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Alkaloids of Abuta panurensis Eichler: In silico and in vitro study of acetylcholinesterase inhibition, cytotoxic and immunomodulatory activities

Natural products obtained from species of the genus Abuta (Menispermaceae) are known as ethnobotanicals that are attracting increasing attention due to a wide range of their pharmacological properties. In this study, the alkaloids stepharine and 5-N-methylmaytenine were first isolated from branches...

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Autores principales: da Silva Mesquita, Rochelly, Kyrylchuk, Andrii, Costa de Oliveira, Regiane, Costa Sá, Ingrity Suelen, Coutinho Borges Camargo, Gabriel, Soares Pontes, Gemilson, Moura Araújo da Silva, Felipe, Saraiva Nunomura, Rita de Cássia, Grafov, Andriy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523975/
https://www.ncbi.nlm.nih.gov/pubmed/32991579
http://dx.doi.org/10.1371/journal.pone.0239364
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author da Silva Mesquita, Rochelly
Kyrylchuk, Andrii
Costa de Oliveira, Regiane
Costa Sá, Ingrity Suelen
Coutinho Borges Camargo, Gabriel
Soares Pontes, Gemilson
Moura Araújo da Silva, Felipe
Saraiva Nunomura, Rita de Cássia
Grafov, Andriy
author_facet da Silva Mesquita, Rochelly
Kyrylchuk, Andrii
Costa de Oliveira, Regiane
Costa Sá, Ingrity Suelen
Coutinho Borges Camargo, Gabriel
Soares Pontes, Gemilson
Moura Araújo da Silva, Felipe
Saraiva Nunomura, Rita de Cássia
Grafov, Andriy
author_sort da Silva Mesquita, Rochelly
collection PubMed
description Natural products obtained from species of the genus Abuta (Menispermaceae) are known as ethnobotanicals that are attracting increasing attention due to a wide range of their pharmacological properties. In this study, the alkaloids stepharine and 5-N-methylmaytenine were first isolated from branches of Abuta panurensis Eichler, an endemic species from the Amazonian rainforest. Structure of the compounds was elucidated by a combination of 1D and 2D NMR spectroscopic and MS and HRMS spectrometric techniques. Interaction of the above-mentioned alkaloids with acetylcholinesterase enzyme and interleukins IL-6 and IL-8 was investigated in silico by molecular docking. The molecules under investigation were able to bind effectively with the active sites of the AChE enzyme, IL-6, and IL-8 showing affinity towards the proteins. Along with the theoretical study, acetylcholinesterase enzyme inhibition, cytotoxic, and immunomodulatory activity of the compounds were assessed by in vitro assays. The data obtained in silico corroborate the results of AChE enzyme inhibition, the IC(50) values of 61.24μM for stepharine and 19.55μM for 5-N-methylmaytenine were found. The compounds showed cytotoxic activity against two tumor cell lines (K562 and U937) with IC(50) values ranging from 11.77 μM to 28.48 μM. The in vitro assays revealed that both alkaloids were non-toxic to Vero and human PBMC cells. As for the immunomodulatory activity, both compounds inhibited the production of IL-6 at similar levels. Stepharine inhibited considerably the production of IL-8 in comparison to 5-N-methylmaytenine, which showed a dose dependent action (inhibitory at the IC(50) dose, and stimulatory at the twofold IC(50) one). Such a behavior may possibly be explained by different binding modes of the alkaloids to the interleukin structural fragments. Occurrence of the polyamine alkaloid 5-N-methylmaytenine was reported for the first time for the Menispermaceae family, as well as the presence of stepharine in A. panurensis.
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spelling pubmed-75239752020-10-06 Alkaloids of Abuta panurensis Eichler: In silico and in vitro study of acetylcholinesterase inhibition, cytotoxic and immunomodulatory activities da Silva Mesquita, Rochelly Kyrylchuk, Andrii Costa de Oliveira, Regiane Costa Sá, Ingrity Suelen Coutinho Borges Camargo, Gabriel Soares Pontes, Gemilson Moura Araújo da Silva, Felipe Saraiva Nunomura, Rita de Cássia Grafov, Andriy PLoS One Research Article Natural products obtained from species of the genus Abuta (Menispermaceae) are known as ethnobotanicals that are attracting increasing attention due to a wide range of their pharmacological properties. In this study, the alkaloids stepharine and 5-N-methylmaytenine were first isolated from branches of Abuta panurensis Eichler, an endemic species from the Amazonian rainforest. Structure of the compounds was elucidated by a combination of 1D and 2D NMR spectroscopic and MS and HRMS spectrometric techniques. Interaction of the above-mentioned alkaloids with acetylcholinesterase enzyme and interleukins IL-6 and IL-8 was investigated in silico by molecular docking. The molecules under investigation were able to bind effectively with the active sites of the AChE enzyme, IL-6, and IL-8 showing affinity towards the proteins. Along with the theoretical study, acetylcholinesterase enzyme inhibition, cytotoxic, and immunomodulatory activity of the compounds were assessed by in vitro assays. The data obtained in silico corroborate the results of AChE enzyme inhibition, the IC(50) values of 61.24μM for stepharine and 19.55μM for 5-N-methylmaytenine were found. The compounds showed cytotoxic activity against two tumor cell lines (K562 and U937) with IC(50) values ranging from 11.77 μM to 28.48 μM. The in vitro assays revealed that both alkaloids were non-toxic to Vero and human PBMC cells. As for the immunomodulatory activity, both compounds inhibited the production of IL-6 at similar levels. Stepharine inhibited considerably the production of IL-8 in comparison to 5-N-methylmaytenine, which showed a dose dependent action (inhibitory at the IC(50) dose, and stimulatory at the twofold IC(50) one). Such a behavior may possibly be explained by different binding modes of the alkaloids to the interleukin structural fragments. Occurrence of the polyamine alkaloid 5-N-methylmaytenine was reported for the first time for the Menispermaceae family, as well as the presence of stepharine in A. panurensis. Public Library of Science 2020-09-29 /pmc/articles/PMC7523975/ /pubmed/32991579 http://dx.doi.org/10.1371/journal.pone.0239364 Text en © 2020 da Silva Mesquita et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
da Silva Mesquita, Rochelly
Kyrylchuk, Andrii
Costa de Oliveira, Regiane
Costa Sá, Ingrity Suelen
Coutinho Borges Camargo, Gabriel
Soares Pontes, Gemilson
Moura Araújo da Silva, Felipe
Saraiva Nunomura, Rita de Cássia
Grafov, Andriy
Alkaloids of Abuta panurensis Eichler: In silico and in vitro study of acetylcholinesterase inhibition, cytotoxic and immunomodulatory activities
title Alkaloids of Abuta panurensis Eichler: In silico and in vitro study of acetylcholinesterase inhibition, cytotoxic and immunomodulatory activities
title_full Alkaloids of Abuta panurensis Eichler: In silico and in vitro study of acetylcholinesterase inhibition, cytotoxic and immunomodulatory activities
title_fullStr Alkaloids of Abuta panurensis Eichler: In silico and in vitro study of acetylcholinesterase inhibition, cytotoxic and immunomodulatory activities
title_full_unstemmed Alkaloids of Abuta panurensis Eichler: In silico and in vitro study of acetylcholinesterase inhibition, cytotoxic and immunomodulatory activities
title_short Alkaloids of Abuta panurensis Eichler: In silico and in vitro study of acetylcholinesterase inhibition, cytotoxic and immunomodulatory activities
title_sort alkaloids of abuta panurensis eichler: in silico and in vitro study of acetylcholinesterase inhibition, cytotoxic and immunomodulatory activities
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523975/
https://www.ncbi.nlm.nih.gov/pubmed/32991579
http://dx.doi.org/10.1371/journal.pone.0239364
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