Rhododendron album Blume inhibits iNOS and COX-2 expression in LPS-stimulated RAW264.7 cells through the downregulation of NF-kappa B signaling
- Authors
- Park, Ji-Won; Kwon, Ok-Kyoung; Kim, Jung-Hee; Oh, Sei-Ryang; Kim, Jae-Hong; Paik, Jin-Hyub; Marwoto, Bambang; Widjhati, Rifatul; Juniarti, Fifit; Irawan, Doddy; Ahn, Kyung-Seop
- Issue Date
- 4월-2015
- Publisher
- SPANDIDOS PUBL LTD
- Keywords
- Rhododendron album Blume; inflammation; lipopolysaccharide; mitogen-activated protein kinases; nuclear factor-kappa B
- Citation
- INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, v.35, no.4, pp.987 - 994
- Indexed
- SCIE
SCOPUS
- Journal Title
- INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
- Volume
- 35
- Number
- 4
- Start Page
- 987
- End Page
- 994
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/94052
- DOI
- 10.3892/ijmm.2015.2107
- ISSN
- 1107-3756
- Abstract
- Rhododendron album Blume (RA) has traditionally been used as an herbal medicine and is considered to have anti-inflammatory properties. In the present study, we screened RA extracts with anti-inflammatory properties. The biological effects of an RA methanol extract (RAME) on inflammation were investigated in lipopolysaccharide (LPS)-stimulated mouse RAW264.7 cells. We investigated the effects of RAME on the production of nitric oxide (NO) and prostaglandin E2 (PGE(2)) in LPS-stimulated RAW264.7 cells. To explore the anti-inflammatory mechanisms of RAME, we measured the mRNA and protein expression of pro-inflammatory mediators induced by RAME in the LPS-stimulated RAW264.7 cells by RT-PCR and western blot analysis, respectively. RAME significantly inhibited the production of NO, PGE(2), interleukin (IL)-6, IL-1 beta and tumor necrosis factor (TNF)-alpha in the LPS-stimulated RAW264.7 cells. It also suppressed the mRNA and protein expression of inducible NO synthase (iNOS), cyclooxygenase-2 (COX-2) and mitogenactivated protein kinases (MAPKs) with a concomitant decrease in the nuclear translocation of nuclear factor-kappa B (NF-kappa B) in the LPS-stimulated RAW264.7 cells. These results indicate that RAME inhibits LPS-induced inflammatory responses. These effects were considered to be strongly associated with the suppression of NF-kappa B activation. We therefore suggest that RAME may be prove to be an effective therapeutic agent for the treatment of inflammatory diseases.
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Collections - College of Life Sciences and Biotechnology > Division of Life Sciences > 1. Journal Articles
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