Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/42592
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dc.creatorJamille Fernandes Lulapt_BR
dc.creatorBruna Mara Aparecida de Carvalho Mesquitapt_BR
dc.creatorLeandro de Freitas Telespt_BR
dc.creatorSérgio Henrique Sousa Santospt_BR
dc.creatorAlfredo Maurício Batista de Paulapt_BR
dc.creatorAndré Luiz Sena Guimaraespt_BR
dc.creatorErivelton Pereira dos Santospt_BR
dc.creatorDeborah de Farias Lelispt_BR
dc.creatorLuís Paulo Oliveirapt_BR
dc.creatorLucyana Conceição Fariaspt_BR
dc.creatorIgor Viana Brandipt_BR
dc.creatorKarla Nayara de Oliveira Santanapt_BR
dc.date.accessioned2022-06-22T12:43:09Z-
dc.date.available2022-06-22T12:43:09Z-
dc.date.issued2017-
dc.citation.volume14pt_BR
dc.citation.issue2pt_BR
dc.citation.spage114pt_BR
dc.citation.epage119pt_BR
dc.identifier.doihttp://doi.org/10.2174/1573408014666171220152537pt_BR
dc.identifier.issn1875-6662pt_BR
dc.identifier.urihttp://hdl.handle.net/1843/42592-
dc.description.resumoBackground: Obesity is an important risk factor for nonalcoholic fatty liver disease which varies from hepatic steatosis to liver cirrhosis. Interventions in weight and metabolic control are important in reducing steatosis risk. Aims: The aim of the present study was to investigate the role of celecoxib in hepatic triacylglycerol deposition in non-alcoholic fatty liver disease exploring the signaling involved in obese mice lipogenesis. Methods: Males FVB/N mice were allocated into three groups and were fed with experimental diets: standard, a high-fat diet or a high-fat diet along with Cox-2 inhibitor treatment (Celecoxib; 100mg/kg of body weight). The body weight, food intake, blood parameters and liver histology were analyzed. Expression of liver lipogenesis-related genes (ACC, PPAR-γ, FAS, SREBP-1c) was evaluated by quantitative real-time PCR. Results: The main findings showed that celecoxib treatment resulted in body weight loss in obese animals, reduced food consumption and decreased triglycerides. ACC, FAS and SREBP1-c mRNA expression was significantly suppressed in HFD+ICOX-2 fed mice. Conclusion: Celecoxib improved lipid metabolism and decreased fat deposition in the liver of obese mice by reducing lipogenesis, which may be a promising therapeutic target for liver disorders, obesity and its comorbidities.pt_BR
dc.languageengpt_BR
dc.publisherUniversidade Federal de Minas Geraispt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentICA - INSTITUTO DE CIÊNCIAS AGRÁRIASpt_BR
dc.publisher.initialsUFMGpt_BR
dc.relation.ispartofCurrent Enzyme Inhibitionpt_BR
dc.rightsAcesso Restritopt_BR
dc.subject.otherAnalgésicospt_BR
dc.subject.otherEnzimaspt_BR
dc.subject.otherInibidores enzimáticospt_BR
dc.subject.otherAgentes anti-inflamatóriospt_BR
dc.subject.otherFígado gordurosopt_BR
dc.subject.otherObesidadept_BR
dc.titleCox enzyme inhibitor, celecoxib, reduces steatosis and liver lipogenesis in high-fat fed micept_BR
dc.typeArtigo de Periódicopt_BR
dc.url.externahttp://www.eurekaselect.com/article/87479pt_BR
dc.identifier.orcidhttps://orcid.org/ 0000-0001-8980-8599pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0001-6714-7996pt_BR
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