Enhanced Carbonyl Stress in a Subpopulation of Schizophrenia

被引:129
作者
Arai, Makoto
Yuzawa, Hiroko [2 ]
Nohara, Izumi
Ohnishi, Tetsuo [3 ]
Obata, Nanako
Iwayama, Yoshimi [3 ]
Haga, Seiichi
Toyota, Tomoko [3 ]
Ujike, Hiroshi [4 ]
Arai, Mayumi
Ichikawa, Tomoe
Nishida, Atsushi
Tanaka, Yoko
Furukawa, Aizo
Aikawa, Yuuzou [5 ]
Kuroda, Osamu [5 ]
Niizato, Kazuhiro [5 ]
Izawa, Ryosuke [5 ]
Nakamura, Kazuhiko [6 ]
Mori, Norio [6 ]
Matsuzawa, Daisuke [7 ]
Hashimoto, Kenji [8 ]
Iyo, Masaomi [9 ]
Sora, Ichiro [10 ]
Matsushita, Masaaki [5 ]
Okazaki, Yuji [5 ]
Yoshikawa, Takeo [3 ,11 ]
Miyata, Toshio [2 ,12 ]
Itokawa, Masanari [1 ,3 ,5 ,11 ]
机构
[1] Tokyo Inst Psychiat, Project Schizophrenia Res, Setagaya Ku, Tokyo 1568585, Japan
[2] Tokai Univ, Inst Med Sci, Kanagawa 2591100, Japan
[3] RIKEN Brain Sci Inst, Lab Mol Psychiat, Saitama, Japan
[4] Okayama Univ, Grad Sch Med & Dent, Dept Neuropsychiat, Okayama, Japan
[5] Tokyo Metropolitan Matsuzawa Hosp, Dept Psychiat, Tokyo, Japan
[6] Hamamatsu Univ Sch Med, Dept Psychiat & Neurol, Hamamatsu, Shizuoka 4312102, Japan
[7] Chiba Univ, Grad Sch Med, Dept Integrat Neurophysiol, Chiba, Japan
[8] Chiba Univ, Ctr Forens Mental Hlth, Div Clin Neurosci, Chiba, Japan
[9] Chiba Univ, Grad Sch Med, Dept Psychiat, Chiba, Japan
[10] Tohoku Univ, Grad Sch Med, Dept Neurosci, Div Psychobiol, Sendai, Miyagi 9808575, Japan
[11] Japan Sci & Technol Agcy, Tokyo, Japan
[12] Tohoku Univ, Grad Sch Med, Ctr Translat & Adv Res Human Dis, Sendai, Miyagi 9808575, Japan
基金
日本学术振兴会;
关键词
GLYCATION END-PRODUCTS; GLYOXALASE-I; OXIDATIVE STRESS; PSYCHIATRIC-DISORDERS; CHROMOSOME; 6P; TRAIT ANXIETY; MOUSE MODEL; SUSCEPTIBILITY; ASSOCIATION; HOMOCYSTEINE;
D O I
10.1001/archgenpsychiatry.2010.62
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Context: Various factors are involved in the pathogenesis of schizophrenia. Accumulation of advanced glycation end products, including pentosidine, results from carbonyl stress, a state featuring an increase in reactive carbonyl compounds (RCOs) and their attendant protein modifications. Vitamin B-6 is known to detoxify RCOs, including advanced glycation end products. Glyoxalase 1 (GLO1) is one of the enzymes required for the cellular detoxification of RCOs. Objectives: To examine whether plasma levels of pentosidine and serum vitamin B-6 are altered in patients with schizophrenia and to evaluate the functionality of GLO1 variations linked to concomitant carbonyl stress. Design: An observational biochemical and genetic analysis study. Setting: Multiple centers in Japan. Participants: One hundred six individuals (45 schizophrenic patients and 61 control subjects) were recruited for biochemical measurements. Deep resequencing of GLO1 derived from peripheral blood or postmortem brain tissue was performed in 1761 patients with schizophrenia and 1921 control subjects. Main Outcome Measures: Pentosidine and vitamin B-6. concentrations were determined by high-performance liquid chromatographic assay. Protein expression and enzymatic activity were quantified in red blood cells and lymphoblastoid cells using Western blot and spectrophotometric techniques. Results: We found that a subpopulation of individuals with schizophrenia exhibit high plasma pentosidine and low serum pyridoxal (vitamin B-6) levels. We also detected genetic and functional alterations in GLO1. Marked reductions in enzymatic activity were associated with pentosidine accumulation and vitamin B-6 depletion, except in some healthy subjects. Most patients with schizophrenia who carried the genetic defects exhibited high pentosidine and low vitamin B-6 levels in contrast with control subjects with the genetic defects, suggesting the existence of compensatory mechanisms. Conclusions: Our findings suggest that GLO1 deficits and carbonyl stress are linked to the development of a certain subtype of schizophrenia. Elevated plasma pentosidine and concomitant low vitamin B-6 levels could be the most cogent and easily measurable biomarkers in schizophrenia and should be helpful for classifying heterogeneous types of schizophrenia on the basis of their biological causes.
引用
收藏
页码:589 / 597
页数:9
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