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Induced Ketosis as a Treatment for Neuroprogressive Disorders: Food for Thought?

Version 3 2024-06-18, 19:21
Version 2 2024-06-04, 12:08
Version 1 2020-03-12, 14:24
journal contribution
posted on 2024-06-18, 19:21 authored by G Morris, BK Puri, A Carvalho, M Maes, Michael BerkMichael Berk, Anu RuusunenAnu Ruusunen, Lisa OliveLisa Olive
AbstractInduced ketosis (or ketone body ingestion) can ameliorate several changes associated with neuroprogressive disorders, including schizophrenia, bipolar disorder, and major depressive disorder. Thus, the effects of glucose hypometabolism can be bypassed through the entry of beta-hydroxybutyrate, providing an alternative source of energy to glucose. The weight of evidence suggests that induced ketosis reduces levels of oxidative stress, mitochondrial dysfunction, and inflammation—core features of the above disorders. There are also data to suggest that induced ketosis may be able to target other molecules and signaling pathways whose levels and/or activity are also known to be abnormal in at least some patients suffering from these illnesses such as peroxisome proliferator-activated receptors, increased activity of the Kelch-like ECH-associated protein/nuclear factor erythroid 2-related factor 2, Sirtuin-1 nuclear factor-κB p65, and nicotinamide adenine dinucleotide (NAD). This review explains the mechanisms by which induced ketosis might reduce mitochondrial dysfunction, inflammation, and oxidative stress in neuropsychiatric disorders and ameliorate abnormal levels of molecules and signaling pathways that also appear to contribute to the pathophysiology of these illnesses. This review also examines safety data relating to induced ketosis over the long term and discusses the design of future studies.

History

Journal

International Journal of Neuropsychopharmacology

Volume

23

Pagination

366-384

Location

England

Open access

  • Yes

ISSN

1461-1457

eISSN

1469-5111

Language

English

Publication classification

C1 Refereed article in a scholarly journal

Issue

6

Publisher

OXFORD UNIV PRESS