Identification of plant metabolite classes from Waltheria Indica L. extracts regulating inflammatory immune responses via COX-2 inhibition.
Alkaloids
/ analysis
Cyclooxygenase 2
/ metabolism
Cyclooxygenase 2 Inhibitors
/ chemistry
Flavonoids
/ analysis
Immunity
/ drug effects
Malvaceae
/ chemistry
Phenols
/ analysis
Plant Extracts
/ chemistry
Plant Leaves
/ chemistry
Saponins
/ analysis
Secondary Metabolism
Steroids
/ analysis
Triterpenes
/ analysis
Alkaloids
Anti-inflammatory
Cyclooxygenase (COX)
Phenols
Saponins
Secondary metabolites
Steroidal-saponins
Tiliroside
Triterpenoid-saponins
Waltheria indica
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
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
113741Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.