Changes in plasma glycine, L-serine, and D-serine levels in patients with schizophrenia as their clinical symptoms improve: Results from the Juntendo University Schizophrenia Projects (JUSP)

被引:70
作者
Ohnuma, Tohru [1 ]
Sakai, Yoshie [1 ]
Maeshima, Hitoshi [1 ]
Hatano, Tokiko [1 ]
Hanzawa, Ryo [1 ]
Abe, Sawako [1 ]
Kida, Sayaka [1 ]
Shibata, Nobuto [1 ]
Suzuki, Toshihito [1 ]
Arai, Heii [1 ]
机构
[1] Juntendo Univ, Sch Med, JUSP, Dept Psychiat,Bunkyo Ku, Tokyo 1138421, Japan
关键词
Glutamate; Glycine; Plasma; Schizophrenia; Serine; Symptom;
D O I
10.1016/j.pnpbp.2008.07.022
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: Based on the hypothesis of NMDA receptor hypofunction in schizophrenia, plasma glycine, L-serine, and D-serine levels have been studied, since they could serve as biological markers. However, changes over time in the levels of these amino acids in schizophrenic patients have not been investigated. To clarify the mean plasma glycine, L-serine, and D-serine levels in patients with schizophrenia, levels of these amino acids were compared between healthy controls and patients with schizophrenia. The plasma levels of these amino acids during the clinical course of schizophrenia were also compared. Methods: Eighty-nine Japanese patients with schizophrenia and 50 age- and gender-matched healthy controls were studied. Plasma glycine, L-serine, and D-serine levels and their ratios were measured twice, during the acute stage and during the remission stage, using high-performance liquid chromatography. Results: The admission plasma glycine, L-serine, and D-serine levels of schizophrenic patients were higher than those of healthy controls. There were no significant differences between drug-naive patients and healthy controls in the admission levels of the plasma amino acids, but chronically medicated patients had higher admission plasma glycine and D-serine levels. Only the D-serine level and the D-/L-serine ratio were markedly significantly increased in schizophrenic patients from the time of admission to the time of discharge as their clinical symptoms improved. in addition, the increase in the Plasma D-serine levels of drug-naive patients was correlated with improvements in positive symptoms. Conclusions: Plasma amino acid levels, especially D-serine levels, could be useful as a "therapeutic" or "clinical state" marker in patients with acute schizophrenia. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1905 / 1912
页数:8
相关论文
共 68 条
[1]   Spatial memory deficits induced by perinatal treatment of rats with PCP and reversal effect of D-serine [J].
Andersen, JD ;
Pouzet, B .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (06) :1080-1090
[2]   PLASMA SERINE IN SCHIZOPHRENICS AND CONTROLS MEASURED BY GAS-CHROMATOGRAPHY MASS-SPECTROMETRY [J].
BARUAH, S ;
WAZIRI, R ;
HEGWOOD, TS ;
MALLIS, LM .
PSYCHIATRY RESEARCH, 1991, 37 (03) :261-270
[3]   Preferred stereoselective brain uptake of D-serine -: a modulator of glutamatergic neurotransmission [J].
Bauer, D ;
Hamacher, K ;
Bröer, S ;
Pauleit, D ;
Palm, C ;
Zilles, K ;
Coenen, HH ;
Langen, KJ .
NUCLEAR MEDICINE AND BIOLOGY, 2005, 32 (08) :793-797
[4]  
BECH P, 1986, ACTA PSYCHIAT SCAND, V73, P1
[5]   A CSF and postmortem brain study of D-serine metabolic parameters in schizophrenia [J].
Bendikov, Inna ;
Nadri, Carmit ;
Amar, Shirly ;
Panizzutti, Rogerio ;
De Miranda, Joari ;
Wolosker, Herman ;
Agam, Galila .
SCHIZOPHRENIA RESEARCH, 2007, 90 (1-3) :41-51
[6]  
BURNET PW, 2008, SCHIZOPHR RES
[7]   Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia [J].
Chumakov, I ;
Blumenfeld, M ;
Guerassimenko, O ;
Cavarec, L ;
Palicio, M ;
Abderrahim, H ;
Bougueleret, L ;
Barry, C ;
Tanaka, H ;
La Rosa, P ;
Puech, A ;
Tahri, N ;
Cohen-Akenine, A ;
Delabrosse, S ;
Lissarrague, S ;
Picard, FP ;
Maurice, K ;
Essioux, L ;
Millasseau, P ;
Grel, P ;
Debailleul, V ;
Simon, AM ;
Caterina, D ;
Dufaure, I ;
Malekzadeh, K ;
Belova, M ;
Luan, JJ ;
Bouillot, M ;
Sambucy, JL ;
Primas, G ;
Saumier, M ;
Boubkiri, N ;
Martin-Saumier, S ;
Nasroune, M ;
Peixoto, H ;
Delaye, A ;
Pinchot, V ;
Bastucci, M ;
Guillou, S ;
Chevillon, M ;
Sainz-Fuertes, R ;
Meguenni, S ;
Aurich-Costa, J ;
Cherif, D ;
Gimalac, A ;
Van Duijn, C ;
Gauvreau, D ;
Quelette, G ;
Fortier, I ;
Realson, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (21) :13675-13680
[8]   Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample [J].
Corvin, A. ;
McGhee, K. A. ;
Murphy, K. ;
Donohoe, G. ;
Nangle, J. M. ;
Schwaiger, S. ;
Kenny, N. ;
Clarke, S. ;
Meagher, D. ;
Quinn, J. ;
Scully, P. ;
Baldwin, P. ;
Browne, D. ;
Walsh, C. ;
Waddington, J. L. ;
Morris, D. W. ;
Gill, M. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2007, 144B (07) :949-953
[9]   G72/G30 in schizophrenia and bipolar disorder: Review and meta-analysis [J].
Detera-Wadleigh, Sevilla D. ;
McMahon, Francis J. .
BIOLOGICAL PSYCHIATRY, 2006, 60 (02) :106-114
[10]   D-cycloserine added to risperidone in patients with primary negative symptoms of schizophrenia [J].
Evins, AE ;
Amico, E ;
Posever, TA ;
Toker, R ;
Goff, DC .
SCHIZOPHRENIA RESEARCH, 2002, 56 (1-2) :19-23