精神分裂症和双相情感障碍的线粒体复合体I缺乏及其药物影响。

Molecular Neuropsychiatry Pub Date : 2018-02-01 Epub Date: 2017-11-30 DOI:10.1159/000484348
Brandi L Rollins, Ling Morgan, Brooke E Hjelm, Adolfo Sequeira, Alan F Schatzberg, Jack D Barchas, Francis S Lee, Rick M Myers, Stanley J Watson, Huda Akil, Steven G Potkin, William E Bunney, Marquis P Vawter
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引用次数: 36

摘要

精神分裂症(SZ)和双相情感障碍(BD)的受试者显示线粒体复合体i的蛋白质和转录水平下降,体外研究结果表明抗精神病药物和抗抑郁药物可能与此有关。我们测量了BD、SZ和对照组中复合物I的活性,抗精神病和抗抑郁药物的存在,线粒体DNA (mtDNA)拷贝数,以及大脑中mtDNA“常见缺失”。与对照组相比,SZ患者前额叶皮层复合体I活性降低了45% (p = 0.02),而BD患者无显著差异。与未检测到精神药物水平的合并病例(SZ和BD)相比,可检测到精神药物的合并病例(SZ和BD)复合体I活性显著降低(p = 0.01)。与成人发病年龄的受试者相比,青少年发病年龄和精神药物治疗的受试者复合物I活性降低(p < 0.05)。SZ组和BD组mtDNA拷贝数均显著高于对照组(p < 0.05);然而,共同的删除负担没有改变。在SZ脑组织中发现复合物I缺乏,精神药物可能在线粒体功能障碍中起作用。需要对无药物首发精神病患者进行研究,以阐明线粒体病理生理是否独立于药物作用而发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Mitochondrial Complex I Deficiency in Schizophrenia and Bipolar Disorder and Medication Influence.

Subjects with schizophrenia (SZ) and bipolar disorder (BD) show decreased protein and transcript levels for mitochondrial complex I. In vitro results suggest antipsychotic and antidepressant drugs may be responsible. We measured complex I activity in BD, SZ, and controls and presence of antipsychotic and antidepressant medications, mitochondrial DNA (mtDNA) copy number, and the mtDNA "common deletion" in the brain. Complex I activity in the prefrontal cortex was decreased by 45% in SZ compared to controls (p = 0.02), while no significant difference was found in BD. Complex I activity was significantly decreased (p = 0.01) in pooled cases (SZ and BD) that had detectable psychotropic medications and drugs compared to pooled cases with no detectable levels. Subjects with age at onset in their teens and psychotropic medications showed decreased (p < 0.05) complex I activity compared to subjects with an adult age at onset. Both SZ and BD groups displayed significant increases (p < 0.05) in mtDNA copy number compared to controls; however, common deletion burden was not altered. Complex I deficiency is found in SZ brain tissue, and psychotropic medications may play a role in mitochondrial dysfunction. Studies of medication-free first-episode psychosis patients are needed to elucidate whether mitochondrial pathophysiology occurs independent of medication effects.

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