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Adenosine A(1) Receptor-Mediated Attenuation of Reciprocal Dendro-Dendritic Inhibition in the Mouse Olfactory Bulb
It is well described that A(1) adenosine receptors inhibit synaptic transmission at excitatory synapses in the brain, but the effect of adenosine on reciprocal synapses has not been studied so far. In the olfactory bulb, the majority of synapses are reciprocal dendro-dendritic synapses mediating rec...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775233/ https://www.ncbi.nlm.nih.gov/pubmed/29379418 http://dx.doi.org/10.3389/fncel.2017.00435 |
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author | Schulz, Kristina Rotermund, Natalie Grzelka, Katarzyna Benz, Jan Lohr, Christian Hirnet, Daniela |
author_facet | Schulz, Kristina Rotermund, Natalie Grzelka, Katarzyna Benz, Jan Lohr, Christian Hirnet, Daniela |
author_sort | Schulz, Kristina |
collection | PubMed |
description | It is well described that A(1) adenosine receptors inhibit synaptic transmission at excitatory synapses in the brain, but the effect of adenosine on reciprocal synapses has not been studied so far. In the olfactory bulb, the majority of synapses are reciprocal dendro-dendritic synapses mediating recurrent inhibition. We studied the effect of A(1) receptor activation on recurrent dendro-dendritic inhibition in mitral cells using whole-cell patch-clamp recordings. Adenosine reduced dendro-dendritic inhibition in wild-type, but not in A(1) receptor knock-out mice. Both NMDA receptor-mediated and AMPA receptor-mediated dendro-dendritic inhibition were attenuated by adenosine, indicating that reciprocal synapses between mitral cells and granule cells as well as parvalbumin interneurons were targeted by A(1) receptors. Adenosine reduced glutamatergic self-excitation and inhibited N-type and P/Q-type calcium currents, but not L-type calcium currents in mitral cells. Attenuated glutamate release, due to A(1) receptor-mediated calcium channel inhibition, resulted in impaired dendro-dendritic inhibition. In behavioral tests we tested the ability of wild-type and A(1) receptor knock-out mice to find a hidden piece of food. Knock-out mice were significantly faster in locating the food. Our results indicate that A(1) adenosine receptors attenuates dendro-dendritic reciprocal inhibition and suggest that they affect odor information processing. |
format | Online Article Text |
id | pubmed-5775233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57752332018-01-29 Adenosine A(1) Receptor-Mediated Attenuation of Reciprocal Dendro-Dendritic Inhibition in the Mouse Olfactory Bulb Schulz, Kristina Rotermund, Natalie Grzelka, Katarzyna Benz, Jan Lohr, Christian Hirnet, Daniela Front Cell Neurosci Neuroscience It is well described that A(1) adenosine receptors inhibit synaptic transmission at excitatory synapses in the brain, but the effect of adenosine on reciprocal synapses has not been studied so far. In the olfactory bulb, the majority of synapses are reciprocal dendro-dendritic synapses mediating recurrent inhibition. We studied the effect of A(1) receptor activation on recurrent dendro-dendritic inhibition in mitral cells using whole-cell patch-clamp recordings. Adenosine reduced dendro-dendritic inhibition in wild-type, but not in A(1) receptor knock-out mice. Both NMDA receptor-mediated and AMPA receptor-mediated dendro-dendritic inhibition were attenuated by adenosine, indicating that reciprocal synapses between mitral cells and granule cells as well as parvalbumin interneurons were targeted by A(1) receptors. Adenosine reduced glutamatergic self-excitation and inhibited N-type and P/Q-type calcium currents, but not L-type calcium currents in mitral cells. Attenuated glutamate release, due to A(1) receptor-mediated calcium channel inhibition, resulted in impaired dendro-dendritic inhibition. In behavioral tests we tested the ability of wild-type and A(1) receptor knock-out mice to find a hidden piece of food. Knock-out mice were significantly faster in locating the food. Our results indicate that A(1) adenosine receptors attenuates dendro-dendritic reciprocal inhibition and suggest that they affect odor information processing. Frontiers Media S.A. 2018-01-15 /pmc/articles/PMC5775233/ /pubmed/29379418 http://dx.doi.org/10.3389/fncel.2017.00435 Text en Copyright © 2018 Schulz, Rotermund, Grzelka, Benz, Lohr and Hirnet. 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 Schulz, Kristina Rotermund, Natalie Grzelka, Katarzyna Benz, Jan Lohr, Christian Hirnet, Daniela Adenosine A(1) Receptor-Mediated Attenuation of Reciprocal Dendro-Dendritic Inhibition in the Mouse Olfactory Bulb |
title | Adenosine A(1) Receptor-Mediated Attenuation of Reciprocal Dendro-Dendritic Inhibition in the Mouse Olfactory Bulb |
title_full | Adenosine A(1) Receptor-Mediated Attenuation of Reciprocal Dendro-Dendritic Inhibition in the Mouse Olfactory Bulb |
title_fullStr | Adenosine A(1) Receptor-Mediated Attenuation of Reciprocal Dendro-Dendritic Inhibition in the Mouse Olfactory Bulb |
title_full_unstemmed | Adenosine A(1) Receptor-Mediated Attenuation of Reciprocal Dendro-Dendritic Inhibition in the Mouse Olfactory Bulb |
title_short | Adenosine A(1) Receptor-Mediated Attenuation of Reciprocal Dendro-Dendritic Inhibition in the Mouse Olfactory Bulb |
title_sort | adenosine a(1) receptor-mediated attenuation of reciprocal dendro-dendritic inhibition in the mouse olfactory bulb |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775233/ https://www.ncbi.nlm.nih.gov/pubmed/29379418 http://dx.doi.org/10.3389/fncel.2017.00435 |
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