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Why a d-β-hydroxybutyrate monoester?

Abstract:
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.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1042/bst20190240

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy & Genetics
Sub department:
Physiology Anatomy & Genetics
Role:
Author
ORCID:
0000-0002-9173-7440
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy & Genetics
Sub department:
Physiology Anatomy & Genetics
Role:
Author
ORCID:
0000-0002-3237-7553
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy & Genetics
Sub department:
Physiology Anatomy & Genetics
Role:
Author
ORCID:
0000-0002-0826-9069


Publisher:
Portland Press
Journal:
Biochemical Society Transactions More from this journal
Volume:
48
Issue:
1
Pages:
51-59
Publication date:
2020-02-25
Acceptance date:
2020-02-10
DOI:
EISSN:
1470-8752
ISSN:
0300-5127


Language:
English
Keywords:
Pubs id:
1091028
Local pid:
pubs:1091028
Deposit date:
2020-03-04

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