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Celecoxib modulates renin-angiotensin system in the adipose tissue of obese mice

Authors :
Aline Hilzenderguer
Alfredo Maurício Batista de Paula
Deborah de Farias Lelis
Alanna Fernandes Paraíso
Toni Ramos Alves de Souza
Sérgio Henrique Sousa Santos
Jamille Fernandes Lula
Keila Lopes Mendes
Igor Viana Brandi
André Luiz Sena Guimarães
João Marcus Oliveira Andrade
Lucyana Conceição Farias
Source :
Repositório Institucional da UFMG, Universidade Federal de Minas Gerais (UFMG), instacron:UFMG
Publication Year :
2018
Publisher :
Universidade Federal de Minas Gerais, 2018.

Abstract

Background: the renin-angiotensin system (RAS) is a critical contributing factor to obesity and related diseases. Several studies have shown the relationship of obesity with cyclooxygenase-2. Objectives: based on these facts, we aimed to investigate the celecoxib oral administration (a selective anti-inflammatory inhibitor of cyclooxygenase-2 (ICOX-2)) effects, in mice fed a high-fat diet by assessing the renin-angiotensin system and inflammatory markers expression. Methods: FVB/N male mice were divided into 3 groups and fed with experimental diets, standard, high-fat diet and high-fat diet plus ICOX-2 at a dose of 100mg/kg/body weight. Body weight, food intake, blood parameters and RAS/inflammatory markers expression were assessed. Results: the main findings showed that diet-induced obese mice treated with COX-2 inhibitor showed significantly improved glucose and insulin homeostasis, presented decreased body weight gain and the biochemical analyses revealed reduced triglyceride levels and higher serum HDL-c levels as compared to HFD and ST. These results were accompanied by a downregulation of AGT, ACE, TNF-α and IL-6 expression in the group receiving treatment. Conclusion: taken together, these results indicate that ICOX-2 may exhibit therapeutic potential for obesity via the renin-angiotensin system and inflammation.

Details

Language :
English
Database :
OpenAIRE
Journal :
Repositório Institucional da UFMG, Universidade Federal de Minas Gerais (UFMG), instacron:UFMG
Accession number :
edsair.doi.dedup.....fc2215def6e8171cb5729424e4554eb5