Ammassari-Teule Martine
Laboratory of Psychobiology, Department of Experimental Neuroscience, Santa Lucia Foundation, Rome, Italy.
National Research Council, Institute of Biochemistry and Cell Biology, Rome, Italy.
Front Behav Neurosci. 2022 Jun 23;16:868473. doi: 10.3389/fnbeh.2022.868473. eCollection 2022.
Increasing efforts have been made in the last decades to increase the face validity of Alzheimer's disease (AD) mouse models. Main advancements have consisted in generating AD mutations closer to those identified in humans, enhancing genetic diversity of wild-type backgrounds, and choosing protocols much apt to reveal AD-like cognitive dysfunctions. Nevertheless, two aspects remain less considered: the cognitive specialization of inbred strains used as recipient backgrounds of mutations and the heuristic importance of studying destabilization of memory circuits in pre-symptomatic mice facing cognitive challenges. This article underscores the relevance of these behavioral/experimental aspects by reviewing data which show that (i) inbred mice differ in their innate predisposition to rely on episodic vs. procedural memory, which implicates differential sensitivity to mutations aimed at disrupting temporal lobe-dependent memory, and that (ii) investigating training-driven neural alterations in asymptomatic mutants unveils early synaptic damage, which considerably anticipates detection of AD first signs.
在过去几十年里,人们为提高阿尔茨海默病(AD)小鼠模型的表面效度付出了更多努力。主要进展包括产生更接近人类所发现突变的AD突变、增强野生型背景的遗传多样性,以及选择更适合揭示AD样认知功能障碍的实验方案。然而,仍有两个方面较少被考虑:用作突变受体背景的近交系小鼠的认知特化,以及研究有认知挑战的症状前小鼠记忆回路失稳的启发式重要性。本文通过回顾数据强调了这些行为/实验方面的相关性,这些数据表明:(i)近交系小鼠在依赖情景记忆与程序记忆的先天倾向方面存在差异,这意味着对旨在破坏颞叶依赖性记忆的突变具有不同的敏感性;(ii)研究无症状突变体中训练驱动的神经改变可揭示早期突触损伤,这大大早于AD首发症状的检测。