首页> 外文期刊>Neuropsychopharmacology reports. >Early manifestation of depressive‐like behavior in transgenic mice that express dementia with Lewy body‐linked mutant β‐synuclein
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Early manifestation of depressive‐like behavior in transgenic mice that express dementia with Lewy body‐linked mutant β‐synuclein

机译:用路易体联突变型β-突触核蛋白表达痴呆的转基因小鼠的抑郁样行为的早期表现

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Aim We previously generated transgenic (Tg) mice that expressed P123H β‐synuclein (βS), a dementia with Lewy body‐linked mutant βS. Notably, these mice recapitulated neurodegenerative features of Lewy body disease, reflected by motor dysfunction, greater protein aggregation, and memory impairment. Since recent studies suggested that non‐motor symptoms, such as depression, might be manifested in the prodromal stage of Lewy body disease, the main objective of the present study was to investigate the early expression of behavior in P123H βS Tg mice. Methods Nest building, locomotor activity, and depressive‐like behavior were assessed using 6‐ to 10‐month‐old male and female P123H βS Tg and wildtype mice. Key Results P123H βS Tg mice exhibited hyperlocomotor activity in a novel environment, a decrease in mobility time in the tail suspension test, and impairments in nest building. Conclusions Importantly, these non‐motor behaviors were manifested before the onset of motor dysfunction, suggesting that P123H βS Tg mice could be a valid model for investigating the early phase of Lewy body disease.
机译:目的我们以前曾产生过表达P123Hβ-突触核蛋白(βS)的转基因(Tg)小鼠,这是一种与路易体联突变βS的痴呆症。值得注意的是,这些小鼠概括了路易体病的神经退行性特征,表现为运动功能障碍,更大的蛋白质聚集和记忆力减退。由于最近的研究表明在路易氏体疾病的前驱阶段可能会出现非运动性症状,例如抑郁,因此本研究的主要目的是研究P123HβSTg小鼠的行为早期表达。方法使用6至10个月大的雄性和雌性P123HβSTg和野生型小鼠评估筑巢,运动能力和抑郁样行为。关键结果P123HβSTg小鼠在新环境中表现出超运动能力,在尾部悬吊试验中活动时间减少,并且筑巢障碍。结论重要的是,这些非运动行为在运动功能障碍发作之前就已经表现出来,这表明P123HβSTg小鼠可能是研究路易氏体病早期阶段的有效模型。

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