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Int. braz. j. urol ; 41(5): 1008-1013, Sept.-Oct. 2015. tab
Artigo em Inglês | LILACS | ID: lil-767054

RESUMO

ABSTRACT Objective: In this study, anti-inflammatory effects of Royal Jelly were investigated by inducing renal inflammation in rats with the use of ethylene glycol. For this purpose, the calcium oxalate urolithiasis model was obtained by feeding rats with ethylene glycol in drinking water. Materials and Methods: The rats were divided in five study groups. The 1st group was determined as the control group. The rats in the 2nd group received ethylene glycol (1%) in drinking water. The rats in the 3rd group were daily fed with Royal Jelly by using oral gavage. The 4th group was determined as the preventive group and the rats were fed with ethylene glycol (1%) in drinking water while receiving Royal Jelly via oral gavage. The 5th group was determined as the therapeutic group and received ethylene glycol in drinking water during the first 2 weeks of the study and Royal Jelly via oral gavage during the last 2 weeks of the study. Results: At the end of the study, proinflammatory/anti-inflammatory cytokines, TNF-α, IL-1β and IL-18 levels in blood and renal tissue samples from the rats used in the application were measured. Conclusion: The results have shown that ethylene glycol does induce inflammation and renal damage. This can cause the formation of reactive oxygen species. Royal Jelly is also considered to have anti-inflammatory effects due to its possible antiradical and antioxidative effects. It can have positive effects on both the prevention of urolithiasis and possible inflammation during the existing urolithiasis and support the medical treatment.


Assuntos
Animais , Masculino , Anti-Inflamatórios/farmacologia , Ácidos Graxos/farmacologia , Nefrolitíase/induzido quimicamente , Nefrolitíase/tratamento farmacológico , Anti-Inflamatórios/uso terapêutico , Ensaio de Imunoadsorção Enzimática , Etilenoglicol , Ácidos Graxos/uso terapêutico , /análise , Interleucina-1beta/análise , Nefrite/induzido quimicamente , Nefrite/tratamento farmacológico , Estresse Oxidativo/efeitos dos fármacos , Ratos Sprague-Dawley , Reprodutibilidade dos Testes , Fatores de Tempo , Resultado do Tratamento , Fator de Necrose Tumoral alfa/análise
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