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Delphinidin and cyanidin inhibit PDGF AB ‐induced VEGF release in vascular smooth muscle cells by preventing activation of p38 MAPK and JNK
Author(s) -
Oak MH,
Bedoui J E,
Madeira S V F,
Chalupsky K,
SchiniKerth V B
Publication year - 2006
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0706843
Subject(s) - delphinidin , cyanidin , vascular smooth muscle , mapk/erk pathway , chemistry , platelet derived growth factor receptor , p38 mitogen activated protein kinases , biochemistry , reactive oxygen species , microbiology and biotechnology , phosphorylation , biology , growth factor , endocrinology , antioxidant , receptor , smooth muscle
Background and purpose: Red wine polyphenols (RWPs) inhibit the expression of vascular endothelial growth factor (VEGF), a major pro‐angiogenic and pro‐atherosclerotic factor, in vascular smooth muscle cells (VSMCs). The aim of this study was to identify which red wine polyphenols were inhibitory and to determine the mechanism underlying the inhibitory effects. Experimental approach: Release of VEGF stimulated by platelet derived growth factor AB (PDGF AB ), from human aortic VSMCs was measured by immunoassay and phosphorylation of kinases by Western blot analysis. The direct antioxidant properties of polyphenols were determined by electron paramagnetic resonance and the cellular formation of reactive oxygen species (ROS) by dichlorofluorescein. Key results: The inhibitory effect of RWPs on PDGF AB ‐induced release of VEGF was mimicked by delphinidin but not by quercetin, catechins, resveratrol, gallic acid or caffeic acid. In the anthocyanin class, not only delphinidin but also cyanidin prevented VEGF release whereas malvidin and peonidin were without effect. RWPs, delphinidin and cyanidin directly scavenged ROS and prevented the PDGF AB ‐induced formation of ROS in VSMCs. Malvidin and peonidin did not scavenge ROS but prevented the cellular formation of ROS. Although the p38 MAPK, ERK1/2 and JNK pathways have been involved in the PDGF AB ‐induced expression of VEGF, in our experiments, only phosphorylation of p38 MAPK and JNK was inhibited by RWPs, delphinidin and cyanidin. Conclusions and implications: Anthocyanins presenting a hydroxyl residue at position 3′ are able to inhibit PDGF AB ‐induced VEGF expression by preventing activation of p38 MAPK and JNK in VSMCs. British Journal of Pharmacology (2006) 149 , 283–290. doi: 10.1038/sj.bjp.0706843

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