Éder Marcolin
Universidade Federal do Rio Grande do Sul
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Arquivos De Gastroenterologia | 2011
Éder Marcolin; Luiz Felipe Forgiarini; Juliana Tieppo; Alexandre Simões Dias; Luiz Antonio Rodrigues de Freitas; Norma Anair Possa Marroni
CONTEXT Non-alcoholic steatohepatitis is a disease with a high incidence, difficult diagnosis, and as yet no effective treatment. So, the use of experimental models for non-alcoholic steatohepatitis induction and the study of its routes of development have been studied. OBJECTIVES This study was designed to develop an experimental model of non-alcoholic steatohepatitis based on a methionine- and choline-deficient diet that is manufactured in Brazil so as to evaluate the liver alterations resulting from the disorder. METHODS Thirty male C57BL6 mice divided in two groups (n = 15) were used: the experimental group fed a methionine- and choline-deficient diet manufactured by Brazilian company PragSoluções®, and the control group fed a normal diet, for a period of 2 weeks. The animals were then killed by exsanguination to sample blood for systemic biochemical analyses, and subsequently submitted to laparotomy with total hepatectomy and preparation of the material for histological analysis. The statistical analysis was done using the Students t-test for independent samples, with significance level of 5%. RESULTS The mice that received the methionine- and choline-deficient diet showed weight loss and significant increase in hepatic damage enzymes, as well as decreased systemic levels of glycemia, triglycerides, total cholesterol, HDL and VLDL. The diagnosis of non-alcoholic steatohepatitis was performed in 100% of the mice that were fed the methionine- and choline-deficient diet. All non-alcoholic steatohepatitis animals showed some degree of macrovesicular steatosis, ballooning, and inflammatory process. None of the animals which were fed the control diet presented histological alterations. All non-alcoholic steatohepatitis animals showed significantly increased lipoperoxidation and antioxidant enzyme GSH activity. CONCLUSION The low cost and easily accessible methionine- and choline-deficient diet explored in this study is highly effective in inducing steatosis and steatohepatitis in animal model, alterations that are similar to those observed in human livers.
BioMed Research International | 2012
Graziella Rodrigues; Fábio Cangeri Di Naso; Marilene Porawski; Éder Marcolin; Nelson A. Kretzmann; Alexandre de Barros Falcão Ferraz; Marc François Richter; Claudio Augusto Marroni; Norma Anair Possa Marroni
Croton cajucara Benth is a plant found in Amazonia, Brazil and the bark and leaf infusion of this plant have been popularly used to treat diabetes and hepatic disorders. The present study was designed to evaluate the oxidative stress as well as the therapeutic effect of Croton cajucara Benth (1.5 mL of the C. cajucara extract i.g.) in rats with streptozotocin-induced diabetes. Croton cajucara Benth was tested as an aqueous extract for its phytochemical composition, and its antioxidant activity in vitro was also evaluated. Lipid peroxidation and superoxide dismutase, catalase, and glutathione reductase activities were measured in the hepatic tissue, as well as the presence activation of p65 (NF-κB), through western blot. Phytochemical screening of Croton cajucara Benth detected the presence of flavonoids, coumarins and alkaloids. The extract exhibited a significant antioxidant activity in the DPPH-scavenging and the hypoxanthine/xanthine oxidase assays. Liver lipid peroxidation increased in diabetic animals followed by a reduction in the Croton-cajucara-Benth-treated group. There was activation of p65 nuclear expression in the diabetic animals, which was attenuated in the animals receiving the Croton cajucara Benth aqueous extract. The liver tissue in diabetic rats showed oxidative alterations related to the streptozotocin treatment. In conclusion the Croton cajucara Benth aqueus extract treatment effectively reduced the oxidative stress and contributed to tissue recovery.
Journal of Nutrition | 2012
Éder Marcolin; Beatriz San-Miguel; Daniela Vallejo; Juliana Tieppo; Norma Anair Possa Marroni; Javier González-Gallego; María J. Tuñón
Basic & Clinical Pharmacology & Toxicology | 2013
Éder Marcolin; Luiz Felipe Forgiarini; Graziella Rodrigues; Juliana Tieppo; Greice Stefani Borghetti; Valquiria Linck Bassani; Jaqueline Nascimento Picada; Norma Anair Possa Marroni
Archive | 2009
Luiz Felipe Forgiarini; Éder Marcolin; Greice Stefani Borghetti; Javier González-Gallego; Juliana Tieppo; Valéria Bassani
Archive | 2008
Luiz Felipe Forgiarini; Éder Marcolin; Graziella Rodrigues; Marc François Richter
Archive | 2008
Elisa Simon; Éder Marcolin; Vanessa Baldissera; Rodrigo Noronha de Mello; Carén Todi; Alexandre de Barros Falcão Ferraz; Marc François Richter
Archive | 2007
Graziela Smaniotto Rodrigues; Éder Marcolin; Silvia Bona; Marilene Porawski; Themis Reverbel da Silveira; Norma Anair Possa Marroni
Archive | 2007
Rodrigo Noronha de Mello; Éder Marcolin; Giovani Cignachi; Luiz Antonio Graciolli; Norma Anair Possa Marroni
Revista de Iniciação Científica da ULBRA | 2006
Larissa Sgaria Pacheco; Éder Marcolin; Dinara Jaqueline Moura; Norma Anair Possa Marroni; Jenifer Saffi; Marc François Richter