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 |
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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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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.</description><identifier>ISSN: 0887-2082</identifier><identifier>EISSN: 1522-7146</identifier><identifier>DOI: 10.1002/jbt.2570090506</identifier><identifier>PMID: 7853361</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>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</subject><ispartof>Journal of biochemical toxicology, 1994-10, Vol.9 (5), p.261-268</ispartof><rights>Copyright © 1994 Wiley‐Liss, Inc., A Wiley Company</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3786-e246bc9c565d84af44a0b22df07c5b8ba30fc2da092c82907a7f00f2938dd21d3</citedby><cites>FETCH-LOGICAL-c3786-e246bc9c565d84af44a0b22df07c5b8ba30fc2da092c82907a7f00f2938dd21d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjbt.2570090506$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbt.2570090506$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7853361$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dehlawi, Mohamed S.</creatorcontrib><creatorcontrib>Eldefrawi, Amira T.</creatorcontrib><creatorcontrib>Eldefrawi, Mohyee E.</creatorcontrib><creatorcontrib>Anis, Nabil A.</creatorcontrib><creatorcontrib>Valdes, James J.</creatorcontrib><title>Choline derivatives and sodium fluoride protect acetylcholinesterase against irreversible inhibition and aging by DFP and paraoxon</title><title>Journal of biochemical toxicology</title><addtitle>J. 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. 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.</description><subject>Acetylcholinesterase - drug effects</subject><subject>Acetylcholinesterase - metabolism</subject><subject>Acetylcholinesterase/Aging</subject><subject>Acetylcholinesterase/Protectants</subject><subject>Biosensor/Acetylcholinesterase</subject><subject>Choline - metabolism</subject><subject>Choline - pharmacology</subject><subject>DFP/Acetylcholinesterase Protection</subject><subject>Enzymes, Immobilized</subject><subject>Isoflurophate - toxicity</subject><subject>NaF/Acetylcho-linesterase Protection</subject><subject>Organophosphate Inhibitors</subject><subject>Paraoxon - toxicity</subject><subject>Paraoxon/ Acetylcholinesterase inhibition</subject><subject>Phosphorylation</subject><subject>Sodium Fluoride - pharmacology</subject><issn>0887-2082</issn><issn>1522-7146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtO6zAQQC0EgvLYskPyD6RM7CR2llBouQhdEALBzho_UgxpUtlpodv75fQSBGLFaqSZOWdxCDlMYZgCsONn3Q1ZLgBKyKHYIIM0ZywRaVZskgFIKRIGku2Q3RifAUACl9tkW8ic8yIdkH-jp7b2jaPWBb_Ezi9dpNhYGlvrFzNa1Ys2eOvoPLSdMx1F47pVbXoqdi5gdBSn6JvYUR-CW7oQva4d9c2T177zbfMhxKlvplSv6Nn45mMxx4DtW9vsk60K6-gOPuceuR-f340ukqvryZ_RyVViuJBF4lhWaFOavMitzLDKMgTNmK1AmFxLjRwqwyxCyYxkJQgUFUDFSi6tZanle2TYe01oYwyuUvPgZxhWKgX1v6Vat1TfLdfAUQ_MF3rm7Nf7Z7z1vezvr752q19s6vL07oc76Vm_bvj2xWJ4UYXgIlcPfyfqQrDx4-VtqQr-DsMjksY</recordid><startdate>199410</startdate><enddate>199410</enddate><creator>Dehlawi, Mohamed S.</creator><creator>Eldefrawi, Amira T.</creator><creator>Eldefrawi, Mohyee E.</creator><creator>Anis, Nabil A.</creator><creator>Valdes, James J.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199410</creationdate><title>Choline derivatives and sodium fluoride protect acetylcholinesterase against irreversible inhibition and aging by DFP and paraoxon</title><author>Dehlawi, Mohamed S. ; Eldefrawi, Amira T. ; Eldefrawi, Mohyee E. ; Anis, Nabil A. ; Valdes, James J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3786-e246bc9c565d84af44a0b22df07c5b8ba30fc2da092c82907a7f00f2938dd21d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Acetylcholinesterase - drug effects</topic><topic>Acetylcholinesterase - metabolism</topic><topic>Acetylcholinesterase/Aging</topic><topic>Acetylcholinesterase/Protectants</topic><topic>Biosensor/Acetylcholinesterase</topic><topic>Choline - metabolism</topic><topic>Choline - pharmacology</topic><topic>DFP/Acetylcholinesterase Protection</topic><topic>Enzymes, Immobilized</topic><topic>Isoflurophate - toxicity</topic><topic>NaF/Acetylcho-linesterase Protection</topic><topic>Organophosphate Inhibitors</topic><topic>Paraoxon - toxicity</topic><topic>Paraoxon/ Acetylcholinesterase inhibition</topic><topic>Phosphorylation</topic><topic>Sodium Fluoride - pharmacology</topic><toplevel>online_resources</toplevel><creatorcontrib>Dehlawi, Mohamed S.</creatorcontrib><creatorcontrib>Eldefrawi, Amira T.</creatorcontrib><creatorcontrib>Eldefrawi, Mohyee E.</creatorcontrib><creatorcontrib>Anis, Nabil A.</creatorcontrib><creatorcontrib>Valdes, James J.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of biochemical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dehlawi, Mohamed S.</au><au>Eldefrawi, Amira T.</au><au>Eldefrawi, Mohyee E.</au><au>Anis, Nabil A.</au><au>Valdes, James J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Choline derivatives and sodium fluoride protect acetylcholinesterase against irreversible inhibition and aging by DFP and paraoxon</atitle><jtitle>Journal of biochemical toxicology</jtitle><addtitle>J. Biochem. Toxicol</addtitle><date>1994-10</date><risdate>1994</risdate><volume>9</volume><issue>5</issue><spage>261</spage><epage>268</epage><pages>261-268</pages><issn>0887-2082</issn><eissn>1522-7146</eissn><abstract>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.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7853361</pmid><doi>10.1002/jbt.2570090506</doi><tpages>8</tpages></addata></record> |
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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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