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The amino acid metabolism pathway of peripheral T lymphocytes and ketamine-induced schizophrenia-like phenotype.

Peipei Wang, Linzhi Jiang, Junmei Hu, Zihan Jiang, Yu Zhang, Congliang Chen, Yanchen Lin, Mi Su, Xia Wang, Linchuan Liao

Journal of psychiatry & neuroscience : JPN January 1, 2024 DOI: 10.1503/jpn-240038 via PubMed

Summary

AI-generated from the abstract

In a mouse model of schizophrenia induced by ketamine, the number of peripheral CD3+ T cells increased. Analysis of metabolites in these immune cells and in plasma showed that amino acid metabolism was substantially altered, with elevated levels of glycine, alanine, asparagine, and aspartic acid. The precise amino acid metabolism pathway driving the schizophrenia-like phenotype has not yet been identified. The findings suggest that the metabolic profile of peripheral immune cells could provide biomarkers for diagnosing and treating psychiatric diseases.

Study at a glance

Characteristics Observational study Peer reviewed
Population Ketamine-treated mouse model of schizophrenia
Intervention Ketamine
Keywords Schizophrenia research Amino acid metabolism Immunology Neuroscience Ketamine studies
Citations 1
Key finding Peripheral CD3+ T cell count increased and levels of glycine, alanine, asparagine, and aspartic acid were elevated in the plasma of a ketamine-induced schizophrenia mouse model.

Abstract

The intricate interplay between peripheral adaptive immune cells and the central nervous system (CNS) has garnered increasing recognition. Given that alterations in cell quantities often translate into modifications in metabolite profiles and that these metabolic changes can potentially traverse the bloodstream and enter the CNS, thereby modulating the progression of mental illnesses, we sought to explore the metabolic profiles of peripheral immune cells in a ketamine-treated mouse model of schizophrenia. We used flow cytometry to scrutinize the alterations in peripheral adaptive immune cells in a ketamine-induced schizophrenia mouse model. Subsequently, we implemented an untargeted metabolomic approach with ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) to detect the metabolite profiles of peripheral abnormal lymphocytes and identify differential metabolites present in plasma. We then employed targeted metabolomics using UPLC-MS/MS to quantify the common differential metabolites detected in mouse plasma. Flow cytometry analysis detected a notable increase in the count of peripheral CD3+ T cells in a ketamine-induced schizophrenia mouse model. Subsequent untargeted metabolomics analysis revealed that the amino acid metabolism pathway underwent substantial alterations. A detailed quantification of 22 amino acid profiles in the peripheral plasma indicated significant elevation in the levels of glycine, alanine, asparagine, and aspartic acid. Our ongoing research has yet to conclusively identify the precise amino acid metabolism pathway that serves as the pivotal factor in the manifestation of the schizophrenia-like phenotype induced by ketamine. The peripheral amino acid metabolism pathway is involved in the ketamine-induced schizophrenia-like phenotype. The metabolic profile of peripheral immune cells could provide accurate biomarkers for the diagnosis and treatment of psychiatric diseases.

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