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狨猴和猕猴认知衰老的平行模式。

Parallel patterns of cognitive aging in marmosets and macaques.

作者信息

Vanderlip Casey R, Jutras Megan L, Asch Payton A, Zhu Stephanie Y, Lerma Monica N, Buffalo Elizabeth A, Glavis-Bloom Courtney

机构信息

Department of Neurobiology and Behavior, University of California Irvine, Irvine, CA, USA.

Department of Physiology and Biophysics, University of Washington School of Medicine, Seattle, WA, USA.

出版信息

bioRxiv. 2024 Jul 23:2024.07.22.604411. doi: 10.1101/2024.07.22.604411.

Abstract

As humans age, some experience cognitive impairment while others do not. When impairment does occur, it is not expressed uniformly across cognitive domains and varies in severity across individuals. Translationally relevant model systems are critical for understanding the neurobiological drivers of this variability, which is essential to uncovering the mechanisms underlying the brain's susceptibility to the effects of aging. As such, non-human primates are particularly important due to shared behavioral, neuroanatomical, and age-related neuropathological features with humans. For many decades, macaque monkeys have served as the primary non-human primate model for studying the neurobiology of cognitive aging. More recently, the common marmoset has emerged as an advantageous model for this work due to its short lifespan that facilitates longitudinal studies. Despite their growing popularity as a model, whether marmosets exhibit patterns of age-related cognitive impairment comparable to those observed in macaques and humans remains unexplored. To address this major limitation for the development and evaluation of the marmoset as a model of cognitive aging, we directly compared working memory ability as a function of age in macaques and marmosets on the identical working memory task. Our results demonstrate that marmosets and macaques exhibit remarkably similar age-related working memory deficits, highlighting the value of the marmoset as a model for cognitive aging research within the neuroscience community.

摘要

随着人类年龄的增长,有些人会出现认知障碍,而另一些人则不会。当出现认知障碍时,它在各个认知领域的表现并不一致,而且个体之间的严重程度也有所不同。与转化研究相关的模型系统对于理解这种变异性的神经生物学驱动因素至关重要,而这对于揭示大脑易受衰老影响的潜在机制必不可少。因此,由于与人类具有共同的行为、神经解剖学和与年龄相关的神经病理学特征,非人类灵长类动物尤为重要。几十年来,猕猴一直是研究认知衰老神经生物学的主要非人类灵长类动物模型。最近,普通狨猴因其较短的寿命便于进行纵向研究而成为这项工作的有利模型。尽管它们作为模型越来越受欢迎,但狨猴是否表现出与猕猴和人类中观察到的类似的与年龄相关的认知障碍模式仍未得到探索。为了解决将狨猴开发和评估为认知衰老模型的这一主要限制,我们在相同的工作记忆任务上直接比较了猕猴和狨猴作为年龄函数的工作记忆能力。我们的结果表明,狨猴和猕猴表现出非常相似的与年龄相关的工作记忆缺陷,突出了狨猴作为神经科学界认知衰老研究模型的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e80/11291085/186a4d9634ac/nihpp-2024.07.22.604411v1-f0001.jpg

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