Protective effect of simvastatin in the cyclophosphamide-induced hemohrragic cystitis in rats

Autores: Anna Carolina Batista Dantas, Francisco Fábio de Araújo Batista-Júnior, Larissa Freitas Macedo, Mariana Noronha Castro Mendes, Ítalo Medeiros Azevedo, Aldo Cunha Medeiros

Data de publicação: 2010/2

Publicações: Acta cirurgica brasileira

Volume: 25 | Edição: 1 | Páginas: 43-46

Editora: Acta Cirúrgica Brasileira/SOBRADPEC

PURPOSE: Cyclophosphamide (CYP) is an antineoplastic agent used for the treatment of many neoplastic and inflammatory diseases. Hemorrhagic cystitis is a frequent side effect of CYP. Several studies show that simvastatin has important pleiotropic (anti-inflammatory and immunomodulatory) effects. The purpose of the study was to investigate the effect of simvastatin on bladder, ureter and kidney injury caused by CYP.METHODS: Adult male Wistar rats were randomly divided into three groups. The CYP/SIM group received simvastatin microemulsion by gavage during 7 days (10 mg/kg body wt) before the administration of CYP and the CYP/SAL group rats received saline 0.9%. The control rats were not treated. After that, all rats were treated with a single dose of CYP 200 mg/kg body wt intraperitoneally. The rats were killed 24 h after CYP administration. Plasma cytokines (TNF-α, IL-1β, IL-6) were measured by ELISA. Macro and light microscopic study was performed in the bladder, kidney and ureter.RESULTS: In the bladders of CYP/SIMV treated rats edema of lamina propria with epithelial and sub-epithelial hemorrhage were lower than in CYP/SAL treated rats. The scores for macroscopic and microscopic evaluation of bladder and ureter were significantly lower in CYP/SIMV rats than in CYP/SAL rats. The kidney was not affected. The expression of TNF-α, IL-1β and IL-6 was significatly lower in CF/SINV rats (164.8±22, 44.8±8 and 52.4±13) than in CF/SAL rats (378.5±66, 122.9±26 e 123.6±18), respectively.CONCLUSION: The results of the current study suggest that simvastatin pretreatment attenuated CYP-induced urotelium inflammation …

Fonte: http://www.scielo.br/scielo.php?pid=S0102-86502010000100011&script=sci_arttext&tlng=ES

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