RESUMEN
Neglected Tropical Diseases are a significant concern as they encompass various infections caused by pathogens prevalent in tropical regions. The limited and often highly toxic treatment options for these diseases necessitate the exploration of new therapeutic candidates. In the present study, the lignan methylpiperitol was isolated after several chromatographic steps from Persea fulva L.â E. Koop (Lauraceae) and its leishmanicidal and trypanocidal activities were evaluated using inâ vitro and inâ silico approaches. The chemical structure of methylpiperitol was defined by NMR and MS spectral data analysis. The antiprotozoal activity of methylpiperitol was determined inâ vitro and indicated potency against trypomastigote forms of Trypanosoma cruzi (EC50 of 4.5±1.1â mM) and amastigote forms of Leishmania infantum (EC50 of 4.1±0.5â mM), with no mammalian cytotoxicity against NCTC cells (CC50>200â mM). Molecular docking studies were conducted using six T. cruzi and four Leishmania. The results indicate that for the molecular target hypoxanthine phosphoribosyl transferase in T. cruzi and piteridine reductase 1 of L. infatum, the methylpiperitol obtained better results than the crystallographic ligand. Therefore, the lignan methylpiperitol, isolated from P. fulva holds potential for the development of new prototypes for the treatment of Neglected Tropical Diseases, especially leishmaniasis.
Asunto(s)
Leishmania infantum , Lignanos , Simulación del Acoplamiento Molecular , Trypanosoma cruzi , Lignanos/farmacología , Lignanos/aislamiento & purificación , Lignanos/química , Trypanosoma cruzi/efectos de los fármacos , Leishmania infantum/efectos de los fármacos , Pruebas de Sensibilidad Parasitaria , Antiprotozoarios/farmacología , Antiprotozoarios/química , Antiprotozoarios/aislamiento & purificación , Animales , Relación Estructura-Actividad , Estructura Molecular , Relación Dosis-Respuesta a Droga , Tripanocidas/farmacología , Tripanocidas/química , Tripanocidas/aislamiento & purificaciónRESUMEN
The new alkene lactone, (3E)-5,6-dihydro-5-(hydroxymethyl)-3-docdecylidenefuran-3(4H)-one (1), named majoranolide B, and three alkene lactones known as majorenolide (2), majoranolide (3) and majorynolide (4) were obtained from the aerial parts of Persea fulva (Lauraceae). The structures were elucidated in light of extensive spectroscopic analysis, including 1D, 2D NMR (1H, 13C, 1H-1H-COSY, HMBC and HSQC) and HR-ESI-MS. These compounds were screened for their in vitro antiproliferative activity in rat C6 glioma and astrocyte cells using MTT assay and in silico by molecular docking against targets that play a central role in controlling glioma cell cycle progression. Majoranolide (3) is the most active compound with IC50 6.69⯵M against C6 glioma cells, followed by the compounds 1 (IC50 9.06⯵M), 2 (IC50 12.04⯵M) and 4 (IC50 41.90⯵M). The alkene lactones 1-3 exhibited lower toxicity in non-tumor cells when compared to glioma cells. Molecular docking results showed that majoranolide establishes hydrogen bonds with all targets through its α,ß-unsaturated-γ-lactone moiety, whereas the long-chain alkyl group binds by means of several hydrophobic bonds. In the present study, it can be concluded from the anti-proliferative activity of isolates against C6 glioma cells that lactone constituents from P. fulva could have a great potential for the control of C6 glioma cells.