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Multitarget anti-parasitic activities of isoquinoline alkaloids isolated from Hippeastrum aulicum (Amaryllidaceae)
•Amaryllidaceae species exhibit a substantial presence of alkaloids distinguished by their structures and bioactive properties.•Eleven alkaloids were previously isolated from Hippeastrum aulicum (Ker Gawl.) Herb, and five of them were now tested against trypanosoma cruzi and Leishmania infantum.•Hae...
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Published in: | Phytomedicine (Stuttgart) 2024-06, Vol.128, p.155414-155414, Article 155414 |
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creator | Bessa, Carliani Dal Piero Betzel Feu, Amanda Eiriz de Menezes, Renata Priscila Barros Scotti, Marcus Tullius Lima, Julia Maria Godoi Lima, Marta Lopes Tempone, Andre Gustavo de Andrade, Jean Paulo Bastida, Jaume Borges, Warley de Souza |
description | •Amaryllidaceae species exhibit a substantial presence of alkaloids distinguished by their structures and bioactive properties.•Eleven alkaloids were previously isolated from Hippeastrum aulicum (Ker Gawl.) Herb, and five of them were now tested against trypanosoma cruzi and Leishmania infantum.•Haemanthamine and lycorine showed multitarget antiparasitic activity through in silico and in vitro analysis.•7‑methoxy-O-methyllycorenine exhibited higher activity against T. cruzi trypomastigotes.
Chagas disease and leishmaniasis affect a significant portion of the Latin American population and still lack efficient treatments. In this context, natural products emerge as promising compounds for developing more effective therapies, aiming to mitigate side effects and drug resistance. Notably, species from the Amaryllidaceae family emerge as potential reservoirs of antiparasitic agents due to the presence of diverse biologically active alkaloids.
To assess the anti-Trypanosoma cruzi and anti-Leishmania infantum activity of five isolated alkaloids from Hippeastrum aulicum Herb. (Amaryllidaceae) against different life stages of the parasites using in silico and in vitro assays. Furthermore, molecular docking was employed to evaluate the interaction of the most active alkaloids.
Five natural isoquinoline alkaloids isolated in suitable quantities for in vitro testing underwent preliminary in silico analysis to predict their potential efficacy against Trypanosoma cruzi (amastigote and trypomastigote forms) and Leishmania infantum (amastigote and promastigote forms). The in vitro antiparasitic activity and mammalian cytotoxicity were investigated with a subsequent comparison of both analysis (in silico and in vitro) findings. Additionally, this study employed the molecular docking technique, utilizing cruzain (T. cruzi) and sterol 14α-demethylase (CYP51, L. infantum) as crucial biological targets for parasite survival, specifically focusing on compounds that exhibited promising activities against both parasites.
Through computational techniques, it was identified that the alkaloids haemanthamine (1) and lycorine (8) were the most active against T. cruzi (amastigote and trypomastigote) and L. infantum (amastigote and promastigote), while also revealing unprecedented activity of alkaloid 7‑methoxy-O-methyllycorenine (6). The in vitro analysis confirmed the in silico tests, in which compound 1 presented the best activities against the promastigote and amastigote forms of L. |
doi_str_mv | 10.1016/j.phymed.2024.155414 |
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Chagas disease and leishmaniasis affect a significant portion of the Latin American population and still lack efficient treatments. In this context, natural products emerge as promising compounds for developing more effective therapies, aiming to mitigate side effects and drug resistance. Notably, species from the Amaryllidaceae family emerge as potential reservoirs of antiparasitic agents due to the presence of diverse biologically active alkaloids.
To assess the anti-Trypanosoma cruzi and anti-Leishmania infantum activity of five isolated alkaloids from Hippeastrum aulicum Herb. (Amaryllidaceae) against different life stages of the parasites using in silico and in vitro assays. Furthermore, molecular docking was employed to evaluate the interaction of the most active alkaloids.
Five natural isoquinoline alkaloids isolated in suitable quantities for in vitro testing underwent preliminary in silico analysis to predict their potential efficacy against Trypanosoma cruzi (amastigote and trypomastigote forms) and Leishmania infantum (amastigote and promastigote forms). The in vitro antiparasitic activity and mammalian cytotoxicity were investigated with a subsequent comparison of both analysis (in silico and in vitro) findings. Additionally, this study employed the molecular docking technique, utilizing cruzain (T. cruzi) and sterol 14α-demethylase (CYP51, L. infantum) as crucial biological targets for parasite survival, specifically focusing on compounds that exhibited promising activities against both parasites.
Through computational techniques, it was identified that the alkaloids haemanthamine (1) and lycorine (8) were the most active against T. cruzi (amastigote and trypomastigote) and L. infantum (amastigote and promastigote), while also revealing unprecedented activity of alkaloid 7‑methoxy-O-methyllycorenine (6). The in vitro analysis confirmed the in silico tests, in which compound 1 presented the best activities against the promastigote and amastigote forms of L. infantum with half-maximal inhibitory concentration (IC50) 0.6 µM and 1.78 µM, respectively. Compound 8 exhibited significant activity against the amastigote form of T. cruzi (IC50 7.70 µM), and compound 6 demonstrated activity against the trypomastigote forms of T. cruzi and amastigote of L. infantum, with IC50 values of 89.55 and 86.12 µM, respectively. Molecular docking analyses indicated that alkaloids 1 and 8 exhibited superior interaction energies compared to the inhibitors.
The hitherto unreported potential of compound 6 against T. cruzi trypomastigotes and L. infantum amastigotes is now brought to the forefront. Furthermore, the acquired dataset signifies that the isolated alkaloids 1 and 8 from H. aulicum might serve as prototypes for subsequent structural refinements aimed at the exploration of novel leads against both T. cruzi and L. infantum parasites.
[Display omitted]</description><identifier>ISSN: 0944-7113</identifier><identifier>EISSN: 1618-095X</identifier><identifier>DOI: 10.1016/j.phymed.2024.155414</identifier><identifier>PMID: 38503155</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Alkaloids ; Alkaloids - chemistry ; Alkaloids - isolation & purification ; Alkaloids - pharmacology ; Amaryllidaceae ; Amaryllidaceae - chemistry ; Animals ; Antiparasitic Agents - chemistry ; Antiparasitic Agents - isolation & purification ; Antiparasitic Agents - pharmacology ; Antiprotozoal Agents - chemistry ; Antiprotozoal Agents - isolation & purification ; Antiprotozoal Agents - pharmacology ; Chagas disease ; Hippeastrum aulicum ; Humans ; Isoquinolines - chemistry ; Isoquinolines - isolation & purification ; Isoquinolines - pharmacology ; Leishmania ; Leishmania infantum - drug effects ; Molecular Docking Simulation ; Multitarget ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Trypanosoma cruzi ; Trypanosoma cruzi - drug effects</subject><ispartof>Phytomedicine (Stuttgart), 2024-06, Vol.128, p.155414-155414, Article 155414</ispartof><rights>2024 Elsevier GmbH</rights><rights>Copyright © 2024 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c311t-4b2448c260077d5c472e8c85f52309883e86dd7289000d6c77a91b5c88909bd93</cites><orcidid>0000-0003-4475-1028 ; 0000-0002-1680-5319</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38503155$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bessa, Carliani Dal Piero Betzel</creatorcontrib><creatorcontrib>Feu, Amanda Eiriz</creatorcontrib><creatorcontrib>de Menezes, Renata Priscila Barros</creatorcontrib><creatorcontrib>Scotti, Marcus Tullius</creatorcontrib><creatorcontrib>Lima, Julia Maria Godoi</creatorcontrib><creatorcontrib>Lima, Marta Lopes</creatorcontrib><creatorcontrib>Tempone, Andre Gustavo</creatorcontrib><creatorcontrib>de Andrade, Jean Paulo</creatorcontrib><creatorcontrib>Bastida, Jaume</creatorcontrib><creatorcontrib>Borges, Warley de Souza</creatorcontrib><title>Multitarget anti-parasitic activities of isoquinoline alkaloids isolated from Hippeastrum aulicum (Amaryllidaceae)</title><title>Phytomedicine (Stuttgart)</title><addtitle>Phytomedicine</addtitle><description>•Amaryllidaceae species exhibit a substantial presence of alkaloids distinguished by their structures and bioactive properties.•Eleven alkaloids were previously isolated from Hippeastrum aulicum (Ker Gawl.) Herb, and five of them were now tested against trypanosoma cruzi and Leishmania infantum.•Haemanthamine and lycorine showed multitarget antiparasitic activity through in silico and in vitro analysis.•7‑methoxy-O-methyllycorenine exhibited higher activity against T. cruzi trypomastigotes.
Chagas disease and leishmaniasis affect a significant portion of the Latin American population and still lack efficient treatments. In this context, natural products emerge as promising compounds for developing more effective therapies, aiming to mitigate side effects and drug resistance. Notably, species from the Amaryllidaceae family emerge as potential reservoirs of antiparasitic agents due to the presence of diverse biologically active alkaloids.
To assess the anti-Trypanosoma cruzi and anti-Leishmania infantum activity of five isolated alkaloids from Hippeastrum aulicum Herb. (Amaryllidaceae) against different life stages of the parasites using in silico and in vitro assays. Furthermore, molecular docking was employed to evaluate the interaction of the most active alkaloids.
Five natural isoquinoline alkaloids isolated in suitable quantities for in vitro testing underwent preliminary in silico analysis to predict their potential efficacy against Trypanosoma cruzi (amastigote and trypomastigote forms) and Leishmania infantum (amastigote and promastigote forms). The in vitro antiparasitic activity and mammalian cytotoxicity were investigated with a subsequent comparison of both analysis (in silico and in vitro) findings. Additionally, this study employed the molecular docking technique, utilizing cruzain (T. cruzi) and sterol 14α-demethylase (CYP51, L. infantum) as crucial biological targets for parasite survival, specifically focusing on compounds that exhibited promising activities against both parasites.
Through computational techniques, it was identified that the alkaloids haemanthamine (1) and lycorine (8) were the most active against T. cruzi (amastigote and trypomastigote) and L. infantum (amastigote and promastigote), while also revealing unprecedented activity of alkaloid 7‑methoxy-O-methyllycorenine (6). The in vitro analysis confirmed the in silico tests, in which compound 1 presented the best activities against the promastigote and amastigote forms of L. infantum with half-maximal inhibitory concentration (IC50) 0.6 µM and 1.78 µM, respectively. Compound 8 exhibited significant activity against the amastigote form of T. cruzi (IC50 7.70 µM), and compound 6 demonstrated activity against the trypomastigote forms of T. cruzi and amastigote of L. infantum, with IC50 values of 89.55 and 86.12 µM, respectively. Molecular docking analyses indicated that alkaloids 1 and 8 exhibited superior interaction energies compared to the inhibitors.
The hitherto unreported potential of compound 6 against T. cruzi trypomastigotes and L. infantum amastigotes is now brought to the forefront. Furthermore, the acquired dataset signifies that the isolated alkaloids 1 and 8 from H. aulicum might serve as prototypes for subsequent structural refinements aimed at the exploration of novel leads against both T. cruzi and L. infantum parasites.
[Display omitted]</description><subject>Alkaloids</subject><subject>Alkaloids - chemistry</subject><subject>Alkaloids - isolation & purification</subject><subject>Alkaloids - pharmacology</subject><subject>Amaryllidaceae</subject><subject>Amaryllidaceae - chemistry</subject><subject>Animals</subject><subject>Antiparasitic Agents - chemistry</subject><subject>Antiparasitic Agents - isolation & purification</subject><subject>Antiparasitic Agents - pharmacology</subject><subject>Antiprotozoal Agents - chemistry</subject><subject>Antiprotozoal Agents - isolation & purification</subject><subject>Antiprotozoal Agents - pharmacology</subject><subject>Chagas disease</subject><subject>Hippeastrum aulicum</subject><subject>Humans</subject><subject>Isoquinolines - chemistry</subject><subject>Isoquinolines - isolation & purification</subject><subject>Isoquinolines - pharmacology</subject><subject>Leishmania</subject><subject>Leishmania infantum - drug effects</subject><subject>Molecular Docking Simulation</subject><subject>Multitarget</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Trypanosoma cruzi</subject><subject>Trypanosoma cruzi - drug effects</subject><issn>0944-7113</issn><issn>1618-095X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kMtu1TAQhq0K1B7avgFCWZZFDrbjxPYGqaoKrVTEBiR2lo89gTk4F2ynUt8eR2m3Xc1o5v_n8hHyntE9o6z7dNzPf54G8HtOudizthVMnJAd65iqqW5_vSE7qoWoJWPNGXmX0pFSJrSkp-SsUS1timVH4rclZMw2_oZc2TFjPdtoE2Z0lXUZH0sGqZr6CtP0b8FxCjhCZcNfGyb0aS0Hm8FXfZyG6g7nGWzKcRkquwR0JV5dDzY-hYDeOrDw8YK87W1IcPkcz8nPL7c_bu7qh-9f72-uH2rXMJZrceBCKMc7SqX0rROSg3Kq7VveUK1UA6rzXnKlKaW-c1JazQ6tU6WgD1435-RqmzvHcjmkbAZMDkKwI0xLMlxLLmkjhSpSsUldnFKK0Js54nq1YdSstM3RbLTNSttstIvtw_OG5bD2XkwveIvg8yaA8ucjQjTJIYwOPEZw2fgJX9_wH_6wk9Q</recordid><startdate>202406</startdate><enddate>202406</enddate><creator>Bessa, Carliani Dal Piero Betzel</creator><creator>Feu, Amanda Eiriz</creator><creator>de Menezes, Renata Priscila Barros</creator><creator>Scotti, Marcus Tullius</creator><creator>Lima, Julia Maria Godoi</creator><creator>Lima, Marta Lopes</creator><creator>Tempone, Andre Gustavo</creator><creator>de Andrade, Jean Paulo</creator><creator>Bastida, Jaume</creator><creator>Borges, Warley de Souza</creator><general>Elsevier GmbH</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4475-1028</orcidid><orcidid>https://orcid.org/0000-0002-1680-5319</orcidid></search><sort><creationdate>202406</creationdate><title>Multitarget anti-parasitic activities of isoquinoline alkaloids isolated from Hippeastrum aulicum (Amaryllidaceae)</title><author>Bessa, Carliani Dal Piero Betzel ; Feu, Amanda Eiriz ; de Menezes, Renata Priscila Barros ; Scotti, Marcus Tullius ; Lima, Julia Maria Godoi ; Lima, Marta Lopes ; Tempone, Andre Gustavo ; de Andrade, Jean Paulo ; Bastida, Jaume ; Borges, Warley de Souza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-4b2448c260077d5c472e8c85f52309883e86dd7289000d6c77a91b5c88909bd93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Alkaloids</topic><topic>Alkaloids - chemistry</topic><topic>Alkaloids - isolation & purification</topic><topic>Alkaloids - pharmacology</topic><topic>Amaryllidaceae</topic><topic>Amaryllidaceae - chemistry</topic><topic>Animals</topic><topic>Antiparasitic Agents - chemistry</topic><topic>Antiparasitic Agents - isolation & purification</topic><topic>Antiparasitic Agents - pharmacology</topic><topic>Antiprotozoal Agents - chemistry</topic><topic>Antiprotozoal Agents - isolation & purification</topic><topic>Antiprotozoal Agents - pharmacology</topic><topic>Chagas disease</topic><topic>Hippeastrum aulicum</topic><topic>Humans</topic><topic>Isoquinolines - chemistry</topic><topic>Isoquinolines - isolation & purification</topic><topic>Isoquinolines - pharmacology</topic><topic>Leishmania</topic><topic>Leishmania infantum - drug effects</topic><topic>Molecular Docking Simulation</topic><topic>Multitarget</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Trypanosoma cruzi</topic><topic>Trypanosoma cruzi - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bessa, Carliani Dal Piero Betzel</creatorcontrib><creatorcontrib>Feu, Amanda Eiriz</creatorcontrib><creatorcontrib>de Menezes, Renata Priscila Barros</creatorcontrib><creatorcontrib>Scotti, Marcus Tullius</creatorcontrib><creatorcontrib>Lima, Julia Maria Godoi</creatorcontrib><creatorcontrib>Lima, Marta Lopes</creatorcontrib><creatorcontrib>Tempone, Andre Gustavo</creatorcontrib><creatorcontrib>de Andrade, Jean Paulo</creatorcontrib><creatorcontrib>Bastida, Jaume</creatorcontrib><creatorcontrib>Borges, Warley de Souza</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Phytomedicine (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bessa, Carliani Dal Piero Betzel</au><au>Feu, Amanda Eiriz</au><au>de Menezes, Renata Priscila Barros</au><au>Scotti, Marcus Tullius</au><au>Lima, Julia Maria Godoi</au><au>Lima, Marta Lopes</au><au>Tempone, Andre Gustavo</au><au>de Andrade, Jean Paulo</au><au>Bastida, Jaume</au><au>Borges, Warley de Souza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multitarget anti-parasitic activities of isoquinoline alkaloids isolated from Hippeastrum aulicum (Amaryllidaceae)</atitle><jtitle>Phytomedicine (Stuttgart)</jtitle><addtitle>Phytomedicine</addtitle><date>2024-06</date><risdate>2024</risdate><volume>128</volume><spage>155414</spage><epage>155414</epage><pages>155414-155414</pages><artnum>155414</artnum><issn>0944-7113</issn><eissn>1618-095X</eissn><abstract>•Amaryllidaceae species exhibit a substantial presence of alkaloids distinguished by their structures and bioactive properties.•Eleven alkaloids were previously isolated from Hippeastrum aulicum (Ker Gawl.) Herb, and five of them were now tested against trypanosoma cruzi and Leishmania infantum.•Haemanthamine and lycorine showed multitarget antiparasitic activity through in silico and in vitro analysis.•7‑methoxy-O-methyllycorenine exhibited higher activity against T. cruzi trypomastigotes.
Chagas disease and leishmaniasis affect a significant portion of the Latin American population and still lack efficient treatments. In this context, natural products emerge as promising compounds for developing more effective therapies, aiming to mitigate side effects and drug resistance. Notably, species from the Amaryllidaceae family emerge as potential reservoirs of antiparasitic agents due to the presence of diverse biologically active alkaloids.
To assess the anti-Trypanosoma cruzi and anti-Leishmania infantum activity of five isolated alkaloids from Hippeastrum aulicum Herb. (Amaryllidaceae) against different life stages of the parasites using in silico and in vitro assays. Furthermore, molecular docking was employed to evaluate the interaction of the most active alkaloids.
Five natural isoquinoline alkaloids isolated in suitable quantities for in vitro testing underwent preliminary in silico analysis to predict their potential efficacy against Trypanosoma cruzi (amastigote and trypomastigote forms) and Leishmania infantum (amastigote and promastigote forms). The in vitro antiparasitic activity and mammalian cytotoxicity were investigated with a subsequent comparison of both analysis (in silico and in vitro) findings. Additionally, this study employed the molecular docking technique, utilizing cruzain (T. cruzi) and sterol 14α-demethylase (CYP51, L. infantum) as crucial biological targets for parasite survival, specifically focusing on compounds that exhibited promising activities against both parasites.
Through computational techniques, it was identified that the alkaloids haemanthamine (1) and lycorine (8) were the most active against T. cruzi (amastigote and trypomastigote) and L. infantum (amastigote and promastigote), while also revealing unprecedented activity of alkaloid 7‑methoxy-O-methyllycorenine (6). The in vitro analysis confirmed the in silico tests, in which compound 1 presented the best activities against the promastigote and amastigote forms of L. infantum with half-maximal inhibitory concentration (IC50) 0.6 µM and 1.78 µM, respectively. Compound 8 exhibited significant activity against the amastigote form of T. cruzi (IC50 7.70 µM), and compound 6 demonstrated activity against the trypomastigote forms of T. cruzi and amastigote of L. infantum, with IC50 values of 89.55 and 86.12 µM, respectively. Molecular docking analyses indicated that alkaloids 1 and 8 exhibited superior interaction energies compared to the inhibitors.
The hitherto unreported potential of compound 6 against T. cruzi trypomastigotes and L. infantum amastigotes is now brought to the forefront. Furthermore, the acquired dataset signifies that the isolated alkaloids 1 and 8 from H. aulicum might serve as prototypes for subsequent structural refinements aimed at the exploration of novel leads against both T. cruzi and L. infantum parasites.
[Display omitted]</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>38503155</pmid><doi>10.1016/j.phymed.2024.155414</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-4475-1028</orcidid><orcidid>https://orcid.org/0000-0002-1680-5319</orcidid></addata></record> |
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subjects | Alkaloids Alkaloids - chemistry Alkaloids - isolation & purification Alkaloids - pharmacology Amaryllidaceae Amaryllidaceae - chemistry Animals Antiparasitic Agents - chemistry Antiparasitic Agents - isolation & purification Antiparasitic Agents - pharmacology Antiprotozoal Agents - chemistry Antiprotozoal Agents - isolation & purification Antiprotozoal Agents - pharmacology Chagas disease Hippeastrum aulicum Humans Isoquinolines - chemistry Isoquinolines - isolation & purification Isoquinolines - pharmacology Leishmania Leishmania infantum - drug effects Molecular Docking Simulation Multitarget Plant Extracts - chemistry Plant Extracts - pharmacology Trypanosoma cruzi Trypanosoma cruzi - drug effects |
title | Multitarget anti-parasitic activities of isoquinoline alkaloids isolated from Hippeastrum aulicum (Amaryllidaceae) |
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