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dc.contributor.authorÇetinkunar, Süleyman
dc.contributor.authorTokgöz, Serhat
dc.contributor.authorBilgin, Bülent Çağlar
dc.contributor.authorErdem, Hasan
dc.contributor.authorAktimur, Recep
dc.contributor.authorCan, Serpil
dc.contributor.authorPolat, Yılmaz
dc.contributor.authorSözen, Selim
dc.date.accessioned2022-05-11T14:39:53Z
dc.date.available2022-05-11T14:39:53Z
dc.date.issued2015
dc.identifier.issn1940-5901
dc.identifier.urihttps://hdl.handle.net/20.500.11776/8782
dc.description.abstractAim: Silymarin from Silybum marianum was found to reduce liver injury. The aim of the present study was to investigate the effects of silymarin on hepatic regeneration in partially hepatectomized rats. Methods: Thirty Wistar-Albino rats were divided into 3 groups of 10 animals as sham, control and experimental groups. In the sham group (n= 10) abdominal incision was closed after laparotomy. In the control group (n= 10), the rats underwent 70% hepatectomy after laparotomy. In the experimental group (n= 10) after partial 70% hepatectomy, silymarin (200 mg/kg/d) were given to rats for 10 days. Rats in three groups were sacrificed on 10 days. Aspartate (AST) and alanine transaminase (ALT), gamma glutamyl transferase (GGT), ALP, LDH and total bilirubin levels were measured using intracardiac blood samples. Tissue malondialdehyde (MDA) and tissue glutathion (GSH) and Superoxide dismutase (SOD) levels were measured. To reveal the increase in the mass of the remnant liver tissue in the control and experimental groups relative weight of the liver was calculated. Histopathological analysis of the liver was performed using a semi-quantitative scoring system. Results: A statistically significant difference among three groups was not shown for AST and ALT levels. A statistically significant difference was found between the groups as for total bilirubin and gamma glutamyl transferase levels. Increases in relative liver weights were seen with time in Groups 2 and 3. A statistically significant difference was not found for tissue malondialdehyde, Glutathion and Superoxide dismutase levels between hepatectomy and hepatectomy + silymarin groups. On liver tissue sections of the rats in the hepatectomy + silymarin group, increased regeneration and lipid peroxidation were observed accompanied by decreased antioxidant response. Conclusion: It has been observed that silymarin with many established functions such as antiproliferative, anti-inflammatory and energy antioxidant effects, does not contributed to proliferative regeneration of the liver-which has very important metabolic functions -after partial hepatectomy; instead it will decrease serum levels of transaminases.en_US
dc.language.isoengen_US
dc.publisherE-Century Publishing Corpen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSilymarinen_US
dc.subjecthepatic regenerationen_US
dc.subjecthepatectomyen_US
dc.subjectLiver-Regenerationen_US
dc.subjectRat-Liveren_US
dc.subjectLipid-Peroxidationen_US
dc.subjectOxidative Stressen_US
dc.subjectInjuryen_US
dc.subjectSilibininen_US
dc.subjectDiseasesen_US
dc.subjectSizeen_US
dc.titleThe effect of silymarin on hepatic regeneration after partial hepatectomy: is silymarin effective in hepatic regeneration?en_US
dc.typearticleen_US
dc.relation.ispartofInternational Journal of Clinical and Experimental Medicineen_US
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalıen_US
dc.authorid0000-0003-2716-6222
dc.authorid0000-0002-9121-536X
dc.authorid0000-0002-9121-536X
dc.authorid0000-0003-2006-9198
dc.authorid0000-0001-9111-2734
dc.identifier.volume8en_US
dc.identifier.issue2en_US
dc.identifier.startpage2578en_US
dc.identifier.endpage2585en_US
dc.institutionauthorSözen, Selim
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorwosidtokgöz, serhat/F-1573-2016
dc.authorwosidErol, Huseyin Serkan/Q-3962-2019
dc.authorwosidSözen, Selim/ABA-6337-2020
dc.authorwosidErol, Huseyin Serkan/B-5793-2016
dc.authorwosidCetinkunar, Suleyman/AFP-2813-2022
dc.identifier.wosWOS:000355306000120en_US
dc.identifier.pmid25932204en_US


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