Shepherd A, Tyebji S, Hannan A J, Burrows E L
Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre, University of Melbourne, Parkville, VIC, 3010, Australia.
Department of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC, 3010, Australia.
J Mol Neurosci. 2016 Nov;60(3):371-382. doi: 10.1007/s12031-016-0837-1. Epub 2016 Sep 16.
Cognitive dysfunction appears as a core feature of dementia, which includes its most prevalent form, Alzheimer's disease (AD), as well as vascular dementia, frontotemporal dementia, and other brain disorders. AD alone affects more than 45 million people worldwide, with growing prevalence in aging populations. There is no cure, and therapeutic options remain limited. Gene-edited and transgenic animal models, expressing disease-specific gene mutations, illuminate pathogenic mechanisms leading to cognitive decline in AD and other forms of dementia. To date, cognitive tests in AD mouse models have not been directly relevant to the clinical presentation of AD, providing challenges for translation of findings to the clinic. Touchscreen testing in mice has enabled the assessment of specific cognitive domains in mice that are directly relevant to impairments described in human AD patients. In this review, we provide context for how cognitive decline is measured in the clinic, describe traditional methods for assessing cognition in mice, and outline novel approaches, including the use of the touchscreen platform for cognitive testing. We highlight the limitations of traditional memory-testing paradigms in mice, particularly their capacity for direct translation into cognitive testing of patients. While it is not possible to expect direct translation in testing methodologies, we can aim to develop tests that engage similar neural substrates in both humans and mice. Ultimately, that would enable us to better predict efficacy across species and therefore improve the chances that a treatment that works in mice will also work in the clinic.
认知功能障碍是痴呆症的核心特征,痴呆症包括其最常见的形式——阿尔茨海默病(AD),以及血管性痴呆、额颞叶痴呆和其他脑部疾病。仅AD在全球就影响着超过4500万人,且在老年人群中的患病率不断上升。目前尚无治愈方法,治疗选择仍然有限。表达疾病特异性基因突变的基因编辑和转基因动物模型,揭示了导致AD和其他形式痴呆症认知衰退的致病机制。迄今为止,AD小鼠模型中的认知测试与AD的临床表现没有直接关联,这给将研究结果转化到临床带来了挑战。小鼠的触摸屏测试能够评估小鼠中与人类AD患者所描述的损伤直接相关的特定认知领域。在本综述中,我们介绍了临床上如何测量认知衰退,描述了评估小鼠认知的传统方法,并概述了新方法,包括使用触摸屏平台进行认知测试。我们强调了小鼠传统记忆测试范式的局限性,特别是它们直接转化为患者认知测试的能力。虽然不可能期望测试方法直接转化,但我们可以致力于开发在人类和小鼠中涉及相似神经基质的测试。最终,这将使我们能够更好地预测跨物种的疗效,从而提高在小鼠中有效的治疗方法在临床上也有效的可能性。