Cargando…
A new ketogenic formulation improves functional outcome and reduces tissue loss following traumatic brain injury in adult mice
Rationale: Traumatic brain injury (TBI) leads to neurological impairment, with no satisfactory treatments available. Classical ketogenic diets (KD), which reduce reliance on carbohydrates and provide ketones as fuel, have neuroprotective potential, but their high fat content reduces compliance, and...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681084/ https://www.ncbi.nlm.nih.gov/pubmed/33391479 http://dx.doi.org/10.7150/thno.48995 |
_version_ | 1783612563441844224 |
---|---|
author | Thau-Zuchman, Orli Svendsen, Linda Dyall, Simon C. Paredes-Esquivel, Ursula Rhodes, Molly Priestley, John V. Feichtinger, René G. Kofler, Barbara Lotstra, Susanne Verkuyl, J. Martin Hageman, Robert J. Broersen, Laus M. van Wijk, Nick Silva, Jose P. Tremoleda, Jordi L. Michael-Titus, Adina T. |
author_facet | Thau-Zuchman, Orli Svendsen, Linda Dyall, Simon C. Paredes-Esquivel, Ursula Rhodes, Molly Priestley, John V. Feichtinger, René G. Kofler, Barbara Lotstra, Susanne Verkuyl, J. Martin Hageman, Robert J. Broersen, Laus M. van Wijk, Nick Silva, Jose P. Tremoleda, Jordi L. Michael-Titus, Adina T. |
author_sort | Thau-Zuchman, Orli |
collection | PubMed |
description | Rationale: Traumatic brain injury (TBI) leads to neurological impairment, with no satisfactory treatments available. Classical ketogenic diets (KD), which reduce reliance on carbohydrates and provide ketones as fuel, have neuroprotective potential, but their high fat content reduces compliance, and experimental evidence suggests they protect juvenile brain against TBI, but not adult brain, which would strongly limit their applicability in TBI. Methods: We designed a new-KD with a fat to carbohydrate plus protein ratio of 2:1, containing medium chain triglycerides (MCT), docosahexaenoic acid (DHA), low glycaemic index carbohydrates, fibres and the ketogenic amino acid leucine, and evaluated its neuroprotective potential in adult TBI. Adult male C57BL6 mice were injured by controlled cortical impact (CCI) and assessed for 70 days, during which they received a control diet or the new-KD. Results: The new-KD, that markedly increased plasma Beta-hydroxybutyrate (β-HB), significantly attenuated sensorimotor deficits and corrected spatial memory deficit. The lesion size, perilesional inflammation and oxidation were markedly reduced. Oligodendrocyte loss appeared to be significantly reduced. TBI activated the mTOR pathway and the new-KD enhanced this increase and increased histone acetylation and methylation. Conclusion: The behavioural improvement and tissue protection provide proof of principle that this new formulation has therapeutic potential in adult TBI. |
format | Online Article Text |
id | pubmed-7681084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-76810842021-01-01 A new ketogenic formulation improves functional outcome and reduces tissue loss following traumatic brain injury in adult mice Thau-Zuchman, Orli Svendsen, Linda Dyall, Simon C. Paredes-Esquivel, Ursula Rhodes, Molly Priestley, John V. Feichtinger, René G. Kofler, Barbara Lotstra, Susanne Verkuyl, J. Martin Hageman, Robert J. Broersen, Laus M. van Wijk, Nick Silva, Jose P. Tremoleda, Jordi L. Michael-Titus, Adina T. Theranostics Research Paper Rationale: Traumatic brain injury (TBI) leads to neurological impairment, with no satisfactory treatments available. Classical ketogenic diets (KD), which reduce reliance on carbohydrates and provide ketones as fuel, have neuroprotective potential, but their high fat content reduces compliance, and experimental evidence suggests they protect juvenile brain against TBI, but not adult brain, which would strongly limit their applicability in TBI. Methods: We designed a new-KD with a fat to carbohydrate plus protein ratio of 2:1, containing medium chain triglycerides (MCT), docosahexaenoic acid (DHA), low glycaemic index carbohydrates, fibres and the ketogenic amino acid leucine, and evaluated its neuroprotective potential in adult TBI. Adult male C57BL6 mice were injured by controlled cortical impact (CCI) and assessed for 70 days, during which they received a control diet or the new-KD. Results: The new-KD, that markedly increased plasma Beta-hydroxybutyrate (β-HB), significantly attenuated sensorimotor deficits and corrected spatial memory deficit. The lesion size, perilesional inflammation and oxidation were markedly reduced. Oligodendrocyte loss appeared to be significantly reduced. TBI activated the mTOR pathway and the new-KD enhanced this increase and increased histone acetylation and methylation. Conclusion: The behavioural improvement and tissue protection provide proof of principle that this new formulation has therapeutic potential in adult TBI. Ivyspring International Publisher 2021-01-01 /pmc/articles/PMC7681084/ /pubmed/33391479 http://dx.doi.org/10.7150/thno.48995 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Thau-Zuchman, Orli Svendsen, Linda Dyall, Simon C. Paredes-Esquivel, Ursula Rhodes, Molly Priestley, John V. Feichtinger, René G. Kofler, Barbara Lotstra, Susanne Verkuyl, J. Martin Hageman, Robert J. Broersen, Laus M. van Wijk, Nick Silva, Jose P. Tremoleda, Jordi L. Michael-Titus, Adina T. A new ketogenic formulation improves functional outcome and reduces tissue loss following traumatic brain injury in adult mice |
title | A new ketogenic formulation improves functional outcome and reduces tissue loss following traumatic brain injury in adult mice |
title_full | A new ketogenic formulation improves functional outcome and reduces tissue loss following traumatic brain injury in adult mice |
title_fullStr | A new ketogenic formulation improves functional outcome and reduces tissue loss following traumatic brain injury in adult mice |
title_full_unstemmed | A new ketogenic formulation improves functional outcome and reduces tissue loss following traumatic brain injury in adult mice |
title_short | A new ketogenic formulation improves functional outcome and reduces tissue loss following traumatic brain injury in adult mice |
title_sort | new ketogenic formulation improves functional outcome and reduces tissue loss following traumatic brain injury in adult mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681084/ https://www.ncbi.nlm.nih.gov/pubmed/33391479 http://dx.doi.org/10.7150/thno.48995 |
work_keys_str_mv | AT thauzuchmanorli anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT svendsenlinda anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT dyallsimonc anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT paredesesquivelursula anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT rhodesmolly anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT priestleyjohnv anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT feichtingerreneg anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT koflerbarbara anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT lotstrasusanne anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT verkuyljmartin anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT hagemanrobertj anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT broersenlausm anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT vanwijknick anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT silvajosep anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT tremoledajordil anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT michaeltitusadinat anewketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT thauzuchmanorli newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT svendsenlinda newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT dyallsimonc newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT paredesesquivelursula newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT rhodesmolly newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT priestleyjohnv newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT feichtingerreneg newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT koflerbarbara newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT lotstrasusanne newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT verkuyljmartin newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT hagemanrobertj newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT broersenlausm newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT vanwijknick newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT silvajosep newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT tremoledajordil newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice AT michaeltitusadinat newketogenicformulationimprovesfunctionaloutcomeandreducestissuelossfollowingtraumaticbraininjuryinadultmice |