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Real-time ex-vivo measurement of brain metabolism using hyperpolarized [1-(13)C]pyruvate
The ability to directly monitor in vivo brain metabolism in real time in a matter of seconds using the dissolution dynamic nuclear polarization technology holds promise to aid the understanding of brain physiology in health and disease. However, translating the hyperpolarized signal observed in the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014998/ https://www.ncbi.nlm.nih.gov/pubmed/29934508 http://dx.doi.org/10.1038/s41598-018-27747-w |
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author | Harris, Talia Azar, Assad Sapir, Gal Gamliel, Ayelet Nardi-Schreiber, Atara Sosna, Jacob Gomori, J. Moshe Katz-Brull, Rachel |
author_facet | Harris, Talia Azar, Assad Sapir, Gal Gamliel, Ayelet Nardi-Schreiber, Atara Sosna, Jacob Gomori, J. Moshe Katz-Brull, Rachel |
author_sort | Harris, Talia |
collection | PubMed |
description | The ability to directly monitor in vivo brain metabolism in real time in a matter of seconds using the dissolution dynamic nuclear polarization technology holds promise to aid the understanding of brain physiology in health and disease. However, translating the hyperpolarized signal observed in the brain to cerebral metabolic rates is not straightforward, as the observed in vivo signals reflect also the influx of metabolites produced in the body, the cerebral blood volume, and the rate of transport across the blood brain barrier. We introduce a method to study rapid metabolism of hyperpolarized substrates in the viable rat brain slices preparation, an established ex vivo model of the brain. By retrospective evaluation of tissue motion and settling from analysis of the signal of the hyperpolarized [1-(13)C]pyruvate precursor, the T(1)s of the metabolites and their rates of production can be determined. The enzymatic rates determined here are in the range of those determined previously with classical biochemical assays and are in agreement with hyperpolarized metabolite relative signal intensities observed in the rodent brain in vivo. |
format | Online Article Text |
id | pubmed-6014998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60149982018-07-06 Real-time ex-vivo measurement of brain metabolism using hyperpolarized [1-(13)C]pyruvate Harris, Talia Azar, Assad Sapir, Gal Gamliel, Ayelet Nardi-Schreiber, Atara Sosna, Jacob Gomori, J. Moshe Katz-Brull, Rachel Sci Rep Article The ability to directly monitor in vivo brain metabolism in real time in a matter of seconds using the dissolution dynamic nuclear polarization technology holds promise to aid the understanding of brain physiology in health and disease. However, translating the hyperpolarized signal observed in the brain to cerebral metabolic rates is not straightforward, as the observed in vivo signals reflect also the influx of metabolites produced in the body, the cerebral blood volume, and the rate of transport across the blood brain barrier. We introduce a method to study rapid metabolism of hyperpolarized substrates in the viable rat brain slices preparation, an established ex vivo model of the brain. By retrospective evaluation of tissue motion and settling from analysis of the signal of the hyperpolarized [1-(13)C]pyruvate precursor, the T(1)s of the metabolites and their rates of production can be determined. The enzymatic rates determined here are in the range of those determined previously with classical biochemical assays and are in agreement with hyperpolarized metabolite relative signal intensities observed in the rodent brain in vivo. Nature Publishing Group UK 2018-06-22 /pmc/articles/PMC6014998/ /pubmed/29934508 http://dx.doi.org/10.1038/s41598-018-27747-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Harris, Talia Azar, Assad Sapir, Gal Gamliel, Ayelet Nardi-Schreiber, Atara Sosna, Jacob Gomori, J. Moshe Katz-Brull, Rachel Real-time ex-vivo measurement of brain metabolism using hyperpolarized [1-(13)C]pyruvate |
title | Real-time ex-vivo measurement of brain metabolism using hyperpolarized [1-(13)C]pyruvate |
title_full | Real-time ex-vivo measurement of brain metabolism using hyperpolarized [1-(13)C]pyruvate |
title_fullStr | Real-time ex-vivo measurement of brain metabolism using hyperpolarized [1-(13)C]pyruvate |
title_full_unstemmed | Real-time ex-vivo measurement of brain metabolism using hyperpolarized [1-(13)C]pyruvate |
title_short | Real-time ex-vivo measurement of brain metabolism using hyperpolarized [1-(13)C]pyruvate |
title_sort | real-time ex-vivo measurement of brain metabolism using hyperpolarized [1-(13)c]pyruvate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014998/ https://www.ncbi.nlm.nih.gov/pubmed/29934508 http://dx.doi.org/10.1038/s41598-018-27747-w |
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