Choline derivatives and sodium fluoride protect acetylcholinesterase against irreversible inhibition and aging by DFP and paraoxon

A light addressable potentiometric sensor was used to measure acetylcholinesterase (AChE) activity in order to evaluate the protective effects of quaternary compounds and NaF against enzyme phosphorylation and aging by two organophosphates. The use of the immobilized AChE made possible the quick rem...

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Veröffentlicht in:Journal of biochemical toxicology 1994-10, Vol.9 (5), p.261-268
Hauptverfasser: Dehlawi, Mohamed S., Eldefrawi, Amira T., Eldefrawi, Mohyee E., Anis, Nabil A., Valdes, James J.
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container_end_page 268
container_issue 5
container_start_page 261
container_title Journal of biochemical toxicology
container_volume 9
creator Dehlawi, Mohamed S.
Eldefrawi, Amira T.
Eldefrawi, Mohyee E.
Anis, Nabil A.
Valdes, James J.
description A light addressable potentiometric sensor was used to measure acetylcholinesterase (AChE) activity in order to evaluate the protective effects of quaternary compounds and NaF against enzyme phosphorylation and aging by two organophosphates. The use of the immobilized AChE made possible the quick removal of reagents (i.e., organophosphate, 2‐pralidoxime, and protectant), thereby permitting accurate determination of AChE activity before and after phosphorylation and aging. Paraoxon was 15‐fold more potent in inhibiting AChE than DFP, while the percent aging following phosphorylation by diiso‐propylfluorophosphate (DFP) was much higher. Sodium fluoride (NaF), the most effective protectant against phosphorylation and aging, and the quaternary ammonium compounds reduced significantly AChE inhibition by DFP and paraoxon, to similar degrees. Even though the percent AChE activity that was lost to aging was reduced by these agents, aging as a percent of phosphorylated AChE was not reduced. Thus, their major effect was in reducing the percent AChE phosphorylation, which consequently resulted in reduction of total aged AChE. The finding that quaternary ammonium compounds protect against phosphorylation is consonant with the proposed presence of the active site of AChE in an aromatic gorge.
doi_str_mv 10.1002/jbt.2570090506
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Biochem. Toxicol</addtitle><description>A light addressable potentiometric sensor was used to measure acetylcholinesterase (AChE) activity in order to evaluate the protective effects of quaternary compounds and NaF against enzyme phosphorylation and aging by two organophosphates. The use of the immobilized AChE made possible the quick removal of reagents (i.e., organophosphate, 2‐pralidoxime, and protectant), thereby permitting accurate determination of AChE activity before and after phosphorylation and aging. Paraoxon was 15‐fold more potent in inhibiting AChE than DFP, while the percent aging following phosphorylation by diiso‐propylfluorophosphate (DFP) was much higher. Sodium fluoride (NaF), the most effective protectant against phosphorylation and aging, and the quaternary ammonium compounds reduced significantly AChE inhibition by DFP and paraoxon, to similar degrees. 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subjects Acetylcholinesterase - drug effects
Acetylcholinesterase - metabolism
Acetylcholinesterase/Aging
Acetylcholinesterase/Protectants
Biosensor/Acetylcholinesterase
Choline - metabolism
Choline - pharmacology
DFP/Acetylcholinesterase Protection
Enzymes, Immobilized
Isoflurophate - toxicity
NaF/Acetylcho-linesterase Protection
Organophosphate Inhibitors
Paraoxon - toxicity
Paraoxon/ Acetylcholinesterase inhibition
Phosphorylation
Sodium Fluoride - pharmacology
title Choline derivatives and sodium fluoride protect acetylcholinesterase against irreversible inhibition and aging by DFP and paraoxon
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