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dc.contributor.authorDogru-Abbasoglu, Semra
dc.contributor.authorUysal, Mujdat
dc.contributor.authorSoluk-Tekkesin, Merva
dc.contributor.authorOlgac, Vakur
dc.contributor.authorGiris, Murat
dc.date.accessioned2021-03-03T18:56:49Z
dc.date.available2021-03-03T18:56:49Z
dc.date.issued2018
dc.identifier.citationGiris M., Dogru-Abbasoglu S., Soluk-Tekkesin M., Olgac V., Uysal M., "Effect of betaine treatment on the regression of existing hepatic triglyceride accumulation and oxidative stress in rats fed on high fructose diet", GENERAL PHYSIOLOGY AND BIOPHYSICS, cilt.37, sa.5, ss.563-570, 2018
dc.identifier.issn0231-5882
dc.identifier.otherav_51e995e2-7a4f-46a2-a3bf-78ac6a5554ed
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/58190
dc.identifier.urihttps://doi.org/10.4149/gpb_2018005x
dc.description.abstractWe investigated whether betaine has any regressive effect on existing high fructose diet (HFrD)-induced insulin resistance, dyslipidemia, inflammation as well as hepatic steatosis and oxidative stress. Rats were fed a HFrD containing 60% fructose for 8 weeks. After 8 weeks, rats were divided into two groups and fed a control diet for an additional 4-week period (regression groups). One of the regression groups received drinking water containing betaine (1%; w/v), having antioxidant and anti-inflammatory actions. HFrD feeding caused insulin resistance, elevated triglyceride (TG) and tumor necrosis factor-alfa (TNF-alpha) levels, alanine aminotransferase (ALT) and aspartate transaminase (AST) activities in serum. This diet increased hepatic TG, thiobarbituric acid reactive substances (TBARS) and diene conjugate (DC) levels, decreased superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities. Marked macro-vesicular steatosis were detected. Serum TNF-alpha and ALT, hepatic TG, TBARS and DC levels and steatosis scores decreased in regression period of HFrD-fed rats. Additionally, serum TNF-alpha, hepatic TG, TBARS and DC levels significantly lower in betaine-treated regressed rats than non-treated regressed group. Our results indicate that betaine treatment may accelerate regression of HFrD-induced hepatic TG accumulation and oxidative stress in rats.
dc.language.isoeng
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyofizik
dc.subjectBiyokimya
dc.subjectFizyoloji
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectFİZYOLOJİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectBİYOFİZİK
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.titleEffect of betaine treatment on the regression of existing hepatic triglyceride accumulation and oxidative stress in rats fed on high fructose diet
dc.typeMakale
dc.relation.journalGENERAL PHYSIOLOGY AND BIOPHYSICS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume37
dc.identifier.issue5
dc.identifier.startpage563
dc.identifier.endpage570
dc.contributor.firstauthorID715937


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