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In situ microwave fixation provides an instantaneous snapshot of the brain metabolome
Brain glucose metabolism is highly heterogeneous among brain regions and continues postmortem. In particular, we demonstrate exhaustion of glycogen and glucose and an increase in lactate production during conventional rapid brain resection and preservation by liquid nitrogen. In contrast, we show th...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163000/ https://www.ncbi.nlm.nih.gov/pubmed/37159672 http://dx.doi.org/10.1016/j.crmeth.2023.100455 |
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author | Juras, Jelena A. Webb, Madison B. Young, Lyndsay E.A. Markussen, Kia H. Hawkinson, Tara R. Buoncristiani, Michael D. Bolton, Kayli E. Coburn, Peyton T. Williams, Meredith I. Sun, Lisa P.Y. Sanders, William C. Bruntz, Ronald C. Conroy, Lindsey R. Wang, Chi Gentry, Matthew S. Smith, Bret N. Sun, Ramon C. |
author_facet | Juras, Jelena A. Webb, Madison B. Young, Lyndsay E.A. Markussen, Kia H. Hawkinson, Tara R. Buoncristiani, Michael D. Bolton, Kayli E. Coburn, Peyton T. Williams, Meredith I. Sun, Lisa P.Y. Sanders, William C. Bruntz, Ronald C. Conroy, Lindsey R. Wang, Chi Gentry, Matthew S. Smith, Bret N. Sun, Ramon C. |
author_sort | Juras, Jelena A. |
collection | PubMed |
description | Brain glucose metabolism is highly heterogeneous among brain regions and continues postmortem. In particular, we demonstrate exhaustion of glycogen and glucose and an increase in lactate production during conventional rapid brain resection and preservation by liquid nitrogen. In contrast, we show that these postmortem changes are not observed with simultaneous animal sacrifice and in situ fixation with focused, high-power microwave. We further employ microwave fixation to define brain glucose metabolism in the mouse model of streptozotocin-induced type 1 diabetes. Using both total pool and isotope tracing analyses, we identified global glucose hypometabolism in multiple brain regions, evidenced by reduced (13)C enrichment into glycogen, glycolysis, and the tricarboxylic acid (TCA) cycle. Reduced glucose metabolism correlated with a marked decrease in GLUT2 expression and several metabolic enzymes in unique brain regions. In conclusion, our study supports the incorporation of microwave fixation for more accurate studies of brain metabolism in rodent models. |
format | Online Article Text |
id | pubmed-10163000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101630002023-05-07 In situ microwave fixation provides an instantaneous snapshot of the brain metabolome Juras, Jelena A. Webb, Madison B. Young, Lyndsay E.A. Markussen, Kia H. Hawkinson, Tara R. Buoncristiani, Michael D. Bolton, Kayli E. Coburn, Peyton T. Williams, Meredith I. Sun, Lisa P.Y. Sanders, William C. Bruntz, Ronald C. Conroy, Lindsey R. Wang, Chi Gentry, Matthew S. Smith, Bret N. Sun, Ramon C. Cell Rep Methods Report Brain glucose metabolism is highly heterogeneous among brain regions and continues postmortem. In particular, we demonstrate exhaustion of glycogen and glucose and an increase in lactate production during conventional rapid brain resection and preservation by liquid nitrogen. In contrast, we show that these postmortem changes are not observed with simultaneous animal sacrifice and in situ fixation with focused, high-power microwave. We further employ microwave fixation to define brain glucose metabolism in the mouse model of streptozotocin-induced type 1 diabetes. Using both total pool and isotope tracing analyses, we identified global glucose hypometabolism in multiple brain regions, evidenced by reduced (13)C enrichment into glycogen, glycolysis, and the tricarboxylic acid (TCA) cycle. Reduced glucose metabolism correlated with a marked decrease in GLUT2 expression and several metabolic enzymes in unique brain regions. In conclusion, our study supports the incorporation of microwave fixation for more accurate studies of brain metabolism in rodent models. Elsevier 2023-04-18 /pmc/articles/PMC10163000/ /pubmed/37159672 http://dx.doi.org/10.1016/j.crmeth.2023.100455 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Report Juras, Jelena A. Webb, Madison B. Young, Lyndsay E.A. Markussen, Kia H. Hawkinson, Tara R. Buoncristiani, Michael D. Bolton, Kayli E. Coburn, Peyton T. Williams, Meredith I. Sun, Lisa P.Y. Sanders, William C. Bruntz, Ronald C. Conroy, Lindsey R. Wang, Chi Gentry, Matthew S. Smith, Bret N. Sun, Ramon C. In situ microwave fixation provides an instantaneous snapshot of the brain metabolome |
title | In situ microwave fixation provides an instantaneous snapshot of the brain metabolome |
title_full | In situ microwave fixation provides an instantaneous snapshot of the brain metabolome |
title_fullStr | In situ microwave fixation provides an instantaneous snapshot of the brain metabolome |
title_full_unstemmed | In situ microwave fixation provides an instantaneous snapshot of the brain metabolome |
title_short | In situ microwave fixation provides an instantaneous snapshot of the brain metabolome |
title_sort | in situ microwave fixation provides an instantaneous snapshot of the brain metabolome |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163000/ https://www.ncbi.nlm.nih.gov/pubmed/37159672 http://dx.doi.org/10.1016/j.crmeth.2023.100455 |
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