Tolerability and first hints for potential efficacy of motor‐cognitive training under inspiratory hypoxia in health and neuropsychiatric disorders: A translational viewpoint

Neuroprotection Pub Date : 2024-06-04 DOI:10.1002/nep3.47
Svea‐Solveig Mennen, Maren Franta, M. Begemann, Justus B. H. Wilke, Roman Schröder, Umer Javed Butt, Jonathan‐Alexis Cortés‐Silva, Umut Çakır, Marie Güra, Markus de Marées, Vinicius Daguano Gastaldi, J. Burtscher, Julie Schanz, Matthias Bohn, M. Burtscher, Andreas Fischer, Luise Poustka, Peter Hammermann, Markus Stadler, Fred Lühder, Manvendra Singh, K. Nave, K. Miskowiak, H. Ehrenreich
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Abstract

Hypoxia is more and more perceived as pivotal physiological driving force, allowing cells in the brain and elsewhere to acclimate to lowered oxygen (O2), and abridged metabolism. The mediating transcription program is induced by inspiratory hypoxia but also by intensive motor‐cognitive tasks, provoking a relative decrease in O2 in relation to the acutely augmented requirement. We termed this fundamental, demand‐dependent drop in O2 availability “functional hypoxia.” Major players in the hypoxia response are hypoxia‐inducible factors (HIFs) and associated prolyl‐hydroxylases. HIFs are transcription factors, stabilized by low O2 accessibility, and control expression of a multitude of genes. Changes in oxygen, however, can also be sensed via other pathways, among them the thiol‐oxidase (2‐aminoethanethiol) dioxygenase. Considering the far‐reaching biological response to hypoxia, hitherto mostly observed in rodents, we initiated a translational project, combining mild to moderate inspiratory with functional hypoxia. We had identified this combination earlier to benefit motor‐cognitive attainment in mice. A total of 20 subjects were included: 13 healthy individuals and 7 patients with depression and/or autism spectrum disorder. Here, we show that motor‐cognitive training under inspiratory hypoxia (12% O2) for 3.5 h daily over 3 weeks is optimally tolerated. We present first signals of beneficial effects on general well‐being, cognitive performance, physical fitness and psychopathology. Erythropoietin in serum increases under hypoxia and flow cytometry analysis of blood reveals several immune cell types to be mildly modulated by hypoxia. To obtain reliable information regarding the “add‐on” value of inspiratory on top of functional hypoxia, induced by motor‐cognitive training, a single‐blind study—with versus without inspiratory hypoxia—is essential and outlined here.
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在吸气性缺氧条件下进行运动认知训练对健康和神经精神疾病的耐受性和潜在疗效的初步提示:转化观点
缺氧越来越被认为是关键的生理驱动力,它使大脑和其他部位的细胞适应氧气(O2)的减少和新陈代谢的减弱。吸气性缺氧会诱发中介转录程序,但高强度的运动-认知任务也会诱发中介转录程序,导致氧气相对于急剧增加的需求量减少。我们将这种基本的、依赖于需求的氧气供应下降称为 "功能性缺氧"。低氧反应的主要参与者是低氧诱导因子(HIFs)和相关的脯氨酰羟化酶。低氧诱导因子是一种转录因子,在低氧条件下会保持稳定,并控制多种基因的表达。不过,氧气的变化也可以通过其他途径感知,其中包括硫醇氧化酶(2-氨基乙硫醇)二氧化酶。考虑到缺氧对生物的深远影响,我们启动了一个转化项目,将轻度至中度吸气与功能性缺氧结合起来。我们早些时候就发现这种组合有益于小鼠的运动认知能力。我们共纳入了 20 名受试者:其中包括 13 名健康人和 7 名抑郁症和/或自闭症谱系障碍患者。在这里,我们展示了在吸气性缺氧(12% O2)条件下,每天进行 3.5 小时、持续 3 周的运动认知训练是可以达到最佳耐受性的。我们首次发现了对一般健康、认知能力、体能和心理病理学产生有益影响的信号。血清中的促红细胞生成素在缺氧条件下会增加,血液的流式细胞仪分析显示,几种免疫细胞类型会受到缺氧的轻微调节。为了获得有关运动认知训练诱导的功能性缺氧基础上吸气 "附加 "价值的可靠信息,单盲研究--有吸气缺氧与无吸气缺氧--是必不可少的,本文对此进行了概述。
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