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From synapses to circuits and back: Bridging levels of understanding in animal models of Alzheimer's disease.从突触到回路再回到突触:在阿尔茨海默病动物模型中连接理解的层次。
Eur J Neurosci. 2022 Nov;56(9):5564-5586. doi: 10.1111/ejn.15636. Epub 2022 Mar 14.
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Aducanumab and the "post-amyloid" era of Alzheimer research?阿杜卡努单抗与阿尔茨海默病研究的“淀粉样蛋白后”时代?
Neuron. 2021 Oct 6;109(19):3045-3047. doi: 10.1016/j.neuron.2021.09.007. Epub 2021 Sep 27.
2
Hippocampal replay reflects specific past experiences rather than a plan for subsequent choice.海马体回放反映的是特定的过去经历,而不是对后续选择的计划。
Neuron. 2021 Oct 6;109(19):3149-3163.e6. doi: 10.1016/j.neuron.2021.07.029. Epub 2021 Aug 26.
3
Divergence in Population Coding for Space between Dorsal and Ventral CA1.空间编码在背侧和腹侧 CA1 之间的群体中出现分歧。
eNeuro. 2021 Sep 7;8(5). doi: 10.1523/ENEURO.0211-21.2021. Print 2021 Sep-Oct.
4
Dynamic and reversible remapping of network representations in an unchanging environment.在不变的环境中动态且可还原的网络表示重映射。
Neuron. 2021 Sep 15;109(18):2967-2980.e11. doi: 10.1016/j.neuron.2021.07.005. Epub 2021 Aug 6.
5
Regulation of Synapse Weakening through Interactions of the Microtubule Associated Protein Tau with PACSIN1.通过微管相关蛋白 Tau 与 PACSIN1 的相互作用调节突触减弱。
J Neurosci. 2021 Aug 25;41(34):7162-7170. doi: 10.1523/JNEUROSCI.3129-20.2021. Epub 2021 Jul 21.
6
Dendritic spines are lost in clusters in Alzheimer's disease.阿尔茨海默病中树突棘会成群丢失。
Sci Rep. 2021 Jun 11;11(1):12350. doi: 10.1038/s41598-021-91726-x.
7
Effects of altered tau expression on dentate granule cell excitability in mice.改变 tau 表达对小鼠齿状回颗粒细胞兴奋性的影响。
Exp Neurol. 2021 Sep;343:113766. doi: 10.1016/j.expneurol.2021.113766. Epub 2021 May 21.
8
Modality-Specific Impairment of Hippocampal CA1 Neurons of Alzheimer's Disease Model Mice.阿尔茨海默病模型小鼠海马 CA1 神经元的模态特异性损伤。
J Neurosci. 2021 Jun 16;41(24):5315-5329. doi: 10.1523/JNEUROSCI.0208-21.2021. Epub 2021 May 12.
9
Four distinct trajectories of tau deposition identified in Alzheimer's disease.阿尔茨海默病中tau 沉积的四种不同轨迹。
Nat Med. 2021 May;27(5):871-881. doi: 10.1038/s41591-021-01309-6. Epub 2021 Apr 29.
10
Alzheimer's pathology causes impaired inhibitory connections and reactivation of spatial codes during spatial navigation.阿尔茨海默病病理学导致在空间导航过程中抑制性连接受损和空间编码重新激活。
Cell Rep. 2021 Apr 20;35(3):109008. doi: 10.1016/j.celrep.2021.109008.

从突触到回路再回到突触:在阿尔茨海默病动物模型中连接理解的层次。

From synapses to circuits and back: Bridging levels of understanding in animal models of Alzheimer's disease.

机构信息

Department of Neuroscience, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.

Neuroscience Graduate Program, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.

出版信息

Eur J Neurosci. 2022 Nov;56(9):5564-5586. doi: 10.1111/ejn.15636. Epub 2022 Mar 14.

DOI:10.1111/ejn.15636
PMID:35244297
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10926359/
Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by behavioural changes that include memory loss and cognitive decline and is associated with the appearance of amyloid-β plaques and neurofibrillary tangles throughout the brain. Although aspects of the disease percolate across multiple levels of neuronal organization, from the cellular to the behavioural, it is increasingly clear that circuits are a critical junction between the cellular pathology and the behavioural phenotypes that bookend these levels of analyses. In this review, we discuss critical aspects of neural circuit research, beginning with synapses and progressing to network activity and how they influence our understanding of disease processed in AD.

摘要

阿尔茨海默病(AD)是一种神经退行性疾病,其特征是行为改变,包括记忆丧失和认知能力下降,并且与大脑中出现淀粉样β斑块和神经原纤维缠结有关。尽管该疾病的各个方面都涉及到神经元组织的多个层次,从细胞到行为,但越来越明显的是,回路是细胞病理学与行为表型之间的关键连接点,这些表型是这些分析水平的两端。在这篇综述中,我们讨论了神经回路研究的关键方面,从突触开始,一直到网络活动,以及它们如何影响我们对 AD 中疾病过程的理解。