Treatment of adriamycin-induced nephropathy with erythropoietin and G-CSF


Autoria(s): Andrade, Luís Gustavo Modelli de; Marlene Viero, Rosa; Cordeiro de Carvalho, Maria Fernanda
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

27/05/2014

27/05/2014

01/05/2013

Resumo

Background: Granulocyte colony-stimulating factor (G-CSF) and Erythropoietin (EPO) are known to stimulate the growth and differentiation of progenitor cells to prevent acute renal injury. This study aimed to assess the use of growth factors to mobilize stem cell in a mouse model of adriamycin-induced chronic kidney disease. Methods: All animals were injected with adriamycin for kidney injury and allocated into three treatment groups (G-CSF, EPO and G-CSF + EPO), and a control group (adriamycin alone). Results: Number of atrophic sites, glomerulosclerosis rate and interstitial fibrosis severity score were assessed in all groups. In all treatment groups, histologic parameters did not significantly differ, but were lower than in the control group (P<.001). Scal and CD34 expressions among treatment groups showed no statistically significant difference, but were higher than in the control group (P<.0001). CD105 expression was higher in EPO and G+EPO as compared to G-CSF and the control group (P<.0001), with no statistically significant difference between the latter two groups (P = NS). Conclusion: G-CSF and EPO had a histologic protective effect, while treatment with EPO + G-CSF had no additive effects in a model of adriamycin-induced chronic kidney disease. © 2013 Societá Italiana di Nefrologia.

Formato

534-539

Identificador

http://dx.doi.org/10.5301/jn.5000200

Journal of Nephrology, v. 26, n. 3, p. 534-539, 2013.

1121-8428

1724-6059

http://hdl.handle.net/11449/75315

10.5301/jn.5000200

WOS:000322053900016

2-s2.0-84877987195

Idioma(s)

eng

Relação

Journal of Nephrology

Direitos

closedAccess

Palavras-Chave #Adriamycin #Erythropoietin #G-CSF #Mobilization #Nephropathy #Stem cell #alfaepoetina #ataxin 1 #CD34 antigen #doxorubicin #endoglin #recombinant erythropoietin #recombinant granulocyte colony stimulating factor #unclassified drug #animal experiment #animal model #animal tissue #atrophy #chronic kidney disease #controlled study #disease severity #drug effect #glomerulosclerosis #histopathology #kidney fibrosis #male #mouse #nonhuman #protein expression #renal protection #scoring system #stem cell mobilization
Tipo

info:eu-repo/semantics/article