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Heme Oxygenase-1 mRNA Expression in Egyptian Patients With Chronic Liver Disease

BACKGROUND: Chronic liver disease (CLD) is a global medical problem. This disease is associated with increased hepatic oxidative stress. One of the antioxidant enzymes that protect cells against this stress is heme oxygenase-1 (HO-1). OBJECTIVES: This study aimed to investigate the mRNA expression o...

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Autores principales: Bessa, Sahar Saad El-Din, Mohamed Ali, Ehab Mostafa, Abd El-Wahab, Abeer El-Sayed, Nor El-Din, Sherif Abd El-Monem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3360938/
https://www.ncbi.nlm.nih.gov/pubmed/22690236
http://dx.doi.org/10.5812/hepatmon.846
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author Bessa, Sahar Saad El-Din
Mohamed Ali, Ehab Mostafa
Abd El-Wahab, Abeer El-Sayed
Nor El-Din, Sherif Abd El-Monem
author_facet Bessa, Sahar Saad El-Din
Mohamed Ali, Ehab Mostafa
Abd El-Wahab, Abeer El-Sayed
Nor El-Din, Sherif Abd El-Monem
author_sort Bessa, Sahar Saad El-Din
collection PubMed
description BACKGROUND: Chronic liver disease (CLD) is a global medical problem. This disease is associated with increased hepatic oxidative stress. One of the antioxidant enzymes that protect cells against this stress is heme oxygenase-1 (HO-1). OBJECTIVES: This study aimed to investigate the mRNA expression of HO-1 in Egyptian patients with CLD and its relation to oxidative stress biomarkers. PATIENTS AND METHODS: Levels of serum ferritin, carboxyhemoglobin, malondialdehyde (MDA), and erythrocyte-reduced glutathione (GSH) were measured, and HO-1 mRNA expression was detected in 45 CLD patients (15 with nonalcoholic steatohepatitis [NASH], 15 with chronic hepatitis C, and 15 with liver cirrhosis) and 15 healthy controls. RESULTS: HO-1 mRNA expression was increased in patients with NASH, chronic hepatitis C, and liver cirrhosis compared to controls. The expression in cirrhotic patients was significantly higher than that in patients with NASH and chronic hepatitis C. Compared to controls, patients with NASH, chronic hepatitis C, and liver cirrhosis had higher levels of ferritin, carboxyhemoglobin, and MDA and lower levels of GSH. HO-1 mRNA expression was positively correlated with levels of carboxyhemoglobin, serum ferritin, and serum MDA and negatively correlated with levels of erythrocyte GSH in CLD patients. CONCLUSIONS: HO-1 mRNA expression was significantly increased in CLD patients, and the increase reflected the severity of the disease. The significant relationship between the increased HO-1 expression and oxidative stress biomarkers in patients with CLD suggests that HO-1 may play an important role in protecting the liver from oxidative stress-dependent damage. Therefore, induction of HO-1 could be a novel therapeutic option for CLD.
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spelling pubmed-33609382012-06-11 Heme Oxygenase-1 mRNA Expression in Egyptian Patients With Chronic Liver Disease Bessa, Sahar Saad El-Din Mohamed Ali, Ehab Mostafa Abd El-Wahab, Abeer El-Sayed Nor El-Din, Sherif Abd El-Monem Hepat Mon Original Article BACKGROUND: Chronic liver disease (CLD) is a global medical problem. This disease is associated with increased hepatic oxidative stress. One of the antioxidant enzymes that protect cells against this stress is heme oxygenase-1 (HO-1). OBJECTIVES: This study aimed to investigate the mRNA expression of HO-1 in Egyptian patients with CLD and its relation to oxidative stress biomarkers. PATIENTS AND METHODS: Levels of serum ferritin, carboxyhemoglobin, malondialdehyde (MDA), and erythrocyte-reduced glutathione (GSH) were measured, and HO-1 mRNA expression was detected in 45 CLD patients (15 with nonalcoholic steatohepatitis [NASH], 15 with chronic hepatitis C, and 15 with liver cirrhosis) and 15 healthy controls. RESULTS: HO-1 mRNA expression was increased in patients with NASH, chronic hepatitis C, and liver cirrhosis compared to controls. The expression in cirrhotic patients was significantly higher than that in patients with NASH and chronic hepatitis C. Compared to controls, patients with NASH, chronic hepatitis C, and liver cirrhosis had higher levels of ferritin, carboxyhemoglobin, and MDA and lower levels of GSH. HO-1 mRNA expression was positively correlated with levels of carboxyhemoglobin, serum ferritin, and serum MDA and negatively correlated with levels of erythrocyte GSH in CLD patients. CONCLUSIONS: HO-1 mRNA expression was significantly increased in CLD patients, and the increase reflected the severity of the disease. The significant relationship between the increased HO-1 expression and oxidative stress biomarkers in patients with CLD suggests that HO-1 may play an important role in protecting the liver from oxidative stress-dependent damage. Therefore, induction of HO-1 could be a novel therapeutic option for CLD. Kowsar 2012-04 2012-04-30 /pmc/articles/PMC3360938/ /pubmed/22690236 http://dx.doi.org/10.5812/hepatmon.846 Text en Copyright © 2012, Kowsar Corp. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Bessa, Sahar Saad El-Din
Mohamed Ali, Ehab Mostafa
Abd El-Wahab, Abeer El-Sayed
Nor El-Din, Sherif Abd El-Monem
Heme Oxygenase-1 mRNA Expression in Egyptian Patients With Chronic Liver Disease
title Heme Oxygenase-1 mRNA Expression in Egyptian Patients With Chronic Liver Disease
title_full Heme Oxygenase-1 mRNA Expression in Egyptian Patients With Chronic Liver Disease
title_fullStr Heme Oxygenase-1 mRNA Expression in Egyptian Patients With Chronic Liver Disease
title_full_unstemmed Heme Oxygenase-1 mRNA Expression in Egyptian Patients With Chronic Liver Disease
title_short Heme Oxygenase-1 mRNA Expression in Egyptian Patients With Chronic Liver Disease
title_sort heme oxygenase-1 mrna expression in egyptian patients with chronic liver disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3360938/
https://www.ncbi.nlm.nih.gov/pubmed/22690236
http://dx.doi.org/10.5812/hepatmon.846
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