Literature DB >> 20226539

Plasma alanine levels increase in patients with schizophrenia as their clinical symptoms improve-Results from the Juntendo University Schizophrenia Projects (JUSP).

Tokiko Hatano1, Tohru Ohnuma, Yoshie Sakai, Nobuto Shibata, Hitoshi Maeshima, Ryo Hanzawa, Toshihito Suzuki, Heii Arai.   

Abstract

UNLABELLED: Since oral administration of d-alanine, an agonist that binds to the glycine site of N-methyl-d-aspartate (NMDA) receptors, improves the positive and cognitive symptoms of patients with schizophrenia, measurement of endogenous plasma alanine levels could serve as a clinical marker for schizophrenia severity and improvement. Mean plasma alanine levels were compared in healthy controls and patients with schizophrenia during the clinical course of the disease.
METHODS: eighty-one Japanese patients with schizophrenia and 50 age- and gender-matched healthy controls were studied. Plasma alanine levels were measured twice, during the acute stage and during the remission stage, using high-performance liquid chromatography. On admission, lower plasma alanine levels in patients with schizophrenia were accompanied by more severe schizophrenic symptoms, especially positive symptoms. The plasma alanine levels in patients with schizophrenia increased significantly from the time of admission to discharge, when they were significantly higher than control levels. An increase in plasma alanine levels from the acute stage to the remission stage of schizophrenia was correlated with improvement in symptoms. Drug-naïve patients did not show a significant difference in plasma alanine levels when compared with healthy controls. The measurement of plasma alanine levels may be a therapeutic marker for schizophrenia. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20226539     DOI: 10.1016/j.psychres.2010.02.014

Source DB:  PubMed          Journal:  Psychiatry Res        ISSN: 0165-1781            Impact factor:   3.222


  7 in total

1.  Meta-analysis of the efficacy of adjunctive NMDA receptor modulators in chronic schizophrenia.

Authors:  Surendra P Singh; Vidhi Singh
Journal:  CNS Drugs       Date:  2011-10-01       Impact factor: 5.749

2.  Significance of measurements of peripheral carbonyl stress markers in a cross-sectional and longitudinal study in patients with acute-stage schizophrenia.

Authors:  Narimasa Katsuta; Tohru Ohnuma; Hitoshi Maeshima; Yuto Takebayashi; Motoyuki Higa; Mayu Takeda; Toru Nakamura; Shohei Nishimon; Takahiro Sannohe; Yuri Hotta; Ryo Hanzawa; Ryoko Higashiyama; Nobuto Shibata; Heii Arai
Journal:  Schizophr Bull       Date:  2014-01-21       Impact factor: 9.306

3.  Metabolomics mapping changed after olanzapine therapy in drug-naive schizophrenia patients-the significant impact of gene polymorphisms.

Authors:  Bensu Karahalil; Aylin Elkama; Mehmet Ak; Emirhan Nemutlu
Journal:  Toxicol Res (Camb)       Date:  2022-06-01       Impact factor: 2.680

Review 4.  Rational and Translational Implications of D-Amino Acids for Treatment-Resistant Schizophrenia: From Neurobiology to the Clinics.

Authors:  Andrea de Bartolomeis; Licia Vellucci; Mark C Austin; Giuseppe De Simone; Annarita Barone
Journal:  Biomolecules       Date:  2022-06-29

5.  Comparative Metagenomics and Metabolomes Reveals Abnormal Metabolism Activity Is Associated with Gut Microbiota in Alzheimer's Disease Mice.

Authors:  Peilin Sun; Hua Zhu; Xue Li; Weixiong Shi; Yaxi Guo; Xiaopeng Du; Ling Zhang; Lei Su; Chuan Qin
Journal:  Int J Mol Sci       Date:  2022-09-30       Impact factor: 6.208

6.  Modulating D-amino acid oxidase (DAAO) substrate specificity through facilitated solvent access.

Authors:  Kalyanasundaram Subramanian; Artur Góra; Ruud Spruijt; Karolina Mitusińska; Maria Suarez-Diez; Vitor Martins Dos Santos; Peter J Schaap
Journal:  PLoS One       Date:  2018-06-15       Impact factor: 3.240

7.  Analysis of Gut Microbiota and Their Metabolic Potential in Patients with Schizophrenia Treated with Olanzapine: Results from a Six-Week Observational Prospective Cohort Study.

Authors:  Justyna Pełka-Wysiecka; Mariusz Kaczmarczyk; Agata Bąba-Kubiś; Paweł Liśkiewicz; Michał Wroński; Karolina Skonieczna-Żydecka; Wojciech Marlicz; Błażej Misiak; Teresa Starzyńska; Jolanta Kucharska-Mazur; Igor Łoniewski; Jerzy Samochowiec
Journal:  J Clin Med       Date:  2019-10-03       Impact factor: 4.241

  7 in total

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