The administration of surfactant decreased oxidative stress in lungs of mice exposed to cigarette smoke
The alveolar surfactant, which composition consists of a unique and complex mixture of lipids and proteins, has immunomodulatory action. This study aimed to evaluate the effects of exogenous surfactant on pulmonary inflammatory response in mice exposed to cigarette smoke (CS). Twenty-four mice C57BL...
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creator | Machado, Dafne Fernandes Campos, Keila Karine Duarte da Silva, Natália Pereira de Oliveira Ramos, Camila Cangussú, Sílvia Dantas de Paula Costa, Guilherme Talvani, André Bezerra, Frank Silva |
description | The alveolar surfactant, which composition consists of a unique and complex mixture of lipids and proteins, has immunomodulatory action. This study aimed to evaluate the effects of exogenous surfactant on pulmonary inflammatory response in mice exposed to cigarette smoke (CS). Twenty-four mice C57BL/6 were divided into four groups: control group exposed to ambient air (CG); surfactant treated group (SG); CS exposed group (CSG) and CS exposed group treated with surfactant (CSSG). For five days, CSG and CSSG were exposed to 12 commercial cigarettes/day and SG and CSSG received the surfactant by intranasal instillation. At the end of the experiment, the animals were euthanatized for the collection of bronchoalveolar lavage fluid (BALF) and lungs. The total number of leukocytes in BALF increased in CSG compared to CG, however, there was a decrease in CSSG compared to CSG. There was an increase in lipid peroxidation in SG and CSG compared to CG while there was a decrease in CSSG compared to CSG. Regarding the antioxidant enzymes, the catalase (CAT) activity increased in all groups compared to CG and the superoxide dismutase (SOD) activity decreased in CSG compared to the CG and SG. There was an increase in TNF in SG, CSG and CSSG compared to CG. There was an increase in IL-17 in CSSG compared to CG. There was an increase in CCL5 in SG and CSSG compared to CG. Therefore, our results demonstrated that the administration of exogenous surfactant was able to decrease the oxidative processes in the lungs of mice induced by short-term exposure to CS.
•Short-term exposure to cigarette smoke causes oxidative damage;•The exogenous surfactant decreased the influx of leukocytes in BALF in a mouse model of cigarette-smoke;•Exogenous surfactant administration has not been shown to be able to reduce the inflammatory mediators;•Our results showed that administration of exogenous surfactant was able to reestablish SOD activity. |
doi_str_mv | 10.1016/j.intimp.2017.11.023 |
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•Short-term exposure to cigarette smoke causes oxidative damage;•The exogenous surfactant decreased the influx of leukocytes in BALF in a mouse model of cigarette-smoke;•Exogenous surfactant administration has not been shown to be able to reduce the inflammatory mediators;•Our results showed that administration of exogenous surfactant was able to reestablish SOD activity.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2017.11.023</identifier><identifier>PMID: 29174925</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Alveoli ; Animals ; Anti-oxidant ; Antioxidants ; Bronchoalveolar Lavage Fluid - immunology ; Bronchus ; Catalase ; Catalase - metabolism ; Cigarette smoke ; Cigarette Smoking - adverse effects ; Cigarettes ; Exogeneous surfactant ; Exposure ; Immunomodulation ; Inflammation ; Inflammatory response ; Interleukin 17 ; Interleukin-17 - metabolism ; Leukocytes ; Leukocytes - immunology ; Lipid Peroxidation ; Lipids ; Lung - metabolism ; Lung - pathology ; Lung inflammation ; Lungs ; Male ; Mice ; Mice, Inbred C57BL ; Oxidative Stress ; Peroxidation ; Proteins ; Pulmonary Surfactants - administration & dosage ; Redox imbalance ; Smoke ; Smoking ; Superoxide dismutase ; Superoxide Dismutase - metabolism ; Surfactants ; Tobacco smoke ; Tumor necrosis factor ; Tumor Necrosis Factor-alpha - metabolism</subject><ispartof>International immunopharmacology, 2018-01, Vol.54, p.275-279</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Jan 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-1cba1f1bbe6b001593b6333bd343e73c629de9add35f6722531003cb551d3d583</citedby><cites>FETCH-LOGICAL-c436t-1cba1f1bbe6b001593b6333bd343e73c629de9add35f6722531003cb551d3d583</cites><orcidid>0000-0002-0804-5196</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.intimp.2017.11.023$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29174925$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Machado, Dafne Fernandes</creatorcontrib><creatorcontrib>Campos, Keila Karine Duarte</creatorcontrib><creatorcontrib>da Silva, Natália Pereira</creatorcontrib><creatorcontrib>de Oliveira Ramos, Camila</creatorcontrib><creatorcontrib>Cangussú, Sílvia Dantas</creatorcontrib><creatorcontrib>de Paula Costa, Guilherme</creatorcontrib><creatorcontrib>Talvani, André</creatorcontrib><creatorcontrib>Bezerra, Frank Silva</creatorcontrib><title>The administration of surfactant decreased oxidative stress in lungs of mice exposed to cigarette smoke</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>The alveolar surfactant, which composition consists of a unique and complex mixture of lipids and proteins, has immunomodulatory action. This study aimed to evaluate the effects of exogenous surfactant on pulmonary inflammatory response in mice exposed to cigarette smoke (CS). Twenty-four mice C57BL/6 were divided into four groups: control group exposed to ambient air (CG); surfactant treated group (SG); CS exposed group (CSG) and CS exposed group treated with surfactant (CSSG). For five days, CSG and CSSG were exposed to 12 commercial cigarettes/day and SG and CSSG received the surfactant by intranasal instillation. At the end of the experiment, the animals were euthanatized for the collection of bronchoalveolar lavage fluid (BALF) and lungs. The total number of leukocytes in BALF increased in CSG compared to CG, however, there was a decrease in CSSG compared to CSG. There was an increase in lipid peroxidation in SG and CSG compared to CG while there was a decrease in CSSG compared to CSG. Regarding the antioxidant enzymes, the catalase (CAT) activity increased in all groups compared to CG and the superoxide dismutase (SOD) activity decreased in CSG compared to the CG and SG. There was an increase in TNF in SG, CSG and CSSG compared to CG. There was an increase in IL-17 in CSSG compared to CG. There was an increase in CCL5 in SG and CSSG compared to CG. Therefore, our results demonstrated that the administration of exogenous surfactant was able to decrease the oxidative processes in the lungs of mice induced by short-term exposure to CS.
•Short-term exposure to cigarette smoke causes oxidative damage;•The exogenous surfactant decreased the influx of leukocytes in BALF in a mouse model of cigarette-smoke;•Exogenous surfactant administration has not been shown to be able to reduce the inflammatory mediators;•Our results showed that administration of exogenous surfactant was able to reestablish SOD activity.</description><subject>Alveoli</subject><subject>Animals</subject><subject>Anti-oxidant</subject><subject>Antioxidants</subject><subject>Bronchoalveolar Lavage Fluid - immunology</subject><subject>Bronchus</subject><subject>Catalase</subject><subject>Catalase - metabolism</subject><subject>Cigarette smoke</subject><subject>Cigarette Smoking - adverse effects</subject><subject>Cigarettes</subject><subject>Exogeneous surfactant</subject><subject>Exposure</subject><subject>Immunomodulation</subject><subject>Inflammation</subject><subject>Inflammatory response</subject><subject>Interleukin 17</subject><subject>Interleukin-17 - metabolism</subject><subject>Leukocytes</subject><subject>Leukocytes - immunology</subject><subject>Lipid Peroxidation</subject><subject>Lipids</subject><subject>Lung - metabolism</subject><subject>Lung - pathology</subject><subject>Lung inflammation</subject><subject>Lungs</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Oxidative Stress</subject><subject>Peroxidation</subject><subject>Proteins</subject><subject>Pulmonary Surfactants - administration & dosage</subject><subject>Redox imbalance</subject><subject>Smoke</subject><subject>Smoking</subject><subject>Superoxide dismutase</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Surfactants</subject><subject>Tobacco smoke</subject><subject>Tumor necrosis factor</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90U2PFCEQBmBiNO66-g-MIfHipVsKGmguJmbjV7KJl_VMaKgeGaebEejN-u9lMqsHD56ow1NFpV5CXgLrgYF6u-_jWuNy7DkD3QP0jItH5BJGPXagmXzcaql0J7UyF-RZKXvWIBvgKbngBvRguLwku9vvSF1Y4hpLza7GtNI007Ll2fnq1koD-oyuYKDpPoYm7pA2iqXQuNLDtu7KqWOJHineH9NJ1kR93LmMtTa8pB_4nDyZ3aHgi4f3inz7-OH2-nN38_XTl-v3N50fhKod-MnBDNOEamrrSiMmJYSYghgEauEVNwGNC0HIWWnOpQDGhJ-khCCCHMUVeXOee8zp54al2iUWj4eDWzFtxYJRxnBtRtbo63_oPm15bdtZzgbFhBqZamo4K59TKRlne8xxcfmXBWZPQdi9PQdhT0FYANuCaG2vHoZv04Lhb9Ofyzfw7gywXeMuYrbFR1w9hpjRVxtS_P8PvwHacZwP</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Machado, Dafne Fernandes</creator><creator>Campos, Keila Karine Duarte</creator><creator>da Silva, Natália Pereira</creator><creator>de Oliveira Ramos, Camila</creator><creator>Cangussú, Sílvia Dantas</creator><creator>de Paula Costa, Guilherme</creator><creator>Talvani, André</creator><creator>Bezerra, Frank Silva</creator><general>Elsevier B.V</general><general>Elsevier BV</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>7QO</scope><scope>7T5</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0804-5196</orcidid></search><sort><creationdate>201801</creationdate><title>The administration of surfactant decreased oxidative stress in lungs of mice exposed to cigarette smoke</title><author>Machado, Dafne Fernandes ; Campos, Keila Karine Duarte ; da Silva, Natália Pereira ; de Oliveira Ramos, Camila ; Cangussú, Sílvia Dantas ; de Paula Costa, Guilherme ; Talvani, André ; Bezerra, Frank Silva</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-1cba1f1bbe6b001593b6333bd343e73c629de9add35f6722531003cb551d3d583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Alveoli</topic><topic>Animals</topic><topic>Anti-oxidant</topic><topic>Antioxidants</topic><topic>Bronchoalveolar Lavage Fluid - immunology</topic><topic>Bronchus</topic><topic>Catalase</topic><topic>Catalase - metabolism</topic><topic>Cigarette smoke</topic><topic>Cigarette Smoking - adverse effects</topic><topic>Cigarettes</topic><topic>Exogeneous surfactant</topic><topic>Exposure</topic><topic>Immunomodulation</topic><topic>Inflammation</topic><topic>Inflammatory response</topic><topic>Interleukin 17</topic><topic>Interleukin-17 - metabolism</topic><topic>Leukocytes</topic><topic>Leukocytes - immunology</topic><topic>Lipid Peroxidation</topic><topic>Lipids</topic><topic>Lung - metabolism</topic><topic>Lung - pathology</topic><topic>Lung inflammation</topic><topic>Lungs</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Oxidative Stress</topic><topic>Peroxidation</topic><topic>Proteins</topic><topic>Pulmonary Surfactants - administration & dosage</topic><topic>Redox imbalance</topic><topic>Smoke</topic><topic>Smoking</topic><topic>Superoxide dismutase</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Surfactants</topic><topic>Tobacco smoke</topic><topic>Tumor necrosis factor</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Machado, Dafne Fernandes</creatorcontrib><creatorcontrib>Campos, Keila Karine Duarte</creatorcontrib><creatorcontrib>da Silva, Natália Pereira</creatorcontrib><creatorcontrib>de Oliveira Ramos, Camila</creatorcontrib><creatorcontrib>Cangussú, Sílvia Dantas</creatorcontrib><creatorcontrib>de Paula Costa, Guilherme</creatorcontrib><creatorcontrib>Talvani, André</creatorcontrib><creatorcontrib>Bezerra, Frank Silva</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Machado, Dafne Fernandes</au><au>Campos, Keila Karine Duarte</au><au>da Silva, Natália Pereira</au><au>de Oliveira Ramos, Camila</au><au>Cangussú, Sílvia Dantas</au><au>de Paula Costa, Guilherme</au><au>Talvani, André</au><au>Bezerra, Frank Silva</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The administration of surfactant decreased oxidative stress in lungs of mice exposed to cigarette smoke</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2018-01</date><risdate>2018</risdate><volume>54</volume><spage>275</spage><epage>279</epage><pages>275-279</pages><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>The alveolar surfactant, which composition consists of a unique and complex mixture of lipids and proteins, has immunomodulatory action. This study aimed to evaluate the effects of exogenous surfactant on pulmonary inflammatory response in mice exposed to cigarette smoke (CS). Twenty-four mice C57BL/6 were divided into four groups: control group exposed to ambient air (CG); surfactant treated group (SG); CS exposed group (CSG) and CS exposed group treated with surfactant (CSSG). For five days, CSG and CSSG were exposed to 12 commercial cigarettes/day and SG and CSSG received the surfactant by intranasal instillation. At the end of the experiment, the animals were euthanatized for the collection of bronchoalveolar lavage fluid (BALF) and lungs. The total number of leukocytes in BALF increased in CSG compared to CG, however, there was a decrease in CSSG compared to CSG. There was an increase in lipid peroxidation in SG and CSG compared to CG while there was a decrease in CSSG compared to CSG. Regarding the antioxidant enzymes, the catalase (CAT) activity increased in all groups compared to CG and the superoxide dismutase (SOD) activity decreased in CSG compared to the CG and SG. There was an increase in TNF in SG, CSG and CSSG compared to CG. There was an increase in IL-17 in CSSG compared to CG. There was an increase in CCL5 in SG and CSSG compared to CG. Therefore, our results demonstrated that the administration of exogenous surfactant was able to decrease the oxidative processes in the lungs of mice induced by short-term exposure to CS.
•Short-term exposure to cigarette smoke causes oxidative damage;•The exogenous surfactant decreased the influx of leukocytes in BALF in a mouse model of cigarette-smoke;•Exogenous surfactant administration has not been shown to be able to reduce the inflammatory mediators;•Our results showed that administration of exogenous surfactant was able to reestablish SOD activity.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29174925</pmid><doi>10.1016/j.intimp.2017.11.023</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-0804-5196</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alveoli Animals Anti-oxidant Antioxidants Bronchoalveolar Lavage Fluid - immunology Bronchus Catalase Catalase - metabolism Cigarette smoke Cigarette Smoking - adverse effects Cigarettes Exogeneous surfactant Exposure Immunomodulation Inflammation Inflammatory response Interleukin 17 Interleukin-17 - metabolism Leukocytes Leukocytes - immunology Lipid Peroxidation Lipids Lung - metabolism Lung - pathology Lung inflammation Lungs Male Mice Mice, Inbred C57BL Oxidative Stress Peroxidation Proteins Pulmonary Surfactants - administration & dosage Redox imbalance Smoke Smoking Superoxide dismutase Superoxide Dismutase - metabolism Surfactants Tobacco smoke Tumor necrosis factor Tumor Necrosis Factor-alpha - metabolism |
title | The administration of surfactant decreased oxidative stress in lungs of mice exposed to cigarette smoke |
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