scholarly journals Gallic Acid Inhibits Histamine Release and Pro-inflammatory Cytokine Production in Mast Cells

2005 ◽  
Vol 91 (1) ◽  
pp. 123-131 ◽  
Author(s):  
Sang-Hyun Kim ◽  
Chang-Duk Jun ◽  
Kyongho Suk ◽  
Byung-Ju Choi ◽  
Hyunjeung Lim ◽  
...  
2004 ◽  
Vol 27 (1) ◽  
pp. 34-37 ◽  
Author(s):  
Mi-Sun Kim ◽  
In-Young Choi ◽  
Si-Hyeong Lee ◽  
Seung-Heon Hong ◽  
Taekyun Shin ◽  
...  

Endocrinology ◽  
2003 ◽  
Vol 144 (9) ◽  
pp. 4080-4086 ◽  
Author(s):  
Hyun-Ja Jeong ◽  
Ho-Jeong Na ◽  
Seung-Heon Hong ◽  
Hyung-Min Kim

Abstract Mast cell accumulation can be causally related to several allergic inflammations. Previous work has demonstrated that glucocorticoids decreased tissue mast cell number, and stem cell factor (SCF)-induced migration of mast cells required p38 MAPK activation. In the present study we investigated the effects of dexamethasone on SCF-induced migration of rat peritoneal mast cells (RPMCs). SCF significantly induced the migration of RPMCs at 4 h. Dexamethasone dose-dependently inhibited SCF-induced migration of RPMCs (∼90.1% at 100 nm; P < 0.05). The MAPK p38 inhibitor SB203580 (20 μm) also inhibited the SCF-induced migration. The ability of SCF to enhance morphological alteration and filamentous actin formation was also abolished by treatment with dexamethasone. Dexamethasone inhibited SCF-induced p38 MAPK activation to near-basal levels and induced MAPK phosphatase-1 expression. In addition, SCF-induced inflammatory cytokine production was significantly inhibited by treatment with dexamethasone or SB203580 (P < 0.01). Our results show that dexamethasone potently regulates SCF-induced migration, p38 MAPK activation, and inflammatory cytokine production through the expression of MKP-1 protein in RPMCs. Such modulation may have functional consequences during dexamethasone treatment, especially mast cell-mediated allergic inflammation disorders.


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