Next Article in Journal
Salix daphnoides: A Screening for Oligomeric and Polymeric Proanthocyanidins
Next Article in Special Issue
Cordyceps militaris (L.) Link Fruiting Body Reduces the Growth of a Non-Small Cell Lung Cancer Cell Line by Increasing Cellular Levels of p53 and p21
Previous Article in Journal
Discovery of 5-(5,5-Dimethylbutenolide-3-ethylidene)-2-amino-imidazolinone Derivatives as Fungicidal Agents
Previous Article in Special Issue
Isolation and Identification of Cytotoxic Compounds from Aeschynomene fascicularis, a Mayan Medicinal Plant
Open AccessArticle

Identification of Eupatilin from Artemisia argyi as a Selective PPARα Agonist Using Affinity Selection Ultrafiltration LC-MS

1
Laboratory of Biomodulation, Natural Products Research Institute, Korea Institute of Science and Technology, Gangneung 210-340, Korea
2
Laboratory of Natural Skinomics, Natural Products Research Institute, Korea Institute of Science and Technology, 290 Daejeon-dong, Gangneung-si, Gangwon-do 210-340, Korea
*
Author to whom correspondence should be addressed.
Academic Editor: Isabel C. F. R. Ferreira
Molecules 2015, 20(8), 13753-13763; https://doi.org/10.3390/molecules200813753
Received: 7 May 2015 / Revised: 20 July 2015 / Accepted: 23 July 2015 / Published: 28 July 2015
(This article belongs to the Collection Bioactive Compounds)
Peroxisome proliferator-activated receptors (PPARs) are key nuclear receptors and therapeutic targets for the treatment of metabolic diseases through the regulation of insulin resistance, diabetes, and dyslipidemia. Although a few drugs that target PPARs have been approved, more diverse and novel PPAR ligands are necessary to improve the safety and efficacy of available drugs. To expedite the search for new natural agonists of PPARs, we developed a screening assay based on ultrafiltration liquid chromatography-mass spectrometry (LC-MS) that is compatible with complex samples such as dietary foods or botanical extracts. The known PPARα and/or PPARγ ligands resveratrol and rosiglitazone were used as positive controls to validate the developed method. When applied to the screening of an Artemisia argyi extract, eupatilin was identified as a selective PPARα ligand. A PPAR competitive binding assay based on FRET detection also confirmed eupatilin as a selective PPARα agonist exhibiting a binding affinity of 1.18 μM (IC50). Furthermore, eupatilin activation of the transcriptional activity of PPARα was confirmed using a cell-based transactivation assay. Thus, ultrafiltration LC-MS is a suitable assay for the identification of PPAR ligands in complex matrixes such as extracts of dietary foods and botanicals. View Full-Text
Keywords: PPARα; eupatilin; Artemisia argyi; ultrafiltration LC-MS PPARα; eupatilin; Artemisia argyi; ultrafiltration LC-MS
Show Figures

Graphical abstract

MDPI and ACS Style

Choi, Y.; Jung, Y.; Kim, S.-N. Identification of Eupatilin from Artemisia argyi as a Selective PPARα Agonist Using Affinity Selection Ultrafiltration LC-MS. Molecules 2015, 20, 13753-13763.

Show more citation formats Show less citations formats

Article Access Map by Country/Region

1
Only visits after 24 November 2015 are recorded.
Search more from Scilit
 
Search
Back to TopTop