Management of hyperglycaemia by ethyl acetate extract of balanites aegyptiaca (Desert date)

dc.contributor.authoral-Malki, Abdulrahman Labeed
dc.contributor.authorBarbour, Elie K.
dc.contributor.authorAbualnaja, Khalid Omer
dc.contributor.authorMoselhy, S. S.
dc.contributor.departmentDepartment of Agriculture
dc.contributor.facultyFaculty of Agricultural and Food Sciences (FAFS)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:18:02Z
dc.date.available2025-01-24T12:18:02Z
dc.date.issued2015
dc.description.abstractReactive oxygen species play a significant role in the pathogenesis of retinopathy in diabetes patients. The current study aimed to assess the effect of ethyl acetate extract (EAE) from Balanites aegyptiaca (10, 25 or 50 mg/kg b.w.) in experimental diabetic rats. To achieve this aim, five groups of male rats were included: control, diabetic, and diabetic rats treated with 10, 25, and 50 μg/kg b.w. of EAE for eight weeks. Our results suggests a protective role of EAE against oxidative stress induced by streptozocine. EAE treatment produced a reduction in blood glucose levels, HbA1c, malondialdehyde and vascular endothelial growth factor (VEGF) in diabetic retina (p < 0.001), as well as an enhancement in antioxidant capacity against streptozocine-induced oxidative stress. Tumor necrosis factor alpha (TNF-α), interleukin (IL-1β) and vascular endothelial growth factor (VEGF) were significantly reduced in diabetic rats treated with EAE, compared with untreated diabetic rats. Analysis of EAE by GC-MS indicated the presence of β-sistosterol. Overall, EAE modulates oxidative stress induced by streptozocine and enhances antioxidant activity, which may provide additional endothelial protection in retina of diabetic rats. These results hold great promise in the management of diabetic complications. © 2015 by the authors.
dc.identifier.doihttps://doi.org/10.3390/molecules200814425
dc.identifier.eid2-s2.0-84941242908
dc.identifier.pmid26262605
dc.identifier.urihttp://hdl.handle.net/10938/33871
dc.language.isoen
dc.publisherMDPI AG
dc.relation.ispartofMolecules
dc.sourceScopus
dc.subjectAntidiabetic
dc.subjectBalanites aegyptiaca
dc.subjectEthyl acetate extract
dc.subjectInflammatory cytokines
dc.subjectAcetates
dc.subjectAnimals
dc.subjectBalanites
dc.subjectBlood glucose
dc.subjectDiabetes mellitus, experimental
dc.subjectDiabetic retinopathy
dc.subjectDisease models, animal
dc.subjectDose-response relationship, drug
dc.subjectHyperglycemia
dc.subjectMale
dc.subjectOxidative stress
dc.subjectPlant extracts
dc.subjectRats
dc.subjectReactive oxygen species
dc.subjectAcetic acid derivative
dc.subjectAcetic acid ethyl ester
dc.subjectGlucose blood level
dc.subjectPlant extract
dc.subjectReactive oxygen metabolite
dc.subjectAnimal
dc.subjectBlood
dc.subjectChemistry
dc.subjectDisease model
dc.subjectDose response
dc.subjectDrug effects
dc.subjectIsolation and purification
dc.subjectMetabolism
dc.subjectRat
dc.subjectNutrition
dc.titleManagement of hyperglycaemia by ethyl acetate extract of balanites aegyptiaca (Desert date)
dc.typeArticle

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