Intestinal permeability assessed by 51Cr-EDTA in rats with CCl4 - induced cirrhosis

CONTEXT: The straight relationship between cirrhosis and impaired intestinal barrier has not been elucidated yet. OBJECTIVES: To verify 51Cr-EDTA-intestinal permeability in rats with CCl4-induced cirrhosis and controls. METHOD: Fifty male Wistar rats weighing 150-180 g were separated in three groups: 25 animals received CCl4 0.25 mL/kg with olive oil by gavage with 12 g/rat/day food restriction for 10 weeks (CCl4-induced cirrhosis); 12 received the same food restriction for 10 weeks (CCl4-non exposed). Other 13 rats received indomethacin 15 mg/kg by gavage as positive control of intestinal inflammation. RESULTS: The median (25-75 interquartile range) 51Cr-EDTA-IP values of cirrhotic and CCl4-non exposed rats were 0.90% (0.63-1.79) and 0.90% (0.60-1.52) respectively, without significant difference (P = 0.65). Animals from indomethacin group showed 51Cr-EDTA-IP, median 7.3% (5.1-14.7), significantly higher than cirrhotic and CCl4-non exposed rats (P<0.001). CONCLUSION: This study showed the lack of difference between 51Cr-EDTA-intestinal permeability in rats with and without cirrhosis. Further studies are necessary to better clarify the relationship between intestinal permeability and cirrhosis.

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Main Authors: Ramos,Ana Regina L., Matte,Ursula, Goldani,Helena Ayako Sueno, Oliveira,Osmar L. M., Vieira,Sandra Maria Gonçalves, Silveira,Themis Reverbel da
Format: Digital revista
Language:English
Published: Instituto Brasileiro de Estudos e Pesquisas de Gastroenterologia e Outras Especialidades - IBEPEGE. 2010
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032010000200014
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spelling oai:scielo:S0004-280320100002000142010-09-22Intestinal permeability assessed by 51Cr-EDTA in rats with CCl4 - induced cirrhosisRamos,Ana Regina L.Matte,UrsulaGoldani,Helena Ayako SuenoOliveira,Osmar L. M.Vieira,Sandra Maria GonçalvesSilveira,Themis Reverbel da Intestinal absorption Edetic acid Liver cirrhosis, experimental Rats CONTEXT: The straight relationship between cirrhosis and impaired intestinal barrier has not been elucidated yet. OBJECTIVES: To verify 51Cr-EDTA-intestinal permeability in rats with CCl4-induced cirrhosis and controls. METHOD: Fifty male Wistar rats weighing 150-180 g were separated in three groups: 25 animals received CCl4 0.25 mL/kg with olive oil by gavage with 12 g/rat/day food restriction for 10 weeks (CCl4-induced cirrhosis); 12 received the same food restriction for 10 weeks (CCl4-non exposed). Other 13 rats received indomethacin 15 mg/kg by gavage as positive control of intestinal inflammation. RESULTS: The median (25-75 interquartile range) 51Cr-EDTA-IP values of cirrhotic and CCl4-non exposed rats were 0.90% (0.63-1.79) and 0.90% (0.60-1.52) respectively, without significant difference (P = 0.65). Animals from indomethacin group showed 51Cr-EDTA-IP, median 7.3% (5.1-14.7), significantly higher than cirrhotic and CCl4-non exposed rats (P<0.001). CONCLUSION: This study showed the lack of difference between 51Cr-EDTA-intestinal permeability in rats with and without cirrhosis. Further studies are necessary to better clarify the relationship between intestinal permeability and cirrhosis.info:eu-repo/semantics/openAccessInstituto Brasileiro de Estudos e Pesquisas de Gastroenterologia e Outras Especialidades - IBEPEGE. Arquivos de Gastroenterologia v.47 n.2 20102010-06-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032010000200014en10.1590/S0004-28032010000200014
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libraryname SciELO
language English
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author Ramos,Ana Regina L.
Matte,Ursula
Goldani,Helena Ayako Sueno
Oliveira,Osmar L. M.
Vieira,Sandra Maria Gonçalves
Silveira,Themis Reverbel da
spellingShingle Ramos,Ana Regina L.
Matte,Ursula
Goldani,Helena Ayako Sueno
Oliveira,Osmar L. M.
Vieira,Sandra Maria Gonçalves
Silveira,Themis Reverbel da
Intestinal permeability assessed by 51Cr-EDTA in rats with CCl4 - induced cirrhosis
author_facet Ramos,Ana Regina L.
Matte,Ursula
Goldani,Helena Ayako Sueno
Oliveira,Osmar L. M.
Vieira,Sandra Maria Gonçalves
Silveira,Themis Reverbel da
author_sort Ramos,Ana Regina L.
title Intestinal permeability assessed by 51Cr-EDTA in rats with CCl4 - induced cirrhosis
title_short Intestinal permeability assessed by 51Cr-EDTA in rats with CCl4 - induced cirrhosis
title_full Intestinal permeability assessed by 51Cr-EDTA in rats with CCl4 - induced cirrhosis
title_fullStr Intestinal permeability assessed by 51Cr-EDTA in rats with CCl4 - induced cirrhosis
title_full_unstemmed Intestinal permeability assessed by 51Cr-EDTA in rats with CCl4 - induced cirrhosis
title_sort intestinal permeability assessed by 51cr-edta in rats with ccl4 - induced cirrhosis
description CONTEXT: The straight relationship between cirrhosis and impaired intestinal barrier has not been elucidated yet. OBJECTIVES: To verify 51Cr-EDTA-intestinal permeability in rats with CCl4-induced cirrhosis and controls. METHOD: Fifty male Wistar rats weighing 150-180 g were separated in three groups: 25 animals received CCl4 0.25 mL/kg with olive oil by gavage with 12 g/rat/day food restriction for 10 weeks (CCl4-induced cirrhosis); 12 received the same food restriction for 10 weeks (CCl4-non exposed). Other 13 rats received indomethacin 15 mg/kg by gavage as positive control of intestinal inflammation. RESULTS: The median (25-75 interquartile range) 51Cr-EDTA-IP values of cirrhotic and CCl4-non exposed rats were 0.90% (0.63-1.79) and 0.90% (0.60-1.52) respectively, without significant difference (P = 0.65). Animals from indomethacin group showed 51Cr-EDTA-IP, median 7.3% (5.1-14.7), significantly higher than cirrhotic and CCl4-non exposed rats (P<0.001). CONCLUSION: This study showed the lack of difference between 51Cr-EDTA-intestinal permeability in rats with and without cirrhosis. Further studies are necessary to better clarify the relationship between intestinal permeability and cirrhosis.
publisher Instituto Brasileiro de Estudos e Pesquisas de Gastroenterologia e Outras Especialidades - IBEPEGE.
publishDate 2010
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032010000200014
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