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PLoS One ; 13(4): e0196195, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29689077

RESUMEN

With the goal of identifying neuroactive secondary metabolites from microalgae, a microscale in vivo zebrafish bioassay for antiseizure activity was used to evaluate bioactivities of the diatom Skeletonema marinoi, which was recently revealed as being a promising source of drug-like small molecules. A freeze-dried culture of S. marinoi was extracted by solvents with increasing polarities (hexane, dichloromethane, methanol and water) and these extracts were screened for anticonvulsant activity using a larval zebrafish epilepsy model with seizures induced by the GABAA antagonist pentylenetetrazole. The methanolic extract of S. marinoi exhibited significant anticonvulsant activity and was chosen for bioassay-guided fractionation, which associated the bioactivity with minor constituents. The key anticonvulsant constituent was identified as the nucleoside inosine, a well-known adenosine receptor agonist with previously reported antiseizure activities in mice and rat epilepsy models, but not reported to date as a bioactive constituent of microalgae. In addition, a UHPLC-HRMS metabolite profiling was used for dereplication of the other constituents of S. marinoi. Structures of the isolated compounds were elucidated by nuclear magnetic resonance and high-resolution spectrometry. These results highlight the potential of zebrafish-based screening and bioassay-guided fractionation to identify neuroactive marine natural products.


Asunto(s)
Anticonvulsivantes/uso terapéutico , Diatomeas/química , Inosina/uso terapéutico , Pentilenotetrazol/efectos adversos , Convulsiones/tratamiento farmacológico , Animales , Anticonvulsivantes/química , Anticonvulsivantes/aislamiento & purificación , Fraccionamiento Químico , Modelos Animales de Enfermedad , Inosina/química , Inosina/aislamiento & purificación , Espectroscopía de Resonancia Magnética , Estructura Molecular , Convulsiones/inducido químicamente , Pez Cebra
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