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The Treatment of Prednisone in Mild Diabetic Rats: Biochemical Parameters and Cell Response

dc.contributor.authorMachado, Mariana P. R. [UNESP]
dc.contributor.authorSchavinski, Aline Z.
dc.contributor.authorDeluque, Amanda L.
dc.contributor.authorVolpato, Gustavo T.
dc.contributor.authorCampos, Kleber E.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de Mato Grosso do Sul (UFMS)
dc.date.accessioned2020-12-10T20:01:26Z
dc.date.available2020-12-10T20:01:26Z
dc.date.issued2020-01-01
dc.description.abstractBackground: Limited studies have been canied out with prednisone (PRED) in treatment by glucose intolerant individuals, even in this model the animals presented low blood glucose levels at adulthood, by the high regenerative capacity of beta-cell. Objective: The aim was to evaluate the effects of the treatment of PRED in mild diabetes on biochemical and immunological biomarkers. Methods: Rats were randomly divided into four groups: control (C), treated control C+PRED (treatment of 1.25 mg/Kg/day PRED); diabetic DM (mild diabetes) and treated diabetic DM PRED (treatment with same dose as C+PRED group). Untreated groups received vehicle, adjusted volume to body weight. The treatment lasted 21 days and measured body weight, food and water intake, and glycemia weekly. In the 3rd week, the Oral Glucose Tolerance Test (OGTT) and the Insulin Tolerance Test (ITT) was performed. On the last day, the rats were killed and the blood was collected for biochemical analyzes, leukogram and imm.unoglobulin G levels. Results: There was a significant decrease in body weight in mild diabetes; however, the treatment in diabetic groups increased food intake, glycemia, and the number of total leukocytes, lymphocytes and neutrophils. On the other hand, it decreased the levels of triglycerides, high -density and very low density lipoproteins. In addition, diabetic groups showed glucose intolerance and mild insulin resistance, confirming that this model induces glucose intolerant in adult life. Conclusion: The results showed that the use of prednisone is not recommended for glucose intolerant individuals and should he replaced in order to not to aggravate this condition.en
dc.description.affiliationSao Paulo State Univ UNESP, Inst Biosci, Postgrad Program Pharmacol & Biotechnol, Botucatu, SP, Brazil
dc.description.affiliationUniv Sao Paulo, Fac Med Ribeirao Preto, Dept Physiol, Sao Paulo, Brazil
dc.description.affiliationFed Univ Mato Grosso UFMT, Inst Biol Sci & Hlth, Lab Syst Physiol & Reprod Toxicol, Barra Do Garcas, Mato Grosso, Brazil
dc.description.affiliationUnespSao Paulo State Univ UNESP, Inst Biosci, Postgrad Program Pharmacol & Biotechnol, Botucatu, SP, Brazil
dc.description.sponsorshipFundacao de Amparo a Pesquisa do Estado de Mato Grosso (FAPEMAT), Cuiaba, Brazil (2014-2016)
dc.description.sponsorshipIdFundacao de Amparo a Pesquisa do Estado de Mato Grosso (FAPEMAT), Cuiaba, Brazil (2014-2016): 002 - 004/2015
dc.description.sponsorshipIdFundacao de Amparo a Pesquisa do Estado de Mato Grosso (FAPEMAT), Cuiaba, Brazil (2014-2016): 36016.541.21414.17082016
dc.format.extent797-805
dc.identifierhttp://dx.doi.org/10.2174/1871530319bb6191204130007
dc.identifier.citationEndocrine Metabolic & Immune Disorders-drug Targets. Sharjah: Bentham Science Publ Ltd, v. 20, n. 5, p. 797-805, 2020.
dc.identifier.doi10.2174/1871530319bb6191204130007
dc.identifier.issn1871-5303
dc.identifier.urihttp://hdl.handle.net/11449/196952
dc.identifier.wosWOS:000538153000016
dc.language.isoeng
dc.publisherBentham Science Publ Ltd
dc.relation.ispartofEndocrine Metabolic & Immune Disorders-drug Targets
dc.sourceWeb of Science
dc.subjectDiabetes
dc.subjectglucocorticoids
dc.subjectglycometabolism
dc.subjectimmunosuppressant
dc.subjectlipometabolism
dc.subjectprednisone
dc.titleThe Treatment of Prednisone in Mild Diabetic Rats: Biochemical Parameters and Cell Responseen
dc.typeArtigopt
dcterms.rightsHolderBentham Science Publ Ltd
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentFarmacologia - IBBpt

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