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dc.contributor.authorBeydogan, Alisa Bahar
dc.contributor.authorCoskun, Zeynep Mine
dc.contributor.authorBolkent, Sema
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T15:55:28Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T15:55:28Z
dc.date.issued2019
dc.identifier.issn0022-3573
dc.identifier.issn2042-7158
dc.identifier.urihttps://dx.doi.org/10.1111/jphp.13042
dc.identifier.urihttp://hdl.handle.net/11446/2036
dc.descriptionWOS: 000457750000012en_US
dc.descriptionPubMed ID: 30427077en_US
dc.description.abstractObjectives A large amount of fructose is metabolized in the liver and causes hepatic functional damage. Delta(9)-tetrahydrocannabinol (THC) is known as a therapeutic agent for clinical and experimental applications. The study aims to investigate the effects of THC treatment on inflammation, lipid profiles and oxidative stress in rat liver with hyperinsulinemia. Methods Sprague-Dawley rats were divided into groups: control, fructose (10% fructose in drinking water for 12 weeks), THC (1.5 mg/kg/day for the last 4 weeks, intraperitoneally) and fructose+THC groups. Biochemical parameters were measured spectrophotometrically. ELISA method was used for insulin measurement. Apoptosis and inflammation markers were detected by the streptavidin-biotin peroxidase method. Key findings The consumptions of food and fluid are inversely proportional to fructose and non-fructose groups. Insulin levels were the highest in fructose group. The reduced glutathione-S-transferase level significantly increased in fructose + THC group compared with fructose group. Total cholesterol level in the fructose + THC group was higher than the fructose group. Caspase-3 and NF-kappa beta immunopositive cell numbers increased in fructose + THC rats compared with fructose group. The number of IL-6 immunopositive cell decreased in fructose + THC group compared with fructose group. Conclusions According to the result, long-term and low-dose THC administration may reduce hyperinsulinemia and inflammation in rats to some extent.en_US
dc.description.sponsorshipScientific Research Projects Coordination Unit of Istanbul University [50228]en_US
dc.description.sponsorshipThis study was supported by the Scientific Research Projects Coordination Unit of Istanbul University. Project no: 50228.en_US
dc.language.isoengen_US
dc.publisherWILEYen_US
dc.identifier.doi10.1111/jphp.13042en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectfructoseen_US
dc.subjecthyperinsulinemiaen_US
dc.subjectinflammationen_US
dc.subjectliveren_US
dc.subjecttetrahydrocannabinolen_US
dc.titleThe protective effects of Delta(9)-tetrahydrocannabinol against inflammation and oxidative stress in rat liver with fructose-induced hyperinsulinemiaen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF PHARMACY AND PHARMACOLOGYen_US
dc.departmentDBÜen_US
dc.identifier.issue3en_US
dc.identifier.volume71en_US
dc.identifier.startpage408en_US
dc.identifier.endpage416en_US
dc.contributor.authorID0000-0001-8463-5561en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Beydogan, Alisa Bahar -- Bolkent, Sema] Istanbul Univ, Fac Cerrahpasa Med, Dept Med Biol, TR-34098 Istanbul, Turkey -- [Coskun, Zeynep Mine] Istanbul Bilim Univ, Fac Arts & Sci, Dept Mol Biol & Genet, Istanbul, Turkeyen_US


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