CIRRHOSIS INDUCES APOPTOSIS IN RENAL TISSUE THROUGH INTRACELLULAR OXIDATIVE STRESS

Background Renal failure is a frequent and serious complication in patients with decompensated cirrhosis. Objectives We aimed to evaluate the renal oxidative stress, cell damage and impaired cell function in animal model of cirrhosis. Methods Secondary biliary cirrhosis was induced in rats by ligati...

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Main Authors: Keli Cristina Simões da SILVEIRA, Cassiana Macagnan VIAU, Josiane Raskopf COLARES, Jenifer SAFFI, Norma Possa MARRONI, Marilene PORAWSKI
Format: Article
Language:English
Published: Instituto Brasileiro de Estudos e Pesquisas de Gastroenterologia (IBEPEGE) 2015-03-01
Series:Arquivos de Gastroenterologia
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Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032015000100014&lng=en&tlng=en
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author Keli Cristina Simões da SILVEIRA
Cassiana Macagnan VIAU
Josiane Raskopf COLARES
Jenifer SAFFI
Norma Possa MARRONI
Marilene PORAWSKI
author_facet Keli Cristina Simões da SILVEIRA
Cassiana Macagnan VIAU
Josiane Raskopf COLARES
Jenifer SAFFI
Norma Possa MARRONI
Marilene PORAWSKI
author_sort Keli Cristina Simões da SILVEIRA
collection DOAJ
description Background Renal failure is a frequent and serious complication in patients with decompensated cirrhosis. Objectives We aimed to evaluate the renal oxidative stress, cell damage and impaired cell function in animal model of cirrhosis. Methods Secondary biliary cirrhosis was induced in rats by ligation of the common bile duct. We measured TBARS, ROS and mitochondrial membrane potential in kidney as markers of oxidative stress, and activities of the antioxidant enzymes. Relative cell viability was determined by trypan blue dye-exclusion assay. Annexin V-PE was used with a vital dye, 7-AAD, to distinguish apoptotic from necrotic cells and comet assay was used for determined DNA integrity in single cells. Results In bile duct ligation animals there was significant increase in the kidney lipoperoxidation and an increase of the level of intracellular ROS. There was too an increase in the activity of all antioxidant enzymes evaluated in the kidney. The percentage viability was above 90% in the control group and in bile duct ligation was 64.66% and the dominant cell death type was apoptosis. DNA damage was observed in the bile duct ligation. There was a decreased in the mitochondrial membrane potential from 71.40% ± 6.35% to 34.48% ± 11.40% in bile duct ligation. Conclusions These results indicate that intracellular increase of ROS cause damage in the DNA and apoptosis getting worse the renal function in cirrhosis.
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spelling doaj.art-029b0340ab5b417eb5a6cb09b3a73ac92022-12-21T22:59:26ZengInstituto Brasileiro de Estudos e Pesquisas de Gastroenterologia (IBEPEGE)Arquivos de Gastroenterologia1678-42192015-03-01521657110.1590/S0004-28032015000100014S0004-28032015000100014CIRRHOSIS INDUCES APOPTOSIS IN RENAL TISSUE THROUGH INTRACELLULAR OXIDATIVE STRESSKeli Cristina Simões da SILVEIRACassiana Macagnan VIAUJosiane Raskopf COLARESJenifer SAFFINorma Possa MARRONIMarilene PORAWSKIBackground Renal failure is a frequent and serious complication in patients with decompensated cirrhosis. Objectives We aimed to evaluate the renal oxidative stress, cell damage and impaired cell function in animal model of cirrhosis. Methods Secondary biliary cirrhosis was induced in rats by ligation of the common bile duct. We measured TBARS, ROS and mitochondrial membrane potential in kidney as markers of oxidative stress, and activities of the antioxidant enzymes. Relative cell viability was determined by trypan blue dye-exclusion assay. Annexin V-PE was used with a vital dye, 7-AAD, to distinguish apoptotic from necrotic cells and comet assay was used for determined DNA integrity in single cells. Results In bile duct ligation animals there was significant increase in the kidney lipoperoxidation and an increase of the level of intracellular ROS. There was too an increase in the activity of all antioxidant enzymes evaluated in the kidney. The percentage viability was above 90% in the control group and in bile duct ligation was 64.66% and the dominant cell death type was apoptosis. DNA damage was observed in the bile duct ligation. There was a decreased in the mitochondrial membrane potential from 71.40% ± 6.35% to 34.48% ± 11.40% in bile duct ligation. Conclusions These results indicate that intracellular increase of ROS cause damage in the DNA and apoptosis getting worse the renal function in cirrhosis.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032015000100014&lng=en&tlng=enCirrose hepáticaInsuficiência renalEstresse oxidativoCitometria de fluxoEspécies reativas de oxigênio
spellingShingle Keli Cristina Simões da SILVEIRA
Cassiana Macagnan VIAU
Josiane Raskopf COLARES
Jenifer SAFFI
Norma Possa MARRONI
Marilene PORAWSKI
CIRRHOSIS INDUCES APOPTOSIS IN RENAL TISSUE THROUGH INTRACELLULAR OXIDATIVE STRESS
Arquivos de Gastroenterologia
Cirrose hepática
Insuficiência renal
Estresse oxidativo
Citometria de fluxo
Espécies reativas de oxigênio
title CIRRHOSIS INDUCES APOPTOSIS IN RENAL TISSUE THROUGH INTRACELLULAR OXIDATIVE STRESS
title_full CIRRHOSIS INDUCES APOPTOSIS IN RENAL TISSUE THROUGH INTRACELLULAR OXIDATIVE STRESS
title_fullStr CIRRHOSIS INDUCES APOPTOSIS IN RENAL TISSUE THROUGH INTRACELLULAR OXIDATIVE STRESS
title_full_unstemmed CIRRHOSIS INDUCES APOPTOSIS IN RENAL TISSUE THROUGH INTRACELLULAR OXIDATIVE STRESS
title_short CIRRHOSIS INDUCES APOPTOSIS IN RENAL TISSUE THROUGH INTRACELLULAR OXIDATIVE STRESS
title_sort cirrhosis induces apoptosis in renal tissue through intracellular oxidative stress
topic Cirrose hepática
Insuficiência renal
Estresse oxidativo
Citometria de fluxo
Espécies reativas de oxigênio
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032015000100014&lng=en&tlng=en
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AT cassianamacagnanviau cirrhosisinducesapoptosisinrenaltissuethroughintracellularoxidativestress
AT josianeraskopfcolares cirrhosisinducesapoptosisinrenaltissuethroughintracellularoxidativestress
AT jenifersaffi cirrhosisinducesapoptosisinrenaltissuethroughintracellularoxidativestress
AT normapossamarroni cirrhosisinducesapoptosisinrenaltissuethroughintracellularoxidativestress
AT marileneporawski cirrhosisinducesapoptosisinrenaltissuethroughintracellularoxidativestress