Beneficial Effects of Fractions ofNardostachys jatamansion Lipopolysaccharide-Induced Inflammatory Response

Author:

Bae Gi-Sang1ORCID,Heo Kwang-Ho2,Choi Sun Bok34,Jo Il-Joo34,Kim Dong-Goo34,Shin Joon-Yeon34,Seo Seung-Hee5,Park Kyoung-Chel3,Lee Dong-Sung1,Oh Hyuncheol16,Kim Youn-Chul16,Song Ho-Joon34,Shin Byung-Cheul2,Park Sung-Joo134ORCID

Affiliation:

1. Hanbang Body-Fluid Research Center, Wonkwang University, Iksan, Jeonbuk 540-749, Republic of Korea

2. Department of Rehabilitation Medicine of Korean Medicine, Spine & Joint Center, Pusan National University Korean Medicine Hospital, Yangsan 626-770, Republic of Korea

3. Department of Herbology, School of Oriental Medicine, Wonkwang University, Iksan, Jeonbuk 540-749, Republic of Korea

4. BK21 plus team, Professional Graduate School of Oriental Medicine, Wonkwang University, Iksan, Jeonbuk 540-749, Republic of Korea

5. Department of Beauty, Dongshin University, Naju, Jeonnam 252-17, Republic of Korea

6. College of Pharmacy, Wonkwang University, Iksan 570-749, Republic of Korea

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.

Funder

National Research Foundation of Korea

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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