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A hierarchy of manganese competition and entry in organotypic hippocampal slice cultures

Contrast agents improve clinical and basic research MRI. The manganese ion (Mn(2+)) is an essential, endogenous metal found in cells and it enhances MRI contrast because of its paramagnetic properties. Manganese‐enhanced MRI (MEMRI) has been widely used to image healthy and diseased states of the bo...

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Autores principales: Petrus, Emily, Saar, Galit, Daoust, Alexia, Dodd, Steve, Koretsky, Alan P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988546/
https://www.ncbi.nlm.nih.gov/pubmed/33538073
http://dx.doi.org/10.1002/nbm.4476
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author Petrus, Emily
Saar, Galit
Daoust, Alexia
Dodd, Steve
Koretsky, Alan P.
author_facet Petrus, Emily
Saar, Galit
Daoust, Alexia
Dodd, Steve
Koretsky, Alan P.
author_sort Petrus, Emily
collection PubMed
description Contrast agents improve clinical and basic research MRI. The manganese ion (Mn(2+)) is an essential, endogenous metal found in cells and it enhances MRI contrast because of its paramagnetic properties. Manganese‐enhanced MRI (MEMRI) has been widely used to image healthy and diseased states of the body and the brain in a variety of animal models. There has also been some work in translating the useful properties of MEMRI to humans. Mn(2+) accumulates in brain regions with high neural activity and enters cells via voltage‐dependent channels that flux calcium (Ca(2+)). In addition, metal transporters for zinc (Zn(2+)) and iron (Fe(2+)) can also transport Mn(2+). There is also transfer through channels specific for Mn(2+). Although Mn(2+) accumulates in many tissues including brain, the mechanisms and preferences of its mode of entry into cells are not well characterized. The current study used MRI on living organotypic hippocampal slice cultures to detect which transport mechanisms are preferentially used by Mn(2+) to enter cells. The use of slice culture overcomes the presence of the blood brain barrier, which limits inferences made with studies of the intact brain in vivo. A range of Mn(2+) concentrations were used and their effects on neural activity were assessed to avoid using interfering doses of Mn(2+). Zn(2+) and Fe(2+) were the most efficient competitors for Mn(2+) uptake into the cultured slices, while the presence of Ca(2+) or Ca(2+) channel antagonists had a more moderate effect. Reducing slice activity via excitatory receptor antagonists was also effective at lowering Mn(2+) uptake. In conclusion, a hierarchy of those agents which influence Mn(2+) uptake was established to enhance understanding of how Mn(2+) enters cells in a cultured slice preparation.
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spelling pubmed-79885462021-03-25 A hierarchy of manganese competition and entry in organotypic hippocampal slice cultures Petrus, Emily Saar, Galit Daoust, Alexia Dodd, Steve Koretsky, Alan P. NMR Biomed Research Articles Contrast agents improve clinical and basic research MRI. The manganese ion (Mn(2+)) is an essential, endogenous metal found in cells and it enhances MRI contrast because of its paramagnetic properties. Manganese‐enhanced MRI (MEMRI) has been widely used to image healthy and diseased states of the body and the brain in a variety of animal models. There has also been some work in translating the useful properties of MEMRI to humans. Mn(2+) accumulates in brain regions with high neural activity and enters cells via voltage‐dependent channels that flux calcium (Ca(2+)). In addition, metal transporters for zinc (Zn(2+)) and iron (Fe(2+)) can also transport Mn(2+). There is also transfer through channels specific for Mn(2+). Although Mn(2+) accumulates in many tissues including brain, the mechanisms and preferences of its mode of entry into cells are not well characterized. The current study used MRI on living organotypic hippocampal slice cultures to detect which transport mechanisms are preferentially used by Mn(2+) to enter cells. The use of slice culture overcomes the presence of the blood brain barrier, which limits inferences made with studies of the intact brain in vivo. A range of Mn(2+) concentrations were used and their effects on neural activity were assessed to avoid using interfering doses of Mn(2+). Zn(2+) and Fe(2+) were the most efficient competitors for Mn(2+) uptake into the cultured slices, while the presence of Ca(2+) or Ca(2+) channel antagonists had a more moderate effect. Reducing slice activity via excitatory receptor antagonists was also effective at lowering Mn(2+) uptake. In conclusion, a hierarchy of those agents which influence Mn(2+) uptake was established to enhance understanding of how Mn(2+) enters cells in a cultured slice preparation. John Wiley and Sons Inc. 2021-02-03 2021-04 /pmc/articles/PMC7988546/ /pubmed/33538073 http://dx.doi.org/10.1002/nbm.4476 Text en Published 2021. This article is a U.S. Government work and is in the public domain in the USA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Petrus, Emily
Saar, Galit
Daoust, Alexia
Dodd, Steve
Koretsky, Alan P.
A hierarchy of manganese competition and entry in organotypic hippocampal slice cultures
title A hierarchy of manganese competition and entry in organotypic hippocampal slice cultures
title_full A hierarchy of manganese competition and entry in organotypic hippocampal slice cultures
title_fullStr A hierarchy of manganese competition and entry in organotypic hippocampal slice cultures
title_full_unstemmed A hierarchy of manganese competition and entry in organotypic hippocampal slice cultures
title_short A hierarchy of manganese competition and entry in organotypic hippocampal slice cultures
title_sort hierarchy of manganese competition and entry in organotypic hippocampal slice cultures
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988546/
https://www.ncbi.nlm.nih.gov/pubmed/33538073
http://dx.doi.org/10.1002/nbm.4476
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