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Properties of Taurine Release in Glucose-Free Media in Hippocampal Slices from Developing and Adult Mice

The release of preloaded [(3)H]taurine from hippocampal slices from developing 7-day-old and young adult 3-month-old mice was studied in a superfusion system in the absence of glucose. These hypoglycemic conditions enhanced the release at both ages, the effect being markedly greater in developing mi...

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Autores principales: Oja, Simo S., Saransaari, Pirjo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540997/
https://www.ncbi.nlm.nih.gov/pubmed/26347028
http://dx.doi.org/10.1155/2015/254583
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author Oja, Simo S.
Saransaari, Pirjo
author_facet Oja, Simo S.
Saransaari, Pirjo
author_sort Oja, Simo S.
collection PubMed
description The release of preloaded [(3)H]taurine from hippocampal slices from developing 7-day-old and young adult 3-month-old mice was studied in a superfusion system in the absence of glucose. These hypoglycemic conditions enhanced the release at both ages, the effect being markedly greater in developing mice. A depolarizing K(+) concentration accentuated the release, which indicates that it was partially mediated by exocytosis. The anion channel blockers were inhibitory, witnessing the contribution of ion channels. NO-generating agents fomented the release as a sign of the participation of excitatory amino acid receptors. The other second messenger systems were apparently less efficient. The much greater taurine release could be a reason for the well-known greater tolerance of developing nervous tissue to lack of glucose.
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spelling pubmed-45409972015-09-06 Properties of Taurine Release in Glucose-Free Media in Hippocampal Slices from Developing and Adult Mice Oja, Simo S. Saransaari, Pirjo J Amino Acids Research Article The release of preloaded [(3)H]taurine from hippocampal slices from developing 7-day-old and young adult 3-month-old mice was studied in a superfusion system in the absence of glucose. These hypoglycemic conditions enhanced the release at both ages, the effect being markedly greater in developing mice. A depolarizing K(+) concentration accentuated the release, which indicates that it was partially mediated by exocytosis. The anion channel blockers were inhibitory, witnessing the contribution of ion channels. NO-generating agents fomented the release as a sign of the participation of excitatory amino acid receptors. The other second messenger systems were apparently less efficient. The much greater taurine release could be a reason for the well-known greater tolerance of developing nervous tissue to lack of glucose. Hindawi Publishing Corporation 2015 2015-08-05 /pmc/articles/PMC4540997/ /pubmed/26347028 http://dx.doi.org/10.1155/2015/254583 Text en Copyright © 2015 S. S. Oja and P. Saransaari. https://creativecommons.org/licenses/by/3.0/ 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
Oja, Simo S.
Saransaari, Pirjo
Properties of Taurine Release in Glucose-Free Media in Hippocampal Slices from Developing and Adult Mice
title Properties of Taurine Release in Glucose-Free Media in Hippocampal Slices from Developing and Adult Mice
title_full Properties of Taurine Release in Glucose-Free Media in Hippocampal Slices from Developing and Adult Mice
title_fullStr Properties of Taurine Release in Glucose-Free Media in Hippocampal Slices from Developing and Adult Mice
title_full_unstemmed Properties of Taurine Release in Glucose-Free Media in Hippocampal Slices from Developing and Adult Mice
title_short Properties of Taurine Release in Glucose-Free Media in Hippocampal Slices from Developing and Adult Mice
title_sort properties of taurine release in glucose-free media in hippocampal slices from developing and adult mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540997/
https://www.ncbi.nlm.nih.gov/pubmed/26347028
http://dx.doi.org/10.1155/2015/254583
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