Integrated Restoration of Cellular Hydration, Signaling, and Inflammation in Agingp

Aging is frequently accompanied by a paradoxical physiological state in which individuals experience chronic dehydration, tissue dryness, and declining cellular function despite adequate or increased water intake. This phenomenon, herein described as cellular water resistance, is increasingly observed alongside chronic low-grade inflammation, impaired cellular signaling, mitochondrial decline, and reduced autophagic capacity. This paper proposes a unified, natural, non-pharmacological framework to address these interconnected dysfunctions simultaneously. Rather than treating hydration failure, inflammation, or aging-related decline as isolated problems, the framework integrates structured hydration, signal-supported electrolyte modulation, inflammation downregulation, autophagy activation, and regulatory reset. The work synthesizes physiological principles, aging biology, and exploratory regulatory concepts to present a practical, pre-clinical intervention model aimed at restoring cellular receptivity, functional signaling, and systemic resilience. No clinical claims are made; the paper is intended to support research discussion, protocol development, and ethical evaluation.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-01-23
DOI
https://doi.org/10.5281/zenodo.18346515
Primary Topic
Hydrogen's biological and therapeutic effects
Type
article
Field-Weighted Citation Impact
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article

Integrated Restoration of Cellular Hydration, Signaling, and Inflammation in Agingp

Sumeru Ray
Zenodo (CERN European Organization for Nuclear Research)
Hydrogen's biological and therapeutic effects
article

Integrated Restoration of Cellular Hydration, Signaling, and Inflammation in Agingp

Sumeru Ray
article en

Abstract

Aging is frequently accompanied by a paradoxical physiological state in which individuals experience chronic dehydration, tissue dryness, and declining cellular function despite adequate or increased water intake. This phenomenon, herein described as cellular water resistance, is increasingly observed alongside chronic low-grade inflammation, impaired cellular signaling, mitochondrial decline, and reduced autophagic capacity. This paper proposes a unified, natural, non-pharmacological framework to address these interconnected dysfunctions simultaneously. Rather than treating hydration failure, inflammation, or aging-related decline as isolated problems, the framework integrates structured hydration, signal-supported electrolyte modulation, inflammation downregulation, autophagy activation, and regulatory reset. The work synthesizes physiological principles, aging biology, and exploratory regulatory concepts to present a practical, pre-clinical intervention model aimed at restoring cellular receptivity, functional signaling, and systemic resilience. No clinical claims are made; the paper is intended to support research discussion, protocol development, and ethical evaluation.

Zenodo (CERN European Organization for Nuclear Research)
Mahle (Austria) (AT)
Openalex Percentile: Top 80%
Hydrogen's biological and therapeutic effects
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Integrated Restoration of Cellular Hydration, Signaling, and Inflammation in Agingp — Sumeru Ray · Zenodo (CERN European Organization for Nuclear Research) (2026) | TGRS Research Map | TGRS