Planta Med 2004; 70(9): 823-827
DOI: 10.1055/s-2004-827230
Original Paper
Biochemistry and Molecular Biology
© Georg Thieme Verlag KG Stuttgart · New York

Cinnamaldehyde and 2-Methoxycinnamaldehyde as NF-κB Inhibitors from Cinnamomum cassia

Alavala Matta Reddy1 , Jee Hee Seo2 , Shi Yong Ryu2 , Yeong Shik Kim3 , Young Sup Kim2 , Kyung Rak Min1 , Youngsoo Kim1
  • 1College of Pharmacy and Research Center for Bioresource and Health, Chungbuk National University, Cheongju, Korea
  • 2Korea Research Institute of Chemical Technology, Taejeon, Korea
  • 3Natural Products Research Institute, Seoul National University, Seoul, Korea
Further Information

Publication History

Received: January 22, 2004

Accepted: June 4, 2004

Publication Date:
23 September 2004 (online)

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Abstract

Nuclear factor (NF)-κB is a transcription factor regulating the expression of inflammatory and immune genes. In the present study, an extract from stem bark of Cinnamomum cassia Blume (Lauraceae) was discovered to have an inhibitory effect on LPS-induced NF-κB transcriptional activity, which was determined using macrophages RAW 264.7 transfected stably with an alkaline phosphatase reporter construct containing four copies of the NF-κB binding κB sequence. Following activity-guided fractionation, trans-cinnamaldehyde and 2-methoxycinnamaldehyde were identified as the NF-κB inhibitors from C. cassia with IC50 values of 43 μM and 31 μM, respectively. As a positive control, caffeic acid phenethyl ester (CAPE) showed an IC50 value of 2 μM on NF-κB transcriptional activity. Both trans-cinnamaldehyde and 2-methoxycinnamaldehyde inhibited LPS-induced DNA binding activity of NF-κB in addition to NF-κB transcriptional activity.

References

Prof. Dr. Youngsoo Kim

College of Pharmacy

Chungbuk National University

Cheongju 361-763

Korea

Phone: +82-43-261-2823

Fax: +82-43-268-2732

Email: youngsoo@chungbuk.ac.kr