as a key enactor of top‐down attentional behavior and may serve as a beneficial therapeutic target. |
format | Online Article Text |
id | pubmed-8340833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83408332021-08-11 Chemogenetic suppression of anterior cingulate cortical neurons projecting to the visual cortex disrupts attentional behavior in mice Norman, Kevin J. Koike, Hiroyuki McCraney, Sarah E. Garkun, Yury Bateh, Julia Falk, Elisa N. Im, Susanna Caro, Keaven Demars, Michael P. Morishita, Hirofumi Neuropsychopharmacol Rep Original Articles AIM: Attention is a goal‐directed cognitive process that facilitates the detection of task‐relevant sensory stimuli from dynamic environments. Anterior cingulate cortical area (ACA) is known to play a key role in attentional behavior, but the specific circuits mediating attention remain largely unknown. As ACA modulates sensory processing in the visual cortex (VIS), we aim to test a hypothesis that frontal top‐down neurons projecting from ACA to VIS (ACA(VIS)) contributes to visual attention behavior through chemogenetic approach. METHODS: Adult, male mice were trained to perform the 5‐choice serial reaction time task (5CSRTT) using a touchscreen system. An intersectional viral approach was used to selectively express inhibitory designer receptors exclusively activated by designer drugs (iDREADD) or a static fluorophore (mCherry) in ACA(VIS) neurons. Mice received counterbalanced injections (i.p.) of the iDREADD ligand (clozapine‐N‐oxide; CNO) or vehicle (saline) prior to 5CSRTT testing. Finally, mice underwent progressive ratio testing and open field testing following CNO or saline administration. RESULTS: Chemogenetic suppression of ACA(VIS) neuron activity decreased correct task performance during the 5CSRTT mainly driven by an increase in omission and a trending decrease in accuracy with no change in behavioral outcomes associated with motivation, impulsivity, or compulsivity. Breakpoint during the progressive ratio task and distance moved in the open field test were unaffected by ACA(VIS) neuron suppression. CNO administration itself had no effect on task performance in mCherry‐expressing mice. CONCLUSION: These results identify long‐range frontal‐sensory ACA(VIS) projection neurons as a key enactor of top‐down attentional behavior and may serve as a beneficial therapeutic target. John Wiley and Sons Inc. 2021-05-06 /pmc/articles/PMC8340833/ /pubmed/33955711 http://dx.doi.org/10.1002/npr2.12176 Text en © 2021 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Society of Neuropsychopharmacology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Norman, Kevin J. Koike, Hiroyuki McCraney, Sarah E. Garkun, Yury Bateh, Julia Falk, Elisa N. Im, Susanna Caro, Keaven Demars, Michael P. Morishita, Hirofumi Chemogenetic suppression of anterior cingulate cortical neurons projecting to the visual cortex disrupts attentional behavior in mice |
title | Chemogenetic suppression of anterior cingulate cortical neurons projecting to the visual cortex disrupts attentional behavior in mice |
title_full | Chemogenetic suppression of anterior cingulate cortical neurons projecting to the visual cortex disrupts attentional behavior in mice |
title_fullStr | Chemogenetic suppression of anterior cingulate cortical neurons projecting to the visual cortex disrupts attentional behavior in mice |
title_full_unstemmed | Chemogenetic suppression of anterior cingulate cortical neurons projecting to the visual cortex disrupts attentional behavior in mice |
title_short | Chemogenetic suppression of anterior cingulate cortical neurons projecting to the visual cortex disrupts attentional behavior in mice |
title_sort | chemogenetic suppression of anterior cingulate cortical neurons projecting to the visual cortex disrupts attentional behavior in mice |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340833/ https://www.ncbi.nlm.nih.gov/pubmed/33955711 http://dx.doi.org/10.1002/npr2.12176 |
work_keys_str_mv | AT normankevinj chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice AT koikehiroyuki chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice AT mccraneysarahe chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice AT garkunyury chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice AT batehjulia chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice AT falkelisan chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice AT imsusanna chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice AT carokeaven chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice AT demarsmichaelp chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice AT morishitahirofumi chemogeneticsuppressionofanteriorcingulatecorticalneuronsprojectingtothevisualcortexdisruptsattentionalbehaviorinmice |