2023, Number 1
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Acta de Otorrinolaringología CCC 2023; 51 (1)
Virtual screening of secondary metabolites of Origanum vulgare and marjoram against NaV1.7 as promising anesthetics associated with the auditory neurosensory pathway
Vélez-Duncan CA, Uribe-Escobar A, Pineda-Alemán R, Contreras-Puentes N, Alviz-Amador A
Language: Spanish
References: 26
Page: 29-34
PDF size: 275.71 Kb.
ABSTRACT
Introduction: In general, oregano is a medicinal plant used in rural areas of the colombian
Caribbean coast to treat conditions of the respiratory system and external
ear due to its potential anti-inflammatory, analgesic and antiseptic effect, however,
it has not been validated through clinical trials.
Objective: To carry out a virtual
screening based on molecular coupling of secondary metabolites identified in Origanum
vulgare and marjoram against the Nav1.7 receptor to evaluate the potential
anesthetic effect at the level of the external ear.
Method: This is an in-silico study
with a virtual molecular docking screening approach, for which the AutoDock Vina
software was used and the Swiss Institute of Bioinformatics (http://www.sib.swiss)
online tool SwissADME was used for pharmacokinetic predictions. Additionally,
the in-silico toxicity of the molecules was evaluated using the GUSAR-Online server.
Results: Of the 99 molecules that were evaluated by molecular coupling, it was
shown that the highest affinities with respect to the Nav1.7 channel were chlorogenic
acid, rutin, luteolin, luteoside and apigenin, where affinity energies were presented
with the binding site in the central pore of the channel at values between -5.40 ±
0.00 to -5.57 ± 0.06 kcal/mol, which according to the ADMET and GUSAR analysis,
only chlorogenic acid, luteolin and apigenin are good potential candidates for
anesthetic drugs complying with the 5 rules of Lipinsky.
Conclusion: Based on the
phytochemical studies of O. vulgare and marjoram that have reported the secondary
metabolites present in the extracts of these plants, their coupling to the Nav1.7 channel
expressed in the neurosensory pathway of the ear was evidenced in this in-silico
study. It was also shown that chlorogenic acid, luteolin and apigenin could be potential
local anesthetic drugs for ear conditions.
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