Preventive and therapeutic effect of anti-IL-17 in an experimental model of elastase-induced lung injury in C57Bl6 mice
Chronic obstructive pulmonary disease (COPD) is an important health care issue, and IL-17 can modulate inflammatory responses. We evaluated preventive and therapeutic effect of anti-interleukin (IL)-17 in a model of lung injury induced by elastase, using 32 male C57Bl6 mice, divided into 4 groups: S...
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creator | Fukuzaki, Silvia Righetti, Renato Fraga Santos, Tabata Maruyama Dos Camargo, Leandro do Nascimento Aristóteles, Luciana R C R B Souza, Flavia C R Garrido, Aurelio C Saraiva-Romanholo, Beatriz Mangueira Leick, Edna Aparecida Prado, Carla Máximo Martins, Mílton de Arruda Tibério, Iolanda de Fátima Lopes Calvo |
description | Chronic obstructive pulmonary disease (COPD) is an important health care issue, and IL-17 can modulate inflammatory responses. We evaluated preventive and therapeutic effect of anti-interleukin (IL)-17 in a model of lung injury induced by elastase, using 32 male C57Bl6 mice, divided into 4 groups: SAL, ELASTASE CONTROL (EC), ELASTASE + PREVENTIVE ANTI-IL-17 (EP), and ELASTASE + THERAPEUTIC ANTI-IL-17 (ET). On the 29th day, animals were anesthetized with thiopental, tracheotomized, and placed on a ventilator to evaluate lung mechanical, exhaled nitric oxide (eNO), and total cells of bronchoalveolar lavage fluid was collected. We performed histological techniques, and linear mean intercept (Lm) was analyzed. Both treatments with anti-IL-17 decreased respiratory resistance and elastance, airway resistance, elastance of pulmonary parenchyma, eNO, and Lm compared with EC. There was reduction in total cells and macrophages in ET compared with EC. Both treatments decreased nuclear factor-кB, inducible nitric oxide synthase, matrix metalloproteinase (MMP)-9, MMP-12, transforming growth factor-β, tumor necrosis factor-α, neutrophils, IL-1β, isoprostane, and IL-17 in airways and alveolar septa; collagen fibers, decorin and lumican in airways; and elastic fibers and fibronectin in alveolar septa compared with EC. There was reduction of collagen fibers in alveolar septa and biglycan in airways in EP and a reduction of eNO synthase in airways in ET. In conclusion, both treatments with anti-IL-17 contributed to improve most of parameters evaluated in inflammation and extracellular matrix remodeling in this model of lung injury. |
doi_str_mv | 10.1152/ajpcell.00017.2020 |
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We evaluated preventive and therapeutic effect of anti-interleukin (IL)-17 in a model of lung injury induced by elastase, using 32 male C57Bl6 mice, divided into 4 groups: SAL, ELASTASE CONTROL (EC), ELASTASE + PREVENTIVE ANTI-IL-17 (EP), and ELASTASE + THERAPEUTIC ANTI-IL-17 (ET). On the 29th day, animals were anesthetized with thiopental, tracheotomized, and placed on a ventilator to evaluate lung mechanical, exhaled nitric oxide (eNO), and total cells of bronchoalveolar lavage fluid was collected. We performed histological techniques, and linear mean intercept (Lm) was analyzed. Both treatments with anti-IL-17 decreased respiratory resistance and elastance, airway resistance, elastance of pulmonary parenchyma, eNO, and Lm compared with EC. There was reduction in total cells and macrophages in ET compared with EC. Both treatments decreased nuclear factor-кB, inducible nitric oxide synthase, matrix metalloproteinase (MMP)-9, MMP-12, transforming growth factor-β, tumor necrosis factor-α, neutrophils, IL-1β, isoprostane, and IL-17 in airways and alveolar septa; collagen fibers, decorin and lumican in airways; and elastic fibers and fibronectin in alveolar septa compared with EC. There was reduction of collagen fibers in alveolar septa and biglycan in airways in EP and a reduction of eNO synthase in airways in ET. In conclusion, both treatments with anti-IL-17 contributed to improve most of parameters evaluated in inflammation and extracellular matrix remodeling in this model of lung injury.</description><identifier>ISSN: 0363-6143</identifier><identifier>EISSN: 1522-1563</identifier><identifier>DOI: 10.1152/ajpcell.00017.2020</identifier><identifier>PMID: 33326311</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Bronchoalveolar Lavage Fluid ; Disease Models, Animal ; Inflammation - metabolism ; Interleukin-17 - metabolism ; Lung - metabolism ; Lung Injury - metabolism ; Macrophages - metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Neutrophils - metabolism ; Nitric Oxide Synthase Type II - metabolism ; Pancreatic Elastase - metabolism ; Pulmonary Disease, Chronic Obstructive - metabolism</subject><ispartof>American Journal of Physiology: Cell Physiology, 2021-03, Vol.320 (3), p.C341-C354</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c303t-4a1a4351f314c00f67cf98c3e7e15d76abb034f6a41b3a98ce211fbebac3e1583</citedby><cites>FETCH-LOGICAL-c303t-4a1a4351f314c00f67cf98c3e7e15d76abb034f6a41b3a98ce211fbebac3e1583</cites><orcidid>0000-0003-1300-0512</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33326311$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fukuzaki, Silvia</creatorcontrib><creatorcontrib>Righetti, Renato Fraga</creatorcontrib><creatorcontrib>Santos, Tabata Maruyama Dos</creatorcontrib><creatorcontrib>Camargo, Leandro do Nascimento</creatorcontrib><creatorcontrib>Aristóteles, Luciana R C R B</creatorcontrib><creatorcontrib>Souza, Flavia C R</creatorcontrib><creatorcontrib>Garrido, Aurelio C</creatorcontrib><creatorcontrib>Saraiva-Romanholo, Beatriz Mangueira</creatorcontrib><creatorcontrib>Leick, Edna Aparecida</creatorcontrib><creatorcontrib>Prado, Carla Máximo</creatorcontrib><creatorcontrib>Martins, Mílton de Arruda</creatorcontrib><creatorcontrib>Tibério, Iolanda de Fátima Lopes Calvo</creatorcontrib><title>Preventive and therapeutic effect of anti-IL-17 in an experimental model of elastase-induced lung injury in C57Bl6 mice</title><title>American Journal of Physiology: Cell Physiology</title><addtitle>Am J Physiol Cell Physiol</addtitle><description>Chronic obstructive pulmonary disease (COPD) is an important health care issue, and IL-17 can modulate inflammatory responses. We evaluated preventive and therapeutic effect of anti-interleukin (IL)-17 in a model of lung injury induced by elastase, using 32 male C57Bl6 mice, divided into 4 groups: SAL, ELASTASE CONTROL (EC), ELASTASE + PREVENTIVE ANTI-IL-17 (EP), and ELASTASE + THERAPEUTIC ANTI-IL-17 (ET). On the 29th day, animals were anesthetized with thiopental, tracheotomized, and placed on a ventilator to evaluate lung mechanical, exhaled nitric oxide (eNO), and total cells of bronchoalveolar lavage fluid was collected. We performed histological techniques, and linear mean intercept (Lm) was analyzed. Both treatments with anti-IL-17 decreased respiratory resistance and elastance, airway resistance, elastance of pulmonary parenchyma, eNO, and Lm compared with EC. There was reduction in total cells and macrophages in ET compared with EC. Both treatments decreased nuclear factor-кB, inducible nitric oxide synthase, matrix metalloproteinase (MMP)-9, MMP-12, transforming growth factor-β, tumor necrosis factor-α, neutrophils, IL-1β, isoprostane, and IL-17 in airways and alveolar septa; collagen fibers, decorin and lumican in airways; and elastic fibers and fibronectin in alveolar septa compared with EC. There was reduction of collagen fibers in alveolar septa and biglycan in airways in EP and a reduction of eNO synthase in airways in ET. In conclusion, both treatments with anti-IL-17 contributed to improve most of parameters evaluated in inflammation and extracellular matrix remodeling in this model of lung injury.</description><subject>Animals</subject><subject>Bronchoalveolar Lavage Fluid</subject><subject>Disease Models, Animal</subject><subject>Inflammation - metabolism</subject><subject>Interleukin-17 - metabolism</subject><subject>Lung - metabolism</subject><subject>Lung Injury - metabolism</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Neutrophils - metabolism</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Pancreatic Elastase - metabolism</subject><subject>Pulmonary Disease, Chronic Obstructive - metabolism</subject><issn>0363-6143</issn><issn>1522-1563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMtOwzAQRS0EgvL4ARbISzYpHo9jt0uoeEmVYAHryHHGkCov4oTH3-NAYTUa3XNHmsPYKYg5QCov7KZzVFVzIQSYuRRS7LBZDGQCqcZdNhOoMdGg8IAdhrCJnJJ6uc8OEFFqBJixj8ee3qkZynfitin48Eq97WgcSsfJe3IDb31MhjK5XydgeNnEjdNnR31Zx6KteN0WVE0YVTYMNlBSNsXoqODV2LzExmbsv6biKjVXleZ16eiY7XlbBTrZziP2fHP9tLpL1g-396vLdeJQ4JAoC1ZhCh5BOSG8Ns4vFw7JEKSF0TbPBSqvrYIcbUxIAvicchsZSBd4xM5_73Z9-zZSGLK6DJM121A7hkwqIxZLo4yJqPxFXd-G0JPPuvii7b8yENkkPNsKz36EZ5PwWDrb3h_zmor_yp9h_AZV5H3V</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Fukuzaki, Silvia</creator><creator>Righetti, Renato Fraga</creator><creator>Santos, Tabata Maruyama Dos</creator><creator>Camargo, Leandro do Nascimento</creator><creator>Aristóteles, Luciana R C R B</creator><creator>Souza, Flavia C R</creator><creator>Garrido, Aurelio C</creator><creator>Saraiva-Romanholo, Beatriz Mangueira</creator><creator>Leick, Edna Aparecida</creator><creator>Prado, Carla Máximo</creator><creator>Martins, Mílton de Arruda</creator><creator>Tibério, Iolanda de Fátima Lopes Calvo</creator><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><orcidid>https://orcid.org/0000-0003-1300-0512</orcidid></search><sort><creationdate>20210301</creationdate><title>Preventive and therapeutic effect of anti-IL-17 in an experimental model of elastase-induced lung injury in C57Bl6 mice</title><author>Fukuzaki, Silvia ; Righetti, Renato Fraga ; Santos, Tabata Maruyama Dos ; Camargo, Leandro do Nascimento ; Aristóteles, Luciana R C R B ; Souza, Flavia C R ; Garrido, Aurelio C ; Saraiva-Romanholo, Beatriz Mangueira ; Leick, Edna Aparecida ; Prado, Carla Máximo ; Martins, Mílton de Arruda ; Tibério, Iolanda de Fátima Lopes Calvo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c303t-4a1a4351f314c00f67cf98c3e7e15d76abb034f6a41b3a98ce211fbebac3e1583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Bronchoalveolar Lavage Fluid</topic><topic>Disease Models, Animal</topic><topic>Inflammation - metabolism</topic><topic>Interleukin-17 - metabolism</topic><topic>Lung - metabolism</topic><topic>Lung Injury - metabolism</topic><topic>Macrophages - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Neutrophils - metabolism</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>Pancreatic Elastase - metabolism</topic><topic>Pulmonary Disease, Chronic Obstructive - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fukuzaki, Silvia</creatorcontrib><creatorcontrib>Righetti, Renato Fraga</creatorcontrib><creatorcontrib>Santos, Tabata Maruyama Dos</creatorcontrib><creatorcontrib>Camargo, Leandro do Nascimento</creatorcontrib><creatorcontrib>Aristóteles, Luciana R C R B</creatorcontrib><creatorcontrib>Souza, Flavia C R</creatorcontrib><creatorcontrib>Garrido, Aurelio C</creatorcontrib><creatorcontrib>Saraiva-Romanholo, Beatriz Mangueira</creatorcontrib><creatorcontrib>Leick, Edna Aparecida</creatorcontrib><creatorcontrib>Prado, Carla Máximo</creatorcontrib><creatorcontrib>Martins, Mílton de Arruda</creatorcontrib><creatorcontrib>Tibério, Iolanda de Fátima Lopes Calvo</creatorcontrib><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 Physiology: Cell Physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fukuzaki, Silvia</au><au>Righetti, Renato Fraga</au><au>Santos, Tabata Maruyama Dos</au><au>Camargo, Leandro do Nascimento</au><au>Aristóteles, Luciana R C R B</au><au>Souza, Flavia C R</au><au>Garrido, Aurelio C</au><au>Saraiva-Romanholo, Beatriz Mangueira</au><au>Leick, Edna Aparecida</au><au>Prado, Carla Máximo</au><au>Martins, Mílton de Arruda</au><au>Tibério, Iolanda de Fátima Lopes Calvo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preventive and therapeutic effect of anti-IL-17 in an experimental model of elastase-induced lung injury in C57Bl6 mice</atitle><jtitle>American Journal of Physiology: Cell Physiology</jtitle><addtitle>Am J Physiol Cell Physiol</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>320</volume><issue>3</issue><spage>C341</spage><epage>C354</epage><pages>C341-C354</pages><issn>0363-6143</issn><eissn>1522-1563</eissn><abstract>Chronic obstructive pulmonary disease (COPD) is an important health care issue, and IL-17 can modulate inflammatory responses. We evaluated preventive and therapeutic effect of anti-interleukin (IL)-17 in a model of lung injury induced by elastase, using 32 male C57Bl6 mice, divided into 4 groups: SAL, ELASTASE CONTROL (EC), ELASTASE + PREVENTIVE ANTI-IL-17 (EP), and ELASTASE + THERAPEUTIC ANTI-IL-17 (ET). On the 29th day, animals were anesthetized with thiopental, tracheotomized, and placed on a ventilator to evaluate lung mechanical, exhaled nitric oxide (eNO), and total cells of bronchoalveolar lavage fluid was collected. We performed histological techniques, and linear mean intercept (Lm) was analyzed. Both treatments with anti-IL-17 decreased respiratory resistance and elastance, airway resistance, elastance of pulmonary parenchyma, eNO, and Lm compared with EC. There was reduction in total cells and macrophages in ET compared with EC. Both treatments decreased nuclear factor-кB, inducible nitric oxide synthase, matrix metalloproteinase (MMP)-9, MMP-12, transforming growth factor-β, tumor necrosis factor-α, neutrophils, IL-1β, isoprostane, and IL-17 in airways and alveolar septa; collagen fibers, decorin and lumican in airways; and elastic fibers and fibronectin in alveolar septa compared with EC. There was reduction of collagen fibers in alveolar septa and biglycan in airways in EP and a reduction of eNO synthase in airways in ET. In conclusion, both treatments with anti-IL-17 contributed to improve most of parameters evaluated in inflammation and extracellular matrix remodeling in this model of lung injury.</abstract><cop>United States</cop><pmid>33326311</pmid><doi>10.1152/ajpcell.00017.2020</doi><orcidid>https://orcid.org/0000-0003-1300-0512</orcidid></addata></record> |
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subjects | Animals Bronchoalveolar Lavage Fluid Disease Models, Animal Inflammation - metabolism Interleukin-17 - metabolism Lung - metabolism Lung Injury - metabolism Macrophages - metabolism Male Mice Mice, Inbred C57BL Neutrophils - metabolism Nitric Oxide Synthase Type II - metabolism Pancreatic Elastase - metabolism Pulmonary Disease, Chronic Obstructive - metabolism |
title | Preventive and therapeutic effect of anti-IL-17 in an experimental model of elastase-induced lung injury in C57Bl6 mice |
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