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2-methoxycinnamaldehyde reduces IL-1beta-induced prostaglandin production in rat cerebral endothelial cells.

Abstract
Prostaglandin E2 (PGE2) works as a common final mediator of the febrile. Guizhi-Tang, one of the most famous traditional Chinese medical formula used to treat influenza, common cold and other pyretic conditions, was previously reported to reduce the production of PGE 2 in rats. 2-Methoxycinnamaldehyde is a principle compound isolated from Guizhi-Tang. The aim of the present study was to investigate the effects of 2-methoxycinnamaldehyde on PGE2 production of rat cerebral endothelial cells (CECs). 2-Methoxycinnamaldehyde dose-dependently inhibited interleukin (IL)-1beta-induced PGE2 production in CECs with IC50 values of 174 microM. IL-1beta stimulation increased the protein, activity and mRNA expression of cyclooxygenase (COX)-2 but not COX-1. 2-Methoxycinnamaldehyde reduced IL-1beta-induced protein and activity of COX-2, but did not influence the COX-2 mRNA expression. Our results show that prostaglandin production in CECs during stimulated conditions is sensitive to inhibition by 2-methoxycinnamaldehyde and suggest that 2-methoxycinnamaldehyde may reduce COX-2 protein level and activity but not COX-2 mRNA.
AuthorsJian-You Guo, Hai-Ru Huo, Yuan-Xiao Yang, Cang-Hai Li, Hong-Bin Liu, Bao-Sheng Zhao, Lan-Fang Li, Yue-Ying Ma, Shu-Ying Guo, Ting-Liang Jiang
JournalBiological & pharmaceutical bulletin (Biol Pharm Bull) Vol. 29 Issue 11 Pg. 2214-21 (Nov 2006) ISSN: 0918-6158 [Print] Japan
PMID17077517 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Analgesics, Non-Narcotic
  • Cinnamates
  • Drugs, Chinese Herbal
  • Interleukin-1beta
  • Membrane Proteins
  • RNA, Messenger
  • von Willebrand Factor
  • 2-methoxycinnamaldehyde
  • Acrolein
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Dinoprostone
Topics
  • Acrolein (analogs & derivatives, chemistry, isolation & purification, pharmacology)
  • Analgesics, Non-Narcotic (chemistry, isolation & purification, pharmacology)
  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Cerebral Cortex (blood supply)
  • Cinnamates (chemistry, isolation & purification, pharmacology)
  • Cyclooxygenase 2 (genetics, metabolism)
  • Dinoprostone (biosynthesis)
  • Dose-Response Relationship, Drug
  • Drugs, Chinese Herbal (chemistry, isolation & purification, pharmacology)
  • Endothelium, Vascular (cytology, drug effects, metabolism)
  • Enzyme-Linked Immunosorbent Assay
  • Interleukin-1beta (pharmacology)
  • Membrane Proteins (antagonists & inhibitors, genetics, metabolism)
  • RNA, Messenger (genetics, metabolism)
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction
  • von Willebrand Factor (analysis)

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