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dc.contributor.authorArslan, Rana
dc.contributor.authorBor, Zeynep
dc.contributor.authorBektaş, Nurcan
dc.contributor.authorMeriçli, Ali Hikmet
dc.contributor.authorÖztürk, Yusuf
dc.date.accessioned2019-10-19T14:16:23Z
dc.date.available2019-10-19T14:16:23Z
dc.date.issued2011
dc.identifier.issn0049-3848
dc.identifier.urihttps://dx.doi.org/10.1016/j.thromres.2010.11.028
dc.identifier.urihttps://hdl.handle.net/11421/13146
dc.descriptionWOS: 000287479800008en_US
dc.descriptionPubMed ID: 21183208en_US
dc.description.abstractIntroduction: Crataegus species (common name is Hawthorn) are medicinal plants, which have flavonoids, triterpene acids, proanthocyanidins, and organic acids as main constituents, used in the treatment of cardiovascular diseases. One of the main causes of multiple cardiovascular diseases is intravascular thrombosis and current agents, which are used for the treatment and prevention of thrombosis, have some side effects. Therefore, new antithrombotic and thrombolytic agents are still needed. Materials and Methods: Antithrombotic function of ethanol extract of Crataegus orientalis (COE) leaves was investigated in carrageenan-induced mice tail thrombosis model. Mice were injected with 40 mu l (1%) carrageenan (Type I) dissolved in physiological saline by intraplantar administration in the right hind paw. After carrageenan injection, the extract was administered at the doses of 100, 200, and 300 mg/kg. Heparin was used as a positive control (10 and 100 IU). The length of tail-thrombosis was measured at 24th, 48th, and 72nd hours. Results and Conclusion: 100 mg/kg COE and 10 IU heparin were not significant when compared to control groups at the time interval (24-72 h) that results was obtained. At 24th hour, both 200 and 300 mg/kg of COE showed a significant antithrombotic activity (p<0.05 and p<0.01, respectively). However, 200 mg/kg COE lost its significance and there was a decrease in the significance values of 300 mg/kg COE (p<0.05) at 48 and 72 h. From these results, it was concluded that COE significantly inhibited carrageenan-induced mice tail thrombosis in vivo.en_US
dc.description.sponsorshipScientific Research Projects Foundation of Anadolu University, Eskisehir, Turkey [090331]en_US
dc.description.sponsorshipThe authors would like to thank to Prof. Dr. Ali A. Donmez from the Faculty of Science, Hacettepe University, Ankara, Turkey for the collection and identification of the plant and also we would like to thank Dr. Sevda Pirildar for preparing the extract. Financial support for this work through the Scientific Research Projects Foundation of Anadolu University, Eskisehir, Turkey is gratefully acknowledged (Project code no: 090331).en_US
dc.language.isoengen_US
dc.publisherPergamon-Elsevier Science LTDen_US
dc.relation.isversionof10.1016/j.thromres.2010.11.028en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCrataegus Orientalisen_US
dc.subjectCarrageenanen_US
dc.subjectTail Thrombosis Modelen_US
dc.subjectAntithrombotic Effecten_US
dc.titleAntithrombotic effects of ethanol extract of Crataegus orientalis in the carrageenan-induced mice tail thrombosis modelen_US
dc.typearticleen_US
dc.relation.journalThrombosis Researchen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmakoloji Anabilim Dalıen_US
dc.identifier.volume127en_US
dc.identifier.issue3en_US
dc.identifier.startpage210en_US
dc.identifier.endpage213en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorArslan, Rana
dc.contributor.institutionauthorBektaş, Nurcan
dc.contributor.institutionauthorÖztürk, Yusuf


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