Copaifera spp. oleoresins and two isolated compounds (ent-kaurenoic and ent-polyalthic acid) inhibit Toxoplasma gondii growth in vitro.
Samuel Cota TeixeiraGuilherme de SouzaJoed Pires de Lima JuniorAlessandra Monteiro RosiniAryani Felixa Fajardo MartínezThales Alves de Melo FernandesSergio Ricardo AmbrósioRodrigo Cassio Sola VenezianiJairo Kenupp BastosCarlos Henrique Gomes MartinsBellisa Freitas BarbosaEloisa Amália Vieira FerroPublished in: Experimental parasitology (2024)
Toxoplasmosis affects about one-third of the world's population. The disease treatment methods pose several side effects and do not efficiently eliminate the parasite, making the search for new therapeutic approaches necessary. We aimed to assess the anti-Toxoplasma gondii activity of four Copaifera oleoresins (ORs) and two isolated diterpene acids, named ent-kaurenoic and ent-polyalthic acid. We used HeLa cells as an experimental model of toxoplasmosis. Uninfected and infected HeLa cells were submitted to the treatments, and the parasite intracellular proliferation, cytokine levels and ROS production were measured. Also, tachyzoites were pre-treated and the parasite invasion was determined. Finally, an in silico analysis was performed to identify potential parasite targets. Our data show that the non-cytotoxic concentrations of ORs and diterpene acids controlled the invasion and proliferation of T. gondii in HeLa cells, thus highlighting the possible direct action on parasites. In addition, some compounds tested controlled parasite proliferation in an irreversible manner. An additional and non-exclusive mechanism of action involves the modulation of host cell components, by affecting the upregulation of the IL-6. Additionally, molecular docking suggested that ent-polyalthic acid has a high affinity for the active site of the TgCDPK1 protein. Copaifera ORs have great antiparasitic activity against T. gondii, and this effect can be partially explained by the presence of the isolated compounds ent-kaurenoic and ent-polyalthic acid.
Keyphrases
- toxoplasma gondii
- cell cycle arrest
- induced apoptosis
- molecular docking
- signaling pathway
- cell death
- pi k akt
- molecular dynamics simulations
- cell proliferation
- dna damage
- stem cells
- poor prognosis
- single cell
- small molecule
- machine learning
- bone marrow
- risk assessment
- hiv infected
- long non coding rna
- data analysis
- protein protein
- replacement therapy
- combination therapy