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Evaluation of toxicity after one-months treatment with Bauhinia forficata decoction in streptozotocin-induced diabetic rats

dc.contributor.authorPepato, Maria Teresa [UNESP]
dc.contributor.authorBaviera, Amanda Martins [UNESP]
dc.contributor.authorVendramini, Regina Célia [UNESP]
dc.contributor.authorBrunetti, Iguatemy Lourenço [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:21:05Z
dc.date.available2014-05-27T11:21:05Z
dc.date.issued2004-06-08
dc.description.abstractBackground: Previous experiments have shown that a decoction of Bauhinia forficata leaves reduces the changes in carbohydrate and protein metabolism that occur in rats with streptozotocin-induced diabetes. In the present investigation, the serum activities of enzymes known to be reliable toxicity markers were monitored in normal and streptozotocin-diabetic rats to discover whether the use of B. forficata decoction has toxic effects on liver, muscle or pancreas tissue or on renal microcirculation. Methods: An experimental group of normal and streptozotocin-diabetic rats received an aqueous decoction of fresh B. forficata leaves (150 g/L) by mouth for 33 days while a control group of normal and diabetic rats received water for the same length of time. The serum activity of the toxicity markers lactate dehydrogenase, creatine kinase, amylase, angiotensin-converting enzyme and bilirubin were assayed before receiving B. forficata decoction and on day 19 and 33 of treatment. Results: The toxicity markers in normal and diabetic rats were not altered by the diabetes itself nor by treatment with decoction. Whether or not they received B. forficata decoction the normal rats showed a significant increase in serum amylase activity during the experimental period while there was a tendency for the diabetic rats, both treated and untreated with decoction, to have lower serum amylase activities than the normal rats. Conclusions: Administration of an aqueous decoction of B. forficata is a potential treatment for diabetes and does not produce toxic effects measurable with the enzyme markers used in our study. © 2004 Pepato et al; licensee BioMed Central Ltd.en
dc.description.affiliationDepartment of Clinical Analyses Araraquara School of Pharmacy Sao Paulo State University UNESP, Araraquara, SP
dc.description.affiliationUnespDepartment of Clinical Analyses Araraquara School of Pharmacy Sao Paulo State University UNESP, Araraquara, SP
dc.identifierhttp://dx.doi.org/10.1186/1472-6882-4-7
dc.identifier.citationBMC Complementary and Alternative Medicine, v. 4.
dc.identifier.doi10.1186/1472-6882-4-7
dc.identifier.file2-s2.0-10444239190.pdf
dc.identifier.issn1472-6882
dc.identifier.lattes3736475025187750
dc.identifier.lattes7641979287850489
dc.identifier.scopus2-s2.0-10444239190
dc.identifier.urihttp://hdl.handle.net/11449/67764
dc.language.isoeng
dc.relation.ispartofBMC Complementary and Alternative Medicine
dc.relation.ispartofjcr2.109
dc.relation.ispartofsjr0,858
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAmylase
dc.subjectAngiotensin-converting enzyme
dc.subjectBauhinia forficata
dc.subjectBilirubin
dc.subjectCreatine kinase
dc.subjectExtended treatment
dc.subjectLactate dehydrogenase
dc.subjectSerum enzymes
dc.subjectStreptozotocin-diabetic rats
dc.subjectamylase
dc.subjectBauhinia forticata extract
dc.subjectbilirubin
dc.subjectcreatine kinase
dc.subjectdipeptidyl carboxypeptidase
dc.subjectlactate dehydrogenase
dc.subjectplant extract
dc.subjectstreptozocin
dc.subjectunclassified drug
dc.subjectwater
dc.subjectamylase blood level
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectaqueous solution
dc.subjectBauhinia
dc.subjectbilirubin blood level
dc.subjectcontrolled study
dc.subjectcreatine kinase blood level
dc.subjectdiabetes mellitus
dc.subjectenzyme activity
dc.subjectenzyme assay
dc.subjectenzyme blood level
dc.subjectkidney circulation
dc.subjectlactate dehydrogenase blood level
dc.subjectliver toxicity
dc.subjectmale
dc.subjectmicrocirculation
dc.subjectmuscle disease
dc.subjectnephrotoxicity
dc.subjectnonhuman
dc.subjectpancreas disease
dc.subjectplant leaf
dc.subjectrat
dc.subjectstreptozocin diabetes
dc.subjectanimal
dc.subjectchemically induced disorder
dc.subjectexperimental diabetes mellitus
dc.subjectmetabolism
dc.subjectphytotherapy
dc.subjecttoxicity testing
dc.subjectWistar rat
dc.subjectAmylases
dc.subjectAnimals
dc.subjectCreatine Kinase
dc.subjectDiabetes Mellitus, Experimental
dc.subjectL-Lactate Dehydrogenase
dc.subjectMale
dc.subjectPeptidyl-Dipeptidase A
dc.subjectPhytotherapy
dc.subjectPlant Leaves
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectStreptozocin
dc.subjectToxicity Tests, Chronic
dc.titleEvaluation of toxicity after one-months treatment with Bauhinia forficata decoction in streptozotocin-induced diabetic ratsen
dc.typeArtigopt
dcterms.licensehttp://www.biomedcentral.com/about/license
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes3736475025187750[2]
unesp.author.lattes7641979287850489
unesp.author.orcid0000-0003-0987-5295[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt

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