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 |
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container_issue | 5 |
container_start_page | 1912 |
container_title | American journal of respiratory and critical care medicine |
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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 |
format | Article |
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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. HO may be an important endogenous antioxidant enzyme.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/ajrccm.162.5.9909081</identifier><identifier>PMID: 11069834</identifier><language>eng</language><publisher>New York, NY: American Lung Association</publisher><subject>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</subject><ispartof>American journal of respiratory and critical care medicine, 2000-11, Vol.162 (5), p.1912-1918</ispartof><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c280t-53f890b97fa71b884ca7a2bbca71fa7408d1accfdbcf3f785da8f2b80b91ab3c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4025,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=798697$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11069834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Expression of heme oxygenase isoenzymes 1 and 2 in normal and asthmatic airways : Effect of inhaled corticosteroids</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><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.</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 & dosage</subject><subject>Bronchoscopy</subject><subject>Budesonide - administration & dosage</subject><subject>Carbon Monoxide - analysis</subject><subject>Eosinophils - pathology</subject><subject>Glucocorticoids - administration & 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. Drug treatments</subject><subject>Respiratory system</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM2KFDEUhYMozo--gUhAcFdtbqWqk7iToXWEATcK7sKtVGJnqEra3Gqc9unN2IWu7g_fOYuPsVcgNgDb7h3eF-fmDWzbTb8xRhih4Qm7hF72TWeUeFp3oWTTdeb7BbsiuhcCWg3iObsAEFujZXfJaPdwKJ4o5sRz4Hs_e54fTj98QvI8Uvbp92n2xIFjGnnLY-IplxmnvzfSsp9xiY5jLL_wRPw934Xg3fLYFtMeJz9yl0tFMi2-5DjSC_Ys4ET-5Tqv2bePu683t83dl0-fbz7cNa7VYml6GbQRg1EBFQxadw4VtsNQB9RXJ_QI6FwYBxdkULofUYd20DUCOEgnr9nbc--h5J9HT4udIzk_TZh8PpJVrTQKdF_B7gy6komKD_ZQ4ozlZEHYR9n2LNtW2ba3q-wae732H4fZj_9Dq90KvFkBJIdTKJhcpH-cMnprlPwDrO-LrA</recordid><startdate>20001101</startdate><enddate>20001101</enddate><creator>SAM LIM</creator><creator>GRONEBERG, David</creator><creator>FISCHER, Axel</creator><creator>OATES, Timothy</creator><creator>CARAMORI, Gaetano</creator><creator>MATTOS, Waldo</creator><creator>ADCOCK, Ian</creator><creator>BARNES, Peter J</creator><creator>KIAN FAN CHUNG</creator><general>American Lung Association</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20001101</creationdate><title>Expression of heme oxygenase isoenzymes 1 and 2 in normal and asthmatic airways : Effect of inhaled corticosteroids</title><author>SAM LIM ; GRONEBERG, David ; FISCHER, Axel ; OATES, Timothy ; CARAMORI, Gaetano ; MATTOS, Waldo ; ADCOCK, Ian ; BARNES, Peter J ; KIAN FAN CHUNG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c280t-53f890b97fa71b884ca7a2bbca71fa7408d1accfdbcf3f785da8f2b80b91ab3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Administration, Inhalation</topic><topic>Asthma - drug therapy</topic><topic>Asthma - enzymology</topic><topic>Asthma - metabolism</topic><topic>Asthma - pathology</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Bronchi - enzymology</topic><topic>Bronchi - pathology</topic><topic>Bronchodilator Agents - administration & dosage</topic><topic>Bronchoscopy</topic><topic>Budesonide - administration & dosage</topic><topic>Carbon Monoxide - analysis</topic><topic>Eosinophils - pathology</topic><topic>Glucocorticoids - administration & dosage</topic><topic>Heme Oxygenase (Decyclizing) - metabolism</topic><topic>Heme Oxygenase-1</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Isoenzymes - metabolism</topic><topic>Medical sciences</topic><topic>Membrane Proteins</topic><topic>Nitric Oxide - analysis</topic><topic>Pharmacology. 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. 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.</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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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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