Adhesion Molecules in Lung Inflammation from Repeated Glyphosate Exposures
Glyphosate is an active ingredient in herbicides. Exposure to glyphosate-based herbicides has been associated with respiratory dysfunctions in agricultural workers. The ability of inhaled glyphosate to induce lung inflammation is not well understood. Further, the role of adhesion molecules in glypho...
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description | Glyphosate is an active ingredient in herbicides. Exposure to glyphosate-based herbicides has been associated with respiratory dysfunctions in agricultural workers. The ability of inhaled glyphosate to induce lung inflammation is not well understood. Further, the role of adhesion molecules in glyphosate-induced lung inflammation has not been studied. We evaluated lung inflammatory responses from single and repeated glyphosate exposures. Male C57BL/6 mice were intranasally exposed to glyphosate (1 μg/40 μL) for 1 day or once daily for 5 days or 10 days. Lung tissue and bronchoalveolar lavage (BAL) fluid were collected and analyzed. Repeated exposure to glyphosate for 5 days and 10 days resulted in an increase in neutrophils in BAL fluid and higher eosinophil peroxidase levels in lungs, with leukocyte infiltration further confirmed through lung histology. Repetitive exposure to glyphosate increased IL-33 and Th2 cytokines IL-5 and IL-13. A single glyphosate treatment revealed expression for ICAM-1, VCAM-1, and vWF adhesion molecules in the perivascular region of lung sections; with repeated treatment (5 and 10 days), adhesion molecule expression was found in the perivascular, peribronchiolar, and alveolar regions of the lungs. Repetitive exposure to glyphosate induced cellular inflammation in which adhesion molecules may be important to the lung inflammatory process. |
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Exposure to glyphosate-based herbicides has been associated with respiratory dysfunctions in agricultural workers. The ability of inhaled glyphosate to induce lung inflammation is not well understood. Further, the role of adhesion molecules in glyphosate-induced lung inflammation has not been studied. We evaluated lung inflammatory responses from single and repeated glyphosate exposures. Male C57BL/6 mice were intranasally exposed to glyphosate (1 μg/40 μL) for 1 day or once daily for 5 days or 10 days. Lung tissue and bronchoalveolar lavage (BAL) fluid were collected and analyzed. Repeated exposure to glyphosate for 5 days and 10 days resulted in an increase in neutrophils in BAL fluid and higher eosinophil peroxidase levels in lungs, with leukocyte infiltration further confirmed through lung histology. Repetitive exposure to glyphosate increased IL-33 and Th2 cytokines IL-5 and IL-13. A single glyphosate treatment revealed expression for ICAM-1, VCAM-1, and vWF adhesion molecules in the perivascular region of lung sections; with repeated treatment (5 and 10 days), adhesion molecule expression was found in the perivascular, peribronchiolar, and alveolar regions of the lungs. Repetitive exposure to glyphosate induced cellular inflammation in which adhesion molecules may be important to the lung inflammatory process.</description><identifier>ISSN: 1660-4601</identifier><identifier>ISSN: 1661-7827</identifier><identifier>EISSN: 1660-4601</identifier><identifier>DOI: 10.3390/ijerph20085484</identifier><identifier>PMID: 37107767</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adhesion ; Agriculture ; Alveoli ; Analysis ; Animals ; Bronchoalveolar Lavage Fluid ; Bronchus ; Cell Adhesion Molecules ; Cytokines ; Exposure ; Farmworkers ; Glyphosate ; Herbicides ; Herbicides - metabolism ; Herbicides - toxicity ; Histology ; Inflammation ; Inflammation - metabolism ; Intercellular adhesion molecule 1 ; Intercellular Adhesion Molecule-1 - adverse effects ; Intercellular Adhesion Molecule-1 - metabolism ; Interleukin 13 ; Interleukin 5 ; Laboratory animals ; Lavage ; Leukocytes ; Leukocytes (eosinophilic) ; Leukocytes (neutrophilic) ; Lung - metabolism ; Lungs ; Lymphocytes T ; Male ; Mice ; Mice, Inbred C57BL ; Occupational exposure ; Peroxidase ; Pneumonia - chemically induced ; Pneumonia - metabolism ; Protocol ; Vascular cell adhesion molecule 1</subject><ispartof>International journal of environmental research and public health, 2023-04, Vol.20 (8), p.5484</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4014-49303e8be11a6b9cc2220810b539cc69c99119b5d14e0931346d402ee1d3c5023</citedby><cites>FETCH-LOGICAL-c4014-49303e8be11a6b9cc2220810b539cc69c99119b5d14e0931346d402ee1d3c5023</cites><orcidid>0000-0003-0416-8946 ; 0000-0002-0106-2540</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138447/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138447/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37107767$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pandher, Upkardeep</creatorcontrib><creatorcontrib>Kirychuk, Shelley</creatorcontrib><creatorcontrib>Schneberger, David</creatorcontrib><creatorcontrib>Thompson, Brooke</creatorcontrib><creatorcontrib>Aulakh, Gurpreet</creatorcontrib><creatorcontrib>Sethi, R S</creatorcontrib><creatorcontrib>Singh, Baljit</creatorcontrib><title>Adhesion Molecules in Lung Inflammation from Repeated Glyphosate Exposures</title><title>International journal of environmental research and public health</title><addtitle>Int J Environ Res Public Health</addtitle><description>Glyphosate is an active ingredient in herbicides. Exposure to glyphosate-based herbicides has been associated with respiratory dysfunctions in agricultural workers. The ability of inhaled glyphosate to induce lung inflammation is not well understood. Further, the role of adhesion molecules in glyphosate-induced lung inflammation has not been studied. We evaluated lung inflammatory responses from single and repeated glyphosate exposures. Male C57BL/6 mice were intranasally exposed to glyphosate (1 μg/40 μL) for 1 day or once daily for 5 days or 10 days. Lung tissue and bronchoalveolar lavage (BAL) fluid were collected and analyzed. Repeated exposure to glyphosate for 5 days and 10 days resulted in an increase in neutrophils in BAL fluid and higher eosinophil peroxidase levels in lungs, with leukocyte infiltration further confirmed through lung histology. Repetitive exposure to glyphosate increased IL-33 and Th2 cytokines IL-5 and IL-13. A single glyphosate treatment revealed expression for ICAM-1, VCAM-1, and vWF adhesion molecules in the perivascular region of lung sections; with repeated treatment (5 and 10 days), adhesion molecule expression was found in the perivascular, peribronchiolar, and alveolar regions of the lungs. Repetitive exposure to glyphosate induced cellular inflammation in which adhesion molecules may be important to the lung inflammatory process.</description><subject>Adhesion</subject><subject>Agriculture</subject><subject>Alveoli</subject><subject>Analysis</subject><subject>Animals</subject><subject>Bronchoalveolar Lavage Fluid</subject><subject>Bronchus</subject><subject>Cell Adhesion Molecules</subject><subject>Cytokines</subject><subject>Exposure</subject><subject>Farmworkers</subject><subject>Glyphosate</subject><subject>Herbicides</subject><subject>Herbicides - metabolism</subject><subject>Herbicides - toxicity</subject><subject>Histology</subject><subject>Inflammation</subject><subject>Inflammation - metabolism</subject><subject>Intercellular adhesion molecule 1</subject><subject>Intercellular Adhesion Molecule-1 - adverse effects</subject><subject>Intercellular Adhesion Molecule-1 - metabolism</subject><subject>Interleukin 13</subject><subject>Interleukin 5</subject><subject>Laboratory animals</subject><subject>Lavage</subject><subject>Leukocytes</subject><subject>Leukocytes (eosinophilic)</subject><subject>Leukocytes (neutrophilic)</subject><subject>Lung - metabolism</subject><subject>Lungs</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Occupational exposure</subject><subject>Peroxidase</subject><subject>Pneumonia - chemically induced</subject><subject>Pneumonia - metabolism</subject><subject>Protocol</subject><subject>Vascular cell adhesion molecule 1</subject><issn>1660-4601</issn><issn>1661-7827</issn><issn>1660-4601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkU1vFDEMhiMEol9cOaKRuHDZYk8yHzmhVVXaoq0qIXqOMhnPblaZZEh2KvrvyYpSWlTlEDt-_Eb2y9h7hFPOJXy2W4rTpgRoK9GKV-wQ6xoWogZ8_SQ-YEcpbQF4K2r5lh3wBqFp6uaQfVv2G0o2-OI6ODKzo1RYX6xmvy6u_OD0OOrdvjzEMBbfaSK9o764cPfTJqQcF-e_ppDmSOmEvRm0S_Tu4T5mt1_Pf5xdLlY3F1dny9XCCECxEJIDp7YjRF130piyLKFF6Cqek1oaKRFlV_UoCCRHLupeQEmEPTcVlPyYffmjO83dSL0hv4vaqSnaUcd7FbRVzyvebtQ63CkEzAsQTVb49KAQw8-Z0k6NNhlyTnsKc1JlC43ECgVm9ON_6DbM0ef59lRdlbxt2n_UWjtS1g8hf2z2omrZVCgxjwiZOn2Byqen0ZrgabD5_aUGE0NKkYbHIRHU3n713P7c8OHpah7xv37z3-QSqa8</recordid><startdate>20230412</startdate><enddate>20230412</enddate><creator>Pandher, Upkardeep</creator><creator>Kirychuk, Shelley</creator><creator>Schneberger, David</creator><creator>Thompson, Brooke</creator><creator>Aulakh, Gurpreet</creator><creator>Sethi, R S</creator><creator>Singh, Baljit</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0416-8946</orcidid><orcidid>https://orcid.org/0000-0002-0106-2540</orcidid></search><sort><creationdate>20230412</creationdate><title>Adhesion Molecules in Lung Inflammation from Repeated Glyphosate Exposures</title><author>Pandher, Upkardeep ; 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Exposure to glyphosate-based herbicides has been associated with respiratory dysfunctions in agricultural workers. The ability of inhaled glyphosate to induce lung inflammation is not well understood. Further, the role of adhesion molecules in glyphosate-induced lung inflammation has not been studied. We evaluated lung inflammatory responses from single and repeated glyphosate exposures. Male C57BL/6 mice were intranasally exposed to glyphosate (1 μg/40 μL) for 1 day or once daily for 5 days or 10 days. Lung tissue and bronchoalveolar lavage (BAL) fluid were collected and analyzed. Repeated exposure to glyphosate for 5 days and 10 days resulted in an increase in neutrophils in BAL fluid and higher eosinophil peroxidase levels in lungs, with leukocyte infiltration further confirmed through lung histology. Repetitive exposure to glyphosate increased IL-33 and Th2 cytokines IL-5 and IL-13. A single glyphosate treatment revealed expression for ICAM-1, VCAM-1, and vWF adhesion molecules in the perivascular region of lung sections; with repeated treatment (5 and 10 days), adhesion molecule expression was found in the perivascular, peribronchiolar, and alveolar regions of the lungs. Repetitive exposure to glyphosate induced cellular inflammation in which adhesion molecules may be important to the lung inflammatory process.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37107767</pmid><doi>10.3390/ijerph20085484</doi><orcidid>https://orcid.org/0000-0003-0416-8946</orcidid><orcidid>https://orcid.org/0000-0002-0106-2540</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adhesion Agriculture Alveoli Analysis Animals Bronchoalveolar Lavage Fluid Bronchus Cell Adhesion Molecules Cytokines Exposure Farmworkers Glyphosate Herbicides Herbicides - metabolism Herbicides - toxicity Histology Inflammation Inflammation - metabolism Intercellular adhesion molecule 1 Intercellular Adhesion Molecule-1 - adverse effects Intercellular Adhesion Molecule-1 - metabolism Interleukin 13 Interleukin 5 Laboratory animals Lavage Leukocytes Leukocytes (eosinophilic) Leukocytes (neutrophilic) Lung - metabolism Lungs Lymphocytes T Male Mice Mice, Inbred C57BL Occupational exposure Peroxidase Pneumonia - chemically induced Pneumonia - metabolism Protocol Vascular cell adhesion molecule 1 |
title | Adhesion Molecules in Lung Inflammation from Repeated Glyphosate Exposures |
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