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阿尔茨海默病大鼠模型中海马区的过度兴奋。

Hippocampal hyperactivity in a rat model of Alzheimer's disease.

机构信息

Neuronal Networks Group, German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.

Department of Cellular Neuroscience, Leibniz Institute for Neurobiology, Magdeburg, Germany.

出版信息

J Neurochem. 2021 Jun;157(6):2128-2144. doi: 10.1111/jnc.15323. Epub 2021 Mar 5.

Abstract

Neuronal network dysfunction is a hallmark of Alzheimer's disease (AD). However, the underlying pathomechanisms remain unknown. We analyzed the hippocampal micronetwork in transgenic McGill-R-Thy1-APP rats (APPtg) at the beginning of extracellular amyloid beta (Aβ) deposition. We established two-photon Ca -imaging in vivo in the hippocampus of rats and found hyperactivity of CA1 neurons. Patch-clamp recordings in brain slices in vitro revealed increased neuronal input resistance and prolonged action potential width in CA1 pyramidal neurons. We did neither observe changes in synaptic inhibition, nor in excitation. Our data support the view that increased intrinsic excitability of CA1 neurons may precede inhibitory dysfunction at an early stage of Aβ-deposition and disease progression.

摘要

神经网络功能障碍是阿尔茨海默病(AD)的标志。然而,其潜在的发病机制尚不清楚。我们在细胞外淀粉样β(Aβ)沉积开始时分析了转基因 McGill-R-Thy1-APP 大鼠(APPtg)的海马微网络。我们在大鼠海马体中建立了双光子 Ca2+ 成像的活体,并发现 CA1 神经元的过度活跃。在体外脑片中进行的膜片钳记录显示 CA1 锥体神经元的神经元输入电阻增加和动作电位宽度延长。我们既没有观察到突触抑制的变化,也没有观察到兴奋的变化。我们的数据支持这样一种观点,即在 Aβ 沉积和疾病进展的早期阶段,CA1 神经元的固有兴奋性增加可能先于抑制功能障碍。

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