Monensin Suppresses Multiple Features of House Dust Mite-Induced Experimental Asthma in Mice.
- Publisher:
- Springer
- Publication Type:
- Journal Article
- Citation:
- Inflammation, 2025, 48, (2), pp. 806-819
- Issue Date:
- 2025-07-03
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Field | Value | Language |
---|---|---|
dc.contributor.author | Allam, VSRR | |
dc.contributor.author | Akula, S | |
dc.contributor.author | Waern, I | |
dc.contributor.author | Taha, S | |
dc.contributor.author | Wernersson, S | |
dc.contributor.author | Pejler, G | |
dc.date.accessioned | 2025-07-15T06:02:09Z | |
dc.date.available | 2024-06-25 | |
dc.date.available | 2025-07-15T06:02:09Z | |
dc.date.issued | 2025-07-03 | |
dc.identifier.citation | Inflammation, 2025, 48, (2), pp. 806-819 | |
dc.identifier.issn | 0360-3997 | |
dc.identifier.issn | 1573-2576 | |
dc.identifier.uri | http://hdl.handle.net/10453/188316 | |
dc.description.abstract | Despite intense efforts to develop efficient therapeutic regimes for asthma, there is a large demand for novel treatment strategies in this disease. Here we evaluated the impact of monensin, a drug with potent anti-mast cell effects, in a mouse model of asthma. Allergic airway inflammation was induced by sensitization of mice with house dust mite (HDM) antigen, and effects of monensin on airway hyperreactivity and inflammatory parameters were studied. Following intraperitoneal administration, monensin did not suppress airway hyperreactivity but was shown to have anti-inflammatory properties, as manifested by reduced eosinophil- and lymphocyte infiltration into the airway lumen, and by suppressed inflammation of the lung tissue. After intranasal instillation, monensin exhibited similar anti-inflammatory effects as seen after intraperitoneal administration. Moreover, intranasally administered monensin was demonstrated to suppress goblet cell hyperplasia, and to cause a reduction in the expression of genes coding for key inflammatory markers. Further, monensin blocked mast cell degranulation in the airways of allergen-sensitized mice. Together, this study reveals that monensin has the capacity to suppress key pathological events associated with allergic airway inflammation. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | Springer | |
dc.relation.ispartof | Inflammation | |
dc.relation.isbasedon | 10.1007/s10753-024-02090-7 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 1107 Immunology | |
dc.subject.classification | Immunology | |
dc.subject.classification | 3204 Immunology | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Asthma | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Pyroglyphidae | |
dc.subject.mesh | Monensin | |
dc.subject.mesh | Disease Models, Animal | |
dc.subject.mesh | Mast Cells | |
dc.subject.mesh | Mice, Inbred BALB C | |
dc.subject.mesh | Anti-Inflammatory Agents | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Cell Degranulation | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Mast Cells | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Mice, Inbred BALB C | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Pyroglyphidae | |
dc.subject.mesh | Asthma | |
dc.subject.mesh | Disease Models, Animal | |
dc.subject.mesh | Monensin | |
dc.subject.mesh | Anti-Inflammatory Agents | |
dc.subject.mesh | Cell Degranulation | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Asthma | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Pyroglyphidae | |
dc.subject.mesh | Monensin | |
dc.subject.mesh | Disease Models, Animal | |
dc.subject.mesh | Mast Cells | |
dc.subject.mesh | Mice, Inbred BALB C | |
dc.subject.mesh | Anti-Inflammatory Agents | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Cell Degranulation | |
dc.title | Monensin Suppresses Multiple Features of House Dust Mite-Induced Experimental Asthma in Mice. | |
dc.type | Journal Article | |
utslib.citation.volume | 48 | |
utslib.location.activity | United States | |
utslib.for | 1107 Immunology | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Health | |
utslib.copyright.status | open_access | * |
pubs.consider-herdc | false | |
dc.rights.license | This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/ | |
dc.date.updated | 2025-07-15T06:01:56Z | |
pubs.issue | 2 | |
pubs.publication-status | Published online | |
pubs.volume | 48 | |
utslib.citation.issue | 2 |
Abstract:
Despite intense efforts to develop efficient therapeutic regimes for asthma, there is a large demand for novel treatment strategies in this disease. Here we evaluated the impact of monensin, a drug with potent anti-mast cell effects, in a mouse model of asthma. Allergic airway inflammation was induced by sensitization of mice with house dust mite (HDM) antigen, and effects of monensin on airway hyperreactivity and inflammatory parameters were studied. Following intraperitoneal administration, monensin did not suppress airway hyperreactivity but was shown to have anti-inflammatory properties, as manifested by reduced eosinophil- and lymphocyte infiltration into the airway lumen, and by suppressed inflammation of the lung tissue. After intranasal instillation, monensin exhibited similar anti-inflammatory effects as seen after intraperitoneal administration. Moreover, intranasally administered monensin was demonstrated to suppress goblet cell hyperplasia, and to cause a reduction in the expression of genes coding for key inflammatory markers. Further, monensin blocked mast cell degranulation in the airways of allergen-sensitized mice. Together, this study reveals that monensin has the capacity to suppress key pathological events associated with allergic airway inflammation.
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