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Feed-Forward versus Feedback Inhibition in a Basic Olfactory Circuit

Inhibitory interneurons play critical roles in shaping the firing patterns of principal neurons in many brain systems. Despite difference in the anatomy or functions of neuronal circuits containing inhibition, two basic motifs repeatedly emerge: feed-forward and feedback. In the locust, it was propo...

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Autores principales: Kee, Tiffany, Sanda, Pavel, Gupta, Nitin, Stopfer, Mark, Bazhenov, Maxim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601731/
https://www.ncbi.nlm.nih.gov/pubmed/26458212
http://dx.doi.org/10.1371/journal.pcbi.1004531
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author Kee, Tiffany
Sanda, Pavel
Gupta, Nitin
Stopfer, Mark
Bazhenov, Maxim
author_facet Kee, Tiffany
Sanda, Pavel
Gupta, Nitin
Stopfer, Mark
Bazhenov, Maxim
author_sort Kee, Tiffany
collection PubMed
description Inhibitory interneurons play critical roles in shaping the firing patterns of principal neurons in many brain systems. Despite difference in the anatomy or functions of neuronal circuits containing inhibition, two basic motifs repeatedly emerge: feed-forward and feedback. In the locust, it was proposed that a subset of lateral horn interneurons (LHNs), provide feed-forward inhibition onto Kenyon cells (KCs) to maintain their sparse firing—a property critical for olfactory learning and memory. But recently it was established that a single inhibitory cell, the giant GABAergic neuron (GGN), is the main and perhaps sole source of inhibition in the mushroom body, and that inhibition from this cell is mediated by a feedback (FB) loop including KCs and the GGN. To clarify basic differences in the effects of feedback vs. feed-forward inhibition in circuit dynamics we here use a model of the locust olfactory system. We found both inhibitory motifs were able to maintain sparse KCs responses and provide optimal odor discrimination. However, we further found that only FB inhibition could create a phase response consistent with data recorded in vivo. These findings describe general rules for feed-forward versus feedback inhibition and suggest GGN is potentially capable of providing the primary source of inhibition to the KCs. A better understanding of how inhibitory motifs impact post-synaptic neuronal activity could be used to reveal unknown inhibitory structures within biological networks.
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spelling pubmed-46017312015-10-20 Feed-Forward versus Feedback Inhibition in a Basic Olfactory Circuit Kee, Tiffany Sanda, Pavel Gupta, Nitin Stopfer, Mark Bazhenov, Maxim PLoS Comput Biol Research Article Inhibitory interneurons play critical roles in shaping the firing patterns of principal neurons in many brain systems. Despite difference in the anatomy or functions of neuronal circuits containing inhibition, two basic motifs repeatedly emerge: feed-forward and feedback. In the locust, it was proposed that a subset of lateral horn interneurons (LHNs), provide feed-forward inhibition onto Kenyon cells (KCs) to maintain their sparse firing—a property critical for olfactory learning and memory. But recently it was established that a single inhibitory cell, the giant GABAergic neuron (GGN), is the main and perhaps sole source of inhibition in the mushroom body, and that inhibition from this cell is mediated by a feedback (FB) loop including KCs and the GGN. To clarify basic differences in the effects of feedback vs. feed-forward inhibition in circuit dynamics we here use a model of the locust olfactory system. We found both inhibitory motifs were able to maintain sparse KCs responses and provide optimal odor discrimination. However, we further found that only FB inhibition could create a phase response consistent with data recorded in vivo. These findings describe general rules for feed-forward versus feedback inhibition and suggest GGN is potentially capable of providing the primary source of inhibition to the KCs. A better understanding of how inhibitory motifs impact post-synaptic neuronal activity could be used to reveal unknown inhibitory structures within biological networks. Public Library of Science 2015-10-12 /pmc/articles/PMC4601731/ /pubmed/26458212 http://dx.doi.org/10.1371/journal.pcbi.1004531 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Kee, Tiffany
Sanda, Pavel
Gupta, Nitin
Stopfer, Mark
Bazhenov, Maxim
Feed-Forward versus Feedback Inhibition in a Basic Olfactory Circuit
title Feed-Forward versus Feedback Inhibition in a Basic Olfactory Circuit
title_full Feed-Forward versus Feedback Inhibition in a Basic Olfactory Circuit
title_fullStr Feed-Forward versus Feedback Inhibition in a Basic Olfactory Circuit
title_full_unstemmed Feed-Forward versus Feedback Inhibition in a Basic Olfactory Circuit
title_short Feed-Forward versus Feedback Inhibition in a Basic Olfactory Circuit
title_sort feed-forward versus feedback inhibition in a basic olfactory circuit
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601731/
https://www.ncbi.nlm.nih.gov/pubmed/26458212
http://dx.doi.org/10.1371/journal.pcbi.1004531
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