Journal
JOURNAL OF NEUROINFLAMMATION
Volume 18, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s12974-021-02260-6
Keywords
Schizophrenia; Cortico-cerebellar-thalamic-cortical circuit; Kynurenine pathway; 5-Hydroxyindoleacetic acid; Monoamine oxidase A; PANSS scale
Categories
Funding
- MINECO-FEDER Funds [SAF2016-75500-R]
- Miguel Servet grant [MS16/00153-CP16/00153]
- Instituto de Salud Carlos III (Spanish Ministry of Health)-General Branch Evaluation and Promotion of Health Research
- European Regional Development Fund (ERDF)
- Predoctoral Fellowship Program from ISCIII (PFIS) [FI19/00080]
- CIBERSAM
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The study found alterations in the kynurenine pathway in the prefrontal cortex and cerebellum of individuals with schizophrenia, highlighting associations with inflammatory mediators, monoamine metabolism, and symptomatology of the disorder.
Background The cortico-cerebellar-thalamic-cortical circuit has been implicated in the emergence of psychotic symptoms in schizophrenia (SZ). The kynurenine pathway (KP) has been linked to alterations in glutamatergic and monoaminergic neurotransmission and to SZ symptomatology through the production of the metabolites quinolinic acid (QA) and kynurenic acid (KYNA). Methods This work describes alterations in KP in the post-mortem prefrontal cortex (PFC) and cerebellum (CB) of 15 chronic SZ patients and 14 control subjects in PFC and 13 control subjects in CB using immunoblot for protein levels and ELISA for interleukins and QA and KYNA determinations. Monoamine metabolites were analysed by high-performance liquid chromatography and SZ symptomatology was assessed by Positive and Negative Syndrome Scale (PANSS). The association of KP with inflammatory mediators, monoamine metabolism and SZ symptomatology was explored. Results In the PFC, the presence of the anti-inflammatory cytokine IL-10 together with IDO2 and KATII enzymes decreased in SZ, while TDO and KMO enzyme expression increased. A network interaction analysis showed that in the PFC IL-10 was coupled to the QA branch of the kynurenine pathway (TDO-KMO-QA), whereas IL-10 associated with KMO in CB. KYNA in the CB inversely correlated with negative and general PANSS psychopathology. Although there were no changes in monoamine metabolite content in the PFC in SZ, a network interaction analysis showed associations between dopamine and methoxyhydroxyphenylglycol degradation metabolite. Direct correlations were found between general PANSS psychopathology and the serotonin degradation metabolite, 5-hydroxyindoleacetic acid. Interestingly, KYNA in the CB inversely correlated with 5-hydroxyindoleacetic acid in the PFC. Conclusions Thus, this work found alterations in KP in two brain areas belonging to the cortico-cerebellar-thalamic-cortical circuit associated with SZ symptomatology, with a possible impact across areas in 5-HT degradation.
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