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长期给予 P301S 转基因小鼠辅酶 Q10 后的行为改善。

Behavioral improvement after chronic administration of coenzyme Q10 in P301S transgenic mice.

机构信息

Weill Cornell Medical College, Department of Neurology and Neuroscience, New York, NY, USA.

出版信息

J Alzheimers Dis. 2012;28(1):173-82. doi: 10.3233/JAD-2011-111190.

Abstract

Coenzyme Q10 is a key component of the electron transport chain which plays an essential role in ATP production and also has antioxidant effects. Neuroprotective effects of coenzyme Q10 have been reported in both in vitro and in vivo models of neurodegenerative diseases. However, its effects have not been studied in cells or in animals with tau induced pathology. In this report, we administered coenzyme Q10 to transgenic mice with the P301S tau mutation, which causes fronto-temporal dementia in man. These mice develop tau hyperphosphorylation and neurofibrillary tangles in the brain. Coenzyme Q10 improved survival and behavioral deficits in the P301S mice. There was a modest reduction in phosphorylated tau in the cortex of P301S mice. We also examined the effects of coenzyme Q10 treatment on the electron transport chain enzymes, the mitochondrial antioxidant enzymes, and the tricarboxylic acid cycle. There was a significant increase in complex I activity and protein levels, and a reduction in lipid peroxidation. Our data show that coenzyme Q10 significantly improved behavioral deficits and survival in transgenic mice with the P301S tau mutation, upregulated key enzymes of the electron transport chain, and reduced oxidative stress.

摘要

辅酶 Q10 是电子传递链的关键组成部分,在 ATP 产生中起着至关重要的作用,并且具有抗氧化作用。辅酶 Q10 在神经退行性疾病的体外和体内模型中都具有神经保护作用。然而,它在诱导tau 病理的细胞或动物中的作用尚未得到研究。在本报告中,我们给携带 P301S 突变 tau 的转基因小鼠(该突变导致人类额颞叶痴呆)施用了辅酶 Q10。这些小鼠的大脑中出现 tau 过度磷酸化和神经纤维缠结。辅酶 Q10 改善了 P301S 小鼠的存活和行为缺陷。P301S 小鼠皮质中的磷酸化 tau 略有减少。我们还研究了辅酶 Q10 治疗对电子传递链酶、线粒体抗氧化酶和三羧酸循环的影响。复合物 I 的活性和蛋白水平显著增加,脂质过氧化减少。我们的数据表明,辅酶 Q10 显著改善了携带 P301S 突变 tau 的转基因小鼠的行为缺陷和存活率,上调了电子传递链的关键酶,并减少了氧化应激。

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