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Ketone body β-hydroxybutyrate (BHB) preserves mitochondrial bioenergetics

The ketogenic diet is an emerging therapeutic approach for refractory epilepsy, as well as certain rare and neurodegenerative disorders. The main ketone body, β-hydroxybutyrate (BHB), is the primary energy substrate endogenously produced in a ketogenic diet, however, mechanisms of its therapeutic ac...

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Autores principales: Llorente-Folch, I., Düssmann, H., Watters, O., Connolly, N. M. C., Prehn, Jochen H. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10640643/
https://www.ncbi.nlm.nih.gov/pubmed/37952048
http://dx.doi.org/10.1038/s41598-023-46776-8
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author Llorente-Folch, I.
Düssmann, H.
Watters, O.
Connolly, N. M. C.
Prehn, Jochen H. M.
author_facet Llorente-Folch, I.
Düssmann, H.
Watters, O.
Connolly, N. M. C.
Prehn, Jochen H. M.
author_sort Llorente-Folch, I.
collection PubMed
description The ketogenic diet is an emerging therapeutic approach for refractory epilepsy, as well as certain rare and neurodegenerative disorders. The main ketone body, β-hydroxybutyrate (BHB), is the primary energy substrate endogenously produced in a ketogenic diet, however, mechanisms of its therapeutic actions remain unknown. Here, we studied the effects of BHB on mitochondrial energetics, both in non-stimulated conditions and during glutamate-mediated hyperexcitation. We found that glutamate-induced hyperexcitation stimulated mitochondrial respiration in cultured cortical neurons, and that this response was greater in cultures supplemented with BHB than with glucose. BHB enabled a stronger and more sustained maximal uncoupled respiration, indicating that BHB enables neurons to respond more efficiently to increased energy demands such as induced during hyperexcitation. We found that cytosolic Ca(2+) was required for BHB-mediated enhancement of mitochondrial function, and that this enhancement was independent of the mitochondrial glutamate-aspartate carrier, Aralar/AGC1. Our results suggest that BHB exerts its protective effects against hyperexcitation by enhancing mitochondrial function through a Ca(2+)-dependent, but Aralar/AGC1-independent stimulation of mitochondrial respiration.
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spelling pubmed-106406432023-11-11 Ketone body β-hydroxybutyrate (BHB) preserves mitochondrial bioenergetics Llorente-Folch, I. Düssmann, H. Watters, O. Connolly, N. M. C. Prehn, Jochen H. M. Sci Rep Article The ketogenic diet is an emerging therapeutic approach for refractory epilepsy, as well as certain rare and neurodegenerative disorders. The main ketone body, β-hydroxybutyrate (BHB), is the primary energy substrate endogenously produced in a ketogenic diet, however, mechanisms of its therapeutic actions remain unknown. Here, we studied the effects of BHB on mitochondrial energetics, both in non-stimulated conditions and during glutamate-mediated hyperexcitation. We found that glutamate-induced hyperexcitation stimulated mitochondrial respiration in cultured cortical neurons, and that this response was greater in cultures supplemented with BHB than with glucose. BHB enabled a stronger and more sustained maximal uncoupled respiration, indicating that BHB enables neurons to respond more efficiently to increased energy demands such as induced during hyperexcitation. We found that cytosolic Ca(2+) was required for BHB-mediated enhancement of mitochondrial function, and that this enhancement was independent of the mitochondrial glutamate-aspartate carrier, Aralar/AGC1. Our results suggest that BHB exerts its protective effects against hyperexcitation by enhancing mitochondrial function through a Ca(2+)-dependent, but Aralar/AGC1-independent stimulation of mitochondrial respiration. Nature Publishing Group UK 2023-11-11 /pmc/articles/PMC10640643/ /pubmed/37952048 http://dx.doi.org/10.1038/s41598-023-46776-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Llorente-Folch, I.
Düssmann, H.
Watters, O.
Connolly, N. M. C.
Prehn, Jochen H. M.
Ketone body β-hydroxybutyrate (BHB) preserves mitochondrial bioenergetics
title Ketone body β-hydroxybutyrate (BHB) preserves mitochondrial bioenergetics
title_full Ketone body β-hydroxybutyrate (BHB) preserves mitochondrial bioenergetics
title_fullStr Ketone body β-hydroxybutyrate (BHB) preserves mitochondrial bioenergetics
title_full_unstemmed Ketone body β-hydroxybutyrate (BHB) preserves mitochondrial bioenergetics
title_short Ketone body β-hydroxybutyrate (BHB) preserves mitochondrial bioenergetics
title_sort ketone body β-hydroxybutyrate (bhb) preserves mitochondrial bioenergetics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10640643/
https://www.ncbi.nlm.nih.gov/pubmed/37952048
http://dx.doi.org/10.1038/s41598-023-46776-8
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