| Literature DB >> 32506121 |
Martina Ulivieri1, Joanna Monika Wierońska2, Luana Lionetto3, Katiuscia Martinello1, Paulina Cieslik2, Agnieszka Chocyk2, Martina Curto4,5,6, Luisa Di Menna1, Luisa Iacovelli7, Anna Traficante1, Francesca Liberatore7, Giada Mascio1, Nico Antenucci7, Giuseppe Giannino8, Matteo Vergassola9, Anna Pittaluga9,10, Valeria Bruno1,7, Giuseppe Battaglia1,7, Sergio Fucile1,7, Maurizio Simmaco3, Ferdinando Nicoletti1,7, Andrzej Pilc2, Francesco Fazio1.
Abstract
Cinnabarinic acid (CA) is a kynurenine metabolite that activates mGlu4 metabotropic glutamate receptors. Using a highly sensitive ultra-performance liquid chromatography/tandem mass spectrometry (UPLC/MS-MS) method, we found that CA is present in trace amounts in human brain tissue. CA levels were largely reduced in the prefrontal cortex (PFC) of individuals affected by schizophrenia. This reduction did not correlate with age, sex, duration of the disease, and duration and type of antipsychotic medication and might, therefore, represent a trait of schizophrenia. Interestingly, systemic treatment with low doses of CA (<1 mg/kg, i.p.) showed robust efficacy in several behavioral tests useful to study antipsychotic-like activity in mice and rats and attenuated MK-801-evoked glutamate release. CA failed to display antipsychotic-like activity and inhibit excitatory synaptic transmission in mice lacking mGlu4 receptors. These findings suggest that CA is a potent endogenous antipsychotic-like molecule and reduced CA levels in the PFC might contribute to the pathophysiology of schizophrenia.Entities:
Keywords: HPLC-mass; MK-801; behavior; electrophysiology; endogenous metabolite; human tissue; kynurenine pathway; mass; metabotropic glutamate receptor; mood disorder
Year: 2020 PMID: 32506121 PMCID: PMC7846105 DOI: 10.1093/schbul/sbaa074
Source DB: PubMed Journal: Schizophr Bull ISSN: 0586-7614 Impact factor: 9.306