نمایش مختصر رکورد

dc.contributor.authorSolomon, Onosheen_US
dc.contributor.authorRabiu Saidu Umar, Wasaguen_US
dc.contributor.authorSanusi Wara, Hassanen_US
dc.contributor.authorSadiq Yakubu, Abubakaren_US
dc.contributor.authorMichael Azubuike, Madusolumouen_US
dc.contributor.authorAsugu Mary, Mbahien_US
dc.contributor.authorLouis, Hitleren_US
dc.date.accessioned1399-07-08T17:22:53Zfa_IR
dc.date.accessioned2020-09-29T17:22:53Z
dc.date.available1399-07-08T17:22:53Zfa_IR
dc.date.available2020-09-29T17:22:53Z
dc.date.issued2018-10-01en_US
dc.date.issued1397-07-09fa_IR
dc.date.submitted2018-11-12en_US
dc.date.submitted1397-08-21fa_IR
dc.identifier.citationSolomon, Onoshe, Rabiu Saidu Umar, Wasagu, Sanusi Wara, Hassan, Sadiq Yakubu, Abubakar, Michael Azubuike, Madusolumou, Asugu Mary, Mbahi, Louis, Hitler. (2018). Antiulcerogenic Activity of methanol extract and solvent fractions of Stem Bark of Lannea acida (A. Rich) Against Ethanol-Induced Gastric Mucosal Injury in Albino Rats. Progress in Chemical and Biochemical Research, 1(1), 29-39. doi: 10.29088/SAMI/PCBR.2018.1.2939en_US
dc.identifier.issn2676-7090
dc.identifier.issn2645-6133
dc.identifier.urihttps://dx.doi.org/10.29088/SAMI/PCBR.2018.1.2939
dc.identifier.urihttp://www.pcbiochemres.com/article_80788.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/19638
dc.description.abstractPeptic ulcer disease is one of the most prevalent gastrointestinal disorders causing tremendous human suffering worldwide. The present study was designed to evaluate the antiulcerogenic activity of the methanol and solvent stem bark fractions (hexane, ethyl acetate and butanol) and elucidate their possible antiulcerogenic mechanisms. The antiulcerogenic mechanisms were investigated by estimation of Superoxide dismutase (SOD), Glutathione (GSH), Catalase (CAT), Vitamins A, C and E,  Malondialdehyde (MDA) and involvement of K<sub>ATP</sub> channel. Pretreatment with the methanol extract and solvent fractions produce significant reductions in ulcer index in a dose dependent manner. Ethylacetate fraction (EtyAc) showed the highest antiulcer activity. Elevated MDA and decreased levels of SOD, GSH, CAT, Vitamin A, C and E observed in ulcer control groups were significantly decreased and increased respectively in the EtyAc fraction treated groups. Antiulcer activity of the EtyAc fraction was blocked upon coadministration with glibenclamide; a K<sub>ATP</sub> channel blocker. The stem bark extract of <em>Lannea acida</em> possess antiulcerogenic activity and the mechanisms seems to involve antioxidant activity and K<sub>ATP</sub> channel opening.en_US
dc.format.extent2544
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherSami Publishing Companyen_US
dc.relation.ispartofProgress in Chemical and Biochemical Researchen_US
dc.relation.isversionofhttps://dx.doi.org/10.29088/SAMI/PCBR.2018.1.2939
dc.subjectAntiulcerogenicen_US
dc.subjectLannea acidaen_US
dc.subjectMechanism, Ethanolen_US
dc.subjectGastricen_US
dc.subjectMucosalen_US
dc.subjectAlbino Ratsen_US
dc.titleAntiulcerogenic Activity of methanol extract and solvent fractions of Stem Bark of Lannea acida (A. Rich) Against Ethanol-Induced Gastric Mucosal Injury in Albino Ratsen_US
dc.typeTexten_US
dc.typeOriginal Research Articleen_US
dc.contributor.departmentDepartment of Biochemistry, Usmanu Danfodiyo University, Sokoto, Nigeria.en_US
dc.contributor.departmentDepartment of Biochemistry, Usmanu Danfodiyo University, Sokoto, Nigeria.en_US
dc.contributor.departmentDepartment of Biochemistry, Usmanu Danfodiyo University, Sokoto, Nigeria.en_US
dc.contributor.departmentDepartment of Veterinary Medicine and Surgery, Usmanu Danfodiyo University, Sokoto, Nigeria.en_US
dc.contributor.departmentDepartment of Biochemistry, School of Life sciences, Modibbo Adama University of Technology, Yola, Nigeria.en_US
dc.contributor.departmentDepartment of Biological Sciences, Federal University Kashere, Gombe, Nigeria.en_US
dc.contributor.departmentCAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Centre for Excellence in Nanoscience, National Centre for Nanoscience and Technology, University of Chinese Academy of Sciences, Beijing 100191, Chinaen_US
dc.citation.volume1
dc.citation.issue1
dc.citation.spage29
dc.citation.epage39
nlai.contributor.orcid0000-0002-0286-2865


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