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Ketamine and Zinc: Treatment of Anorexia Nervosa Via Dual NMDA Receptor Modulation

Anorexia nervosa is a disorder associated with serious adverse health outcomes, for which there is currently considerable treatment ineffectiveness. Characterised by restrictive eating behaviours, distorted body image perceptions and excessive physical activity, there is growing recognition anorexia...

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Autores principales: Mitchell, Jules S., Hermens, Daniel F., Bennett, Maxwell R., Can, Adem T., Lagopoulos, Jim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911496/
https://www.ncbi.nlm.nih.gov/pubmed/36681939
http://dx.doi.org/10.1007/s40263-022-00984-4
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author Mitchell, Jules S.
Hermens, Daniel F.
Bennett, Maxwell R.
Can, Adem T.
Lagopoulos, Jim
author_facet Mitchell, Jules S.
Hermens, Daniel F.
Bennett, Maxwell R.
Can, Adem T.
Lagopoulos, Jim
author_sort Mitchell, Jules S.
collection PubMed
description Anorexia nervosa is a disorder associated with serious adverse health outcomes, for which there is currently considerable treatment ineffectiveness. Characterised by restrictive eating behaviours, distorted body image perceptions and excessive physical activity, there is growing recognition anorexia nervosa is associated with underlying dysfunction in excitatory and inhibitory neurometabolite metabolism and signalling. This narrative review critically explores the role of N-methyl-d-aspartate receptor-mediated excitatory and inhibitory neurometabolite dysfunction in anorexia nervosa and its associated biomarkers. The existing magnetic resonance spectroscopy literature in anorexia nervosa is reviewed and we outline the brain region-specific neurometabolite changes that have been reported and their connection to anorexia nervosa psychopathology. Considering the proposed role of dysfunctional neurotransmission in anorexia nervosa, the potential utility of zinc supplementation and sub-anaesthetic doses of ketamine in normalising this is discussed with reference to previous research in anorexia nervosa and other neuropsychiatric conditions. The rationale for future research to investigate the combined use of low-dose ketamine and zinc supplementation to potentially extend the therapeutic benefits in anorexia nervosa is subsequently explored and promising biological markers for assessing and potentially predicting treatment response are outlined.
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spelling pubmed-99114962023-02-11 Ketamine and Zinc: Treatment of Anorexia Nervosa Via Dual NMDA Receptor Modulation Mitchell, Jules S. Hermens, Daniel F. Bennett, Maxwell R. Can, Adem T. Lagopoulos, Jim CNS Drugs Review Article Anorexia nervosa is a disorder associated with serious adverse health outcomes, for which there is currently considerable treatment ineffectiveness. Characterised by restrictive eating behaviours, distorted body image perceptions and excessive physical activity, there is growing recognition anorexia nervosa is associated with underlying dysfunction in excitatory and inhibitory neurometabolite metabolism and signalling. This narrative review critically explores the role of N-methyl-d-aspartate receptor-mediated excitatory and inhibitory neurometabolite dysfunction in anorexia nervosa and its associated biomarkers. The existing magnetic resonance spectroscopy literature in anorexia nervosa is reviewed and we outline the brain region-specific neurometabolite changes that have been reported and their connection to anorexia nervosa psychopathology. Considering the proposed role of dysfunctional neurotransmission in anorexia nervosa, the potential utility of zinc supplementation and sub-anaesthetic doses of ketamine in normalising this is discussed with reference to previous research in anorexia nervosa and other neuropsychiatric conditions. The rationale for future research to investigate the combined use of low-dose ketamine and zinc supplementation to potentially extend the therapeutic benefits in anorexia nervosa is subsequently explored and promising biological markers for assessing and potentially predicting treatment response are outlined. Springer International Publishing 2023-01-22 2023 /pmc/articles/PMC9911496/ /pubmed/36681939 http://dx.doi.org/10.1007/s40263-022-00984-4 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Review Article
Mitchell, Jules S.
Hermens, Daniel F.
Bennett, Maxwell R.
Can, Adem T.
Lagopoulos, Jim
Ketamine and Zinc: Treatment of Anorexia Nervosa Via Dual NMDA Receptor Modulation
title Ketamine and Zinc: Treatment of Anorexia Nervosa Via Dual NMDA Receptor Modulation
title_full Ketamine and Zinc: Treatment of Anorexia Nervosa Via Dual NMDA Receptor Modulation
title_fullStr Ketamine and Zinc: Treatment of Anorexia Nervosa Via Dual NMDA Receptor Modulation
title_full_unstemmed Ketamine and Zinc: Treatment of Anorexia Nervosa Via Dual NMDA Receptor Modulation
title_short Ketamine and Zinc: Treatment of Anorexia Nervosa Via Dual NMDA Receptor Modulation
title_sort ketamine and zinc: treatment of anorexia nervosa via dual nmda receptor modulation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911496/
https://www.ncbi.nlm.nih.gov/pubmed/36681939
http://dx.doi.org/10.1007/s40263-022-00984-4
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