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dc.contributor.authorÇaylı, Sevil
dc.contributor.authorSati, Leyla
dc.contributor.authorSeval Çelik, Yasemin
dc.contributor.authorTuncer, M. Altug
dc.contributor.authorYaymaci, Bengi
dc.contributor.authorBerkman, Zafer
dc.contributor.authorDemir, Ramazan
dc.date.accessioned2022-05-11T14:34:46Z
dc.date.available2022-05-11T14:34:46Z
dc.date.issued2010
dc.identifier.issn0213-3911
dc.identifier.issn1699-5848
dc.identifier.urihttps://hdl.handle.net/20.500.11776/8084
dc.description.abstractThe preventive and therapeutic effects of Eicosapentaenoic acid (EPA) on diet-induced hyperlipidemia in rabbits have been investigated. Eighteen New Zealand rabbits were randomly divided into three groups of 6 subjects each; experimental group-I (EG-I) was administered a cholesterol rich diet, experimental group-II (EG-II) was treated with EPA (300 mg/kg/d) following a cholesterol-rich diet and the control group (CG) had a standard diet. Blood samples were collected at day 0 and at the 4th and 12th weeks of EG-II to obtain serum levels of total cholesterol (TC), high density lipid-cholesterol (HDL-C), low density lipid-cholesterol (LDL-C) and triglyceride (TG). From each group tissue samples were collected from the carotid artery for immunohistochemistry and electron microscopy. Our results showed that EPA could significantly lower (p<0.001) serum TC, LDL-C, HDLC and TG levels with a reduction of 35%; 55%; 44% and 51%, respectively. Scanning and transmission electron microscopy results revealed that endothelial damage was more prominent in EG-I when compared to EG-II. The ruptured endothelial lining and damaged cellular surface was increased in EG-I when compared to EG-II. Ultrastructural observations showed that after EPA treatment, the degeneration and cellular surface damage on the endothelium were also decreased. These biochemical and ultrastructural results suggest that EPA is a potential drug which significantly lowers the serum lipid profile and partially repairs endothelial dysfunction due to hyperlipidemia.en_US
dc.description.sponsorshipAkdeniz University Research FoundationAkdeniz Universityen_US
dc.description.sponsorshipThis article was produced by a collaborative project between the departments of Cardiovascular Surgery and Cardiology of Kosuyolu State Hospital, Istanbul; and Department of Histology and Embryology, Faculty of Medicine, Akdeniz University, Antalya, and Department of Experimental Laboratory, Cerrahpasa Medical Faculty (Tuncay Altug), Istanbul University, Istanbul, Turkey. This study was partly funded by a grant from Akdeniz University Research Foundation. We would like to thank Gksemin Acar, Gamze Tanriover, Eylem Tuncer for their scientific support and to Sibel Ozer, Arife Demirtop and Hakan Er for their excellent technical assistance.en_US
dc.language.isoengen_US
dc.publisherF Hernandezen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEPAen_US
dc.subjectCholesterolen_US
dc.subjectAtherosclerosisen_US
dc.subjectEndotheliumen_US
dc.subjectUltrastructureen_US
dc.subjectRabbiten_US
dc.subjectAll-Cis-5,8,11,14,17-Icosapentaenoate Epa-Een_US
dc.subjectPolyunsaturated Fatty-Acidsen_US
dc.subjectFish-Oil Supplementationen_US
dc.subjectBlood-Pressureen_US
dc.subjectEthyl All-Cis-5,8,11,14,17-Icosapentaenoateen_US
dc.subjectPlasma-Lipidsen_US
dc.subjectDocosahexaenoic Aciden_US
dc.subjectLipoproteinsen_US
dc.subjectVasculogenesisen_US
dc.subjectAngiogenesisen_US
dc.titleThe effects of Eicosapentaenoic acid on the endothelium of the carotid artery of rabbits on a high-cholesterol dieten_US
dc.typearticleen_US
dc.relation.ispartofHistology and Histopathologyen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Beyin ve Sinir Cerrahisi Ana Bilim Dalıen_US
dc.authorid0000-0002-1801-2021
dc.authorid0000-0002-6516-6285
dc.authorid0000-0003-2465-5389
dc.identifier.volume25en_US
dc.identifier.issue2en_US
dc.identifier.startpage141en_US
dc.identifier.endpage151en_US
dc.institutionauthorBerkman, Zafer
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid35486863400
dc.authorscopusid12645794600
dc.authorscopusid6508378888
dc.authorscopusid57204598049
dc.authorscopusid6602245602
dc.authorscopusid12752602200
dc.authorscopusid7004337877
dc.authorwosidSati, Leyla/C-2489-2016
dc.authorwosidCayli, Sevil/V-2342-2019
dc.identifier.wosWOS:000272839100002en_US
dc.identifier.scopus2-s2.0-75149195561en_US
dc.identifier.pmid20017101en_US


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