Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/85153
Type: Artigo de periódico
Title: Effects Of Immunosuppression With Tacrolimus And Mycophenolate Mofetil On Renal Histology And Function In Single Kidney Rats Submitted To Ischemia And Reperfusion1
Author: Dias P.H.G.F.
Oliveira G.A.
Dias F.G.F.
Gomes R.P.X.
Tambara Filho R.
de Fraga R.
Abstract: PURPOSE: To evaluate renal histological changes and renal function in single kidney rats submitted to renal ischemia-reperfusion and to immunosuppression with tacrolimus and mycophenolate-mofetil. METHODS: Experimental study with 80 Wistar rats distributed into control, Sham and six other groups treated with immunosuppressive drugs. Animals undergoing surgery, right nephrectomy and left renal clamping, killed on the 14th day and analyzed for renal histology, urea and creatinine. RESULTS: The group receiving tacrolimus at higher doses (T3) showed renal histological lesions indicative of early nephrotoxicity, and significant increase in urea and creatinine. The group M (mycophenolate-mofetil alone) and the group M2 (mycophenolate-mofetil combined with half the usual dose of tacrolimus) presented a slight rise in serum urea. The groups using mycophenolate-mofetil alone or combined with tacrolimus showed creatinine levels similar to that of the group T3. CONCLUSIONS: Histologically, the association of injury by ischemia-reperfusion with the use of tacrolimus or mycophenolate-mofetil alone demonstrated a higher rate of renal changes typical of early nephrotoxicity. In laboratory, the combination of injury by ischemia-reperfusion with tacrolimus at higher doses proved to be nephrotoxic.
Editor: Sociedade Brasileira para o Desenvolvimento de Pesquisa em Cirurgia
Rights: aberto
Identifier DOI: 10.1590/S0102-86502015002000007
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-84923653386&partnerID=40&md5=f88e16a75034dfe400fd7f9239e9f9c3
Date Issue: 2015
Appears in Collections:Unicamp - Artigos e Outros Documentos

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