Cargando…

Isolation and Characterization of Phenylpropanoid and Lignan Compounds from Peperomia pellucida [L.] Kunth with Estrogenic Activities

Extracts of Peperomia pellucida [L.] Kunth have previously been demonstrated to have in vivo estrogenic-like effects, thereby functioning as an anti-osteoporotic agent. However, the compounds responsible for these effects have not yet been determined. Therefore, the aim of this study is to isolate a...

Descripción completa

Detalles Bibliográficos
Autores principales: Kartika, I Gusti Agung Ayu, Bang, In Jae, Riani, Catur, Insanu, Muhamad, Kwak, Jong Hwan, Chung, Kyu Hyuck, Adnyana, I Ketut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660628/
https://www.ncbi.nlm.nih.gov/pubmed/33114252
http://dx.doi.org/10.3390/molecules25214914
_version_ 1783609044068466688
author Kartika, I Gusti Agung Ayu
Bang, In Jae
Riani, Catur
Insanu, Muhamad
Kwak, Jong Hwan
Chung, Kyu Hyuck
Adnyana, I Ketut
author_facet Kartika, I Gusti Agung Ayu
Bang, In Jae
Riani, Catur
Insanu, Muhamad
Kwak, Jong Hwan
Chung, Kyu Hyuck
Adnyana, I Ketut
author_sort Kartika, I Gusti Agung Ayu
collection PubMed
description Extracts of Peperomia pellucida [L.] Kunth have previously been demonstrated to have in vivo estrogenic-like effects, thereby functioning as an anti-osteoporotic agent. However, the compounds responsible for these effects have not yet been determined. Therefore, the aim of this study is to isolate and elucidate potential compounds with estrogenic activity. The structures of the isolated compounds were identified using 1D (1)H and (13)C-NMR and confirmed by 2D FT-NMR. The estrogenic activity was evaluated using the E-SCREEN assay, and a molecular docking study was performed to predict the binding affinity of the isolated compounds to estrogen receptors. In this experiment, we successfully isolated three phenylpropanoids and two lignan derivatives, namely, 6-allyl-5-methoxy-1,3-benzodioxol-4-ol (1), pachypostaudin B (2), pellucidin A (3), dillapiole (4), and apiol (5). Among these compounds, the isolation of 1 and 2 from P. pellucida is reported for the first time in this study. Activity assays clearly showed that the ethyl acetate extract and its fractions, subfractions, and isolated compounds exerted estrogenic activity. Methanol fraction of the ethyl acetate extract produced the highest estrogenic activity, while 1 and 2 had partial agonist activity. Some compounds (derivates of dillapiole and pellucidin A) also had, in addition, anti-estrogenic activity. In the docking study, the estrogenic activities of 1–5 appeared to be mediated by a classical ligand-dependent mechanism as suggested by the binding interaction between the compounds and estrogen receptors; binding occurred on Arg 394 and His 524 of the alpha receptor and Arg 346 and His 475 of the beta receptor. In summary, we reveal that P. pellucida is a promising anti-osteoporotic agent due to its estrogenic activity, and the compounds responsible for this activity were found to be lignan and phenylpropanoid derivatives. The presence of other compounds in either the extract or fraction may contribute to a synergistic effect, as suggested by the higher estrogenic activity of the methanol fraction. Hence, we suggest further research on the osteoporotic activity and safety of the identified compounds, especially regarding their effects on estrogen-responsive organs.
format Online
Article
Text
id pubmed-7660628
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-76606282020-11-13 Isolation and Characterization of Phenylpropanoid and Lignan Compounds from Peperomia pellucida [L.] Kunth with Estrogenic Activities Kartika, I Gusti Agung Ayu Bang, In Jae Riani, Catur Insanu, Muhamad Kwak, Jong Hwan Chung, Kyu Hyuck Adnyana, I Ketut Molecules Article Extracts of Peperomia pellucida [L.] Kunth have previously been demonstrated to have in vivo estrogenic-like effects, thereby functioning as an anti-osteoporotic agent. However, the compounds responsible for these effects have not yet been determined. Therefore, the aim of this study is to isolate and elucidate potential compounds with estrogenic activity. The structures of the isolated compounds were identified using 1D (1)H and (13)C-NMR and confirmed by 2D FT-NMR. The estrogenic activity was evaluated using the E-SCREEN assay, and a molecular docking study was performed to predict the binding affinity of the isolated compounds to estrogen receptors. In this experiment, we successfully isolated three phenylpropanoids and two lignan derivatives, namely, 6-allyl-5-methoxy-1,3-benzodioxol-4-ol (1), pachypostaudin B (2), pellucidin A (3), dillapiole (4), and apiol (5). Among these compounds, the isolation of 1 and 2 from P. pellucida is reported for the first time in this study. Activity assays clearly showed that the ethyl acetate extract and its fractions, subfractions, and isolated compounds exerted estrogenic activity. Methanol fraction of the ethyl acetate extract produced the highest estrogenic activity, while 1 and 2 had partial agonist activity. Some compounds (derivates of dillapiole and pellucidin A) also had, in addition, anti-estrogenic activity. In the docking study, the estrogenic activities of 1–5 appeared to be mediated by a classical ligand-dependent mechanism as suggested by the binding interaction between the compounds and estrogen receptors; binding occurred on Arg 394 and His 524 of the alpha receptor and Arg 346 and His 475 of the beta receptor. In summary, we reveal that P. pellucida is a promising anti-osteoporotic agent due to its estrogenic activity, and the compounds responsible for this activity were found to be lignan and phenylpropanoid derivatives. The presence of other compounds in either the extract or fraction may contribute to a synergistic effect, as suggested by the higher estrogenic activity of the methanol fraction. Hence, we suggest further research on the osteoporotic activity and safety of the identified compounds, especially regarding their effects on estrogen-responsive organs. MDPI 2020-10-23 /pmc/articles/PMC7660628/ /pubmed/33114252 http://dx.doi.org/10.3390/molecules25214914 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kartika, I Gusti Agung Ayu
Bang, In Jae
Riani, Catur
Insanu, Muhamad
Kwak, Jong Hwan
Chung, Kyu Hyuck
Adnyana, I Ketut
Isolation and Characterization of Phenylpropanoid and Lignan Compounds from Peperomia pellucida [L.] Kunth with Estrogenic Activities
title Isolation and Characterization of Phenylpropanoid and Lignan Compounds from Peperomia pellucida [L.] Kunth with Estrogenic Activities
title_full Isolation and Characterization of Phenylpropanoid and Lignan Compounds from Peperomia pellucida [L.] Kunth with Estrogenic Activities
title_fullStr Isolation and Characterization of Phenylpropanoid and Lignan Compounds from Peperomia pellucida [L.] Kunth with Estrogenic Activities
title_full_unstemmed Isolation and Characterization of Phenylpropanoid and Lignan Compounds from Peperomia pellucida [L.] Kunth with Estrogenic Activities
title_short Isolation and Characterization of Phenylpropanoid and Lignan Compounds from Peperomia pellucida [L.] Kunth with Estrogenic Activities
title_sort isolation and characterization of phenylpropanoid and lignan compounds from peperomia pellucida [l.] kunth with estrogenic activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660628/
https://www.ncbi.nlm.nih.gov/pubmed/33114252
http://dx.doi.org/10.3390/molecules25214914
work_keys_str_mv AT kartikaigustiagungayu isolationandcharacterizationofphenylpropanoidandlignancompoundsfrompeperomiapellucidalkunthwithestrogenicactivities
AT banginjae isolationandcharacterizationofphenylpropanoidandlignancompoundsfrompeperomiapellucidalkunthwithestrogenicactivities
AT rianicatur isolationandcharacterizationofphenylpropanoidandlignancompoundsfrompeperomiapellucidalkunthwithestrogenicactivities
AT insanumuhamad isolationandcharacterizationofphenylpropanoidandlignancompoundsfrompeperomiapellucidalkunthwithestrogenicactivities
AT kwakjonghwan isolationandcharacterizationofphenylpropanoidandlignancompoundsfrompeperomiapellucidalkunthwithestrogenicactivities
AT chungkyuhyuck isolationandcharacterizationofphenylpropanoidandlignancompoundsfrompeperomiapellucidalkunthwithestrogenicactivities
AT adnyanaiketut isolationandcharacterizationofphenylpropanoidandlignancompoundsfrompeperomiapellucidalkunthwithestrogenicactivities