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Murburn Concept: A Molecular Explanation for Hormetic and Idiosyncratic Dose Responses.


ABSTRACT: Recently, electron transfers and catalyses in a bevy of redox reactions mediated by hemeproteins were explained by murburn concept. The term "murburn" is abstracted from "muredburning" or "mildunrestrictedburning" and connotes a novel "molecule-unbound ion-radical" interaction paradigm. Quite unlike the genetic regulations and protein-level affinity-based controls that govern order and specificity/selectivity in conventional treatments, murburn concept is based on stochastic/thermodynamic regulatory principles. The novel insight necessitates a "reactivity outside the active-site" perspective, because select redox enzymatic activity is obligatorily mediated via diffusible radical/species. Herein, reactions employing key hemeproteins (as exemplified by CYP2E1) establish direct experimental connection between "additive-influenced redox catalysis" and "unusual dose responses" in reductionist and physiological milieu. Thus, direct and conclusive molecular-level experimental evidence is presented, supporting the mechanistic relevance of murburn concept in "maverick" concentration-based effects brought about by additives. Therefore, murburn concept could potentially explain several physiological hormetic and idiosyncratic dose responses.

SUBMITTER: Parashar A 

PROVIDER: S-EPMC5946624 | biostudies-literature | 2018 Apr-Jun

REPOSITORIES: biostudies-literature

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Murburn Concept: A Molecular Explanation for Hormetic and Idiosyncratic Dose Responses.

Parashar Abhinav A   Gideon Daniel Andrew DA   Manoj Kelath Murali KM  

Dose-response : a publication of International Hormesis Society 20180401 2


Recently, electron transfers and catalyses in a bevy of redox reactions mediated by hemeproteins were explained by murburn concept. The term "murburn" is abstracted from "<i>mur</i><i>ed</i><i>burn</i><i>ing</i>" or "<i>m</i><i>ild</i><i>u</i><i>n</i><i>r</i><i>estricted</i><i>burn</i><i>ing</i>" and connotes a novel "<i>m</i><i>olecule-</i><i>u</i><i>nbound ion-</i><i>r</i><i>adical</i>" interaction paradigm. Quite unlike the genetic regulations and protein-level affinity-based controls that go  ...[more]

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