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OZONE DIFFERENTIALLY MODULATES AIRWAY RESPONSIVENESS IN ATOPIC VERSUS NONATOPIC GUINEA PIGS
While acute exposures to ozone (O 3) can alter airway responsiveness, effects from long-term exposures at low concentrations are less clear. This study assessed whether such exposures could induce nonspecific hyperresponsiveness in nonatopic (nonsensitized) guinea pigs and/or could exacerbate the pr...
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Published in: | Inhalation toxicology 2002-05, Vol.14 (5), p.431-457 |
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creator | Schlesinger, Richard B. Cohen, Mitchell D. Gordon, Terry Nadziejko, Christine Zelikoff, Judith T. Sisco, Maureen Regal, Jean F. Ménache, Margaret G. |
description | While acute exposures to ozone (O 3) can alter airway responsiveness, effects from long-term exposures at low concentrations are less clear. This study assessed whether such exposures could induce nonspecific hyperresponsiveness in nonatopic (nonsensitized) guinea pigs and/or could exacerbate the pre-existing hyperresponsive state in atopic (sensitized) animals, and whether gender was a factor modulating any effect of O 3. Responsiveness was measured during and following exposures to 0.1 and 0.3 ppm O 3 for 4 h/day, 4 days/wk for 24 wk in male and female nonsensitized animals, those sensitized to allergen (ovalbumin) prior to initiation of O 3 exposures, and those sensitized concurrently with exposures. Ozone did not produce hyperresponsiveness in nonsensitized animals, but did exacerbate hyperresponsiveness to both specific and nonspecific bronchoprovocation challenges in sensitized animals, an effect that persisted through at least 4 wk after exposures ended. Gender was not a factor modulating response to O 3. Induced effects on responsiveness were not associated with numbers of eosinophils in the lungs nor with any chronic pulmonary inflammatory response, but were correlated with antigen-specific antibodies in blood. This study supports a role for chronic O 3 exposure in the exacerbation of airways dysfunction in a certain segment of the general population, namely, those demonstrating atopy. |
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This study assessed whether such exposures could induce nonspecific hyperresponsiveness in nonatopic (nonsensitized) guinea pigs and/or could exacerbate the pre-existing hyperresponsive state in atopic (sensitized) animals, and whether gender was a factor modulating any effect of O 3. Responsiveness was measured during and following exposures to 0.1 and 0.3 ppm O 3 for 4 h/day, 4 days/wk for 24 wk in male and female nonsensitized animals, those sensitized to allergen (ovalbumin) prior to initiation of O 3 exposures, and those sensitized concurrently with exposures. Ozone did not produce hyperresponsiveness in nonsensitized animals, but did exacerbate hyperresponsiveness to both specific and nonspecific bronchoprovocation challenges in sensitized animals, an effect that persisted through at least 4 wk after exposures ended. Gender was not a factor modulating response to O 3. Induced effects on responsiveness were not associated with numbers of eosinophils in the lungs nor with any chronic pulmonary inflammatory response, but were correlated with antigen-specific antibodies in blood. This study supports a role for chronic O 3 exposure in the exacerbation of airways dysfunction in a certain segment of the general population, namely, those demonstrating atopy.</description><identifier>ISSN: 0895-8378</identifier><identifier>EISSN: 1091-7691</identifier><identifier>DOI: 10.1080/089583701753678562</identifier><identifier>PMID: 12028802</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Airway Resistance - drug effects ; Animals ; Dose-Response Relationship, Drug ; Female ; Guinea Pigs ; Hypersensitivity, Immediate ; Male ; Oxidants, Photochemical - adverse effects ; Ozone - adverse effects ; Sex Factors</subject><ispartof>Inhalation toxicology, 2002-05, Vol.14 (5), p.431-457</ispartof><rights>2002 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2002</rights><rights>Copyright © 2002 Taylor & Francis 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c567t-1c58081757939c19a881077b5a1d460e9d0d8a3c3e363e40e9dd883b6f7c0b5b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,786,790,891,27957,27958</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12028802$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schlesinger, Richard B.</creatorcontrib><creatorcontrib>Cohen, Mitchell D.</creatorcontrib><creatorcontrib>Gordon, Terry</creatorcontrib><creatorcontrib>Nadziejko, Christine</creatorcontrib><creatorcontrib>Zelikoff, Judith T.</creatorcontrib><creatorcontrib>Sisco, Maureen</creatorcontrib><creatorcontrib>Regal, Jean F.</creatorcontrib><creatorcontrib>Ménache, Margaret G.</creatorcontrib><title>OZONE DIFFERENTIALLY MODULATES AIRWAY RESPONSIVENESS IN ATOPIC VERSUS NONATOPIC GUINEA PIGS</title><title>Inhalation toxicology</title><addtitle>Inhal Toxicol</addtitle><description>While acute exposures to ozone (O 3) can alter airway responsiveness, effects from long-term exposures at low concentrations are less clear. This study assessed whether such exposures could induce nonspecific hyperresponsiveness in nonatopic (nonsensitized) guinea pigs and/or could exacerbate the pre-existing hyperresponsive state in atopic (sensitized) animals, and whether gender was a factor modulating any effect of O 3. Responsiveness was measured during and following exposures to 0.1 and 0.3 ppm O 3 for 4 h/day, 4 days/wk for 24 wk in male and female nonsensitized animals, those sensitized to allergen (ovalbumin) prior to initiation of O 3 exposures, and those sensitized concurrently with exposures. Ozone did not produce hyperresponsiveness in nonsensitized animals, but did exacerbate hyperresponsiveness to both specific and nonspecific bronchoprovocation challenges in sensitized animals, an effect that persisted through at least 4 wk after exposures ended. Gender was not a factor modulating response to O 3. Induced effects on responsiveness were not associated with numbers of eosinophils in the lungs nor with any chronic pulmonary inflammatory response, but were correlated with antigen-specific antibodies in blood. This study supports a role for chronic O 3 exposure in the exacerbation of airways dysfunction in a certain segment of the general population, namely, those demonstrating atopy.</description><subject>Airway Resistance - drug effects</subject><subject>Animals</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Guinea Pigs</subject><subject>Hypersensitivity, Immediate</subject><subject>Male</subject><subject>Oxidants, Photochemical - adverse effects</subject><subject>Ozone - adverse effects</subject><subject>Sex Factors</subject><issn>0895-8378</issn><issn>1091-7691</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkdFv0zAQxi0EYmXwD_CA8sRb2NlObEcCpKhzS6SQVE07NHiwHMelmdJkOCnT_ntStQImpPF00t3v--5OH0KvMbzDIOACRBQKygHzkDIuQkaeoAmGCPucRfgpmhwAfyTEGXrR9zcAwIDy5-gMEyBCAJmgb_nXPJPeZTKbyaXMVkmcptfe5_xyncYrWXhxsvwSX3tLWSzyrEiuZCaLwksyL17li2TqXcllsS68LM9Ojfk6yWTsLZJ58RI92-imt69O9RytZ3I1_eSn-TyZxqlvQsYHH5tQgBif4BGNDI60EBg4L0ONq4CBjSqohKaGWsqoDQ6NSghasg03UIYlPUcfj763-3JnK2PbwelG3bp6p9296nStHk7aequ-dz8VibhgIR0N3p4MXPdjb_tB7ere2KbRre32vcIRYQSC8P9gwLAICBlBcgSN6_re2c3vazCoQ3jq3_BG0Zu___gjOaU1Ah-OQN1uOrfTd51rKjXo-6ZzG6dbU_eKPrrg_QP91upm2BrtrLrp9q4dQ3rsvl9-m7M3</recordid><startdate>20020501</startdate><enddate>20020501</enddate><creator>Schlesinger, Richard B.</creator><creator>Cohen, Mitchell D.</creator><creator>Gordon, Terry</creator><creator>Nadziejko, Christine</creator><creator>Zelikoff, Judith T.</creator><creator>Sisco, Maureen</creator><creator>Regal, Jean F.</creator><creator>Ménache, Margaret G.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><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>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7U7</scope><scope>5PM</scope></search><sort><creationdate>20020501</creationdate><title>OZONE DIFFERENTIALLY MODULATES AIRWAY RESPONSIVENESS IN ATOPIC VERSUS NONATOPIC GUINEA PIGS</title><author>Schlesinger, Richard B. ; Cohen, Mitchell D. ; Gordon, Terry ; Nadziejko, Christine ; Zelikoff, Judith T. ; Sisco, Maureen ; Regal, Jean F. ; Ménache, Margaret G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c567t-1c58081757939c19a881077b5a1d460e9d0d8a3c3e363e40e9dd883b6f7c0b5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Airway Resistance - drug effects</topic><topic>Animals</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Guinea Pigs</topic><topic>Hypersensitivity, Immediate</topic><topic>Male</topic><topic>Oxidants, Photochemical - adverse effects</topic><topic>Ozone - adverse effects</topic><topic>Sex Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schlesinger, Richard B.</creatorcontrib><creatorcontrib>Cohen, Mitchell D.</creatorcontrib><creatorcontrib>Gordon, Terry</creatorcontrib><creatorcontrib>Nadziejko, Christine</creatorcontrib><creatorcontrib>Zelikoff, Judith T.</creatorcontrib><creatorcontrib>Sisco, Maureen</creatorcontrib><creatorcontrib>Regal, Jean F.</creatorcontrib><creatorcontrib>Ménache, Margaret G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Toxicology Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Inhalation toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schlesinger, Richard B.</au><au>Cohen, Mitchell D.</au><au>Gordon, Terry</au><au>Nadziejko, Christine</au><au>Zelikoff, Judith T.</au><au>Sisco, Maureen</au><au>Regal, Jean F.</au><au>Ménache, Margaret G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>OZONE DIFFERENTIALLY MODULATES AIRWAY RESPONSIVENESS IN ATOPIC VERSUS NONATOPIC GUINEA PIGS</atitle><jtitle>Inhalation toxicology</jtitle><addtitle>Inhal Toxicol</addtitle><date>2002-05-01</date><risdate>2002</risdate><volume>14</volume><issue>5</issue><spage>431</spage><epage>457</epage><pages>431-457</pages><issn>0895-8378</issn><eissn>1091-7691</eissn><notes>ObjectType-Article-2</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-1</notes><notes>content type line 23</notes><abstract>While acute exposures to ozone (O 3) can alter airway responsiveness, effects from long-term exposures at low concentrations are less clear. This study assessed whether such exposures could induce nonspecific hyperresponsiveness in nonatopic (nonsensitized) guinea pigs and/or could exacerbate the pre-existing hyperresponsive state in atopic (sensitized) animals, and whether gender was a factor modulating any effect of O 3. Responsiveness was measured during and following exposures to 0.1 and 0.3 ppm O 3 for 4 h/day, 4 days/wk for 24 wk in male and female nonsensitized animals, those sensitized to allergen (ovalbumin) prior to initiation of O 3 exposures, and those sensitized concurrently with exposures. Ozone did not produce hyperresponsiveness in nonsensitized animals, but did exacerbate hyperresponsiveness to both specific and nonspecific bronchoprovocation challenges in sensitized animals, an effect that persisted through at least 4 wk after exposures ended. Gender was not a factor modulating response to O 3. Induced effects on responsiveness were not associated with numbers of eosinophils in the lungs nor with any chronic pulmonary inflammatory response, but were correlated with antigen-specific antibodies in blood. This study supports a role for chronic O 3 exposure in the exacerbation of airways dysfunction in a certain segment of the general population, namely, those demonstrating atopy.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>12028802</pmid><doi>10.1080/089583701753678562</doi><tpages>27</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Airway Resistance - drug effects Animals Dose-Response Relationship, Drug Female Guinea Pigs Hypersensitivity, Immediate Male Oxidants, Photochemical - adverse effects Ozone - adverse effects Sex Factors |
title | OZONE DIFFERENTIALLY MODULATES AIRWAY RESPONSIVENESS IN ATOPIC VERSUS NONATOPIC GUINEA PIGS |
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