Multifunctional approaches to provide potential pharmacophores for the pharmacy shelf: Heracleum sphondylium L. subsp. ternatum (Velen.) Brummitt.
Acetylcholinesterase
/ metabolism
Amylases
/ antagonists & inhibitors
Anti-Bacterial Agents
/ chemistry
Antifungal Agents
/ chemistry
Bacteria
/ drug effects
Butyrylcholinesterase
/ metabolism
Enzyme Inhibitors
/ chemistry
Fungi
/ drug effects
Heracleum
/ chemistry
Humans
Microbial Sensitivity Tests
Molecular Docking Simulation
Molecular Structure
Plant Extracts
/ chemistry
Acetylcholinesterase
Antimicrobial
Hogweed
In silico
Industrial uses
Phenolic
Journal
Computational biology and chemistry
ISSN: 1476-928X
Titre abrégé: Comput Biol Chem
Pays: England
ID NLM: 101157394
Informations de publication
Date de publication:
Feb 2019
Feb 2019
Historique:
received:
17
09
2018
revised:
29
10
2018
accepted:
19
11
2018
pubmed:
1
12
2018
medline:
9
4
2019
entrez:
1
12
2018
Statut:
ppublish
Résumé
Heracleum sphondylium L. subsp. ternatum (Velen.) Brummitt. commonly known as "hogweed" is traditionally used to manage several human ailments. This investigation assessed, for the first time, the enzyme inhibitory properties, antioxidant activity, phytochemical profile, antimutagenic, and antimicrobial potential of the ethyl acetate, methanol, and water extracts of H. sphondylium. We also established the possible interactions of identified phenolic compounds with cholinesterases, amylase, glucosidase, and tyrosinase using in silico docking studies. Chlorogenic acid was found in high amounts in the methanol extract of H. sphondylium. The methanol extract was an effective inhibitor of acetylcholinesterase (1.70 mg galantamine equivalent (GALAE)/g extract) while the ethyl acetate extract showed pronounced inhibitory action against butyrylcholinesterase (1.77 mg GALAE/g extract). The extracts exhibited low inhibition against amylase (0.12-0.84 mmol acarbose equivalent (ACAE)/g extract) and a more pronounced inhibition against glucosidase (2.29-3.65 mmol ACAE/g extract). In silico results showed that rutin and quercetin (-70.4 and -72.2 Kcal/mol, for rutin and quercetin respectively) docked to the enzymatic cavity of acetylcholinesterase but these phenolic compounds showed less affinity with butyrylcholinesterase (-15.0 and -5.2 Kcal/mol, for rutin and quercetin respectively). The extracts did not induce any mutations on the bacterial strains, while they have excellent antimutagenic capacity against well-known mutagens (inhibition values 98%, 97% and 96%). The methanol extract (0.78 mg/ml) showed moderate antifungal activity while the ethyl acetate extract (0.78-3.12 mg/ml) showed weak to moderate antimicrobial activity. This study provides valuable baseline data which might serve for the development of future pharmacophores for the management of human ailments.
Identifiants
pubmed: 30500554
pii: S1476-9271(18)30684-4
doi: 10.1016/j.compbiolchem.2018.11.018
pii:
doi:
Substances chimiques
Anti-Bacterial Agents
0
Antifungal Agents
0
Enzyme Inhibitors
0
Plant Extracts
0
Acetylcholinesterase
EC 3.1.1.7
Butyrylcholinesterase
EC 3.1.1.8
Amylases
EC 3.2.1.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
64-73Informations de copyright
Copyright © 2018 Elsevier Ltd. All rights reserved.