In vitro and in silico analysis of galanthine from Zephyranthes carinata as an inhibitor of acetylcholinesterase

Zephyranthes carinata Herb., a specie of the Amaryllidoideae subfamily, has been reported to have inhibitory activity against acetylcholinesterase. However, scientific evidence related to their bioactive alkaloids has been lacking. Thus, this study describes the isolation of the alkaloids of this pl...

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Autores:
Sierra, Karina
De Andrade, Jean Paulo
Angel Villalba, Javier R
Osorio, Edison
Yañéz, Osvaldo
Guaita Martínez, José Manuel
Oleas, Nora H.
García-Beltrán, Olimpo
De S. Borges, Warley
Bastida, Jaume
Osorio, Edison
Cortes, Natalie
Tipo de recurso:
Article of investigation
Fecha de publicación:
2022
Institución:
Universidad de Ibagué
Repositorio:
Repositorio Universidad de Ibagué
Idioma:
eng
OAI Identifier:
oai:repositorio.unibague.edu.co:20.500.12313/5488
Acceso en línea:
https://www.sciencedirect.com/science/article/pii/S075333222200405X
Palabra clave:
Alcaloides de Amaryllidaceae Galantina
Acetylcholinesterase inhibition
Amaryllidaceae alkaloids
Galanthine; Molecular docking
Molecular dynamics
Rights
openAccess
License
http://purl.org/coar/access_right/c_abf2
Description
Summary:Zephyranthes carinata Herb., a specie of the Amaryllidoideae subfamily, has been reported to have inhibitory activity against acetylcholinesterase. However, scientific evidence related to their bioactive alkaloids has been lacking. Thus, this study describes the isolation of the alkaloids of this plant, and their inhibition of the enzymes acetylcholinesterase (eeAChE) and butyrylcholinesterase (eqBuChE), being galanthine the main component. Additionally, haemanthamine, hamayne, lycoramine, lycorine, tazettine, trisphaeridine and vittatine/crinine were also isolated. The results showed that galanthine has significant activity at low micromolar concentrations for eeAChE (IC50 = 1.96 μg/mL). The in-silico study allowed to establish at a molecular level the high affinity and the way galanthine interacts with the active site of the TcAChE enzyme, information that corroborates the result of the experimental IC50. However, according to molecular dynamics (MD) analysis, it is also suggested that galanthine presents a different inhibition mode that the one observed for galanthamine, by presenting interaction with peripheral anionic binding site of the enzyme, which prevents the entrance and exit of molecules from the active site. Thus, in vitro screening assays plus rapid computer development play an essential role in the search for new cholinesterase inhibitors by identifying unknown bio-interactions between bioactive compounds and biological targets. © 2022 The Authors