Chemical Analysis of the Ingredients of 20% Aqueous Ethanol Extract of Nardostachys jatamansi through Phytochemical Study and Evaluation of Anti-Neuroinflammatory Component

Author:

Kim Kwan-Woo123ORCID,Yoon Chi-Su1245,Park Sung-Joo267,Bae Gi-Sang28,Kim Dong-Gu2,Kim Youn-Chul12ORCID,Oh Hyuncheol12ORCID

Affiliation:

1. Institute of Pharmaceutical Research and Development, College of Pharmacy, Wonkwang University, Iksan 54538, Republic of Korea

2. Hanbang Cardio-Renal Syndrome Research Center Wonkwang University, Iksan 54538, Republic of Korea

3. Department of Herbal Crop Research, National Institute of Horticultural and Herbal Science, RDA, Eumseong 27709, Republic of Korea

4. Natural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju 28116, Republic of Korea

5. Department of Chemistry, University of Florida, Gainesville 32611, FL, USA

6. Department of Herbology, School of Korean Medicine, Wonkwang University, Iksan 54538, Republic of Korea

7. Department of Herbal Resources, Professional Graduate School of Oriental Medicine, Wonkwang University, Iksan 54538, Republic of Korea

8. Department of Pharmacology, School of Korean Medicine, Wonkwang University, Iksan 54538, Republic of Korea

Abstract

Nardostachys spp. have been widely used in Asia as a folk medicine. In particular, the extracts of Nardostachys jatamansi, a species that grows in China, India, and Tibet, have been used to treat mental disorders, hyperlipidemia, hypertension, and convulsions. In this investigation, the potential of 20% aqueous ethanol extract of N. jatamansi (NJ20) as a botanical drug was explored by chemically investigating its constituents and its anti-neuroinflammatory effects on lipopolysaccharide- (LPS-) induced in vitro and in vivo models. Nine secondary metabolites were isolated and identified from NJ20, and quantitative analysis of these metabolites revealed desoxo-narchinol A as the major constituent. In LPS-challenged cells, pretreatment with NJ20 inhibited the LPS-induced excessive production of proinflammatory mediators, such as nitric oxide, prostaglandin E2, interleukin- (IL-) 1β, IL-6, and tumor necrosis factor-α. NJ20 also attenuated the overexpression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2. Additionally, pre-intraperitoneal injection of NJ20 downregulated the mRNA overexpression of IL-1β, IL-6, and iNOS in the prefrontal cortex, hypothalamus, and hippocampus of the LPS-stimulated C57BL/c mouse model. Chemical and biological investigations of NJ20 revealed that it is a potential inhibitor of LPS-induced neuroinflammatory responses in microglial cells and mouse models. The major active constituent of NJ20, desoxo-narchinol A, demonstrated anti-neuroinflammatory effects. Hence, our findings indicate that NJ20 may be a promising herbal mixture for developing a functional product and/or herbal drug for treating neuroinflammatory diseases.

Funder

Ministry of Science, ICT and Future Planning

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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