Literature DB >> 27629100

Inverse relationship between brain glucose and ketone metabolism in adults during short-term moderate dietary ketosis: A dual tracer quantitative positron emission tomography study.

Alexandre Courchesne-Loyer1,2, Etienne Croteau1,2, Christian-Alexandre Castellano1, Valérie St-Pierre1,2, Marie Hennebelle1,2, Stephen C Cunnane1,2,3.   

Abstract

Ketones (principally β-hydroxybutyrate and acetoacetate (AcAc)) are an important alternative fuel to glucose for the human brain, but their utilisation by the brain remains poorly understood. Our objective was to use positron emission tomography (PET) to assess the impact of diet-induced moderate ketosis on cerebral metabolic rate of acetoacetate (CMRa) and glucose (CMRglc) in healthy adults. Ten participants (35 ± 15 y) received a very high fat ketogenic diet (KD) (4.5:1; lipid:protein plus carbohydrates) for four days. CMRa and CMRglc were quantified by PET before and after the KD with the tracers, 11C-AcAc and 18F-fluorodeoxyglucose (18F-FDG), respectively. During the KD, plasma ketones increased 8-fold ( p = 0.005) while plasma glucose decreased by 24% ( p = 0.005). CMRa increased 6-fold ( p = 0.005), whereas CMRglc decreased by 20% ( p = 0.014) on the KD. Plasma ketones were positively correlated with CMRa (r = 0.93; p < 0.0001). After four days on the KD, CMRa represented 17% of whole brain energy requirements in healthy adults with a 2-fold difference across brain regions (12-24%). The CMR of ketones (AcAc and β-hydroxybutyrate combined) while on the KD was estimated to represent about 33% of brain energy requirements or approximately double the CMRa. Whether increased ketone availability raises CMR of ketones to the same extent in older people as observed here or in conditions in which chronic brain glucose hypometabolism is present remains to be determined.

Entities:  

Keywords:  Metabolism; acetoacetate; glucose; ketogenic diet; ketone; neuroimaging

Mesh:

Substances:

Year:  2016        PMID: 27629100      PMCID: PMC5531346          DOI: 10.1177/0271678X16669366

Source DB:  PubMed          Journal:  J Cereb Blood Flow Metab        ISSN: 0271-678X            Impact factor:   6.200


  48 in total

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3.  Automated synthesis of 1-[11C]acetoacetate on a TRASIS AIO module.

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Journal:  Appl Radiat Isot       Date:  2017-08-02       Impact factor: 1.513

4.  β-Hydroxybutyrate Boosts Mitochondrial and Neuronal Metabolism but is not Preferred Over Glucose Under Activated Conditions.

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Review 5.  β-Hydroxybutyrate in the Brain: One Molecule, Multiple Mechanisms.

Authors:  Lavanya B Achanta; Caroline D Rae
Journal:  Neurochem Res       Date:  2016-11-08       Impact factor: 3.996

Review 6.  Intermittent metabolic switching, neuroplasticity and brain health.

Authors:  Mark P Mattson; Keelin Moehl; Nathaniel Ghena; Maggie Schmaedick; Aiwu Cheng
Journal:  Nat Rev Neurosci       Date:  2018-01-11       Impact factor: 34.870

7.  The Growth Response to Beta-Hydroxybutyrate in SH-SY5Y Neuroblastoma Cells is Suppressed by Glucose and Pyruvate Supplementation.

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Review 8.  Alternative Fuels in Epilepsy and Amyotrophic Lateral Sclerosis.

Authors:  Tesfaye W Tefera; Kah Ni Tan; Tanya S McDonald; Karin Borges
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9.  Modulation of cerebral ketone metabolism following traumatic brain injury in humans.

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10.  Urinary ketone body loss leads to degeneration of brain white matter in elderly SLC5A8-deficient mice.

Authors:  Laurent Suissa; Virginie Flachon; Jean-Marie Guigonis; Charles-Vivien Olivieri; Fanny Burel-Vandenbos; Julien Guglielmi; Damien Ambrosetti; Matthieu Gérard; Philippe Franken; Jacques Darcourt; Luc Pellerin; Thierry Pourcher; Sabine Lindenthal
Journal:  J Cereb Blood Flow Metab       Date:  2019-09-10       Impact factor: 6.200

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