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首页> 外文期刊>Alzheimer s Research & Therapy >Photobiomodulation with near infrared light mitigates Alzheimer’s disease-related pathology in cerebral cortex – evidence from two transgenic mouse models
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Photobiomodulation with near infrared light mitigates Alzheimer’s disease-related pathology in cerebral cortex – evidence from two transgenic mouse models

机译:用近红外光进行光生物调节可减轻阿尔茨海默氏病与大脑皮层的疾病相关病理-来自两个转基因小鼠模型的证据

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Introduction Previous work has demonstrated the efficacy of irradiating tissue with red to infrared light in mitigating cerebral pathology and degeneration in animal models of stroke, traumatic brain injury, parkinsonism and Alzheimer’s disease (AD). Using mouse models, we explored the neuroprotective effect of near infrared light (NIr) treatment, delivered at an age when substantial pathology is already present in the cerebral cortex. Methods We studied two mouse models with AD-related pathologies: the K369I tau transgenic model (K3), engineered to develop neurofibrillary tangles, and the APPswe/PSEN1dE9 transgenic model (APP/PS1), engineered to develop amyloid plaques. Mice were treated with NIr 20 times over a four-week period and histochemistry was used to quantify AD-related pathological hallmarks and other markers of cell damage in the neocortex and hippocampus. Results In the K3 mice, NIr treatment was associated with a reduction in hyperphosphorylated tau, neurofibrillary tangles and oxidative stress markers (4-hydroxynonenal and 8-hydroxy-2′-deoxyguanosine) to near wildtype levels in the neocortex and hippocampus, and with a restoration of expression of the mitochondrial marker cytochrome c oxidase in surviving neurons. In the APP/PS1 mice, NIr treatment was associated with a reduction in the size and number of amyloid-β plaques in the neocortex and hippocampus. Conclusions Our results, in two transgenic mouse models, suggest that NIr may have potential as an effective, minimally-invasive intervention for mitigating, and even reversing, progressive cerebral degenerations.
机译:引言先前的工作证明了在中风,颅脑外伤,帕金森病和阿尔茨海默氏病(AD)的动物模型中,用红色至红外光照射组织可以减轻脑部病理和变性。使用小鼠模型,我们探索了近红外光(NIr)治疗的神经保护作用,该作用在大脑皮层中已经存在实质性病理的年龄提供。方法我们研究了两种与AD相关的病理模型的小鼠模型:经过设计可开发神经原纤维缠结的K369I tau转基因模型(K3),以及经过设计可开发淀粉样斑块的APPswe / PSEN1dE9转基因模型(APP / PS1)。在四个星期的时间内,用NIr治疗小鼠20次,并使用组织化学方法量化AD相关的病理学标志以及新皮质和海马中细胞损伤的其他标志。结果在K3小鼠中,NIr治疗可将新皮层和海马中的高磷酸化tau,神经原纤维缠结和氧化应激标记物(4-羟基壬烯醛和8-羟基-2'-脱氧鸟苷)降低至接近野生型水平,并且存活神经元中线粒体标记细胞色素C氧化酶表达的恢复。在APP / PS1小鼠中,NIr治疗与新皮层和海马中淀粉样β斑块的大小和数量减少有关。结论在两个转基因小鼠模型中,我们的结果表明,NIr可能作为缓解甚至逆转进行性脑部退化的有效,微创干预手段具有潜力。

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