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Coexistence of perseveration and apathy in the TDP-43 Q331K knock-in mouse model of ALS–FTD

机译:TDP-43 Q331K击球突出和冷漠的共存 - 在ALS-FTD的鼠标模型中

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Perseveration and apathy are two of the most common behavioural and psychological symptoms of dementia (BPSDs) in amyotrophic lateral sclerosis–frontotemporal dementia (ALS–FTD). Availability of a validated and behaviourally characterised animal model is crucial for translational research into BPSD in the FTD context. We behaviourally evaluated the male TDP-43Q331K mouse, an ALS–FTD model with a human-equivalent mutation (TDP-43Q331K) knocked into the endogenous Tardbp gene. We utilised a panel of behavioural tasks delivered using the rodent touchscreen apparatus, including progressive ratio (PR), extinction and visual discrimination/reversal learning (VDR) assays to examine motivation, response inhibition and cognitive flexibility, respectively. Relative to WT littermates, TDP-43Q331K mice exhibited increased responding under a PR schedule. While elevated PR responding is typically an indication of increased motivation for reward, a trial-by-trial response rate analysis revealed that TDP-43Q331K mice exhibited decreased maximal response rate and slower response decay rate, suggestive of reduced motivation and a perseverative behavioural phenotype, respectively. In the extinction assay, TDP-43Q331K mice displayed increased omissions during the early phase of each session, consistent with a deficit in activational motivation. Finally, the VDR task revealed cognitive inflexibility, manifesting as stimulus-bound perseveration. Together, our data indicate that male TDP-43Q331K mice exhibit a perseverative phenotype with some evidence of apathy-like behaviour, similar to BPSDs observed in human ALS–FTD patients. The TDP-43Q331K knock-in mouse therefore has features that recommend it as a useful platform to facilitate translational research into behavioural symptoms in the context of ALS–FTD.
机译:坚持不懈和脾气暴躁是肌营养侧面硬化剂 - 额定痴呆症(ALS-FTD)中痴呆症(BPSDS)中最常见的行为和心理症状的两个。验证和行为特征的动物模型的可用性对于FTD背景下的BPSD转化研究至关重要。我们的行为评估了雄性TDP-43Q331K小鼠,具有敲入内源TARTBP基因的人类当量突变(TDP-43331K)的ALS-FTD模型。我们利用了使用啮齿动物触摸屏设备送出的行为任务面板,包括渐进比(PR),消灭和视觉鉴别/反转学习(VDR)测定分别用于检查动机,反应抑制和认知灵活性。相对于WT凋落物,TDP-43Q331K小鼠在PR日程中表现出增加的响应。虽然升高的PR响应通常是增加奖励动机的指示,但试验响应率分析显示,TDP-43Q331K小鼠表现出降低的最大反应率和较慢的响应衰减率,提示减少动机和持续性行为表型。分别。在消灭检测中,TDP-43Q331K小鼠在每届会议早期期间展示了较省略的遗漏,这一致符合活性动机的赤字。最后,VDR任务揭示了认知的不灵活性,表现为刺激束缚的持久性。我们的数据在一起表明,男性TDP-43Q331K小鼠具有持续性表型,其具有脾气暴躁的行为的证据,类似于在人ALS-FTD患者中观察到的BPSD。因此,TDP-43Q331K敲击鼠标具有推荐它作为一个有用的平台,以便在ALS-FTD的背景下促进平移研究行为症状。

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