Expression of heme oxygenase isoenzymes 1 and 2 in normal and asthmatic airways : Effect of inhaled corticosteroids

Heme oxygenase (HO) is considered to be an antioxidant enzyme that catabolizes heme to produce carbon monoxide (CO) and biliverdin. We determined the expression and distribution of HO-1 and HO-2, two isoenzymes of HO, in the airways of patients with asthma, and determined the effect of inhaled corti...

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Veröffentlicht in:American journal of respiratory and critical care medicine 2000-11, Vol.162 (5), p.1912-1918
Hauptverfasser: SAM LIM, GRONEBERG, David, FISCHER, Axel, OATES, Timothy, CARAMORI, Gaetano, MATTOS, Waldo, ADCOCK, Ian, BARNES, Peter J, KIAN FAN CHUNG
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container_end_page 1918
container_issue 5
container_start_page 1912
container_title American journal of respiratory and critical care medicine
container_volume 162
creator SAM LIM
GRONEBERG, David
FISCHER, Axel
OATES, Timothy
CARAMORI, Gaetano
MATTOS, Waldo
ADCOCK, Ian
BARNES, Peter J
KIAN FAN CHUNG
description Heme oxygenase (HO) is considered to be an antioxidant enzyme that catabolizes heme to produce carbon monoxide (CO) and biliverdin. We determined the expression and distribution of HO-1 and HO-2, two isoenzymes of HO, in the airways of patients with asthma, and determined the effect of inhaled corticosteroid therapy. Immunostaining for both enzymes was widely distributed in the airways' submucosa, particularly in airway epithelium and submucosal macrophages (CD68(+)) as determined by double immunostaining. There was no difference in intensity and extent of staining in biopsies from normal subjects (n = 10) and subjects with asthma (n = 10). Following 1 mo of treatment with inhaled corticosteroids (budesonide 1,600 microg/d), there was no significant change in the expression and distribution of either HO-1 or HO-2 in the airways' submucosa in eight subjects with mild asthma, despite a significant reduction in airway eosinophils and a reduction in bronchial responsiveness to methacholine. Levels of exhaled nitric oxide were significantly reduced, but exhaled CO levels remained unchanged by the treatment. Treatment with a placebo inhaler (n = 8) had no effects on these parameters. Thus, both HO-1 and HO-2 are extensively distributed equally in normal subjects and subjects with asthma, and are not modulated by inhaled corticosteroid therapy in subjects with asthma. HO may be an important endogenous antioxidant enzyme.
doi_str_mv 10.1164/ajrccm.162.5.9909081
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We determined the expression and distribution of HO-1 and HO-2, two isoenzymes of HO, in the airways of patients with asthma, and determined the effect of inhaled corticosteroid therapy. Immunostaining for both enzymes was widely distributed in the airways' submucosa, particularly in airway epithelium and submucosal macrophages (CD68(+)) as determined by double immunostaining. There was no difference in intensity and extent of staining in biopsies from normal subjects (n = 10) and subjects with asthma (n = 10). Following 1 mo of treatment with inhaled corticosteroids (budesonide 1,600 microg/d), there was no significant change in the expression and distribution of either HO-1 or HO-2 in the airways' submucosa in eight subjects with mild asthma, despite a significant reduction in airway eosinophils and a reduction in bronchial responsiveness to methacholine. Levels of exhaled nitric oxide were significantly reduced, but exhaled CO levels remained unchanged by the treatment. Treatment with a placebo inhaler (n = 8) had no effects on these parameters. Thus, both HO-1 and HO-2 are extensively distributed equally in normal subjects and subjects with asthma, and are not modulated by inhaled corticosteroid therapy in subjects with asthma. 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Treatment with a placebo inhaler (n = 8) had no effects on these parameters. Thus, both HO-1 and HO-2 are extensively distributed equally in normal subjects and subjects with asthma, and are not modulated by inhaled corticosteroid therapy in subjects with asthma. HO may be an important endogenous antioxidant enzyme.</description><subject>Administration, Inhalation</subject><subject>Asthma - drug therapy</subject><subject>Asthma - enzymology</subject><subject>Asthma - metabolism</subject><subject>Asthma - pathology</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Bronchi - enzymology</subject><subject>Bronchi - pathology</subject><subject>Bronchodilator Agents - administration &amp; dosage</subject><subject>Bronchoscopy</subject><subject>Budesonide - administration &amp; dosage</subject><subject>Carbon Monoxide - analysis</subject><subject>Eosinophils - pathology</subject><subject>Glucocorticoids - administration &amp; dosage</subject><subject>Heme Oxygenase (Decyclizing) - metabolism</subject><subject>Heme Oxygenase-1</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Isoenzymes - metabolism</subject><subject>Medical sciences</subject><subject>Membrane Proteins</subject><subject>Nitric Oxide - analysis</subject><subject>Pharmacology. 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Drug treatments</topic><topic>Respiratory system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SAM LIM</creatorcontrib><creatorcontrib>GRONEBERG, David</creatorcontrib><creatorcontrib>FISCHER, Axel</creatorcontrib><creatorcontrib>OATES, Timothy</creatorcontrib><creatorcontrib>CARAMORI, Gaetano</creatorcontrib><creatorcontrib>MATTOS, Waldo</creatorcontrib><creatorcontrib>ADCOCK, Ian</creatorcontrib><creatorcontrib>BARNES, Peter J</creatorcontrib><creatorcontrib>KIAN FAN CHUNG</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of respiratory and critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SAM LIM</au><au>GRONEBERG, David</au><au>FISCHER, Axel</au><au>OATES, Timothy</au><au>CARAMORI, Gaetano</au><au>MATTOS, Waldo</au><au>ADCOCK, Ian</au><au>BARNES, Peter J</au><au>KIAN FAN CHUNG</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of heme oxygenase isoenzymes 1 and 2 in normal and asthmatic airways : Effect of inhaled corticosteroids</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>2000-11-01</date><risdate>2000</risdate><volume>162</volume><issue>5</issue><spage>1912</spage><epage>1918</epage><pages>1912-1918</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>Heme oxygenase (HO) is considered to be an antioxidant enzyme that catabolizes heme to produce carbon monoxide (CO) and biliverdin. 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Treatment with a placebo inhaler (n = 8) had no effects on these parameters. Thus, both HO-1 and HO-2 are extensively distributed equally in normal subjects and subjects with asthma, and are not modulated by inhaled corticosteroid therapy in subjects with asthma. HO may be an important endogenous antioxidant enzyme.</abstract><cop>New York, NY</cop><pub>American Lung Association</pub><pmid>11069834</pmid><doi>10.1164/ajrccm.162.5.9909081</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Journals@Ovid Complete; American Thoracic Society (ATS) Journals Online; EZB-FREE-00999 freely available EZB journals
subjects Administration, Inhalation
Asthma - drug therapy
Asthma - enzymology
Asthma - metabolism
Asthma - pathology
Biological and medical sciences
Blotting, Western
Bronchi - enzymology
Bronchi - pathology
Bronchodilator Agents - administration & dosage
Bronchoscopy
Budesonide - administration & dosage
Carbon Monoxide - analysis
Eosinophils - pathology
Glucocorticoids - administration & dosage
Heme Oxygenase (Decyclizing) - metabolism
Heme Oxygenase-1
Humans
Immunohistochemistry
Isoenzymes - metabolism
Medical sciences
Membrane Proteins
Nitric Oxide - analysis
Pharmacology. Drug treatments
Respiratory system
title Expression of heme oxygenase isoenzymes 1 and 2 in normal and asthmatic airways : Effect of inhaled corticosteroids
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