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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
Main Authors: 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
Format: Article
Language:English
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Summary: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.
ISSN:0753-3322
1950-6007
DOI:10.1016/j.biopha.2022.112694