Low circulating adropin concentrations identify vulnerability in learning-dependent cognitive performance in aged rhesus macaques.

IF 13 Q2 GERIATRICS & GERONTOLOGY
Andrew A Butler, James L Graham, Lesly C Ceniceros, Ashlee M Cruz, Ashley D Cunningham, Riya Subedi, Anthony P Brown, Nicholas Dai, Giovanne B Diniz, Peter J Havel, John H Morrison, Erin L Kinnally
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Abstract

Identifying biomarkers that identify vulnerability to age-related cognitive decline is a major priority in aging research. Adropin, a circulating peptide that regulates metabolic and vascular homeostasis, has been associated with cognitive performance in humans, but its relevance across species has remained unclear. Here we report low plasma adropin concentrations associate with poor decision-making in aged rhesus macaques subject to an increasing food choice test paradigm. Animals with higher adropin levels exhibited faster improvement in reaction time and reductions of variability in reaction time, whereas intrinsic performance on simple tasks was preserved. These associations were most apparent under conditions requiring adaptation to novelty or stress, suggesting that adropin may signal cognitive resilience rather than baseline executive capacity. The findings parallel mechanistic data from rodent models linking adropin signaling to mitochondrial function, resistance to oxidative stress, and hippocampal-dependent learning. Together, these results support measurements of circulating adropin as a conserved, translational biomarker of cognitive aging and a potential therapeutic target.

低循环adropin浓度确定了老年恒河猴学习依赖认知表现的脆弱性。
识别识别与年龄相关的认知能力下降易感性的生物标志物是衰老研究的主要重点。Adropin是一种调节代谢和血管稳态的循环肽,与人类的认知能力有关,但其在物种间的相关性尚不清楚。在这里,我们报告了低血浆促肾上腺素浓度与老年恒河猴在增加食物选择测试范式中的不良决策相关。adropin水平较高的动物在反应时间上表现出更快的改善和反应时间变异性的减少,而在简单任务上的内在表现则保持不变。这些关联在需要适应新鲜事物或压力的条件下最为明显,这表明下降可能表明认知弹性,而不是基线执行能力。这些发现与啮齿类动物模型的机制数据相一致,将adropin信号与线粒体功能、抗氧化应激和海马依赖学习联系起来。总之,这些结果支持循环adropin作为认知衰老的保守的翻译生物标志物和潜在的治疗靶点的测量。
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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来源期刊
CiteScore
8.90
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0.00%
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