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Front Mol Biosci. 2016 May 12;3:18. doi: 10.3389/fmolb.2016.00018. eCollection 2016.

Dehydration and Cognition in Geriatrics: A Hydromolecular Hypothesis.

Frontiers in molecular biosciences

Adonis Sfera, Michael Cummings, Carolina Osorio

Affiliations

  1. Department of Psychiatry, Loma Linda UniversityLoma Linda, USA; Patton State HospitalPatton, USA.
  2. Patton State Hospital Patton, USA.
  3. Department of Psychiatry, Loma Linda University Loma Linda, USA.

PMID: 27252943 PMCID: PMC4860410 DOI: 10.3389/fmolb.2016.00018

Abstract

Dehydration is one of the ten most frequent diagnoses responsible for the hospital admission of elderly in the United States. It is associated with increased mortality, morbidity and an estimated cost of 1.14 billion per year (Xiao et al., 2004; Schlanger et al., 2010; Pretorius et al., 2013; Frangeskou et al., 2015). Older individuals are predisposed to dehydration encephalopathy as a result of decreased total body water (TBW) and diminished sensation of thirst. We hypothesize that thirst blunting in older individuals is the result of a defective microRNA-6842-3p failing to silence the expression of the vesicular GABA transporters (VGAT) and alpha 7 cholinergic nicotinic receptors in the subfornical organ (SFO) of the hypothalamus. We hypothesize further that resultant dehydration facilitates protein misfolding and aggregation, predisposing to neurocognitive disorders. We completed a search of predicted microRNA targets, utilizing the public domain tool miRDB and found that microRNA-6842-3p modulates the SLC6A1 and CHRNA7 genes both of which were previously hypothesized to inhibit the thirst sensation by their action on SFO. The primary aim of this article is to answer two questions: Can prevention and correction of dehydration in elderly lower age-related cognitive deterioration? Can exosomal miR-6842 in the peripheral blood predict dehydration encephalopathy in elderly?

Keywords: aquaporins; dehydration; extracellular space; protein conformational dynamics; protein folding

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