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The role of mitochondrial dysfunction in psychiatric disease.

机译:线粒体功能障碍在精神疾病中的作用。

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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.
机译:线粒体呼吸链疾病是一组遗传和临床异质性疾病,由线粒体呼吸的生物化学复杂性和两个基因组(一个线粒体和一个核基因组)编码呼吸链的组成部分引起。这些疾病可以在出生时或以后出现。它们至少部分导致ATP的产生不良。通常,线粒体疾病会影响高能量需求的组织,例如骨骼肌,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,特定的线粒体疾病伴有局灶性脑坏死(利氏病),痴呆症或静态脑病。此外,许多患有线粒体脑脊髓病的儿童表现出更微妙和顽强的体征,包括记忆,知觉和语言的局灶性认知缺陷。某些线粒体疾病患者可能还会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,这可能反映出突触可塑性的缺陷。在线粒体综合征的临床范围内发现精神病学特征。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,例如痴呆,重度抑郁和躁郁症。此外,一些证据表明,精神分裂症涉及线粒体功能障碍,包括脑能量代谢,电子转运链活性和涉及线粒体功能的基因表达的文献记载。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,并讨论功能紊乱的细胞能量代谢的可能机制,这些机制是精神病学主要子集的病理生理基础。

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