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首页> 外文期刊>Scientific reports. >Classification of?α-synuclein-induced changes?in the AAV α-synuclein rat model of Parkinson’s disease using electrophysiological measurements of visual processing
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Classification of?α-synuclein-induced changes?in the AAV α-synuclein rat model of Parkinson’s disease using electrophysiological measurements of visual processing

机译:α-突触核蛋白诱导的变化的分类?在使用电生理学测量的视觉处理中帕金森病的AAVα-突触核蛋白大鼠模型

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Biomarkers suitable for early diagnosis and monitoring disease progression are the cornerstone of developing disease-modifying treatments for neurodegenerative diseases such as Parkinson’s disease (PD). Besides motor complications, PD is also characterized by deficits in visual processing. Here, we investigate how virally-mediated overexpression of α-synuclein in the substantia nigra pars compacta impacts visual processing in a well-established rodent model of PD. After a unilateral injection of vector, human α-synuclein was detected in the striatum and superior colliculus (SC). In parallel, there was a significant delay in the latency of the transient VEPs from the affected side of the SC in late stages of the disease. Inhibition of leucine-rich repeat kinase using PFE360 failed to rescue the VEP delay and instead increased the latency of the VEP waveform. A support vector machine classifier accurately classified rats according to their `disease state’ using frequency-domain data from steady-state visual evoked potentials (SSVEP). Overall, these findings indicate that the latency of the rodent VEP is sensitive to changes mediated by the increased expression of α-synuclein and especially when full overexpression is obtained, whereas the SSVEP facilitated detection of α-synuclein across reflects all stages of PD model progression.
机译:适用于早期诊断和监测疾病进展的生物标志物是发展疾病修饰治疗的神经变性疾病如帕金森病(PD)的基石。除电机并发症外,PD还具有视觉处理的缺陷。在这里,我们研究了真实性的α-突触核蛋白的病症介导的过表达如何在熟悉的PD啮齿动物模型中影响视觉处理。在单侧注射载体后,在纹状体和优异的小学(SC)中检测人α-突触核蛋白。同时,来自疾病的后期患者的受影响的侧面的瞬态VEPS潜伏期存在显着延迟。使用PFE360抑制富含亮氨酸的重复激酶未能拯救VEP延迟,而是增加VEP波形的延迟。支持向量机分类器根据稳态视觉诱发电位(SSVEP)的频率域数据根据其“疾病状态”准确分类大鼠。总体而言,这些发现表明,啮齿动物VEP的潜伏期对由α-突触核蛋白的表达增加介导的变化,特别是当获得完全过表达时,而SSVEP促进α-突触核蛋白的检测反映了PD模型进展的所有阶段。

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