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Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis

BACKGROUND: Oxidative stress, an increase in oxidants and/or a decrease in antioxidant capacity, is one of the potential biochemical mechanisms involved in the pathogenesis of nonalcoholic steatohepatitis. We aimed to investigate the total antioxidant response using a novel automated method in nonal...

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Autores principales: Horoz, Mehmet, Bolukbas, Cengiz, Bolukbas, Fusun F, Sabuncu, Tevfik, Aslan, Mehmet, Sarifakiogullari, Serpil, Gunaydin, Necla, Erel, Ozcan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1308812/
https://www.ncbi.nlm.nih.gov/pubmed/16283935
http://dx.doi.org/10.1186/1471-230X-5-35
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author Horoz, Mehmet
Bolukbas, Cengiz
Bolukbas, Fusun F
Sabuncu, Tevfik
Aslan, Mehmet
Sarifakiogullari, Serpil
Gunaydin, Necla
Erel, Ozcan
author_facet Horoz, Mehmet
Bolukbas, Cengiz
Bolukbas, Fusun F
Sabuncu, Tevfik
Aslan, Mehmet
Sarifakiogullari, Serpil
Gunaydin, Necla
Erel, Ozcan
author_sort Horoz, Mehmet
collection PubMed
description BACKGROUND: Oxidative stress, an increase in oxidants and/or a decrease in antioxidant capacity, is one of the potential biochemical mechanisms involved in the pathogenesis of nonalcoholic steatohepatitis. We aimed to investigate the total antioxidant response using a novel automated method in nonalcoholic steatohepatitis subjects. As a reciprocal measure, we also aimed to determine total peroxide level in the same plasma samples. METHODS: Twenty-two subjects with biopsy proven nonalcoholic steatohepatitis and 22 healthy controls were enrolled. Total antioxidant response and total peroxide level measurements were done in all participants. The ratio percentage of total peroxide level to total antioxidant response was regarded as oxidative stress index. RESULTS: Total antioxidant response of subjects with nonalcoholic steatohepatitis was significantly lower than controls (p < 0.05), while mean total peroxide level and mean oxidative stress index were higher (all p < 0.05). In subjects with nonalcoholic steatohepatitis, fibrosis score was significantly correlated with total peroxide level, total antioxidant response and oxidative stress index (p < 0.05, r = 0.607; p < 0.05, r = -0.506; p < 0.05, r = 0.728, respectively). However, no correlation was observed between necroimflamatory grade and those oxidative status parameters (all p > 0.05). CONCLUSION: Nonalcoholic steatohepatitis is associated with increased oxidant capacity, especially in the presence of liver fibrosis. The novel automated assay is a reliable and easily applicable method for total plasma antioxidant response measurement in nonalcoholic steatohepatitis.
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spelling pubmed-13088122005-12-08 Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis Horoz, Mehmet Bolukbas, Cengiz Bolukbas, Fusun F Sabuncu, Tevfik Aslan, Mehmet Sarifakiogullari, Serpil Gunaydin, Necla Erel, Ozcan BMC Gastroenterol Technical Advance BACKGROUND: Oxidative stress, an increase in oxidants and/or a decrease in antioxidant capacity, is one of the potential biochemical mechanisms involved in the pathogenesis of nonalcoholic steatohepatitis. We aimed to investigate the total antioxidant response using a novel automated method in nonalcoholic steatohepatitis subjects. As a reciprocal measure, we also aimed to determine total peroxide level in the same plasma samples. METHODS: Twenty-two subjects with biopsy proven nonalcoholic steatohepatitis and 22 healthy controls were enrolled. Total antioxidant response and total peroxide level measurements were done in all participants. The ratio percentage of total peroxide level to total antioxidant response was regarded as oxidative stress index. RESULTS: Total antioxidant response of subjects with nonalcoholic steatohepatitis was significantly lower than controls (p < 0.05), while mean total peroxide level and mean oxidative stress index were higher (all p < 0.05). In subjects with nonalcoholic steatohepatitis, fibrosis score was significantly correlated with total peroxide level, total antioxidant response and oxidative stress index (p < 0.05, r = 0.607; p < 0.05, r = -0.506; p < 0.05, r = 0.728, respectively). However, no correlation was observed between necroimflamatory grade and those oxidative status parameters (all p > 0.05). CONCLUSION: Nonalcoholic steatohepatitis is associated with increased oxidant capacity, especially in the presence of liver fibrosis. The novel automated assay is a reliable and easily applicable method for total plasma antioxidant response measurement in nonalcoholic steatohepatitis. BioMed Central 2005-11-11 /pmc/articles/PMC1308812/ /pubmed/16283935 http://dx.doi.org/10.1186/1471-230X-5-35 Text en Copyright © 2005 Horoz et al; licensee BioMed Central Ltd.
spellingShingle Technical Advance
Horoz, Mehmet
Bolukbas, Cengiz
Bolukbas, Fusun F
Sabuncu, Tevfik
Aslan, Mehmet
Sarifakiogullari, Serpil
Gunaydin, Necla
Erel, Ozcan
Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis
title Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis
title_full Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis
title_fullStr Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis
title_full_unstemmed Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis
title_short Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis
title_sort measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1308812/
https://www.ncbi.nlm.nih.gov/pubmed/16283935
http://dx.doi.org/10.1186/1471-230X-5-35
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