{"id":{"repo_id":"vt","oai_identifier":"oai:vtechworks.lib.vt.edu:10919/72984"},"canonical_url":"https://search.dev.ndltd.org/etd/vt/oai:vtechworks.lib.vt.edu:10919/72984","repository":{"repo_id":"vt","name":"Virginia Tech","base_url":"https://vtechworks.lib.vt.edu/oai/request"},"display":{"title":"Response of Peripheral Blood Lymphocytes from RAO-affected Horses to b2-Agonist Stimulation","abstract":"Recurrent airway obstruction (RAO) affects middle-age horses, inducing bronchoconstriction and airway inflammation. Î²2-agonists like salbutamol are used as treatment, promoting airway smooth muscle (ASM) relaxation and bronchodilation. In addition to ASM, inflammatory cells express the Î²2-adrenoreceptors (Î²2-AR). In other species, Î²2-agonists promote peripheral blood lymphocyte (PBL) cytokine expression towards a pro-inflammatory phenotype. RAO horses are a good model for evaluating chronic changes in human asthma. However, little is known about the effect of Î²2-agonist stimulation on equine PBL inflammatory response. The aims of this study were to develop an indirect method to evaluate the response of equine PBLs to Î²2-agonist stimulation, and to compare it between cells from RAO and non-affected horses. Isolated PBLs were activated with ConA and stimulated with salbutamol. Response to agonist binding was indirectly determined using flow cytometric methodology and verified by Western blot. Activated PBLs from RAO horses demonstrated a significant response to Î²2-agonist binding whereas cells from non-affected horses did not. Response of PBLs from RAO horses was attenuated when pre-treated with a Î²2-antagonist but unaffected following pre-treatment with a Î²1-antagonist, indicating that the response of PBLs from these horses to salbutamol binding was mainly through the Î²2-AR. Preliminary investigation of bronchoalveolar lavage (BAL) lymphocytes from RAO horses demonstrated that they also responded to Î²2-agonist binding, while cells from non-affected horses did not. These findings represent a novel tool for further investigation of the role of Î²2-agonist binding in diseases like asthma and RAO, and support the use of this model for future studies.","abstract_html":"Recurrent airway obstruction (RAO) affects middle-age horses, inducing bronchoconstriction and airway inflammation. Î²2-agonists like salbutamol are used as treatment, promoting airway smooth muscle (ASM) relaxation and bronchodilation. In addition to ASM, inflammatory cells express the Î²2-adrenoreceptors (Î²2-AR). In other species, Î²2-agonists promote peripheral blood lymphocyte (PBL) cytokine expression towards a pro-inflammatory phenotype. RAO horses are a good model for evaluating chronic changes in human asthma. However, little is known about the effect of Î²2-agonist stimulation on equine PBL inflammatory response. The aims of this study were to develop an indirect method to evaluate the response of equine PBLs to Î²2-agonist stimulation, and to compare it between cells from RAO and non-affected horses. Isolated PBLs were activated with ConA and stimulated with salbutamol. Response to agonist binding was indirectly determined using flow cytometric methodology and verified by Western blot. Activated PBLs from RAO horses demonstrated a significant response to Î²2-agonist binding whereas cells from non-affected horses did not. Response of PBLs from RAO horses was attenuated when pre-treated with a Î²2-antagonist but unaffected following pre-treatment with a Î²1-antagonist, indicating that the response of PBLs from these horses to salbutamol binding was mainly through the Î²2-AR. Preliminary investigation of bronchoalveolar lavage (BAL) lymphocytes from RAO horses demonstrated that they also responded to Î²2-agonist binding, while cells from non-affected horses did not. These findings represent a novel tool for further investigation of the role of Î²2-agonist binding in diseases like asthma and RAO, and support the use of this model for future studies.","abstract_has_math":false,"creators":["Werner Becker, Marianne Patricia"],"institution":"Virginia Tech","degree_name":"Master of Science","degree_level":"masters","degree_discipline":"Biomedical and Veterinary Sciences","degree_department":"Biomedical and Veterinary Sciences","school":null,"contributors":[],"advisors":[],"committee_chairs":["Buechner-Maxwell, Virginia A."],"committee_members":["Ehrich, Marion F.","Eyre, Peter","Prater, Mary R."],"year":2011,"date_issued":"2011-05-03","date_published":"2011-05-03","updated_at":"2026-07-22T22:18:50Z","subjects":["Horses","VASP","b2-adrenoreceptors"],"languages":["en_US"],"rights":["In Copyright"],"rights_urls":["http://rightsstatements.org/vocab/InC/1.0/"],"identifier_entries":[{"key":"dc:identifier.other","label":"Dc Identifier Other","values":["etd-05162011-162639"],"render_values":[{"text":"etd-05162011-162639","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/10919/72984","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.committeechair","label":"Committee Chair","values":["Buechner-Maxwell, Virginia A."]},{"key":"dc:contributor.committeemember","label":"Committee Member","values":["Ehrich, Marion F.","Eyre, Peter","Prater, Mary R."]},{"key":"dc:contributor.department","label":"Department","values":["Biomedical and Veterinary Sciences"]},{"key":"dc:creator","label":"Author","values":["Werner Becker, Marianne Patricia"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2016-09-22T14:56:38Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2016-09-22T14:56:38Z","2015-04-22"]},{"key":"dc:date.issued","label":"Date","values":["2011-05-03"]},{"key":"dc:publisher","label":"Institution","values":["Virginia Tech"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.dcmitype","label":"Dc Type Dcmitype","values":["Text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biomedical and Veterinary Sciences"]},{"key":"thesis:degree_level","label":"Degree Level","values":["masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Virginia Polytechnic Institute and State University"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Horses","VASP","b2-adrenoreceptors"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en_US"]},{"key":"dc:rights","label":"Dc Rights","values":["In Copyright"]},{"key":"dc:rights.uri","label":"Rights URI","values":["http://rightsstatements.org/vocab/InC/1.0/"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.other","label":"Dc Identifier Other","values":["etd-05162011-162639"]},{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10919/72984"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Recurrent airway obstruction (RAO) affects middle-age horses, inducing bronchoconstriction and airway inflammation. Î²2-agonists like salbutamol are used as treatment, promoting airway smooth muscle (ASM) relaxation and bronchodilation. In addition to ASM, inflammatory cells express the Î²2-adrenoreceptors (Î²2-AR). In other species, Î²2-agonists promote peripheral blood lymphocyte (PBL) cytokine expression towards a pro-inflammatory phenotype. RAO horses are a good model for evaluating chronic changes in human asthma. However, little is known about the effect of Î²2-agonist stimulation on equine PBL inflammatory response. The aims of this study were to develop an indirect method to evaluate the response of equine PBLs to Î²2-agonist stimulation, and to compare it between cells from RAO and non-affected horses. Isolated PBLs were activated with ConA and stimulated with salbutamol. Response to agonist binding was indirectly determined using flow cytometric methodology and verified by Western blot. Activated PBLs from RAO horses demonstrated a significant response to Î²2-agonist binding whereas cells from non-affected horses did not. Response of PBLs from RAO horses was attenuated when pre-treated with a Î²2-antagonist but unaffected following pre-treatment with a Î²1-antagonist, indicating that the response of PBLs from these horses to salbutamol binding was mainly through the Î²2-AR. Preliminary investigation of bronchoalveolar lavage (BAL) lymphocytes from RAO horses demonstrated that they also responded to Î²2-agonist binding, while cells from non-affected horses did not. These findings represent a novel tool for further investigation of the role of Î²2-agonist binding in diseases like asthma and RAO, and support the use of this model for future studies."]},{"key":"dc:description.degree","label":"Dc Description Degree","values":["Master of Science"]},{"key":"dc:title","label":"Title","values":["Response of Peripheral Blood Lymphocytes from RAO-affected Horses to b2-Agonist Stimulation"]}]}],"canonical_facts":{"dc:contributor.committeechair":["Buechner-Maxwell, Virginia A."],"dc:contributor.committeemember":["Ehrich, Marion F.","Eyre, Peter","Prater, Mary R."],"dc:contributor.department":["Biomedical and Veterinary Sciences"],"dc:creator":["Werner Becker, Marianne Patricia"],"dc:date.accessioned":["2016-09-22T14:56:38Z"],"dc:date.available":["2016-09-22T14:56:38Z","2015-04-22"],"dc:date.issued":["2011-05-03"],"dc:description.abstract":["Recurrent airway obstruction (RAO) affects middle-age horses, inducing bronchoconstriction and airway inflammation. Î²2-agonists like salbutamol are used as treatment, promoting airway smooth muscle (ASM) relaxation and bronchodilation. In addition to ASM, inflammatory cells express the Î²2-adrenoreceptors (Î²2-AR). In other species, Î²2-agonists promote peripheral blood lymphocyte (PBL) cytokine expression towards a pro-inflammatory phenotype. RAO horses are a good model for evaluating chronic changes in human asthma. However, little is known about the effect of Î²2-agonist stimulation on equine PBL inflammatory response. The aims of this study were to develop an indirect method to evaluate the response of equine PBLs to Î²2-agonist stimulation, and to compare it between cells from RAO and non-affected horses. Isolated PBLs were activated with ConA and stimulated with salbutamol. Response to agonist binding was indirectly determined using flow cytometric methodology and verified by Western blot. Activated PBLs from RAO horses demonstrated a significant response to Î²2-agonist binding whereas cells from non-affected horses did not. Response of PBLs from RAO horses was attenuated when pre-treated with a Î²2-antagonist but unaffected following pre-treatment with a Î²1-antagonist, indicating that the response of PBLs from these horses to salbutamol binding was mainly through the Î²2-AR. Preliminary investigation of bronchoalveolar lavage (BAL) lymphocytes from RAO horses demonstrated that they also responded to Î²2-agonist binding, while cells from non-affected horses did not. These findings represent a novel tool for further investigation of the role of Î²2-agonist binding in diseases like asthma and RAO, and support the use of this model for future studies."],"dc:description.degree":["Master of Science"],"dc:identifier.other":["etd-05162011-162639"],"dc:identifier.uri":["http://hdl.handle.net/10919/72984"],"dc:language.iso":["en_US"],"dc:publisher":["Virginia Tech"],"dc:rights":["In Copyright"],"dc:rights.uri":["http://rightsstatements.org/vocab/InC/1.0/"],"dc:subject":["Horses","VASP","b2-adrenoreceptors"],"dc:title":["Response of Peripheral Blood Lymphocytes from RAO-affected Horses to b2-Agonist Stimulation"],"dc:type":["Thesis"],"dc:type.dcmitype":["Text"],"thesis:degree_discipline":["Biomedical and Veterinary Sciences"],"thesis:degree_level":["masters"],"thesis:degree_name":["Master of Science"],"thesis:institution_name":["Virginia Polytechnic Institute and State University"]},"updated_at":"2026-07-22T22:18:50Z"}