Identification of plant metabolite classes from Waltheria Indica L. extracts regulating inflammatory immune responses via COX-2 inhibition.


Journal

Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310

Informations de publication

Date de publication:
24 Apr 2021
Historique:
received: 23 10 2020
revised: 11 12 2020
accepted: 19 12 2020
pubmed: 29 12 2020
medline: 4 8 2021
entrez: 28 12 2020
Statut: ppublish

Résumé

Waltheria Indica L. is traditionally used in Africa, South America and Hawaii to treat pain, anemia, diarrhea, epilepsy and inflammatory related diseases. This study aimed to identify extraction parameters to maximize tiliroside yield and to quantitative secondary metabolite composition of Waltheria Indica under various extraction conditions. The extracts were tested for COX-2 inhibition and their activity correlated with the type and quantity of the secondary metabolites. Insight was gained about how extraction parameters influence the extract composition and thus the COX-2 enzymatic inhibitory activity. Powdered leaves of Waltheria Indica were extracted using water, methanol, ethyl acetate and ethanol at different temperatures. Tiliroside was identified by HPLC-HRMS n and quantified using a tiliroside standard. The compound groups of the secondary metabolites were quantified by spectrometric methods. Inhibitory potential of different Waltheria extracts against the COX-2 enzyme was determined using a fluorometric COX-2 inhibition assay. The molecule, tiliroside, exhibited a COX-2 inhibition of 10.4% starting at a concentration of 15 μM and increased in a dose dependent manner up to 51.2% at 150 μM. The ethanolic extract at 30 °C and the ethyl acetate extract at 90 °C inhibited COX-2 with 37.7% and 38.9%, while the methanolic and aqueous extract showed a lower inhibition of 21.9% and 9.2% respectively. The results concerning phenol, alkaloid and tiliroside concentration in the extracts showed no dependence on COX-2 inhibition. The extracts demonstrated a direct correlation of COX-2 inhibitory activity with their triterpenoid-/steroidal-saponin concentration. COX-2 inhibition increased linearly with the concentration of the saponins. The data suggest that Waltheria Indica extracts inhibit the key inflammatory enzyme, COX-2, as a function of triterpenoid- and steroidal-saponin concentration and support the known efficacy of extracted Waltheria Indica leaves as a traditional treatment against inflammation related diseases.

Identifiants

pubmed: 33359867
pii: S0378-8741(20)33629-1
doi: 10.1016/j.jep.2020.113741
pii:
doi:

Substances chimiques

Alkaloids 0
Cyclooxygenase 2 Inhibitors 0
Flavonoids 0
Phenols 0
Plant Extracts 0
Saponins 0
Steroids 0
Triterpenes 0
tiliroside 15M04TXR9M
Cyclooxygenase 2 EC 1.14.99.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113741

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Michael Termer (M)

Department of Pharmaceutics and Biopharmaceutics, Philipps-University of Marburg, Marburg, Germany. Electronic address: michael.termer1@gmail.com.

Christophe Carola (C)

Merck KGaA, BU Performance Materials, Darmstadt, Germany.

Andrew Salazar (A)

Merck KGaA, BU Performance Materials, Darmstadt, Germany.

Cornelia M Keck (CM)

Department of Pharmaceutics and Biopharmaceutics, Philipps-University of Marburg, Marburg, Germany.

Juergen Hemberger (J)

Department of Life Science Engineering, Institute for Biochemical Engineering & Analytics, University of Applied Sciences, Giessen, Germany.

Joerg von Hagen (J)

Department of Life Science Engineering, Institute for Biochemical Engineering & Analytics, University of Applied Sciences, Giessen, Germany; Merck KGaA, BU Performance Materials, Darmstadt, Germany.

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Classifications MeSH