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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/16200
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dc.contributor.authorAbbasi-Al, Ahmed Fahad-
dc.contributor.authorEsmat Ahmed-
dc.contributor.authorMohamadin, Mohamed Ahmed-
dc.contributor.authorAbdel Naim, Ashraf Bahyeldeen-
dc.date.accessioned2023-01-20T05:45:43Z-
dc.date.available2023-01-20T05:45:43Z-
dc.date.issued2018-07-20-
dc.identifier.citationAl-Abbasi, F. A., Esmat, A., Mohamadin, A. M., & Abdel-Naim, A. B. (2018). Role of prostaglandin H synthase in activation of acrylonitrile to cyanide. Pakistan Journal of Pharmaceutical Sciences, 31(4).en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/16200-
dc.description.abstractThe present study aimed at investigating the in-vitro oxidation of acrylonitrile (ACN) to cyanide (CN−) by prostaglandin H synthase (PHS). Detection of CN− is considered a marker for free radical intermediates involved in ACN-induced toxicity. First, most favorable circumstances for ACN oxidation were characterized: pH (4.5), temperature (37ºC) and time of incubation (60 min.). In addition, the concentrations of ACN, PHS and H2O2 in incubation mixtures were assessed for further reaction characterization. The reaction maximum velocity (Vmax) was calculated to be 582.75 pmol CN−/mL/min and the Michaelis-Menten constant (Km) was 149.25 µmol ACN. Adding PHS inhibitors; resveratrol, quercetin, indomethacin or troloc-C to the reaction mixtures significantly reduced the rate of ACN oxidation. In conclusion, the present study demonstrates the ability of PHS to oxidize ACN to CN− and provides a clue for the explanation of ACN target toxicity.en_US
dc.language.isoenen_US
dc.publisherKarachi: Pakistan Botanical Society, University of Karachien_US
dc.subjectAcrylonitrileen_US
dc.subjectprostaglandin H synthaseen_US
dc.subjectcyanide.en_US
dc.titleRole of prostaglandin H synthase in activation of acrylonitrile to cyanideen_US
dc.typeArticleen_US
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