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1.
Mar Drugs ; 17(1)2019 Jan 16.
Artículo en Inglés | MEDLINE | ID: mdl-30654553

RESUMEN

The marine sponge Raspailia bouryesnaultae, collected in South Brazil, was selected for detailed investigation considering the results of a screening that pointed to an in vitro antiproliferative effect against non-small cells of human lung cancer (A549) and anti-herpes activity against Herpes Simplex virus type 1 (KOS and 29R strains) of ethanolic extracts. The fractionation and chemical investigation of the sponge's hexanic fraction led to the isolation and structural elucidation of six clerodane diterpenes. The main component was identified as the already-reported raspailol (1), isolated from a sponge of the same genus collected in New Zealand. The structure of a new diterpene (2) with a rearranged skeleton was established by high-resolution mass spectrometry (HRMS) and 1D and 2D Nuclear magnetic resonance spectroscopy (NMR) experiments, and named here as raspadiene. Furthermore, four diterpenes were elucidated as isomers of clerodane diterpenes previously obtained from plants, namely kerlinic acid (3), kerlinic acid methyl ester (4), annonene (5), and 6-hydroxyannonene (6). They differ in their stereochemistry, since these diterpenes are characterized by a trans ring fusion at the decalin moiety and the relative configuration of the two methyl groups at C-8 and C-9 in a cis relationship (type trans/cis). The Raspailia diterpenes have a cis ring fusion at the decalin moiety, and the two methyl groups at C-8 and C-9 are in a trans relationship (type cis/trans). The isolated compounds were evaluated for their potential antiproliferative effects on human cancer cell line A549, and it was observed that the diterpenes bearing a hydroxyl group at C-6 exhibited moderate cytotoxic activity, with 50% inhibitory concentration (IC50) values lower than 25 µM. The evaluation of the potential anti-herpes activity against Herpes Simplex Virus type 1 (HSV-1, KOS and 29R strains) showed that the more promising results were observed for the new compound 2, since it inhibited HSV-1 (KOS and 29R strains) replication by 83% and 74%, respectively.


Asunto(s)
Antineoplásicos/farmacología , Antivirales/farmacología , Diterpenos de Tipo Clerodano/farmacología , Poríferos/química , Células A549 , Animales , Antineoplásicos/química , Antineoplásicos/aislamiento & purificación , Antivirales/química , Antivirales/aislamiento & purificación , Brasil , Proliferación Celular/efectos de los fármacos , Diterpenos de Tipo Clerodano/química , Diterpenos de Tipo Clerodano/aislamiento & purificación , Ensayos de Selección de Medicamentos Antitumorales , Herpesvirus Humano 1 , Humanos , Concentración 50 Inhibidora , Espectroscopía de Resonancia Magnética , Estructura Molecular , Estereoisomerismo , Replicación Viral/efectos de los fármacos
2.
Mar Drugs ; 11(11): 4176-92, 2013 Oct 29.
Artículo en Inglés | MEDLINE | ID: mdl-24172213

RESUMEN

The n-butanol fraction (BF) obtained from the crude extract of the marine sponge Petromica citrina, the halistanol-enriched fraction (TSH fraction), and the isolated compounds halistanol sulfate (1) and halistanol sulfate C (2), were evaluated for their inhibitory effects on the replication of the Herpes Simplex Virus type 1 (HSV-1, KOS strain) by the viral plaque number reduction assay. The TSH fraction was the most effective against HSV-1 replication (SI = 15.33), whereas compounds 1 (SI = 2.46) and 2 (SI = 1.95) were less active. The most active fraction and these compounds were also assayed to determine the viral multiplication step(s) upon which they act as well as their potential synergistic effects. The anti-HSV-1 activity detected was mediated by the inhibition of virus attachment and by the penetration into Vero cells, the virucidal effect on virus particles, and by the impairment in levels of ICP27 and gD proteins of HSV-1. In summary, these results suggest that the anti-HSV-1 activity of TSH fraction detected is possibly related to the synergic effects of compounds 1 and 2.


Asunto(s)
Antivirales/química , Antivirales/farmacología , Herpesvirus Humano 1/efectos de los fármacos , Poríferos/química , Esteroles/química , Esteroles/farmacología , 1-Butanol/química , Animales , Brasil , Línea Celular , Chlorocebus aethiops , Células Vero , Ensayo de Placa Viral/métodos
3.
Molecules ; 18(5): 5761-78, 2013 May 16.
Artículo en Inglés | MEDLINE | ID: mdl-23681060

RESUMEN

This manuscript describes the evaluation of anti-infective potential in vitro of organic extracts from nine sponges, one ascidian, two octocorals, one bryozoan, and 27 seaweed species collected along the Brazilian coast. Antimicrobial activity was tested against Staphylococcus aureus (ATCC 25923), Enterococcus faecalis (ATCC 29212), Pseudomonas aeruginosa (ATCC 27853), Escherichia coli (ATCC 25922) and Candida albicans (ATCC 10231) by the disk diffusion method. Antiprotozoal activity was evaluated against Leishmania braziliensis (MHOM/BR/96/LSC96-H3) promastigotes and Trypanosoma cruzi (MHOM/BR/00/Y) epimastigotes by MTT assay. Activity against intracellular amastigotes of T. cruzi and L. brasiliensis in murine macrophages was also evaluated. Antiviral activity was tested against Herpes Simplex Virus type 1 (HSV-1, KOS strain) by the plaque number reduction assay (IC50). Cytotoxicity on VERO cells was evaluated by the MTT assay (CC50). The results were expressed as SI = CC50/IC50. The most promising antimicrobial results were obtained against S. aureus and C. albicans with Dragmacidon reticulatum. Among the seaweeds, only Osmundaria obtusiloba showed moderate activity against P. aeruginosa. Concerning antiprotozoal activity, Bugula neritina, Carijoa riseii, Dragmaxia anomala and Haliclona (Halichoclona) sp. showed the most interesting results, mainly against extracellular promastigote forms of L. braziliensis (66, 35.9, 97.2, and 43.6% inhibition, respectively). Moreover, six species of seaweeds Anadyomene saldanhae, Caulerpa cupressoides, Canistrocarpus cervicornis, Dictyota sp., Ochtodes secundiramea, and Padina sp. showed promising results against L. braziliensis (87.9, 51.7, 85.9, 93.3, 99.7, and 80.9% inhibition, respectively), and only Dictyota sp. was effective against T. cruzi (60.4% inhibition). Finally, the antiherpes activity was also evaluated, with Haliclona (Halichoclona) sp. and Petromica citrina showing the best results (SI = 11.9 and SI > 5, respectively). All the active extracts deserve special attention in further studies to chemically characterize the bioactive compounds, and to perform more refined biological assays.


Asunto(s)
Antozoos/química , Antibacterianos , Antiprotozoarios , Citotoxinas , Poríferos/química , Algas Marinas/química , Urocordados/química , Animales , Antibacterianos/química , Antibacterianos/aislamiento & purificación , Antibacterianos/farmacología , Antiprotozoarios/química , Antiprotozoarios/aislamiento & purificación , Antiprotozoarios/farmacología , Bacterias/crecimiento & desarrollo , Brasil , Chlorocebus aethiops , Citotoxinas/química , Citotoxinas/aislamiento & purificación , Citotoxinas/farmacología , Leishmania braziliensis/crecimiento & desarrollo , Trypanosoma cruzi/crecimiento & desarrollo , Células Vero
4.
Biota neotrop. (Online, Ed. port.) ; 7(3): 83-90, 2007. ilus, mapas, tab
Artículo en Inglés | LILACS | ID: lil-477676

RESUMEN

This work provides new information on agelasid sponges found on the continental shelf off northern Brazil. Agelas sceptrum (Lamarck, 1815) and Agelas wiedenmayeri Alcolado, 1984 have their first record for the Brazilian coast. Agelas dispar Duchassaing & Michelotti, 1864 and Agelas schmidti Wilson, 1902, previously recorded from Brazil, are cited for the first time off the mouth of the Amazon River.


Este trabalho fornece novas informações sobre esponjas agelasidas encontradas na costa norte da plataforma continental brasileira. Agelas sceptrum (Lamarck, 1815) e Agelas wiedenmayeri Alcolado, 1984 têm seu primeiro registro para a costa brasileira. Agelas dispar Duchassaing & Michelotti, 1864 e Agelas schmidti Wilson, 1902, registradas anteriormente na costa brasileira, são citadas pela primeira vez ao largo da desembocadura do Rio Amazonas.


Asunto(s)
Costas (Litoral)/análisis , Costas (Litoral)/clasificación , Ecosistema/análisis , Ecosistema/clasificación , Poríferos/anatomía & histología , Poríferos/clasificación , Poríferos/crecimiento & desarrollo
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