نمایش مختصر رکورد

dc.contributor.authorRahimi-Madiseh, Mohammaden_US
dc.contributor.authorKarimian, Paridokhten_US
dc.contributor.authorKafeshani, Marziehen_US
dc.contributor.authorRafieian-Kopaei, Mahmouden_US
dc.date.accessioned1399-07-09T08:22:45Zfa_IR
dc.date.accessioned2020-09-30T08:22:45Z
dc.date.available1399-07-09T08:22:45Zfa_IR
dc.date.available2020-09-30T08:22:45Z
dc.date.issued2017-05-01en_US
dc.date.issued1396-02-11fa_IR
dc.date.submitted2017-05-02en_US
dc.date.submitted1396-02-12fa_IR
dc.identifier.citationRahimi-Madiseh, Mohammad, Karimian, Paridokht, Kafeshani, Marzieh, Rafieian-Kopaei, Mahmoud. (2017). The effects of ethanol extract of Berberis vulgaris fruit on histopathological changes and biochemical markers of the liver damage in diabetic rats. Iranian Journal of Basic Medical Sciences, 20(5), 552-556. doi: 10.22038/ijbms.2017.8681en_US
dc.identifier.issn2008-3866
dc.identifier.issn2008-3874
dc.identifier.urihttps://dx.doi.org/10.22038/ijbms.2017.8681
dc.identifier.urihttp://ijbms.mums.ac.ir/article_8681.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/340295
dc.description.abstract<strong><em>Objective(s)</em></strong>: Various studies have shown that the diabetes is associated with liver failure. The objective of this study was determining the effects of <em>Berberis vulgaris</em> fruit on histopathological and biochemical markers of liver in diabetic rats.<br /> <strong><em>Materials and Methods: </em></strong>In this experimental study, 60 male Wistar rats weighing 200-250 g with free access to water and <em>ad libitum</em> were randomly divided to five twelve-membered groups including healthy control (group 1), diabetic control (group 2, this two groups received distilled water), treated diabetic positive control (group 3) using dose 150 mg/kg/day metformin, and two groups treated with doses 200 (group 4) and 600 (group 5) mg/kg/BW of <em>B. vulgaris</em> extracts via gavage feeding for 8 weeks. Diabetes mellitus was experimentally induced by one dose injection of alloxan 120 mg/kg. This pre-clinical study was performed on 120 mg/kg alloxan induced diabetic rats.<br /> <strong><em>Results:</em></strong> The hepatic steatosis status, liver cholestasis and fibrosis were not changed in group 4 and 5. Glycogen deposition changed mildly and polymorphonuclear neutrophils infiltration changed moderately at group 5. Liver hepatitis changed mildly and severely at group 3 as well as group 5, respectively. Glucose, serum glutamic-oxaloacetic transaminase, serum glutamic pyruvic transaminase, and alkaline phosphatase were lower in high dose group compared to other groups.<br /> <strong><em>Conclusion:</em></strong> Results suggested that <em>B. vulgaris</em> extract can decrease liver damage by influencing hepatic histopathological and biochemical markers in diabetic rats.en_US
dc.format.extent971
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Basic Medical Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ijbms.2017.8681
dc.subjectBerberineen_US
dc.subjectBiochemical markersen_US
dc.subjectDiabetesen_US
dc.subjectHistopathologyen_US
dc.subjectHerbal Medicineen_US
dc.subjectLiver diseasesen_US
dc.titleThe effects of ethanol extract of Berberis vulgaris fruit on histopathological changes and biochemical markers of the liver damage in diabetic ratsen_US
dc.typeTexten_US
dc.contributor.departmentMedical Plants Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iranen_US
dc.contributor.departmentDepartment of Pathology, Shahrekord University of Medical Sciences, Shahrekord, Iranen_US
dc.contributor.departmentDepartment of Clinical Nutrition/Community Nutrition/Food Science & Technology, Food Security Research Center, School of Nutrition & Food Science, Isfahan, Iranen_US
dc.contributor.departmentMedical Plants Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iranen_US
dc.citation.volume20
dc.citation.issue5
dc.citation.spage552
dc.citation.epage556


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