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dc.contributor.authorTokac, Mehmet
dc.contributor.authorBacanli, Merve
dc.contributor.authorDumlu, Ersin Gurkan
dc.contributor.authorAydin, Sevtap
dc.contributor.authorEngin, Merve
dc.contributor.authorBozkurt, Birkan
dc.contributor.authorYalcin, Abdussamed
dc.contributor.authorErel, Ozcan
dc.contributor.authorKilic, Mehmet
dc.contributor.authorBasaran, Nursen
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:39:49Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:39:49Z
dc.date.issued2017
dc.identifier.issn1304-530X
dc.identifier.urihttps://dx.doi.org/10.4274/tjps.49369
dc.identifier.urihttps://hdl.handle.net/20.500.12418/6587
dc.descriptionWOS: 000417379400007en_US
dc.description.abstractObjectives: Pycnogenol (R) (PYC (R)), a standardized extract from the bark of Pinus maritima, consists of different phenolic compounds. PYC (R) has shown to have protective effects on chronic diseases such as diabetes, asthma, cancer, and immune disorders. The aim of this study was to determine the effects of PYC (R) against the DNA damage and biochemical changes in blood, liver, and lung tissues of ischemia-reperfusion (IR)-induced Wistar albino rats. Materials and Methods: A sham group, IR injury-induced group, and IR+PYC (R) group were formed. Ischemia was induced and sustained for 45 min, then the ischemic liver was reperfused, which was sustained for a further 120 min at the end of this period. After anesthesia and before the IR inducement, 100 mg/kg PYC (R) was given to the IR+PYC (R) group through intraperitoneal injections. The total oxidant (TOS) and total antioxidant status (TAS), total thiol levels (TTL), advanced oxidation protein products (AOPP), and biochemical parameters [myeloperoxidase (MPO), aspartate aminotransferase (AST), alanine aminotransferase (ALT) and lactate dehydrogenase (LDH)] in the rats were analyzed using spectrophotometric methods and DNA damage was assessed using single-cell gel electrophoresis. Results: The levels of TOS, TTL, MPO, AOPP, ALT, AST, and LDH were significantly decreased in the IR+PYC (R) group compared with the IR group (p<0.05). The levels of TAS were significantly increased in the IR+PYC (R) group compared with the IR group (p<0.05). PYC (R) reduced the DNA damage when compared with the IR group (p<0.05). Conclusion: The present results suggest that PYC (R) treatment might have a role in the prevention of IR-induced oxidative damage by decreasing DNA damage and increasing antioxidant status.en_US
dc.language.isoengen_US
dc.publisherTURKISH PHARMACISTS ASSOCen_US
dc.relation.isversionof10.4274/tjps.49369en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPycnogenolen_US
dc.subjectischemia reperfusion injuryen_US
dc.subjectDNA damageen_US
dc.titleThe Ameliorative Effects of Pycnogenol (R) on Liver Ischemia-Reperfusion Injury in Ratsen_US
dc.typearticleen_US
dc.relation.journalTURKISH JOURNAL OF PHARMACEUTICAL SCIENCESen_US
dc.contributor.department[Tokac, Mehmet] Yeni Yuzyil Univ, Gaziosmanpasa Hosp, Clin Gen Surg, Fac Med, Istanbul, Turkey -- [Bacanli, Merve -- Aydin, Sevtap -- Basaran, Nursen] Hacettepe Univ, Dept Pharmaceut Toxicol, Fac Pharm, Ankara, Turkey -- [Dumlu, Ersin Gurkan -- Yalcin, Abdussamed -- Kilic, Mehmet] Yildirim Beyazit Univ, Dept Gen Surg, Fac Med, Ankara, Turkey -- [Engin, Merve] Ankara Ataturk Training & Res Hosp, Clin Biochem, Ankara, Turkey -- [Bozkurt, Birkan] Cumhuriyet Univ, Dept Gen Surg, Fac Med, Sivas, Turkey -- [Erel, Ozcan] Yildirim Beyazit Univ, Dept Biochem, Fac Med, Ankara, Turkeyen_US
dc.contributor.authorIDAydin, Sevtap -- 0000-0002-6368-2745en_US
dc.identifier.volume14en_US
dc.identifier.issue3en_US
dc.identifier.endpage263en_US
dc.identifier.startpage257en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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