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Beneficial Effects of Fractions of Nardostachys jatamansi on Lipopolysaccharide-Induced Inflammatory Response

Authors :
Kwang-Ho Heo
Youn-Chul Kim
Sun Bok Choi
Joon-Yeon Shin
Seung-Hee Seo
Kyoung-Chel Park
Gi-Sang Bae
Dong-Sung Lee
Byung-Cheul Shin
Il-Joo Jo
Hyuncheol Oh
Dong-Goo Kim
Ho-Joon Song
Sung-Joo Park
Source :
Evidence-Based Complementary and Alternative Medicine, Vol 2014 (2014), Evidence-based Complementary and Alternative Medicine : eCAM
Publication Year :
2014
Publisher :
Hindawi Limited, 2014.

Abstract

It has been previously shown thatNardostachys jatamansi(NJ) exhibits anti-inflammatory properties against lipopolysaccharide (LPS) challenges. However, the potency of NJ constituents against LPS-induced inflammatory responses has not been examined. In this present study, we determined which NJ extract fractions exhibit inhibitory effects against LPS-induced inflammatory responses. Among the NJ fractions, NJ-1, NJ-3, NJ-4, and NJ-6 inhibited LPS-induced production of NO. The NJ-3, NJ-4, and NJ-6 fractions also inhibited the production of cytokines, such as IL-1β, IL-6, and TNF-α. However, NJ-1, NJ-3, NJ-4, and NJ-6 showed differential inhibitory mechanisms against LPS-induced inflammatory responses. NJ-1, NJ-3, and NJ-4 inhibited LPS-induced activation of c-jun NH2-terminal kinase (JNK) and p38 but did not affect activation of extracellular signal-regulated kinase (ERK) or NF-κB. On the other hand, NJ-6 inhibited activation of MAPKs and NF-κB. In addition,in vivoexperiments revealed that administration of NJ-1, NJ-3, NJ-4, and NJ-6 reduced LPS-induced endotoxin shock, with NJ-6 especially showing a marked protective effect. Taken together, these results provide the evidence for the potential of selective NJ fractions against LPS-induced inflammation. Thus, it will be advantageous to further isolate and determine single effective compounds from these potent fractions.

Details

Language :
English
ISSN :
17414288
Volume :
2014
Database :
OpenAIRE
Journal :
Evidence-Based Complementary and Alternative Medicine
Accession number :
edsair.doi.dedup.....13aa41588f3904a40c09f35b17766084