One-carbon metabolism and schizophrenia: current challenges and future directions

被引:69
作者
Krebs, M. O. [1 ,2 ]
Bellon, Alfredo [1 ,2 ]
Mainguy, Gaell [1 ,2 ]
Jay, T. M. [1 ,2 ]
Frieling, Helge [1 ,3 ]
机构
[1] St Anne Hosp, INSERM, U894, CPN, F-75014 Paris, France
[2] Univ Paris 05, Fac Med Paris Descartes, Paris, France
[3] Hannover Med Sch, Dept Psychiat Socialpsychiat & Psychotherapy, D-3000 Hannover, Germany
关键词
EXCITOTOXIC NEURONAL INJURY; HOMOCYSTEINE LEVELS; NITRIC-OXIDE; SYNAPTIC PLASTICITY; PLASMA HOMOCYSTEINE; FOLATE-DEFICIENCY; PREFRONTAL CORTEX; BIPOLAR DISORDER; OXIDATIVE STRESS; DNA-METHYLATION;
D O I
10.1016/j.molmed.2009.10.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Schizophrenia is a heterogeneous disease generally considered to result from a combination of heritable and environmental factors. Although its pathophysiology has not been fully determined, biological studies support the involvement of several possible components including altered DNA methylation, abnormal glutamatergic transmission, altered mitochondrial function, folate deficiency and high maternal homocysteine levels. Although these factors have been explored separately, they all involve one-carbon (C1) metabolism. Furthermore, C1 metabolism is well positioned to integrate gene-environment interactions by influencing epigenetic regulation. Here, we discuss the potential roles of C1 metabolism in the pathophysiology of schizophrenia. Understanding the contribution of these mechanisms could yield new therapeutic approaches aiming to counteract disease onset or progression.
引用
收藏
页码:562 / 570
页数:9
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