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Imperatorin Suppresses Degranulation and Eicosanoid Generation in Activated Bone Marrow-Derived Mast Cells
Article in English | WPRIM (Western Pacific) | ID: wpr-36718
Responsible library: WPRO
ABSTRACT
Imperatorin has been known to exert many biological functions including anti-inflammatory activity. In this study, we investigated the inhibitory effects of imperatorin on the production of inflammatory mediators in mouse bone marrow-derived mast cells (BMMC). Imperatorin inhibited degranulation and the generation of eicosanoids (leukotriene C4 (LTC4) and prostaglandin D2 (PGD2)) in IgE/antigen (Ag)-stimulated BMMC. To elucidate the molecular mechanism involved in this process, we investigated the effect of imperatorin on intracellular signaling in BMMC. Biochemical analyses of the IgE/Ag-mediated signaling pathway demonstrated that imperatorin dramatically attenuated degranulation and the production of 5-lipoxygenase-dependent LTC4 and cyclooxygenase-2-dependent PGD2 through the inhibition of intracellular calcium influx/phospholipase Cgamma1, cytosolic phospholipase A2/mitogen-activated protein kinases and/or nuclear factor-kappaB pathways in BMMC. These results suggest that the effects of imperatorin on inhibition of degranulation and eicosanoid generation through the suppression of multiple steps of IgE/Ag-mediated signaling pathways would be beneficial for the prevention of allergic inflammation.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Phospholipases / Protein Kinases / Prostaglandin D2 / Eicosanoids / Calcium / Leukotriene C4 / Mitogen-Activated Protein Kinases / Cytosol / Inflammation / Mast Cells Limits: Animals Language: English Journal: Biomolecules & Therapeutics Year: 2015 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Phospholipases / Protein Kinases / Prostaglandin D2 / Eicosanoids / Calcium / Leukotriene C4 / Mitogen-Activated Protein Kinases / Cytosol / Inflammation / Mast Cells Limits: Animals Language: English Journal: Biomolecules & Therapeutics Year: 2015 Document type: Article
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