Cargando…

Why a d-β-hydroxybutyrate monoester?

Much of the world's prominent and burdensome chronic diseases, such as diabetes, Alzheimer's, and heart disease, are caused by impaired metabolism. By acting as both an efficient fuel and a powerful signalling molecule, the natural ketone body, d-β-hydroxybutyrate (βHB), may help circumven...

Descripción completa

Detalles Bibliográficos
Autores principales: Soto-Mota, Adrian, Norwitz, Nicholas G., Clarke, Kieran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065286/
https://www.ncbi.nlm.nih.gov/pubmed/32096539
http://dx.doi.org/10.1042/BST20190240
_version_ 1783505037805223936
author Soto-Mota, Adrian
Norwitz, Nicholas G.
Clarke, Kieran
author_facet Soto-Mota, Adrian
Norwitz, Nicholas G.
Clarke, Kieran
author_sort Soto-Mota, Adrian
collection PubMed
description Much of the world's prominent and burdensome chronic diseases, such as diabetes, Alzheimer's, and heart disease, are caused by impaired metabolism. By acting as both an efficient fuel and a powerful signalling molecule, the natural ketone body, d-β-hydroxybutyrate (βHB), may help circumvent the metabolic malfunctions that aggravate some diseases. Historically, dietary interventions that elevate βHB production by the liver, such as high-fat diets and partial starvation, have been used to treat chronic disease with varying degrees of success, owing to the potential downsides of such diets. The recent development of an ingestible βHB monoester provides a new tool to quickly and accurately raise blood ketone concentration, opening a myriad of potential health applications. The βHB monoester is a salt-free βHB precursor that yields only the biologically active d-isoform of the metabolite, the pharmacokinetics of which have been studied, as has safety for human consumption in athletes and healthy volunteers. This review describes fundamental concepts of endogenous and exogenous ketone body metabolism, the differences between the βHB monoester and other exogenous ketones and summarises the disease-specific biochemical and physiological rationales behind its clinical use in diabetes, neurodegenerative diseases, heart failure, sepsis related muscle atrophy, migraine, and epilepsy. We also address the limitations of using the βHB monoester as an adjunctive nutritional therapy and areas of uncertainty that could guide future research.
format Online
Article
Text
id pubmed-7065286
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Portland Press Ltd.
record_format MEDLINE/PubMed
spelling pubmed-70652862020-03-18 Why a d-β-hydroxybutyrate monoester? Soto-Mota, Adrian Norwitz, Nicholas G. Clarke, Kieran Biochem Soc Trans Review Articles Much of the world's prominent and burdensome chronic diseases, such as diabetes, Alzheimer's, and heart disease, are caused by impaired metabolism. By acting as both an efficient fuel and a powerful signalling molecule, the natural ketone body, d-β-hydroxybutyrate (βHB), may help circumvent the metabolic malfunctions that aggravate some diseases. Historically, dietary interventions that elevate βHB production by the liver, such as high-fat diets and partial starvation, have been used to treat chronic disease with varying degrees of success, owing to the potential downsides of such diets. The recent development of an ingestible βHB monoester provides a new tool to quickly and accurately raise blood ketone concentration, opening a myriad of potential health applications. The βHB monoester is a salt-free βHB precursor that yields only the biologically active d-isoform of the metabolite, the pharmacokinetics of which have been studied, as has safety for human consumption in athletes and healthy volunteers. This review describes fundamental concepts of endogenous and exogenous ketone body metabolism, the differences between the βHB monoester and other exogenous ketones and summarises the disease-specific biochemical and physiological rationales behind its clinical use in diabetes, neurodegenerative diseases, heart failure, sepsis related muscle atrophy, migraine, and epilepsy. We also address the limitations of using the βHB monoester as an adjunctive nutritional therapy and areas of uncertainty that could guide future research. Portland Press Ltd. 2020-02-28 2020-02-25 /pmc/articles/PMC7065286/ /pubmed/32096539 http://dx.doi.org/10.1042/BST20190240 Text en © 2020 The Author(s) https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . Open access for this article was enabled by the participation of University of Oxford in an all-inclusive Read & Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with JISC.
spellingShingle Review Articles
Soto-Mota, Adrian
Norwitz, Nicholas G.
Clarke, Kieran
Why a d-β-hydroxybutyrate monoester?
title Why a d-β-hydroxybutyrate monoester?
title_full Why a d-β-hydroxybutyrate monoester?
title_fullStr Why a d-β-hydroxybutyrate monoester?
title_full_unstemmed Why a d-β-hydroxybutyrate monoester?
title_short Why a d-β-hydroxybutyrate monoester?
title_sort why a d-β-hydroxybutyrate monoester?
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065286/
https://www.ncbi.nlm.nih.gov/pubmed/32096539
http://dx.doi.org/10.1042/BST20190240
work_keys_str_mv AT sotomotaadrian whyadbhydroxybutyratemonoester
AT norwitznicholasg whyadbhydroxybutyratemonoester
AT clarkekieran whyadbhydroxybutyratemonoester