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Diospyros kaki calyx inhibits immediate-type hypersensitivity via the reduction of mast cell activation.
- Source :
- Pharmaceutical Biology; Dec2017, Vol. 55 Issue 1, p1946-1953, 8p
- Publication Year :
- 2017
-
Abstract
- Context:Diospyros kakiL. (Ebenaceae) fruit is widely distributed in Asia and is known to exert anti-inflammatory and antithrombotic effects. Objective:We evaluated the inhibitory effect of aqueous extract ofD. kakicalyx (AEDKC) on mast cell-mediated immediate-type hypersensitivity and underlying mechanism of action. Materials and methods:Forin vivo, ovalbumin (OVA)-induced active systemic anaphylaxis (ASA) and immunoglobulin (Ig) E-mediated passive cutaneous anaphylaxis (PCA) models were used. In the ASA, AEDKC (1–100 mg/kg) was orally administered 3 times during 14 days. In the PCA, AEDKC was orally treated 1 h before the antigen challenge. The control drug dexamethasone was used to compare the effectiveness of AEDKC. Forin vitro, IgE-stimulated RBL-2H3 cells and primary cultured peritoneal mast cells were used to determine the role of AEDKC (0.01–1 mg/mL). Results:Oral administration of AEDKC dose dependently suppressed rectal temperature decrease and increases in serum histamine, total IgE, OVA-specific IgE, and interleukin (IL)-4 in the ASA. In the PCA, AEDKC reduced Evans blue pigmentation. Compared to dexamethasone (10 mg/kg), AEDKC (100 mg/kg) showed similar inhibitory effectsin vivo. AEDKC concentration dependently suppressed the release of histamine and β-hexosaminidase through the reduction of intracellular calcium in mast cells. In addition, AEDKC decreased the expression and secretion of tumour necrosis factor-α and IL-4 by the reduction of nuclear factor-κB. The inhibitory potential of AEDKC (1 mg/mL) was similar with dexamethasone (10 μM)in vitro. Conclusions:We suggest that AEDKC may be a potential candidate for the treatment of mast cell-mediated allergic diseases. [ABSTRACT FROM PUBLISHER]
Details
- Language :
- English
- ISSN :
- 13880209
- Volume :
- 55
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Pharmaceutical Biology
- Publication Type :
- Academic Journal
- Accession number :
- 126815830
- Full Text :
- https://doi.org/10.1080/13880209.2017.1354386