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In vivo anti-ulcerogenic effect of okra (Abelmoschus esculentus) on ethanol-induced acute gastric mucosal lesions

dc.contributor.authorOrtac, Deniz
dc.contributor.authorCemek, Mustafa
dc.contributor.authorKaraca, Turan
dc.contributor.authorBuyukokuroglu, Mehmet E.
dc.contributor.authorOzdemir, Zafer O.
dc.contributor.authorKocaman, Ayse Tuba
dc.contributor.authorGones, Sadik
dc.date.accessioned2026-06-27T14:12:42Z
dc.date.issued2018
dc.description.abstractContext: Okra, Abelmoschus esculentus (L.) (Malvaceae), is a medicinal plant widely used in Turkish traditional medicine for the treatment of various diseases such as ulcers and gastritis. Objective: In the present study, we evaluated the gastroprotective effect of okra against ethanol-induced acute gastric mucosal injury in animal models. Materials and methods: Wistar rats were treated with 500, 250 or 100 mg/kg okra; 20 mg/kg famotidine (Fam); and 75 mg/kg quercetin (Que). Following a 60 min period, all the rats were given 1 mL of ethanol (80%). One hour after the administration of ethanol, all groups were sacrificed. Results: At 5000 mg/kg, the extract produced (okra) no signs of toxicity in animals. Okra 500, 250, 100, Fam 20 and Que 75 inhibited ulcer formation by 81.0, 67.5, 67.0, 76.3 and 72.4%, respectively. Okra 500 significantly decreased edema, hemorrhage and inflammation scores compared with the ethanol group (p < 0.05). The oxidant levels decreased significantly in the all study groups compared within ethanol group (p < 0.001). Serum beta-carotene and retinol levels significantly increased 40.2 and 45.4% in the okra 500 group. In okra 500, 250 and Fam 20 groups, apoptosis significantly decreased (p < 0.001), while okra 500, 250 and Fam 20 groups showed a higher percentage of cell proliferation compared with the ethanol group (p < 0.001). Discussion and conclusions: Our in vivo data indicate that okra has a gastroprotective effect against ethanol and could reduce the gastric ulcer as seen from biochemical and histopathological results. We suggest that okra could be a possible therapeutic antiulcer agent.en
dc.description.sponsorshipYildiz Technical University research fund [2015-07-04-KAP02]
dc.description.urihttps://doi.org/10.1080/13880209.2018.1442481
dc.identifier.doi10.1080/13880209.2018.1442481
dc.identifier.eissn1744-5116
dc.identifier.endpage175
dc.identifier.issn1388-0209
dc.identifier.issue1
dc.identifier.pubmed29513129
dc.identifier.startpage165
dc.identifier.urihttps://hdl.handle.net/20.500.14981/58002
dc.identifier.volume56
dc.identifier.wos000426940500001
dc.language.isoeng
dc.publisherTAYLOR & FRANCIS LTD
dc.relation.ispartofPHARMACEUTICAL BIOLOGY
dc.rightsopenAccess
dc.subjectGastroprotection
dc.subjectapoptosis
dc.subjectgastric ulcer
dc.subjectimmunohistochemistry
dc.subjectulcer index
dc.subjectulcer inhibition
dc.subjectNITRIC-OXIDE
dc.subjectASCORBIC-ACID
dc.subjectRATS
dc.subjectGLUTATHIONE
dc.subjectINJURY
dc.subjectANTIOXIDANT
dc.subjectQUERCETIN
dc.subjectEXPRESSION
dc.subjectDAMAGE
dc.subjectOIL
dc.subjectPlant Sciences
dc.subjectMedical Laboratory Technology
dc.subjectPharmacology & Pharmacy
dc.titleIn vivo anti-ulcerogenic effect of okra (Abelmoschus esculentus) on ethanol-induced acute gastric mucosal lesions
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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