Cargando…

Ketogenesis controls mitochondrial gene expression and rescues mitochondrial bioenergetics after cervical spinal cord injury in rats

A better understanding of the secondary injury mechanisms that occur after traumatic spinal cord injury (SCI) is essential for the development of novel neuroprotective strategies linked to the restoration of metabolic deficits. We and others have shown that Ketogenic diet (KD), a high fat, moderate...

Descripción completa

Detalles Bibliográficos
Autores principales: Seira, Oscar, Kolehmainen, Kathleen, Liu, Jie, Streijger, Femke, Haegert, Anne, Lebihan, Stéphane, Boushel, Robert, Tetzlaff, Wolfram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357839/
https://www.ncbi.nlm.nih.gov/pubmed/34381166
http://dx.doi.org/10.1038/s41598-021-96003-5
_version_ 1783737221191303168
author Seira, Oscar
Kolehmainen, Kathleen
Liu, Jie
Streijger, Femke
Haegert, Anne
Lebihan, Stéphane
Boushel, Robert
Tetzlaff, Wolfram
author_facet Seira, Oscar
Kolehmainen, Kathleen
Liu, Jie
Streijger, Femke
Haegert, Anne
Lebihan, Stéphane
Boushel, Robert
Tetzlaff, Wolfram
author_sort Seira, Oscar
collection PubMed
description A better understanding of the secondary injury mechanisms that occur after traumatic spinal cord injury (SCI) is essential for the development of novel neuroprotective strategies linked to the restoration of metabolic deficits. We and others have shown that Ketogenic diet (KD), a high fat, moderate in proteins and low in carbohydrates is neuroprotective and improves behavioural outcomes in rats with acute SCI. Ketones are alternative fuels for mitochondrial ATP generation, and can modulate signaling pathways via targeting specific receptors. Here, we demonstrate that ad libitum administration of KD for 7 days after SCI rescued mitochondrial respiratory capacity, increased parameters of mitochondrial biogenesis, affected the regulation of mitochondrial-related genes, and activated the NRF2-dependent antioxidant pathway. This study demonstrates that KD improves post-SCI metabolism by rescuing mitochondrial function and supports the potential of KD for treatment of acute SCI in humans.
format Online
Article
Text
id pubmed-8357839
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-83578392021-08-13 Ketogenesis controls mitochondrial gene expression and rescues mitochondrial bioenergetics after cervical spinal cord injury in rats Seira, Oscar Kolehmainen, Kathleen Liu, Jie Streijger, Femke Haegert, Anne Lebihan, Stéphane Boushel, Robert Tetzlaff, Wolfram Sci Rep Article A better understanding of the secondary injury mechanisms that occur after traumatic spinal cord injury (SCI) is essential for the development of novel neuroprotective strategies linked to the restoration of metabolic deficits. We and others have shown that Ketogenic diet (KD), a high fat, moderate in proteins and low in carbohydrates is neuroprotective and improves behavioural outcomes in rats with acute SCI. Ketones are alternative fuels for mitochondrial ATP generation, and can modulate signaling pathways via targeting specific receptors. Here, we demonstrate that ad libitum administration of KD for 7 days after SCI rescued mitochondrial respiratory capacity, increased parameters of mitochondrial biogenesis, affected the regulation of mitochondrial-related genes, and activated the NRF2-dependent antioxidant pathway. This study demonstrates that KD improves post-SCI metabolism by rescuing mitochondrial function and supports the potential of KD for treatment of acute SCI in humans. Nature Publishing Group UK 2021-08-11 /pmc/articles/PMC8357839/ /pubmed/34381166 http://dx.doi.org/10.1038/s41598-021-96003-5 Text en © The Author(s) 2021 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
Seira, Oscar
Kolehmainen, Kathleen
Liu, Jie
Streijger, Femke
Haegert, Anne
Lebihan, Stéphane
Boushel, Robert
Tetzlaff, Wolfram
Ketogenesis controls mitochondrial gene expression and rescues mitochondrial bioenergetics after cervical spinal cord injury in rats
title Ketogenesis controls mitochondrial gene expression and rescues mitochondrial bioenergetics after cervical spinal cord injury in rats
title_full Ketogenesis controls mitochondrial gene expression and rescues mitochondrial bioenergetics after cervical spinal cord injury in rats
title_fullStr Ketogenesis controls mitochondrial gene expression and rescues mitochondrial bioenergetics after cervical spinal cord injury in rats
title_full_unstemmed Ketogenesis controls mitochondrial gene expression and rescues mitochondrial bioenergetics after cervical spinal cord injury in rats
title_short Ketogenesis controls mitochondrial gene expression and rescues mitochondrial bioenergetics after cervical spinal cord injury in rats
title_sort ketogenesis controls mitochondrial gene expression and rescues mitochondrial bioenergetics after cervical spinal cord injury in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357839/
https://www.ncbi.nlm.nih.gov/pubmed/34381166
http://dx.doi.org/10.1038/s41598-021-96003-5
work_keys_str_mv AT seiraoscar ketogenesiscontrolsmitochondrialgeneexpressionandrescuesmitochondrialbioenergeticsaftercervicalspinalcordinjuryinrats
AT kolehmainenkathleen ketogenesiscontrolsmitochondrialgeneexpressionandrescuesmitochondrialbioenergeticsaftercervicalspinalcordinjuryinrats
AT liujie ketogenesiscontrolsmitochondrialgeneexpressionandrescuesmitochondrialbioenergeticsaftercervicalspinalcordinjuryinrats
AT streijgerfemke ketogenesiscontrolsmitochondrialgeneexpressionandrescuesmitochondrialbioenergeticsaftercervicalspinalcordinjuryinrats
AT haegertanne ketogenesiscontrolsmitochondrialgeneexpressionandrescuesmitochondrialbioenergeticsaftercervicalspinalcordinjuryinrats
AT lebihanstephane ketogenesiscontrolsmitochondrialgeneexpressionandrescuesmitochondrialbioenergeticsaftercervicalspinalcordinjuryinrats
AT boushelrobert ketogenesiscontrolsmitochondrialgeneexpressionandrescuesmitochondrialbioenergeticsaftercervicalspinalcordinjuryinrats
AT tetzlaffwolfram ketogenesiscontrolsmitochondrialgeneexpressionandrescuesmitochondrialbioenergeticsaftercervicalspinalcordinjuryinrats