Synthetic organic food colouring agents and their degraded products: effects on human and rat cholinesterases
Most synthetic coloured additives are carcinogenic, teratogenic and cause allergic reactions. In this study, the effects of synthetic azo dyes (sunset yellow FCF and carmoisine), as well as their degraded products (sulphanilic acid and naphthionic acid), on both true and pseudo-cholinesterases (ChEs...
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Veröffentlicht in: | British journal of biomedical science 2004-01, Vol.61 (3), p.128-132 |
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description | Most synthetic coloured additives are carcinogenic, teratogenic and cause allergic reactions. In this study, the effects of synthetic azo dyes (sunset yellow FCF and carmoisine), as well as their degraded products (sulphanilic acid and naphthionic acid), on both true and pseudo-cholinesterases (ChEs) are studied. The results indicate that the synthetic azo dyes and their degraded products inhibit both human true and pseudo-ChE activities in vitro. The concentration of coloured additive that cause 50% inhibition (IC
50
) and enzyme inhibitor dissociation constant (K
i
) show that sunset yellow FCF produces greater inhibition of both true and pseudo-ChEs than does carmoisine and sulphanilic acid, while naphthionic acid produces greater inhibition of pseudo-ChE only. K
i
indicates that the affinity of sulphanilic acid for both true and pseudo-ChEs is higher than the other three inhibitors. Inhibition of both true and pseudo-ChEs by sunset yellow FCF is of mixed (competitive and non-competitive) type, but carmoisine and sulphanilic acid are non-competitive. Naphthionic acid produces a competitive inhibition kinetic with plasma ChE only. This inhibition is abolished by dialysis, indicating that their effects are reversible. The effects of sunset yellow FCF, carmoisine, sulphanilic acid and naphthionic acid on rat true and pseudo-ChEs are investigated. The data clearly show that there is a significant decrease in enzyme activity. Sulphanilic acid and sunset yellow FCF are the most potent in vivo inhibitors of true ChE and pseudo-ChE, respectively. |
doi_str_mv | 10.1080/09674845.2004.11732657 |
format | Article |
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50
) and enzyme inhibitor dissociation constant (K
i
) show that sunset yellow FCF produces greater inhibition of both true and pseudo-ChEs than does carmoisine and sulphanilic acid, while naphthionic acid produces greater inhibition of pseudo-ChE only. K
i
indicates that the affinity of sulphanilic acid for both true and pseudo-ChEs is higher than the other three inhibitors. Inhibition of both true and pseudo-ChEs by sunset yellow FCF is of mixed (competitive and non-competitive) type, but carmoisine and sulphanilic acid are non-competitive. Naphthionic acid produces a competitive inhibition kinetic with plasma ChE only. This inhibition is abolished by dialysis, indicating that their effects are reversible. The effects of sunset yellow FCF, carmoisine, sulphanilic acid and naphthionic acid on rat true and pseudo-ChEs are investigated. The data clearly show that there is a significant decrease in enzyme activity. Sulphanilic acid and sunset yellow FCF are the most potent in vivo inhibitors of true ChE and pseudo-ChE, respectively.</description><identifier>ISSN: 0967-4845</identifier><identifier>EISSN: 2474-0896</identifier><identifier>DOI: 10.1080/09674845.2004.11732657</identifier><identifier>PMID: 15462257</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Adult ; Animals ; Azo Compounds - pharmacology ; Carmoisine ; Cholinesterases ; Cholinesterases - blood ; Dialysis ; Food Coloring Agents - metabolism ; Food Coloring Agents - pharmacology ; Humans ; Male ; Naphthalenesulfonates - pharmacology ; Naphthionic acid ; Rats ; Sulfanilic Acids - pharmacology ; Sulphanilic acid ; Sunset yellow</subject><ispartof>British journal of biomedical science, 2004-01, Vol.61 (3), p.128-132</ispartof><rights>Copyright 2004 Taylor and Francis Group LLC 2004</rights><rights>Copyright Step Communications Ltd. 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-19291edcf0c145ce7569e7fa42fcc32a3636b6ef92495800d212e67a199480c33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15462257$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Osman, M.Y.</creatorcontrib><creatorcontrib>Sharaf, I.A.</creatorcontrib><creatorcontrib>Osman, H.M.Y.</creatorcontrib><creatorcontrib>El-Khouly, Z.A.</creatorcontrib><creatorcontrib>Ahmed, E.I.</creatorcontrib><title>Synthetic organic food colouring agents and their degraded products: effects on human and rat cholinesterases</title><title>British journal of biomedical science</title><addtitle>Br J Biomed Sci</addtitle><description>Most synthetic coloured additives are carcinogenic, teratogenic and cause allergic reactions. In this study, the effects of synthetic azo dyes (sunset yellow FCF and carmoisine), as well as their degraded products (sulphanilic acid and naphthionic acid), on both true and pseudo-cholinesterases (ChEs) are studied. The results indicate that the synthetic azo dyes and their degraded products inhibit both human true and pseudo-ChE activities in vitro. The concentration of coloured additive that cause 50% inhibition (IC
50
) and enzyme inhibitor dissociation constant (K
i
) show that sunset yellow FCF produces greater inhibition of both true and pseudo-ChEs than does carmoisine and sulphanilic acid, while naphthionic acid produces greater inhibition of pseudo-ChE only. K
i
indicates that the affinity of sulphanilic acid for both true and pseudo-ChEs is higher than the other three inhibitors. Inhibition of both true and pseudo-ChEs by sunset yellow FCF is of mixed (competitive and non-competitive) type, but carmoisine and sulphanilic acid are non-competitive. Naphthionic acid produces a competitive inhibition kinetic with plasma ChE only. This inhibition is abolished by dialysis, indicating that their effects are reversible. The effects of sunset yellow FCF, carmoisine, sulphanilic acid and naphthionic acid on rat true and pseudo-ChEs are investigated. The data clearly show that there is a significant decrease in enzyme activity. Sulphanilic acid and sunset yellow FCF are the most potent in vivo inhibitors of true ChE and pseudo-ChE, respectively.</description><subject>Adult</subject><subject>Animals</subject><subject>Azo Compounds - pharmacology</subject><subject>Carmoisine</subject><subject>Cholinesterases</subject><subject>Cholinesterases - blood</subject><subject>Dialysis</subject><subject>Food Coloring Agents - metabolism</subject><subject>Food Coloring Agents - pharmacology</subject><subject>Humans</subject><subject>Male</subject><subject>Naphthalenesulfonates - pharmacology</subject><subject>Naphthionic acid</subject><subject>Rats</subject><subject>Sulfanilic Acids - pharmacology</subject><subject>Sulphanilic acid</subject><subject>Sunset yellow</subject><issn>0967-4845</issn><issn>2474-0896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkE1PxCAQhonR6Lr6Fwzx3hUoheLNGL8SEw_qmSAMuzUtKLQx--9l3TUePc0cnpl35kHojJIFJS25IEpI3vJmwQjhC0plzUQj99CMcckr0iqxj2YbqNpQR-g453dCqGJSHKIj2nDBWCNnaHheh3EFY2dxTEsTSvUxOmxjH6fUhSU2SwhjxiY4XMAuYQfLZBw4_JGim-yYLzF4D6XBMeDVNJjwQyczYruKfRcgj5BMhnyCDrzpM5zu6hy93t68XN9Xj093D9dXj5WtFRurcqai4KwnlvLGgmyEAukNZ97ampla1OJNgFeMq6YlxDHKQEhDleItsXU9R-fbveXEz6nE6_fyTSiRmjHZtlKwpkBiC9kUc07g9UfqBpPWmhK9kax_JeuNZP0ruQye7bZPbwO4v7Gd1QJcbYEu-JgG8xVT7_Ro1n1MPplgu6zrf0K-AY1RjKs</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>Osman, M.Y.</creator><creator>Sharaf, I.A.</creator><creator>Osman, H.M.Y.</creator><creator>El-Khouly, Z.A.</creator><creator>Ahmed, E.I.</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>EHMNL</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope></search><sort><creationdate>20040101</creationdate><title>Synthetic organic food colouring agents and their degraded products: effects on human and rat cholinesterases</title><author>Osman, M.Y. ; Sharaf, I.A. ; Osman, H.M.Y. ; El-Khouly, Z.A. ; Ahmed, E.I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-19291edcf0c145ce7569e7fa42fcc32a3636b6ef92495800d212e67a199480c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Animals</topic><topic>Azo Compounds - pharmacology</topic><topic>Carmoisine</topic><topic>Cholinesterases</topic><topic>Cholinesterases - blood</topic><topic>Dialysis</topic><topic>Food Coloring Agents - metabolism</topic><topic>Food Coloring Agents - pharmacology</topic><topic>Humans</topic><topic>Male</topic><topic>Naphthalenesulfonates - pharmacology</topic><topic>Naphthionic acid</topic><topic>Rats</topic><topic>Sulfanilic Acids - pharmacology</topic><topic>Sulphanilic acid</topic><topic>Sunset yellow</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Osman, M.Y.</creatorcontrib><creatorcontrib>Sharaf, I.A.</creatorcontrib><creatorcontrib>Osman, H.M.Y.</creatorcontrib><creatorcontrib>El-Khouly, Z.A.</creatorcontrib><creatorcontrib>Ahmed, E.I.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>UK & Ireland Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><jtitle>British journal of biomedical science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Osman, M.Y.</au><au>Sharaf, I.A.</au><au>Osman, H.M.Y.</au><au>El-Khouly, Z.A.</au><au>Ahmed, E.I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthetic organic food colouring agents and their degraded products: effects on human and rat cholinesterases</atitle><jtitle>British journal of biomedical science</jtitle><addtitle>Br J Biomed Sci</addtitle><date>2004-01-01</date><risdate>2004</risdate><volume>61</volume><issue>3</issue><spage>128</spage><epage>132</epage><pages>128-132</pages><issn>0967-4845</issn><eissn>2474-0896</eissn><abstract>Most synthetic coloured additives are carcinogenic, teratogenic and cause allergic reactions. In this study, the effects of synthetic azo dyes (sunset yellow FCF and carmoisine), as well as their degraded products (sulphanilic acid and naphthionic acid), on both true and pseudo-cholinesterases (ChEs) are studied. The results indicate that the synthetic azo dyes and their degraded products inhibit both human true and pseudo-ChE activities in vitro. The concentration of coloured additive that cause 50% inhibition (IC
50
) and enzyme inhibitor dissociation constant (K
i
) show that sunset yellow FCF produces greater inhibition of both true and pseudo-ChEs than does carmoisine and sulphanilic acid, while naphthionic acid produces greater inhibition of pseudo-ChE only. K
i
indicates that the affinity of sulphanilic acid for both true and pseudo-ChEs is higher than the other three inhibitors. Inhibition of both true and pseudo-ChEs by sunset yellow FCF is of mixed (competitive and non-competitive) type, but carmoisine and sulphanilic acid are non-competitive. Naphthionic acid produces a competitive inhibition kinetic with plasma ChE only. This inhibition is abolished by dialysis, indicating that their effects are reversible. The effects of sunset yellow FCF, carmoisine, sulphanilic acid and naphthionic acid on rat true and pseudo-ChEs are investigated. The data clearly show that there is a significant decrease in enzyme activity. Sulphanilic acid and sunset yellow FCF are the most potent in vivo inhibitors of true ChE and pseudo-ChE, respectively.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>15462257</pmid><doi>10.1080/09674845.2004.11732657</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Adult Animals Azo Compounds - pharmacology Carmoisine Cholinesterases Cholinesterases - blood Dialysis Food Coloring Agents - metabolism Food Coloring Agents - pharmacology Humans Male Naphthalenesulfonates - pharmacology Naphthionic acid Rats Sulfanilic Acids - pharmacology Sulphanilic acid Sunset yellow |
title | Synthetic organic food colouring agents and their degraded products: effects on human and rat cholinesterases |
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