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Moringa fruit inhibits LPS-induced NO/iNOS expression through suppressing the NF-κB activation in RAW264.7 cells

  • Hyo Jin Lee
  • , Yun Jeong Jeong
  • , Tae Sung Lee
  • , Yoon Yub Park
  • , Whi Gun Chae
  • , Il Kyung Chung
  • , Hyeun Wook Chang
  • , Cheorl Ho Kim
  • , Yung Hyun Choi
  • , Wun Jae Kim
  • , Sung Kwon Moon
  • , Young Chae Chang
  • The Catholic University of Korea
  • Catholic University of Daegu
  • Yeungnam University
  • Sungkyunkwan University
  • Dongeui University
  • Chungbuk National University
  • Chung-Ang University

Research output: Contribution to journalArticlepeer-review

34 Scopus citations

Abstract

In this study, we evaluated the anti-inflammatory effects of moringa (Moringa oleifera Lam.), a natural biologically active substance, by determining its inhibitory effects on pro-inflammatory mediators in lipopolysaccharide (LPS)-stimulated macrophage RAW264.7 cells. Extracts from different parts of moringa (root, leaf, and fruit) reduced LPS-induced nitric oxide (NO) release in a dose-dependent manner. The moringa fruit extract most effectively inhibited LPS-induced NO production and levels of inducible nitric oxide synthase (iNOS). The moringa fruit extract also was shown to suppress the production of inflammatory cytokines including IL-1β, TNF-α, and IL-6. Furthermore, moringa fruit extract inhibited the cytoplasmic degradation of IκB-α and the nuclear translocation of p65 proteins, resulting in lower levels of NF-κB transactivation. Collectively, the results of this study demonstrate that moringa fruit extract reduces the levels of pro-inflammatory mediators including NO, IL-1β, TNF-α, and IL-6 via the inhibition of NF-κB activation in RAW264.7 cells. These findings reveal, in part, the molecular basis underlying the anti-inflammatory properties of moringa fruit extract.

Original languageEnglish
Pages (from-to)1109-1123
Number of pages15
JournalAmerican Journal of Chinese Medicine
Volume41
Issue number5
DOIs
StatePublished - 2013

Bibliographical note

Funding Information:
This work was supported by the National Research Foundation of Korea (NRF, Personalized Tumor Engineering Research Center) grant funded by the Korea government (MEST) (No. 2008-0062611) and was supported by Basic Science Research Program through National Research Foundation of Korea (NRF) grant funded by the Ministry of Education, Science and Technology (MEST) (No. 2011-0021574).

Keywords

  • COX-2
  • Moringa
  • NF-κB
  • NO
  • iNOS

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