Ketosis regulates K+ ion channels, strengthening brain-wide signaling disrupted by age

Author:

van Nieuwenhuizen Helena12,Chesebro Anthony G.234,Polizu Claire4,Clarke Kieran5,Strey Helmut H.36,Weistuch Corey7,Mujica-Parodi Lilianne R.1236

Affiliation:

1. Department of Physics and Astronomy, Stony Brook University, Stony Brook, NY, United States

2. Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, United States

3. Department of Biomedical Engineering, Stony Brook University, Stony Brook, NY, United States

4. Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, United States

5. Department of Physiology, Oxford University, Oxford, United Kingdom

6. Laufer Center for Physical and Quantitative Biology, Stony Brook University, Stony Brook, NY, United States

7. Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, United States

Abstract

Abstract Aging is associated with impaired signaling between brain regions when measured using resting-state functional magnetic resonance imaging (fMRI). This age-related destabilization and desynchronization of brain networks reverses itself when the brain switches from metabolizing glucose to ketones. Here, we probe the mechanistic basis for these effects. First, we confirmed their robustness across measurement modalities using two datasets acquired from resting-state EEG (Lifespan: standard diet, 20–80 years, N = 201; Metabolic: individually weight-dosed and calorically-matched glucose and ketone ester challenge, μage = 26.9 ±11.2 years, N = 36). Then, using a multiscale conductance-based neural mass model, we identified the unique set of mechanistic parameters consistent with our clinical data. Together, our results implicate potassium (K+) gradient dysregulation as a mechanism for age-related neural desynchronization and its reversal with ketosis, the latter finding of which is consistent with direct measurement of ion channels. As such, the approach facilitates the connection between macroscopic brain activity and cellular-level mechanisms.

Publisher

MIT Press

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3