Spontaneous mammalian models for Alzheimer's disease and dementia.

IF 4.5 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-07-29 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf287
Madeleine Ford, Frank J Gunn-Moore, Mark P Dagleish
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Abstract

Globally, the human population is ageing, and, consequently, the prevalence of major neurocognitive disorders is increasing, resulting in a greater need for novel dementia therapeutic interventions. Animal models are invaluable in studying underlying pathological processes in human diseases and with evidence for rising life expectancy in many domesticated animals studies have investigated neurocognitive disorders in several non-human species. Rodents have been used extensively as animal models, but this review will examine published literature suggesting candidate non-laboratory animal models for studying dementia, especially human Alzheimer's disease. Comparison of the physiological, pathological and clinical features of companion animals, farm animals and marine mammals shows that although many animals develop amyloid plaques and, to lesser degree, hyperphosphorylated tau protein, very few develop neurofibrillary tangles or neuronal loss to the same extent as humans with Alzheimer's disease. Several hypotheses are proposed as to why, as yet, no animals have been found to spontaneously develop Alzheimer's disease-like pathology to the same level as humans but highlight specific aspects where these models may be useful if developed further.

阿尔茨海默病和痴呆症的自发哺乳动物模型。
在全球范围内,人口正在老龄化,因此,主要神经认知障碍的患病率正在增加,导致对新型痴呆症治疗干预措施的更大需求。动物模型在研究人类疾病的潜在病理过程中是非常宝贵的,并且有证据表明许多家养动物的预期寿命正在上升,研究已经调查了几种非人类物种的神经认知障碍。啮齿类动物被广泛用作动物模型,但本综述将检查已发表的文献,提出研究痴呆症,特别是人类阿尔茨海默病的候选非实验室动物模型。通过对伴侣动物、农场动物和海洋哺乳动物的生理、病理和临床特征的比较,可以发现,尽管许多动物会出现淀粉样斑块,并在较小程度上出现tau蛋白的过度磷酸化,但很少有动物会出现与人类阿尔茨海默病相同程度的神经原纤维缠结或神经元丢失。关于为什么到目前为止,还没有发现动物自发地发展成与人类相同水平的阿尔茨海默病样病理,提出了几个假设,但强调了这些模型如果进一步发展可能有用的具体方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.00
自引率
0.00%
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审稿时长
6 weeks
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