Planta Med 2010; 76(3): 251-257
DOI: 10.1055/s-0029-1186142
Pharmacology
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Anti-inflammatory Effects of Madecassic Acid via the Suppression of NF-κB Pathway in LPS-Induced RAW 264.7 Macrophage Cells

Jong-Heon Won1 , Ji-Sun Shin1 , Hee-Juhn Park2 , Hyun-Ju Jung3 , Duck-Jae Koh4 , Baek-Geon Jo4 , Jin-Yong Lee4 , Kijoo Yun5 , Kyung-Tae Lee1
  • 1College of Pharmacy, Kyung-Hee University, Hoegi-Dong, Seoul, Republic of Korea
  • 2Department of Botanical Resources, Sangji University, Wonju, Republic of Korea
  • 3Department of Oriental Pharmacy, Wonkwang University, Sinyong-Dong, Iksan, Republic of Korea
  • 4College of Oriental Medicine, Kyung Hee University, Hoegi-Dong, Seoul, Republic of Korea
  • 5College of Culture and Industry, Gangneung-Wonju National University, Namwon-ro, Wonju, Gangwon, 220-711, Republic of Korea
Further Information

Publication History

received April 23, 2009 revised July 17, 2009

accepted August 15, 2009

Publication Date:
11 September 2009 (online)

Abstract

We have investigated the anti-inflammatory effects of madecassic acid and madecassoside isolated from Centella asiatica (Umbelliferae) on lipopolysaccharide (LPS)-stimulated RAW 264.7 murine macrophage cells. Both madecassic acid and madecassoside inhibited the production of nitric oxide (NO), prostaglandin E2 (PGE2), tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and IL-6. However, madecassic acid more potently suppressed these inflammatory mediators than did madecassoside. Consistent with these observations, madecassic acid inhibited the LPS-induced expression of iNOS and COX-2 at the protein level and of iNOS, COX-2, TNF-α, IL-1β, and IL-6 at the mRNA level in RAW 264.7 macrophage cells, as determined by Western blotting and RT‐PCR, respectively. Furthermore, madecassic acid suppressed the LPS-induced activation of nuclear factor-κB (NF-κB), and this was associated with the abrogation of inhibitory kappa B-α (IκB-α) degradation and with the subsequent blocking of p65 protein translocation to the nucleus. These results suggest that the anti-inflammatory properties of madecassic acid are caused by iNOS, COX-2, TNF-α, IL-1β, and IL-6 inhibition via the downregulation of NF-κB activation in RAW 264.7 macrophage cells.

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Ph.D. Kyung-Tae Lee

Department of Pharmaceutical Biochemistry
College of Pharmacy
Kyung-Hee University

Dongdaemun-Ku, Hoegi-Dong #1

130-701 Seoul

Republic of Korea

Phone: + 82 (0) 29 61 08 60

Fax: + 82 (0) 29 62 08 60

Email: ktlee@khu.ac.kr