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Vol. 60, Issue 3, 507-513, September 2001
School of Traditional Chinese Medicine, Chang Gung University,
Tao-Yuan, Taiwan, Republic of China (Y.-L.C., J.-J.S.); and Institute
of Biomedical Sciences, Academia Sinica, Taipei, Taiwan, Republic of
China (B.-S.W., J.-J.C., D.L.W.)
Wogonin (Wog), an active component of Scutellaria
baicalensis, has antioxidant and anti-inflammatory properties.
Monocyte chemotactic protein-1 (MCP-1), a potent chemoattractant for
monocytes, plays a crucial role in case of early inflammatory
responses, including atherosclerosis. In this study, we investigated
the effect of Wog on phorbol ester (PMA)-induced MCP-1 expression in
human umbilical vein endothelial cells (ECs). The MCP-1 mRNA levels and
MCP-1 release in Wog-treated ECs were measured. Wog inhibited
PMA-induced MCP-1 mRNA levels and MCP-1 secretion in a dose-dependent
manner. The inhibition of MCP-1 induction by Wog is a transcriptional
event, as shown by Wog's significant reduction of both MCP-1 promoter
and 4× 12-O-tetradecanoylphorbol-13-acetate response element-luciferase reporter activities. By electrophoretic mobility assay, Wog significantly reduced the AP-1 binding activity induced by PMA. Furthermore, the PMA-induced extracellular
signal-regulated kinase 1/2 and c-Jun amino-terminal kinase activities
that contributed to AP-1 activity and MCP-1 gene induction were
obviously attenuated after pretreating ECs with Wog. The decrease of
MCP-1 secretion by Wog pretreatment led to a reduction of monocyte
adhesion to ECs. Taken together, our results demonstrate that Wog
inhibits MCP-1 induction in ECs; this inhibition is mediated by
reducing AP-1 transcriptional activity via the attenuation of ERK1/2
and JNK signal transduction pathways. We conclude that Wog has the potential therapeutic development for use in anti-inflammatory and
vascular disorders.
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