{"title":"The role of mitochondrial dysfunction in psychiatric disease","authors":"Fernando Scaglia","doi":"10.1002/ddrr.115","DOIUrl":null,"url":null,"abstract":"<p>Mitochondrial respiratory chain disorders are a group of genetically and clinically heterogeneous disorders caused by the biochemical complexity of mitochondrial respiration and the fact that two genomes, one mitochondrial and one nuclear, encode the components of the respiratory chain. These disorders can manifest at birth or present later in life. They result, at least in part, in defective production of ATP. Typically, mitochondrial disorders affect tissues with high energetic demands such as skeletal muscle, cardiac muscle, and the central nervous system. Neurological dysfunction is the most frequent clinical presentation of these disorders. The central nervous system is highly dependent on oxidative metabolism, and particular mitochondrial disorders are accompanied by focal brain necrosis (Leigh disease), dementia, or static encephalopathy. Furthermore, many children with mitochondrial encephalomyopathies present with more subtle and indolent signs including focal cognitive deficits of memory, perception, and language. Some subjects with mitochondrial disorders may also exhibit nonverbal cognitive impairment, compromised visuospatial abilities, and short-term memory deficits associated with working memory that likely reflect defects in synaptic plasticity. Psychiatric features are found within the clinical spectrum of mitochondrial syndromes. It is increasingly recognized that mitochondrial dysfunction may be associated with neuropsychiatric abnormalities such as dementia, major depression, and bipolar disorder. Furthermore, several lines of evidence suggest that there is involvement of mitochondrial dysfunction in schizophrenia, including documented alterations in brain energy metabolism, electron transport chain activity, and expression of genes involved in mitochondrial function. The purpose of this review article is to summarize the psychiatric features observed in mitochondrial cytopathies and discuss possible mechanisms of dysfunctional cellular energy metabolism that underlie the pathophysiology of major subsets of psychiatric disorders. © 2010 Wiley-Liss, Inc. Dev Disabil Res Rev 2010;16:136–143.</p>","PeriodicalId":55176,"journal":{"name":"Developmental Disabilities Research Reviews","volume":"16 2","pages":"136-143"},"PeriodicalIF":0.0000,"publicationDate":"2010-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/ddrr.115","citationCount":"95","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental Disabilities Research Reviews","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ddrr.115","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 95
Abstract
Mitochondrial respiratory chain disorders are a group of genetically and clinically heterogeneous disorders caused by the biochemical complexity of mitochondrial respiration and the fact that two genomes, one mitochondrial and one nuclear, encode the components of the respiratory chain. These disorders can manifest at birth or present later in life. They result, at least in part, in defective production of ATP. Typically, mitochondrial disorders affect tissues with high energetic demands such as skeletal muscle, cardiac muscle, and the central nervous system. Neurological dysfunction is the most frequent clinical presentation of these disorders. The central nervous system is highly dependent on oxidative metabolism, and particular mitochondrial disorders are accompanied by focal brain necrosis (Leigh disease), dementia, or static encephalopathy. Furthermore, many children with mitochondrial encephalomyopathies present with more subtle and indolent signs including focal cognitive deficits of memory, perception, and language. Some subjects with mitochondrial disorders may also exhibit nonverbal cognitive impairment, compromised visuospatial abilities, and short-term memory deficits associated with working memory that likely reflect defects in synaptic plasticity. Psychiatric features are found within the clinical spectrum of mitochondrial syndromes. It is increasingly recognized that mitochondrial dysfunction may be associated with neuropsychiatric abnormalities such as dementia, major depression, and bipolar disorder. Furthermore, several lines of evidence suggest that there is involvement of mitochondrial dysfunction in schizophrenia, including documented alterations in brain energy metabolism, electron transport chain activity, and expression of genes involved in mitochondrial function. The purpose of this review article is to summarize the psychiatric features observed in mitochondrial cytopathies and discuss possible mechanisms of dysfunctional cellular energy metabolism that underlie the pathophysiology of major subsets of psychiatric disorders. © 2010 Wiley-Liss, Inc. Dev Disabil Res Rev 2010;16:136–143.
线粒体功能障碍在精神疾病中的作用
线粒体呼吸链疾病是一组遗传和临床异质性疾病,由线粒体呼吸的生化复杂性和两个基因组(一个线粒体和一个核)编码呼吸链的组成部分引起。这些疾病可以在出生时表现出来,也可以在以后的生活中出现。它们至少在一定程度上导致ATP产生缺陷。通常,线粒体疾病会影响高能量需求的组织,如骨骼肌、心肌和中枢神经系统。神经功能障碍是这些疾病最常见的临床表现。中枢神经系统高度依赖于氧化代谢,特殊的线粒体疾病可伴有局灶性脑坏死(Leigh病)、痴呆或静态脑病。此外,许多患有线粒体脑肌病的儿童表现出更微妙和惰性的症状,包括记忆、感知和语言的局灶性认知缺陷。一些线粒体疾病患者还可能表现出非语言认知障碍、视觉空间能力受损以及与工作记忆相关的短期记忆缺陷,这些可能反映了突触可塑性的缺陷。在线粒体综合征的临床谱中发现精神病学特征。人们越来越认识到线粒体功能障碍可能与神经精神异常有关,如痴呆、重度抑郁症和双相情感障碍。此外,一些证据表明,精神分裂症与线粒体功能障碍有关,包括记录在案的脑组织能量代谢、电子传递链活性和与线粒体功能有关的基因表达的改变。这篇综述文章的目的是总结在线粒体细胞病变中观察到的精神病学特征,并讨论在精神疾病主要亚群的病理生理学基础上功能失调的细胞能量代谢的可能机制。©2010 Wiley-Liss, IncDev disability Res 2010; 16:36 - 143。
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