Chemical Analysis of the Ingredients of 20% Aqueous Ethanol Extract of Nardostachys jatamansi through Phytochemical Study and Evaluation of Anti-Neuroinflammatory Component.
Kwan-Woo KimChi-Su YoonSung-Joo ParkGi-Sang BaeDong-Gu KimYoun-Chul KimHyuncheol OhPublished in: Evidence-based complementary and alternative medicine : eCAM (2021)
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.
Keyphrases
- lps induced
- inflammatory response
- nitric oxide synthase
- nitric oxide
- mouse model
- lipopolysaccharide induced
- induced apoptosis
- prefrontal cortex
- toll like receptor
- cell cycle arrest
- cell proliferation
- oxidative stress
- anti inflammatory
- ms ms
- rheumatoid arthritis
- blood pressure
- transcription factor
- signaling pathway
- high resolution
- emergency department
- body mass index
- hydrogen peroxide
- skeletal muscle
- type diabetes
- adipose tissue
- cell death
- spinal cord injury
- drug induced
- pi k akt
- blood brain barrier
- immune response