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©2014 Baishideng Publishing Group Inc.
World J Gastroenterol. Nov 28, 2014; 20(44): 16535-16543
Published online Nov 28, 2014. doi: 10.3748/wjg.v20.i44.16535
Published online Nov 28, 2014. doi: 10.3748/wjg.v20.i44.16535
Inhibitor | Mechanism of action | Effects |
SP600125 | Selective and reversible inhibitor of JNK | Dose dependent inhibition of JNK Inhibition of inflammatory genes (COX-2, IFN, IL-2, TNF-α) in vivoReduction of pancreatic inflammatory mediators (TNF-α, IL-1β) in vivo |
CEP1347 | Potent and selective inhibitor of JNK | Dose dependent inhibition of JNK both in vivo than in vitroReduction of inflammatory cytokines |
PD98059 | Inhibitor of ERK 1/2, prevents phosphorylation binding MEK | Protection against inflammatory process in the pancreas in vivo Protective effects probably related to the inhibition of COX-2 |
UO126 | Selective inhibitor of MEK1 and MEK2; it prevents the activation of ERK1/2 | Protection against inflammatory process in the pancreas in vivo |
SB203580 | Selective inhibitor of p38. Inhibition of p38 catalytic activity | Downregulation of the expression of proinflammatory mediators (TNF-α and IL-1β) in vivo |
- Citation: Irrera N, Bitto A, Interdonato M, Squadrito F, Altavilla D. Evidence for a role of mitogen-activated protein kinases in the treatment of experimental acute pancreatitis. World J Gastroenterol 2014; 20(44): 16535-16543
- URL: https://www.wjgnet.com/1007-9327/full/v20/i44/16535.htm
- DOI: https://dx.doi.org/10.3748/wjg.v20.i44.16535