Mitochondrial dysfunction in schizophrenia: an evolutionary perspective

被引:0
作者
Vanessa F. Gonçalves
Ana C. Andreazza
James L. Kennedy
机构
[1] Centre for Addiction and Mental Health,Department of Psychiatry
[2] University of Toronto,Department of Pharmacology
[3] University of Toronto,undefined
[4] Centre for Addiction and Mental Health,undefined
来源
Human Genetics | 2015年 / 134卷
关键词
Mitochondrial Dysfunction; Postmortem Brain Tissue; Alpha Ketoglutarate; Major Depression Disorder; Brain Energy Metabolism;
D O I
暂无
中图分类号
学科分类号
摘要
Schizophrenia (SCZ) is a severe psychiatric illness with a lifetime prevalence of 0.4 %. A disturbance of energy metabolism has been suggested as part of the etiopathogenesis of the disorder. Several lines of evidence have proposed a connection between etiopathogenesis of SCZ and human brain evolution, which was characterized by an increase in the energy requirement, demanding a co-evolution of the mitochondrial system. Mitochondria are key players in brain energy homeostasis and multiple lines of evidence suggest that the system is disrupted in SCZ. In this review, we will describe the current knowledge on pathways/system involved in the human brain evolution as well as the main theories regarding the evolutionary origin of SCZ. We will furthermore discuss the role of mitochondria in the context of brain energy metabolism and its role in the etiopathogenesis of SCZ. Understanding SCZ in the context of human brain evolution opens a new perspective to elucidate pathophysiological mechanisms involved in the origin and/or portions of the complex symptomatology of this severe mental disorder.
引用
收藏
页码:13 / 21
页数:8
相关论文
共 523 条
[41]  
Schork NJ(2008)Metabolic changes in schizophrenia and human brain evolution Genome Biol 9 R124-e17
[42]  
Fanous AH(2004)Molecular evidence for mitochondrial dysfunction in bipolar disorder Arch Gen Psychiatry 61 300-387
[43]  
O’Donovan MC(2013)Mitochondrial dysfunction in autism Semin Pediatr Neurol 20 163-299
[44]  
Niculescu AB(2013)An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer’s disease Neurobiol Aging 34 e13-501
[45]  
Ben-Shachar D(2005)Mitochondrial dysfunction and type 2 diabetes Science 307 384-101
[46]  
Berman KF(2006)Mitochondria at the synapse Neuroscientist 12 291-289
[47]  
Torrey EF(2007)Mitochondrial DNA haplogroups and age at onset of schizophrenia Am J Med Genet B Neuropsychiatr Genet 144B 496-120
[48]  
Daniel DG(2013)The role of mitochondria in the aetiology of insulin resistance and type 2 diabetes Biochim Biophys Acta 9 95-1189
[49]  
Weinberger DR(2011)Proteomics as a tool for understanding schizophrenia Clin Psychopharmacol Neurosci 9 17-2079
[50]  
Bertolin C(2009)Proteome analysis of schizophrenia patients Wernicke’s area reveals an energy metabolism dysregulation BMC Psychiatry 116 275-136