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DC Field | Value | Language |
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dc.contributor.author | Aidoo, Douglas B. | - |
dc.contributor.author | Obiri, David D. | - |
dc.contributor.author | Osafo, Newman | - |
dc.contributor.author | Antwi, Aaron O. | - |
dc.contributor.author | Essel, Leslie B. | - |
dc.contributor.author | Duduyemi, Babatunde M. | - |
dc.contributor.author | Ekor, Martins | - |
dc.date.accessioned | 2023-10-20T10:53:47Z | - |
dc.date.available | 2023-10-20T10:53:47Z | - |
dc.date.issued | 2019 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/9768 | - |
dc.description.abstract | Bergapten (5-methoxypsoralen, 5-MOP) is a plant-derived furocoumarin with demonstrated anti-inflammatory action. *e present study investigated its effects on allergic inflammation in two related pathways of mast cell degranulation. Compound 48/ 80 and lipopolysaccharide (LPS) were used to activate the IgE-independent pathway while bovine serum albumin (BSA) was used as allergen for the IgE-dependent pathway. *e modulatory effect of bergapten on mast cell degranulation, neutrophil extravasation, protein concentration, lung histopathology, and oxidative stress was assessed. Bergapten at 10, 30, and 100 μg/ml for 15 min stabilized mast cells in rat mesenteric tissue from disruption in vitro and when administered in vivo at 3, 10, and 30 mg kg-1 for 1 h protected mice from fatal anaphylaxis induced by compound 48/80. Similarly, treatment of LPS-challenged mice with bergapten (3, 10, and 30 mg kg-1) for 24 h significantly decreased neutrophil infiltration into bronchoalveolar lavage fluid, mean protein concentration, and inflammatory cell infiltration of pulmonary tissues when compared to the saline-treated LPS-challenged control. In addition, lung histology of the bergapten-treated LPS-challenged mice showed significantly less oedema, congestion, and alveolar septa thickening when compared to the saline-treated LPS-challenged disease control. LPS-induced oxidative stress was significantly reduced through increased tissue activities of catalase and superoxide dismutase and reduced malondialdehyde levels on treatment with bergapten. In the triple antigen-induced active anaphylaxis, daily administration of bergapten at 3, 10, and 30 mg kg-1 for 10 days, respectively, protected previously sensitized and challenged mice against anaphylactic shock. Overall, our study demonstrates the ability of bergapten to attenuate allergic airway-induced hypersensitivity in murine models of inflammation, suggesting its possible therapeutic benefit in this condition. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Advances in Pharmacological Sciences | en_US |
dc.subject | Airway-Induced Hypersensitivity | en_US |
dc.subject | Bergapten | en_US |
dc.subject | Murine Models of Inflammation | en_US |
dc.title | Allergic Airway-Induced Hypersensitivity Is Attenuated by Bergapten in Murine Models of Inflammation | en_US |
dc.type | Article | en_US |
Appears in Collections: | School of Medical Sciences |
Files in This Item:
File | Description | Size | Format | |
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Allergic Airway-Induced Hypersensitivity Is Attenuated by Bergapten in Murine Models of Inflammation.pdf | MAIN ARTICLE | 5.18 MB | Adobe PDF | View/Open |
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