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精神分裂症中的线粒体功能障碍:双打击小鼠模型中线粒体呼吸活性的测定

Mitochondrial Dysfunction in Schizophrenia: Determination of Mitochondrial Respiratory Activity in a Two-Hit Mouse Model.

作者信息

Monpays Cécile, Deslauriers Jessica, Sarret Philippe, Grignon Sylvain

机构信息

Department of Pharmacology and Physiology, Faculty of Medicine and Health Sciences, Université de Sherbrooke, 12e avenue Nord, Sherbrooke, QC, J1H 5N4, Canada.

Department of Psychiatry, Centre Hospitalier Universitaire de Sherbrooke, 580 Bowen Sud, Sherbrooke, QC, J1G 2E8, Canada.

出版信息

J Mol Neurosci. 2016 Aug;59(4):440-51. doi: 10.1007/s12031-016-0746-3. Epub 2016 Mar 31.

DOI:10.1007/s12031-016-0746-3
PMID:27034067
Abstract

Schizophrenia is a chronic mental illness in which mitochondrial dysfunction has been suggested. Our laboratory recently developed a juvenile murine two-hit model (THM) of schizophrenia based on the combination of gestational inflammation, followed by juvenile restraint stress. We previously reported that relevant behaviors and neurochemical disturbances, including oxidative stress, were reversed by the antioxidant lipoic acid (LA), thereby pointing to the central role played by oxidative abnormalities and prompting us to investigate mitochondrial function. Mitochondrial activity was determined with the MitoXpress® commercial kit in two schizophrenia-relevant regions (prefrontal cortex (PFC) and striatum). Measurements were performed in state 3, with substrates for complex I- and complex II-induced respiratory activity (IRA). We observed an increase in complex I IRA in the PFC and striatum in both sexes but an increase in complex II activity only in males. LA treatment prevented this increase only in complex II IRA in males. Expression levels of the different respiratory chain complexes, as well as fission/fusion proteins and protein carbonylation, were unchanged. In conclusion, our juvenile schizophrenia THM shows an increase in mitochondrial activity reversed by LA, specifically in complex II IRA in males. Further investigations are required to determine the mechanisms of these modifications.

摘要

精神分裂症是一种慢性精神疾病,其中线粒体功能障碍已被提出。我们实验室最近基于孕期炎症联合幼年限制应激,开发了一种精神分裂症的幼年小鼠双打击模型(THM)。我们之前报道过,包括氧化应激在内的相关行为和神经化学紊乱可被抗氧化剂硫辛酸(LA)逆转,从而指出氧化异常所起的核心作用,并促使我们研究线粒体功能。使用MitoXpress®商业试剂盒在两个与精神分裂症相关的区域(前额叶皮层(PFC)和纹状体)测定线粒体活性。在状态3下进行测量,使用针对复合物I和复合物II诱导的呼吸活性(IRA)的底物。我们观察到,两性的PFC和纹状体中复合物I的IRA均增加,但仅雄性的复合物II活性增加。LA治疗仅能防止雄性复合物II的IRA增加。不同呼吸链复合物以及裂变/融合蛋白和蛋白质羰基化的表达水平未发生变化。总之,我们的幼年精神分裂症THM显示线粒体活性增加,可被LA逆转,特别是雄性的复合物II的IRA。需要进一步研究以确定这些改变的机制。

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本文引用的文献

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Linking early-life NMDAR hypofunction and oxidative stress in schizophrenia pathogenesis.将早期 NMDAR 功能低下与氧化应激联系起来,探索精神分裂症的发病机制。
Nat Rev Neurosci. 2016 Feb;17(2):125-34. doi: 10.1038/nrn.2015.19. Epub 2016 Jan 14.
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Mitochondrial impairment, apoptosis and autophagy in a rat brain as immediate and long-term effects of perinatal phencyclidine treatment - influence of restraint stress.围产期苯环利定治疗对大鼠脑线粒体损伤、凋亡和自噬的即时及长期影响——束缚应激的作用
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Risperidone Attenuates Modified Stress-Re-stress Paradigm-Induced Mitochondrial Dysfunction and Apoptosis in Rats Exhibiting Post-traumatic Stress Disorder-Like Symptoms.
利培酮减轻在表现出创伤后应激障碍样症状的大鼠中,改良应激-再应激范式诱导的线粒体功能障碍和细胞凋亡。
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Potential involvement of the mitochondrial unfolded protein response in depressive-like symptoms in mice.线粒体未折叠蛋白反应在小鼠抑郁样症状中的潜在作用。
Neurosci Lett. 2015 Feb 19;588:166-71. doi: 10.1016/j.neulet.2015.01.006. Epub 2015 Jan 7.
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Mitochondrial dysfunction in schizophrenia: pathways, mechanisms and implications.精神分裂症中的线粒体功能障碍:途径、机制及意义。
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Neuroscience. 2014 Jul 11;272:261-70. doi: 10.1016/j.neuroscience.2014.04.061. Epub 2014 May 9.
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