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Sesquiterpene lactones as potential therapeutic agents against Naegleria fowleri
Naegleria fowleri is the causative agent the primary amoebic meningoencephalitis (PAM), a fatal disease in more than the 90% of the reported cases that affects the central nervous system. The amoeba infects the nasal cavity of mostly children and young adults who report previous aquatic exposure in...
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Published in: | Biomedicine & pharmacotherapy 2022-03, Vol.147, p.112694-112694, Article 112694 |
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creator | Arberas-Jiménez, Iñigo Rizo-Liendo, Aitor Nocchi, Nathália Sifaoui, Ines Chao-Pellicer, Javier Souto, María L. Suárez-Gómez, Blanca Díaz-Marrero, Ana R. Fernández, José J. Piñero, José E. Lorenzo-Morales, Jacob |
description | Naegleria fowleri is the causative agent the primary amoebic meningoencephalitis (PAM), a fatal disease in more than the 90% of the reported cases that affects the central nervous system. The amoeba infects the nasal cavity of mostly children and young adults who report previous aquatic exposure in warm water sources. The rapid progression of the disease and the lack of effective and safety therapeutic options make the search of new anti-amoebic compounds an urgent issue. In this study, twelve sesquiterpene lactones isolated from the zoanthid Palythoa aff. clavata were tested against the trophozoite stage of Naegleria fowleri. Anhydroartemorin (2) and 1(10)Z,4E,14-acetoxy-costunolide (3) showed the best anti-amoeboid activity values with IC50 23.02 ± 1.26 and 28.34 ± 6.27, respectively. In addition, the mechanisms of programmed cell death induction of these two molecules were evaluated with positive results for both compounds. Finally, a structure-activity relationship was analyzed to reveal the dependence of reactivity and lipophilicity on the biological activity. The log P values of the compounds were calculated to postulate them as good candidates to cross the blood-brain barrier, a limiting factor in the development of new anti-Naegleria treatments. Therefore, the mentioned sesquiterpene lactones could be considered as potential PAM therapeutic options in the future.
[Display omitted]
•Three germacrane sesquiterpene lactones showed anti-Naegleria activity.•Anhydroartemorin was the most active molecule with an IC50 of 23.02 μM.•Anhydroartemorin and cis-trans-Costunolide-14-acetate induce PCD in treated amoebae. |
doi_str_mv | 10.1016/j.biopha.2022.112694 |
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[Display omitted]
•Three germacrane sesquiterpene lactones showed anti-Naegleria activity.•Anhydroartemorin was the most active molecule with an IC50 of 23.02 μM.•Anhydroartemorin and cis-trans-Costunolide-14-acetate induce PCD in treated amoebae.</description><identifier>ISSN: 0753-3322</identifier><identifier>EISSN: 1950-6007</identifier><identifier>DOI: 10.1016/j.biopha.2022.112694</identifier><identifier>PMID: 35131659</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Meningoencephalitis ; Naegleria ; Palythoa ; Programmed cell death ; Sesquiterpene lactones</subject><ispartof>Biomedicine & pharmacotherapy, 2022-03, Vol.147, p.112694-112694, Article 112694</ispartof><rights>2022 The Authors</rights><rights>Copyright © 2022 The Authors. Published by Elsevier Masson SAS.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-2e334b47150153cb4d95e05abbad756574e961bce79b4614be419f8f2fa2a3b13</citedby><cites>FETCH-LOGICAL-c408t-2e334b47150153cb4d95e05abbad756574e961bce79b4614be419f8f2fa2a3b13</cites></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/35131659$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arberas-Jiménez, Iñigo</creatorcontrib><creatorcontrib>Rizo-Liendo, Aitor</creatorcontrib><creatorcontrib>Nocchi, Nathália</creatorcontrib><creatorcontrib>Sifaoui, Ines</creatorcontrib><creatorcontrib>Chao-Pellicer, Javier</creatorcontrib><creatorcontrib>Souto, María L.</creatorcontrib><creatorcontrib>Suárez-Gómez, Blanca</creatorcontrib><creatorcontrib>Díaz-Marrero, Ana R.</creatorcontrib><creatorcontrib>Fernández, José J.</creatorcontrib><creatorcontrib>Piñero, José E.</creatorcontrib><creatorcontrib>Lorenzo-Morales, Jacob</creatorcontrib><title>Sesquiterpene lactones as potential therapeutic agents against Naegleria fowleri</title><title>Biomedicine & pharmacotherapy</title><addtitle>Biomed Pharmacother</addtitle><description>Naegleria fowleri is the causative agent the primary amoebic meningoencephalitis (PAM), a fatal disease in more than the 90% of the reported cases that affects the central nervous system. The amoeba infects the nasal cavity of mostly children and young adults who report previous aquatic exposure in warm water sources. The rapid progression of the disease and the lack of effective and safety therapeutic options make the search of new anti-amoebic compounds an urgent issue. In this study, twelve sesquiterpene lactones isolated from the zoanthid Palythoa aff. clavata were tested against the trophozoite stage of Naegleria fowleri. Anhydroartemorin (2) and 1(10)Z,4E,14-acetoxy-costunolide (3) showed the best anti-amoeboid activity values with IC50 23.02 ± 1.26 and 28.34 ± 6.27, respectively. In addition, the mechanisms of programmed cell death induction of these two molecules were evaluated with positive results for both compounds. Finally, a structure-activity relationship was analyzed to reveal the dependence of reactivity and lipophilicity on the biological activity. The log P values of the compounds were calculated to postulate them as good candidates to cross the blood-brain barrier, a limiting factor in the development of new anti-Naegleria treatments. Therefore, the mentioned sesquiterpene lactones could be considered as potential PAM therapeutic options in the future.
[Display omitted]
•Three germacrane sesquiterpene lactones showed anti-Naegleria activity.•Anhydroartemorin was the most active molecule with an IC50 of 23.02 μM.•Anhydroartemorin and cis-trans-Costunolide-14-acetate induce PCD in treated amoebae.</description><subject>Meningoencephalitis</subject><subject>Naegleria</subject><subject>Palythoa</subject><subject>Programmed cell death</subject><subject>Sesquiterpene lactones</subject><issn>0753-3322</issn><issn>1950-6007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kE1Lw0AQhhdRbK3-A5EcvSTud5qLIMUvKCqo52V3M2m3pEm6u1H896ZEPXqaYeZ952UehM4Jzggm8mqTGdd2a51RTGlGCJUFP0BTUgicSozzQzTFuWApY5RO0EkIG4yxkGx-jCZMEEakKKbo5RXCrncRfAcNJLW2sW0gJDokXRuhiU7XSVyD1x300dlEr4bhsF9p14SYPGlY1eCdTqr2c9-coqNK1wHOfuoMvd_dvi0e0uXz_ePiZplajucxpcAYNzwnAhPBrOFlIQALbYwucyFFzqGQxFjIC8Ml4QY4Kap5RStNNTOEzdDleLfz7a6HENXWBQt1rRto-6CopHJe4JzupXyUWt-G4KFSnXdb7b8UwWrPUm3UyFLtWaqR5WC7-EnozRbKP9MvvEFwPQpg-PPDgVfBOmgslM6Djaps3f8J3021h7I</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Arberas-Jiménez, Iñigo</creator><creator>Rizo-Liendo, Aitor</creator><creator>Nocchi, Nathália</creator><creator>Sifaoui, Ines</creator><creator>Chao-Pellicer, Javier</creator><creator>Souto, María L.</creator><creator>Suárez-Gómez, Blanca</creator><creator>Díaz-Marrero, Ana R.</creator><creator>Fernández, José J.</creator><creator>Piñero, José E.</creator><creator>Lorenzo-Morales, Jacob</creator><general>Elsevier Masson SAS</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202203</creationdate><title>Sesquiterpene lactones as potential therapeutic agents against Naegleria fowleri</title><author>Arberas-Jiménez, Iñigo ; Rizo-Liendo, Aitor ; Nocchi, Nathália ; Sifaoui, Ines ; Chao-Pellicer, Javier ; Souto, María L. ; Suárez-Gómez, Blanca ; Díaz-Marrero, Ana R. ; Fernández, José J. ; Piñero, José E. ; Lorenzo-Morales, Jacob</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-2e334b47150153cb4d95e05abbad756574e961bce79b4614be419f8f2fa2a3b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Meningoencephalitis</topic><topic>Naegleria</topic><topic>Palythoa</topic><topic>Programmed cell death</topic><topic>Sesquiterpene lactones</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arberas-Jiménez, Iñigo</creatorcontrib><creatorcontrib>Rizo-Liendo, Aitor</creatorcontrib><creatorcontrib>Nocchi, Nathália</creatorcontrib><creatorcontrib>Sifaoui, Ines</creatorcontrib><creatorcontrib>Chao-Pellicer, Javier</creatorcontrib><creatorcontrib>Souto, María L.</creatorcontrib><creatorcontrib>Suárez-Gómez, Blanca</creatorcontrib><creatorcontrib>Díaz-Marrero, Ana R.</creatorcontrib><creatorcontrib>Fernández, José J.</creatorcontrib><creatorcontrib>Piñero, José E.</creatorcontrib><creatorcontrib>Lorenzo-Morales, Jacob</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedicine & pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arberas-Jiménez, Iñigo</au><au>Rizo-Liendo, Aitor</au><au>Nocchi, Nathália</au><au>Sifaoui, Ines</au><au>Chao-Pellicer, Javier</au><au>Souto, María L.</au><au>Suárez-Gómez, Blanca</au><au>Díaz-Marrero, Ana R.</au><au>Fernández, José J.</au><au>Piñero, José E.</au><au>Lorenzo-Morales, Jacob</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sesquiterpene lactones as potential therapeutic agents against Naegleria fowleri</atitle><jtitle>Biomedicine & pharmacotherapy</jtitle><addtitle>Biomed Pharmacother</addtitle><date>2022-03</date><risdate>2022</risdate><volume>147</volume><spage>112694</spage><epage>112694</epage><pages>112694-112694</pages><artnum>112694</artnum><issn>0753-3322</issn><eissn>1950-6007</eissn><abstract>Naegleria fowleri is the causative agent the primary amoebic meningoencephalitis (PAM), a fatal disease in more than the 90% of the reported cases that affects the central nervous system. The amoeba infects the nasal cavity of mostly children and young adults who report previous aquatic exposure in warm water sources. The rapid progression of the disease and the lack of effective and safety therapeutic options make the search of new anti-amoebic compounds an urgent issue. In this study, twelve sesquiterpene lactones isolated from the zoanthid Palythoa aff. clavata were tested against the trophozoite stage of Naegleria fowleri. Anhydroartemorin (2) and 1(10)Z,4E,14-acetoxy-costunolide (3) showed the best anti-amoeboid activity values with IC50 23.02 ± 1.26 and 28.34 ± 6.27, respectively. In addition, the mechanisms of programmed cell death induction of these two molecules were evaluated with positive results for both compounds. Finally, a structure-activity relationship was analyzed to reveal the dependence of reactivity and lipophilicity on the biological activity. The log P values of the compounds were calculated to postulate them as good candidates to cross the blood-brain barrier, a limiting factor in the development of new anti-Naegleria treatments. Therefore, the mentioned sesquiterpene lactones could be considered as potential PAM therapeutic options in the future.
[Display omitted]
•Three germacrane sesquiterpene lactones showed anti-Naegleria activity.•Anhydroartemorin was the most active molecule with an IC50 of 23.02 μM.•Anhydroartemorin and cis-trans-Costunolide-14-acetate induce PCD in treated amoebae.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>35131659</pmid><doi>10.1016/j.biopha.2022.112694</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Meningoencephalitis Naegleria Palythoa Programmed cell death Sesquiterpene lactones |
title | Sesquiterpene lactones as potential therapeutic agents against Naegleria fowleri |
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