skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: The regulatory effect of SC-236 (4-[5-(4-chlorophenyl)-3-(trifluoromethyl)-1-pyrazol-1-l] benzenesulfonamide) on stem cell factor induced migration of mast cells

Journal Article · · Toxicology and Applied Pharmacology
 [1];  [1];  [1];  [2];  [3];  [3];  [1]
  1. VestibuloCochlear Research Center of Wonkwang University, Iksan, Jeonbuk 570-749 (Korea, Republic of)
  2. Division of Biological Sciences, College of Natural Science, Chounbuk National University, Jeonju, Jeonbuk 561-756 (Korea, Republic of)
  3. College of Oriental Medicine, Kyung Hee University, 1 Hoegi-Dong, Dongdaemun-Gu, Seoul 130-701 (Korea, Republic of)

SC-236 (4-[5-(4-chlorophenyl)-3-(trifluoromethyl)-1-pyrazol-1-]benzenesulfonamide; C{sub 16}H{sub 11}ClF{sub 3}N{sub 3}O{sub 2}S), is a highly selective cyclooxygenase (COX)-2 inhibitor. Recently, there have been reports that SC-236 protects against cartilage damage in addition to reducing inflammation and pain in osteoarthritis. However, the mechanism involved in the inflammatory allergic reaction has not been examined. Mast cells accumulation can be related to inflammatory conditions, including allergic rhinitis, asthma, and rheumatoid arthritis. The aim of the present study is to investigate the effects of SC-236 on stem cell factor (SCF)-induced migration, morphological alteration, and cytokine production of rat peritoneal mast cells (RPMCs). We observed that SCF significantly induced the migration and morphological alteration. The ability of SCF to enhance migration and morphological alteration was abolished by treatment with SC-236. In addition, production of tumor necrosis factor (TNF)-{alpha}, interleukin (IL)-1{beta}, and vascular endothelial growth factor (VEGF) production induced by SCF was significantly inhibited by treatment with SC-236. Previous work has demonstrated that SCF-induced migration and cytokine production of mast cells require p38 MAPK activation. We also showed that SC-236 suppresses the SCF-induced p38 MAPK activation in RPMCs. These data suggest that SC-236 inhibits migration and cytokine production through suppression of p38 MAPK activation. These results provided new insight into the pharmacological actions of SC-236 and its potential therapeutic role in the treatment of inflammatory allergic diseases.

OSTI ID:
20976904
Journal Information:
Toxicology and Applied Pharmacology, Vol. 220, Issue 2; Other Information: DOI: 10.1016/j.taap.2006.12.036; PII: S0041-008X(06)00486-8; Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0041-008X
Country of Publication:
United States
Language:
English

Similar Records

Anti-allergic effects of Lycopus lucidus on mast cell-mediated allergy model
Journal Article · Thu Dec 15 00:00:00 EST 2005 · Toxicology and Applied Pharmacology · OSTI ID:20976904

Acidic environment augments FcεRI-mediated production of IL-6 and IL-13 in mast cells
Journal Article · Fri Aug 28 00:00:00 EDT 2015 · Biochemical and Biophysical Research Communications · OSTI ID:20976904

Cornuside inhibits mast cell-mediated allergic response by down-regulating MAPK and NF-κB signaling pathways
Journal Article · Fri Apr 29 00:00:00 EDT 2016 · Biochemical and Biophysical Research Communications · OSTI ID:20976904