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Relation of oxidant-antioxidant imbalance with disease progression in patients with asthma

CONTEXT: Asthma is a chronic airway disorder which is associated to the inflammatory cells. Inflammatory and immune cells generate more reactive oxygen species in patients suffering from asthma which leads to tissue injury. AIMS: To investigate the role of oxidant-antioxidant imbalance in disease pr...

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Autores principales: Ahmad, Asrar, Shameem, Mohammad, Husain, Qayyum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506103/
https://www.ncbi.nlm.nih.gov/pubmed/23189100
http://dx.doi.org/10.4103/1817-1737.102182
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author Ahmad, Asrar
Shameem, Mohammad
Husain, Qayyum
author_facet Ahmad, Asrar
Shameem, Mohammad
Husain, Qayyum
author_sort Ahmad, Asrar
collection PubMed
description CONTEXT: Asthma is a chronic airway disorder which is associated to the inflammatory cells. Inflammatory and immune cells generate more reactive oxygen species in patients suffering from asthma which leads to tissue injury. AIMS: To investigate the role of oxidant-antioxidant imbalance in disease progression of asthmatic patients. SETTINGS AND DESIGN: In this study, 130 asthmatic patients and 70 healthy controls were documented. METHODS: For this malondialdehyde level, total protein carbonyls, sulfhydryls, activity of superoxide dismutase (SOD), catalase, glutathione peroxidase (GPx), total blood glutathione, and total antioxidant capacity (FRAP) were measured. STATISTICAL ANALYSIS USED: Analysis of the data was done using unpaired student t test and one-way ANOVA analysis. P < 0.05 was considered significant. RESULTS: The present work showed that the systemic levels of MDA (4.19 ± 0.10 nmol/ml, P < 0.001) and protein carbonyls (1.13 ± 0.02 nmol/mg, P < 0.001) were found to be remarkably higher in asthmatic patients while protein sulfhydryls (0.55 ± 0.01 mmol/l, P < 0.05) decreased as compared to controls (2.84 ± 0.12 nmol/ml, 0.79 ± 0.02 nmol/mg and 0.60 ± 0.02 mmol/l, respectively). We also observed decrease in activities of SOD (2047 ± 50.34 U/g Hb, P < 0.05), catalase (4374 ± 67.98 U/g Hb, P < 0.01), and GPx (40.97 ± 1.05 U/g Hb, P < 0.01) in erythrocytes compared to control (2217 ± 60.11 U/g Hb, 4746 ± 89.94 U/g Hb, and 48.37 ± 2.47 U/g Hb, respectively). FRAP level (750.90 ± 21.22 μmol/l, P < 0.05) in plasma was decreased, whereas total blood glutathione increased (0.94 ± 0.02 mmol/l, P < 0.05) as seen in control (840.40 ± 28.39 μmol/l and 0.84 ± 0.04 mmol/l). CONCLUSIONS: This work supports and describes the hypothesis that an imbalance between oxidant-antioxidant is associated to the oxidative stress which plays a significant role in severity of the disease.
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spelling pubmed-35061032012-11-27 Relation of oxidant-antioxidant imbalance with disease progression in patients with asthma Ahmad, Asrar Shameem, Mohammad Husain, Qayyum Ann Thorac Med Original Article CONTEXT: Asthma is a chronic airway disorder which is associated to the inflammatory cells. Inflammatory and immune cells generate more reactive oxygen species in patients suffering from asthma which leads to tissue injury. AIMS: To investigate the role of oxidant-antioxidant imbalance in disease progression of asthmatic patients. SETTINGS AND DESIGN: In this study, 130 asthmatic patients and 70 healthy controls were documented. METHODS: For this malondialdehyde level, total protein carbonyls, sulfhydryls, activity of superoxide dismutase (SOD), catalase, glutathione peroxidase (GPx), total blood glutathione, and total antioxidant capacity (FRAP) were measured. STATISTICAL ANALYSIS USED: Analysis of the data was done using unpaired student t test and one-way ANOVA analysis. P < 0.05 was considered significant. RESULTS: The present work showed that the systemic levels of MDA (4.19 ± 0.10 nmol/ml, P < 0.001) and protein carbonyls (1.13 ± 0.02 nmol/mg, P < 0.001) were found to be remarkably higher in asthmatic patients while protein sulfhydryls (0.55 ± 0.01 mmol/l, P < 0.05) decreased as compared to controls (2.84 ± 0.12 nmol/ml, 0.79 ± 0.02 nmol/mg and 0.60 ± 0.02 mmol/l, respectively). We also observed decrease in activities of SOD (2047 ± 50.34 U/g Hb, P < 0.05), catalase (4374 ± 67.98 U/g Hb, P < 0.01), and GPx (40.97 ± 1.05 U/g Hb, P < 0.01) in erythrocytes compared to control (2217 ± 60.11 U/g Hb, 4746 ± 89.94 U/g Hb, and 48.37 ± 2.47 U/g Hb, respectively). FRAP level (750.90 ± 21.22 μmol/l, P < 0.05) in plasma was decreased, whereas total blood glutathione increased (0.94 ± 0.02 mmol/l, P < 0.05) as seen in control (840.40 ± 28.39 μmol/l and 0.84 ± 0.04 mmol/l). CONCLUSIONS: This work supports and describes the hypothesis that an imbalance between oxidant-antioxidant is associated to the oxidative stress which plays a significant role in severity of the disease. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3506103/ /pubmed/23189100 http://dx.doi.org/10.4103/1817-1737.102182 Text en Copyright: © Annals of Thoracic Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ahmad, Asrar
Shameem, Mohammad
Husain, Qayyum
Relation of oxidant-antioxidant imbalance with disease progression in patients with asthma
title Relation of oxidant-antioxidant imbalance with disease progression in patients with asthma
title_full Relation of oxidant-antioxidant imbalance with disease progression in patients with asthma
title_fullStr Relation of oxidant-antioxidant imbalance with disease progression in patients with asthma
title_full_unstemmed Relation of oxidant-antioxidant imbalance with disease progression in patients with asthma
title_short Relation of oxidant-antioxidant imbalance with disease progression in patients with asthma
title_sort relation of oxidant-antioxidant imbalance with disease progression in patients with asthma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506103/
https://www.ncbi.nlm.nih.gov/pubmed/23189100
http://dx.doi.org/10.4103/1817-1737.102182
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