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Engaging and disengaging recurrent inhibition coincides with sensing and unsensing of a sensory stimulus
Even simple sensory stimuli evoke neural responses that are dynamic and complex. Are the temporally patterned neural activities important for controlling the behavioral output? Here, we investigated this issue. Our results reveal that in the insect antennal lobe, due to circuit interactions, distinc...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457525/ https://www.ncbi.nlm.nih.gov/pubmed/28534502 http://dx.doi.org/10.1038/ncomms15413 |
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author | Saha, Debajit Sun, Wensheng Li, Chao Nizampatnam, Srinath Padovano, William Chen, Zhengdao Chen, Alex Altan, Ege Lo, Ray Barbour, Dennis L. Raman, Baranidharan |
author_facet | Saha, Debajit Sun, Wensheng Li, Chao Nizampatnam, Srinath Padovano, William Chen, Zhengdao Chen, Alex Altan, Ege Lo, Ray Barbour, Dennis L. Raman, Baranidharan |
author_sort | Saha, Debajit |
collection | PubMed |
description | Even simple sensory stimuli evoke neural responses that are dynamic and complex. Are the temporally patterned neural activities important for controlling the behavioral output? Here, we investigated this issue. Our results reveal that in the insect antennal lobe, due to circuit interactions, distinct neural ensembles are activated during and immediately following the termination of every odorant. Such non-overlapping response patterns are not observed even when the stimulus intensity or identities were changed. In addition, we find that ON and OFF ensemble neural activities differ in their ability to recruit recurrent inhibition, entrain field-potential oscillations and more importantly in their relevance to behaviour (initiate versus reset conditioned responses). Notably, we find that a strikingly similar strategy is also used for encoding sound onsets and offsets in the marmoset auditory cortex. In sum, our results suggest a general approach where recurrent inhibition is associated with stimulus ‘recognition' and ‘derecognition'. |
format | Online Article Text |
id | pubmed-5457525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54575252017-06-08 Engaging and disengaging recurrent inhibition coincides with sensing and unsensing of a sensory stimulus Saha, Debajit Sun, Wensheng Li, Chao Nizampatnam, Srinath Padovano, William Chen, Zhengdao Chen, Alex Altan, Ege Lo, Ray Barbour, Dennis L. Raman, Baranidharan Nat Commun Article Even simple sensory stimuli evoke neural responses that are dynamic and complex. Are the temporally patterned neural activities important for controlling the behavioral output? Here, we investigated this issue. Our results reveal that in the insect antennal lobe, due to circuit interactions, distinct neural ensembles are activated during and immediately following the termination of every odorant. Such non-overlapping response patterns are not observed even when the stimulus intensity or identities were changed. In addition, we find that ON and OFF ensemble neural activities differ in their ability to recruit recurrent inhibition, entrain field-potential oscillations and more importantly in their relevance to behaviour (initiate versus reset conditioned responses). Notably, we find that a strikingly similar strategy is also used for encoding sound onsets and offsets in the marmoset auditory cortex. In sum, our results suggest a general approach where recurrent inhibition is associated with stimulus ‘recognition' and ‘derecognition'. Nature Publishing Group 2017-05-23 /pmc/articles/PMC5457525/ /pubmed/28534502 http://dx.doi.org/10.1038/ncomms15413 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Saha, Debajit Sun, Wensheng Li, Chao Nizampatnam, Srinath Padovano, William Chen, Zhengdao Chen, Alex Altan, Ege Lo, Ray Barbour, Dennis L. Raman, Baranidharan Engaging and disengaging recurrent inhibition coincides with sensing and unsensing of a sensory stimulus |
title | Engaging and disengaging recurrent inhibition coincides with sensing and unsensing of a sensory stimulus |
title_full | Engaging and disengaging recurrent inhibition coincides with sensing and unsensing of a sensory stimulus |
title_fullStr | Engaging and disengaging recurrent inhibition coincides with sensing and unsensing of a sensory stimulus |
title_full_unstemmed | Engaging and disengaging recurrent inhibition coincides with sensing and unsensing of a sensory stimulus |
title_short | Engaging and disengaging recurrent inhibition coincides with sensing and unsensing of a sensory stimulus |
title_sort | engaging and disengaging recurrent inhibition coincides with sensing and unsensing of a sensory stimulus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457525/ https://www.ncbi.nlm.nih.gov/pubmed/28534502 http://dx.doi.org/10.1038/ncomms15413 |
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