The Initial Common Pathway of Inflammation, Disease, and Sudden Death
Name
Davidson-2012-The Initial Common P.pdf
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1.19 MB
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Adobe PDF
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Author(s) •
Davidson, Robert M.
Seneff, Stephanie
Date Issued
August 2012
Journal
Entropy
Publisher
MDPI AG
Citation
Davidson, Robert M., and Stephanie Seneff. “The Initial Common Pathway of Inflammation, Disease, and Sudden Death.” Entropy 14.12 (2012): 1399–1442.
Version
Final published version
Abstract
In reviewing the literature pertaining to interfacial water, colloidal stability, and cell membrane function, we are led to propose that a cascade of events that begins with acute exogenous surfactant-induced interfacial water stress can explain the etiology of sudden death syndrome (SDS), as well as many other diseases associated with modern times. A systemic lowering of serum zeta potential mediated by exogenous cationic surfactant administration is the common underlying pathophysiology. The cascade leads to subsequent inflammation, serum sickness, thrombohemorrhagic phenomena, colloidal instability, and ultimately even death. We propose that a sufficient precondition for sudden death is lowered bioavailability of certain endogenous sterol sulfates, sulfated glycolipids, and sulfated glycosaminoglycans, which are essential in maintaining biological equipose, energy metabolism, membrane function, and thermodynamic stability in living organisms. Our literature review provides the basis for the presentation of a novel hypothesis as to the origin of endogenous bio-sulfates which involves energy transduction from sunlight. Our hypothesis is amply supported by a growing body of data showing that parenteral administration of substances that lower serum zeta potential results in kosmotropic cationic and/or chaotropic anionic interfacial water stress, and the resulting cascade.
MIT Department
Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
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Creative Commons Attribution 3.0
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DOI of Published Version
https://doi.org/10.3390/e14081399