The kynurenine pathway: a finger in every pie.


Journal

Molecular psychiatry
ISSN: 1476-5578
Titre abrégé: Mol Psychiatry
Pays: England
ID NLM: 9607835

Informations de publication

Date de publication:
01 2020
Historique:
received: 21 10 2018
accepted: 22 03 2019
revised: 18 03 2019
pubmed: 14 4 2019
medline: 18 11 2020
entrez: 14 4 2019
Statut: ppublish

Résumé

The kynurenine pathway (KP) plays a critical role in generating cellular energy in the form of nicotinamide adenine dinucleotide (NAD+). Because energy requirements are substantially increased during an immune response, the KP is a key regulator of the immune system. Perhaps more importantly in the context of psychiatry, many kynurenines are neuroactive, modulating neuroplasticity and/or exerting neurotoxic effects in part through their effects on NMDA receptor signaling and glutamatergic neurotransmission. As such, it is not surprising that the kynurenines have been implicated in psychiatric illness in the context of inflammation. However, because of their neuromodulatory properties, the kynurenines are not just additional members of a list of inflammatory mediators linked with psychiatric illness, but in preclinical studies have been shown to be necessary components of the behavioral analogs of depression and schizophrenia-like cognitive deficits. Further, as the title suggests, the KP is regulated by, and in turn regulates multiple other physiological systems that are commonly disrupted in psychiatric disorders, including endocrine, metabolic, and hormonal systems. This review provides a broad overview of the mechanistic pathways through which the kynurenines interact with these systems, thus impacting emotion, cognition, pain, metabolic function, and aging, and in so doing potentially increasing the risk of developing psychiatric disorders. Novel therapeutic approaches targeting the KP are discussed. Moreover, electroconvulsive therapy, ketamine, physical exercise, and certain non-steroidal anti-inflammatories have been shown to alter kynurenine metabolism, raising the possibility that kynurenine metabolites may have utility as treatment response or therapeutic monitoring biomarkers.

Identifiants

pubmed: 30980044
doi: 10.1038/s41380-019-0414-4
pii: 10.1038/s41380-019-0414-4
pmc: PMC6790159
mid: NIHMS1525285
doi:

Substances chimiques

NAD 0U46U6E8UK
Kynurenine 343-65-7
Tryptophan 8DUH1N11BX

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

131-147

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM121312
Pays : United States
Organisme : NIMH NIH HHS
ID : R21 MH113871
Pays : United States

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Auteurs

Jonathan Savitz (J)

Laureate Institute for Brain Research, Tulsa, OK, USA. jsavitz@laureateinstitute.org.
Oxley College of Health Sciences, The University of Tulsa, Tulsa, OK, USA. jsavitz@laureateinstitute.org.

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Classifications MeSH