TY - JOUR
T1 - Ellagic acid blocks activation of pancreatic stellate cells
AU - Masamune, Atsushi
AU - Satoh, Masahiro
AU - Kikuta, Kazuhiro
AU - Suzuki, Noriaki
AU - Satoh, Kennichi
AU - Shimosegawa, Tooru
N1 - Funding Information:
This work was supported in part by Grant-in-Aid for Encouragement of Young Scientists from Japan Society for the Promotion of Science (to A.M.), by the Pancreas Research Foundation of Japan (to A.M. and to K. K.), by the Kanae Foundation for Life and Socio-Medical Science (to A.M.) and by the Uehara Memorial Foundation (to A.M.).
PY - 2005/9/15
Y1 - 2005/9/15
N2 - Activated pancreatic stellate cells (PSCs) play a pivotal role in the pathogenesis of pancreatic fibrosis and inflammation. Ellagic acid is a plant-derived polyphenol found in fruits and nuts, and has anti-oxidant and anti-inflammatory properties. But, little is known about the effects of ellagic acid on PSCs as well as on the activation of signal transduction pathways. We here evaluated the effects of ellagic acid on the activation and cell functions of PSCs. PSCs were isolated from rat pancreas tissue and used in their culture-activated, myofibroblast-like phenotype unless otherwise stated. Ellagic acid inhibited platelet-derived growth factor (PDGF)-BB-induced proliferation and migration, interleukin (IL)-1β- and tumor necrosis factor (TNF)-α-induced monocyte chemoattractant protein-1 production, and expression of α-smooth muscle actin and collagen genes. Ellagic acid inhibited PDGF-BB-induced tyrosine phosphorylation of PDGF β-receptor and the downstream activation of extracellular signal-regulated kinase and Akt. Ellagic acid inhibited IL-1β- and TNF-α-induced activation of activator protein-1 and mitogen-activated protein kinases (extracellular signal-regulated kinase, c-Jun N-terminal kinase and p38 mitogen-activated protein kinase), but not of nuclear factor-κB. In addition, ellagic acid inhibited transformation of freshly isolated cells to an activated, myofibroblast-like phenotype. In conclusion, ellagic acid inhibited key cell functions and activation of PSCs.
AB - Activated pancreatic stellate cells (PSCs) play a pivotal role in the pathogenesis of pancreatic fibrosis and inflammation. Ellagic acid is a plant-derived polyphenol found in fruits and nuts, and has anti-oxidant and anti-inflammatory properties. But, little is known about the effects of ellagic acid on PSCs as well as on the activation of signal transduction pathways. We here evaluated the effects of ellagic acid on the activation and cell functions of PSCs. PSCs were isolated from rat pancreas tissue and used in their culture-activated, myofibroblast-like phenotype unless otherwise stated. Ellagic acid inhibited platelet-derived growth factor (PDGF)-BB-induced proliferation and migration, interleukin (IL)-1β- and tumor necrosis factor (TNF)-α-induced monocyte chemoattractant protein-1 production, and expression of α-smooth muscle actin and collagen genes. Ellagic acid inhibited PDGF-BB-induced tyrosine phosphorylation of PDGF β-receptor and the downstream activation of extracellular signal-regulated kinase and Akt. Ellagic acid inhibited IL-1β- and TNF-α-induced activation of activator protein-1 and mitogen-activated protein kinases (extracellular signal-regulated kinase, c-Jun N-terminal kinase and p38 mitogen-activated protein kinase), but not of nuclear factor-κB. In addition, ellagic acid inhibited transformation of freshly isolated cells to an activated, myofibroblast-like phenotype. In conclusion, ellagic acid inhibited key cell functions and activation of PSCs.
KW - MAP kinase
KW - Pancreatic fibrosis
KW - Pancreatic stellate cells
KW - Pancreatitis
KW - Platelet-derived growth factor
KW - Polyphenol
UR - http://www.scopus.com/inward/record.url?scp=23744492100&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=23744492100&partnerID=8YFLogxK
U2 - 10.1016/j.bcp.2005.06.008
DO - 10.1016/j.bcp.2005.06.008
M3 - Article
C2 - 16023081
AN - SCOPUS:23744492100
SN - 0006-2952
VL - 70
SP - 869
EP - 878
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
IS - 6
ER -