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The Effect of Glutamate Receptor Agonists on Mouse Retinal Astrocyte [Ca(2+)](i)
Calcium-imaging techniques were used to determine if mouse retinal astrocytes in situ respond to agonists of ionotropic (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid, AMPA; N-methyl-D-aspartate, NMDA) and metabotropic (S-3,5-dihydroxyphenylglycine, DHPG; trans-1-amino-1,3-cyclopentanedicarbo...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930813/ https://www.ncbi.nlm.nih.gov/pubmed/27413752 http://dx.doi.org/10.1155/2016/8178162 |
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author | Blandford, Stephanie N. Baldridge, William H. |
author_facet | Blandford, Stephanie N. Baldridge, William H. |
author_sort | Blandford, Stephanie N. |
collection | PubMed |
description | Calcium-imaging techniques were used to determine if mouse retinal astrocytes in situ respond to agonists of ionotropic (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid, AMPA; N-methyl-D-aspartate, NMDA) and metabotropic (S-3,5-dihydroxyphenylglycine, DHPG; trans-1-amino-1,3-cyclopentanedicarboxylic acid, ACPD) glutamate receptors. In most cases we found no evidence that retinal astrocyte intracellular calcium ion concentration ([Ca(2+)](i)) increased in response to these glutamate agonists. The one exception was AMPA that increased [Ca(2+)](i) in some, but not all, mouse retinal astrocytes in situ. However, AMPA did not increase [Ca(2+)](i) in mouse retinal astrocytes in vitro, suggesting that the effect of AMPA in situ may be indirect. |
format | Online Article Text |
id | pubmed-4930813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49308132016-07-13 The Effect of Glutamate Receptor Agonists on Mouse Retinal Astrocyte [Ca(2+)](i) Blandford, Stephanie N. Baldridge, William H. Biomed Res Int Research Article Calcium-imaging techniques were used to determine if mouse retinal astrocytes in situ respond to agonists of ionotropic (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid, AMPA; N-methyl-D-aspartate, NMDA) and metabotropic (S-3,5-dihydroxyphenylglycine, DHPG; trans-1-amino-1,3-cyclopentanedicarboxylic acid, ACPD) glutamate receptors. In most cases we found no evidence that retinal astrocyte intracellular calcium ion concentration ([Ca(2+)](i)) increased in response to these glutamate agonists. The one exception was AMPA that increased [Ca(2+)](i) in some, but not all, mouse retinal astrocytes in situ. However, AMPA did not increase [Ca(2+)](i) in mouse retinal astrocytes in vitro, suggesting that the effect of AMPA in situ may be indirect. Hindawi Publishing Corporation 2016 2016-06-19 /pmc/articles/PMC4930813/ /pubmed/27413752 http://dx.doi.org/10.1155/2016/8178162 Text en Copyright © 2016 S. N. Blandford and W. H. Baldridge. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Blandford, Stephanie N. Baldridge, William H. The Effect of Glutamate Receptor Agonists on Mouse Retinal Astrocyte [Ca(2+)](i) |
title | The Effect of Glutamate Receptor Agonists on Mouse Retinal Astrocyte [Ca(2+)](i)
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title_full | The Effect of Glutamate Receptor Agonists on Mouse Retinal Astrocyte [Ca(2+)](i)
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title_fullStr | The Effect of Glutamate Receptor Agonists on Mouse Retinal Astrocyte [Ca(2+)](i)
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title_full_unstemmed | The Effect of Glutamate Receptor Agonists on Mouse Retinal Astrocyte [Ca(2+)](i)
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title_short | The Effect of Glutamate Receptor Agonists on Mouse Retinal Astrocyte [Ca(2+)](i)
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title_sort | effect of glutamate receptor agonists on mouse retinal astrocyte [ca(2+)](i) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930813/ https://www.ncbi.nlm.nih.gov/pubmed/27413752 http://dx.doi.org/10.1155/2016/8178162 |
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