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Modelling the neurodevelopmental pathogenesis in neuropsychiatric disorders. Bioactive kynurenines and their analogues as neuroprotective agents—in celebration of 80th birthday of Professor Peter Riederer

  • Psychiatry and Preclinical Psychiatric Studies - Review Article
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Abstract

Following introduction of the monoamine oxidase type B inhibitor selegiline for the treatment of Parkinson’s disease (PD), discovery of the action mechanism of Alzheimer’s disease-modifying agent memantine, the role of iron in PD, and the loss of electron transport chain complex I in PD, and development of the concept of clinical neuroprotection, Peter Riederer launched one of the most challenging research project neurodevelopmental aspects of neuropsychiatric disorders. The neurodevelopmental theory holds that a disruption of normal brain development in utero or during early life underlies the subsequent emergence of neuropsychiatric symptoms during later life. Indeed, the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition and the International Classification of Diseases, 11th Revision categorize autism spectrum disorder and attention deficit hyperactivity disorder in neurodevelopmental disorders (NDDs). More and more evidence, especially from preclinical studies, is revealing that neurodevelopmental pathology is not limited to the diagnostic class above, but also contributes to the development of other psychiatric disorders such as schizophrenia, bipolar disorder, and obsessive–compulsive disorder as well as neurodegenerative diseases such as PD and Huntington’s disease. Preclinical animal research is taking a lead in understanding the pathomechanisms of NDDs, searching for novel targets, and developing new neuroprotective agents against NDDs. This narrative review discusses emerging evidence of the neurodevelopmental etiology of neuropsychiatric disorders, recent advances in modelling neurodevelopmental pathogenesis, potential strategies of clinical neuroprotection using novel kynurenine metabolites and analogues, and future research direction for NDDs.

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Abbreviations

AA:

Anthranilic acid

ADGL3:

Adhesion G protein-coupled receptor L3

AHR:

Aryl hydrocarbon receptor

ADHD:

Attention deficit hyperactive disorder

ASD:

Autism spectrum disorder

BBB:

Blood-brain barrier

BP:

Bipolar disorder

CNTNAP2:

Contactin-associated protein-like 2

DISC1:

Disrupted in Schizophrenia 1

DSM-5:

Diagnostic and statistical manual of mental disorders, fifth edition

HD:

Huntington’s disease

3-HAA:

3-Hydroxyanthranilic acid

3-HK:

3-Hydroxy-L-kynurenine

IDO:

Indoleamine 2,3-dioxygenase

ICD-11:

International classification of diseases, 11th revision

KYNU:

Kynureninase

KYN:

Kynurenine

KAT:

Kynurenine aminotransferase

KMO:

Kynurenine 3-monooxygenase

KYNA:

Kynurenic acid

MIA:

Maternal immune activation

NMDA:

N-methyl-D-aspartate

NDDs:

Neurodevelopmental disorders

NAD+ :

Nicotinamide adenine dinucleotide

OCD:

Obsessive compulsive disorder

PD:

Parkinson’s disease

poly I:C:

Polyinosinic polycytidylic acid

PTSD:

Post-traumatic stress syndrome

PINK:

Phosphatase and tensin homolog (PTEN)-induced kinase

QA:

Quinolinic acid

SCZ:

Schizophrenia

SHANK3:

Src-homology 3 and multiple ankyrin repeat domains 3

Trp:

Tryptophan

TDO:

Tryptophan 2,3-dioxygenase

VPA:

Valproic acid

XA:

Xanthurenic acid

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Acknowledgements

This work is funded by National Research, Development and Innovation Office [NKFIH-1279-2/2020 TKP 2020], TUDFO/47138-1/2019-ITM, National Scientific Research Fund [OTKA138125], and MTA-JSP-050609. Helga Polyák was supported by the New National Excellence Program of the Ministry for Innovation and Technology from the source of the National Research, Development and Innovation Fund [ÚNKP-21-3] and EFOP-3.6.3-VEKOP-16-2017-00009.

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Correspondence to László Vécsei.

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Tanaka, M., Spekker, E., Szabó, Á. et al. Modelling the neurodevelopmental pathogenesis in neuropsychiatric disorders. Bioactive kynurenines and their analogues as neuroprotective agents—in celebration of 80th birthday of Professor Peter Riederer. J Neural Transm 129, 627–642 (2022). https://doi.org/10.1007/s00702-022-02513-5

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  • DOI: https://doi.org/10.1007/s00702-022-02513-5

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