Artigos Científicos - ICEN

URI Permanente para esta coleçãohttps://repositorio.ufpa.br/handle/2011/2557

Navegar

Agora exibindo 1 - 7 de 7

Acesso aberto (Open Access)
Avaliação do efeito antifúngico do óleo resina e do óleo essencial de copaíba (Copaifera multijuga Hayne)
(2011) DEUS, Ricardo Jorge Amorim de; ALVES, Claudio Nahum; ARRUDA, Mara Silvia Pinheiro
Copaifera multijuga Hayne oil in natura and its fractions were evaluated as to their fungitoxic activities against five filamentous fungus species belonging to the genus Aspergillus and three yeast species of the genus Candida. Oleoresin and essential oil concentrations ranging from 0.08 mg mL-1 to 1.6 mg mL-1 were used for qualitative and quantitative analyses. The samples were placed onto 5mm-diameter paper discs distributed on Sabouraud's medium in Petri dishes inoculated with spores of the microorganisms and incubated at 28ºC for 10 days. A solution containing 1.6 mg mL-1 miconazole nitrate was used as positive control. Qualitative results showed that the oleoresin presented good activity, while a fraction of the essential oil was highly effective against Candida parapsilosis IOC-2882, Aspergillus flavus IOC-3874 and A tamarii IOC-187 with 16.0±1.4 mm, 19.5±2.1 mm and 12.5±3.5 mm inhibition halos, respectively. The quantitative evaluation showed that 0.3 mg mL-1 oleoresin inhibited the growth of Aspergillus flavus and Candida parapsilosis, while 0.08 mg mL-1 of the essential oil fraction reached this same activity.
Acesso aberto (Open Access)
Efeito fungitóxico in vitro do óleo resina e do óleo essencial de copaíba (Copaifera multijuga Hayne)
(2009) DEUS, Ricardo Jorge Amorim de; CARVALHO, Antonio Sergio Costa; BANNA, Débora Ariane Dornelas da Silva; ARRUDA, Mara Silvia Pinheiro; ALVES, Claudio Nahum; SANTOS, Alberdan Silva
In vitro fungitoxic effect of the oil-resin and the essential oil of copaiba (Copaifera multijuga Hayne). Copaifera multijuga Hayne oil, crude and fractions, was evaluated for its in vitro fungitoxic activities against five species of filamentous fungi belonging to the genus Aspergillus and three yeast species of the genus Candida. Oil-resin and essential oil concentrations ranging from 0.008 mg mL-1 to 1.6 mg mL-1 were used in qualitative and quantitative analyses. Samples were placed onto 5mm-diameter paper disks and distributed on Saboraud culture medium in Petri dishes inoculated with conidia and incubated at 28ºC during 10 days. A solution with 1.6 mg mL-1 of miconazole nitrate was used as positive control. Qualitative results indicated that the oil-resin presented good fungistatic activity; however, one of the essential oil fractions was highly effective against Candida parapsilosis IOC-2882, Aspergillus flavus IOC-3874 and A. tamarii IOC- 187, with inhibition halos of 16.0±1.4 mm, 19.5±2.1 mm and 12.5±3.5 mm, respectively. The quantitative evaluation indicated that 0.3 mg mL-1 of the oil-resin inhibited Aspergillus flavus and Candida parapsilosis growth, whereas 0.08 mg mL-1 of the essential oil fraction reached this same activity.
Acesso aberto (Open Access)
Flavonoids from the leaves of Deguelia utilis (Leguminosae): structural elucidation and neuroprotective properties
(2012-10) OLIVEIRA, Dalglish Gomes de; ALMEIDA, Cecília M. C. de; SILVA, Consuelo Yumiko Yoshioka e; ARRUDA, Mara Silvia Pinheiro; ARRUDA, Alberto Cardoso; LOPES, Dielly Catrina Favacho; YAMADA, Elizabeth Sumi; COSTA, Edmar Tavares da; MARTINS FILHO, Arnaldo Jorge; SILVA, Milton Nascimento da
Five new flavonoids, 5,3'-dihydroxy-4'-methoxy-2'',2''-dimethylchromene-(5'',6'':6,7)dihydroflavonol (1), 5,3'-dihydroxy-7,4'-dimethoxy-6,8-dimethylallyl-dihydroflavonol (2), 5,3'-dihydroxy-4'-methoxy-8-allyl-2'',2''-dimethylchromene-(5'',6'':6,7) flavanone (3), 5,3'-dihydroxy-7,4'-dimethoxy-6,8-dimethylallyl-flavanone (4), 3,5,3'-trihydroxy-7,4'-dimethoxy6,8-dimethylallyl-flavanol (5), together with the stilbenes 4-methoxylonchocarpene (6) and lonchocarpene (7) were isolated from the leaves of Deguelia utilis. Their chemical structures were established on the basis of NMR (nuclear magnetic resonance) spectral data and HRESITOF-MS (electrospray ionization-high resolution time-of-flight mass spectrometry). Also, in order to investigate potential cytoprotective effects of these flavonoids, we used a fraction eluted with hexane:EtOAc containing all seven flavonoids, in an in vitro model of neurodegeneration, using hippocampal primary cultures from neonatal (PND2-P3) rats exposed to rotenone, a mitochondrial complex I inhibitor. There was a significant reduction in cell viability (19.4 ± 1.6%) when the cultures were exposed to 30 nmol L-1 rotenone for 72 h. Concomitant exposure of the cultures to the FR3 (5 µg mL-1) and 30 nmol L-1 rotenone resulted in values of cell viability similar to control groups (99.6 ± 4.8%), strongly suggesting a cytoprotective effect for this flavonoid-rich fraction.
Acesso aberto (Open Access)
New isoflavones from the leaves of Vatairea guianensis Aublé
(2013-11) SOUZA, Ronilson Freitas de; MARINHO, Victor Hugo de Souza; SILVA, Geilson Alcantara da; COSTA JUNIOR, Livio Martins; SILVA, Joyce Kelly do Rosário da; BASTOS, Gilmara de Nazareth Tavares; ARRUDA, Alberto Cardoso; SILVA, Milton Nascimento da; ARRUDA, Mara Silvia Pinheiro
Four isoflavones were isolated from Vatairea guianensis Aublé leaves and identified as 5,3'-dihydroxy-4'-methoxy-2",2"-dimethylpyrano-(5",6":8,7)-isoflavone ( 1: ), 5,7-dihydroxy-3',4'-methylenedioxy-8-prenyl-isoflavone ( 2: ), 5,3'-dihydroxy-4'-methoxy-7-O-β-glucopyranoside-8-prenyl-isoflavone ( 3: ) and derrone ( 4: ) together with five triterpenes identified in mixture, lupeol, α-amyrin, β-amyrin, germanicol and betulinic acid. Substances 1: 3: are novel natural products, although 1: and 2: have been cited as synthetic products. However, all these compounds are first reported from this species. Their chemical structures were elucidated based on their 1D and 2D nuclear magnetic resonance (NMR) data and high resolution mass spectrometry. The ethanol extract from the leaves and 1: 3: were evaluated for their potential in scavenging DPPH• (2,2-diphenyl-1-picrylhydrazylradical) and the results showed that the extract presented high activity (IC50 = 6.2 ± 0.4 µg mL-1), while the isolated compounds showed low antioxidant power (IC50 ≥ 29.5 ± 2.5 µg mL-1) when compared to Trolox (IC50 = 4.5 ± 0.4 µg mL-1).
Acesso aberto (Open Access)
A New Prenylisoflavone from the Antifungal Extract of Leaves of Vatairea guianensis Aubl.
(Universidade Federal do Pará, 2017-06) SOUZA, Ronilson Freitas de; SILVA, Geilson Alcantara da; ARRUDA, Alberto Cardoso; SILVA, Milton Nascimento da; SANTOS, Alberdan Silva; GRISÓLIA, Daniella Paternostro de Araújo; SILVA, Moisés Batista da; ARRUDA, Mara Silvia Pinheiro
A new compound, 5,7,3'-trihydroxy-4'-methoxy-8-prenylisoflavone, was isolated from the leaves of Vatairea guianensis Aubl. (Fabaceae), together with two known isoflavones lupiwighteone and 5,7,4'-trihydroxy-3'-methoxy-8-prenylisoflavone. All isolated compounds were characterized based on infrared (IR), UV, 1H and 13C nuclear magnetic resonance (NMR), including 2D NMR analyses and high resolution mass spectrometry. The ethanolic extract from V. guianensis leaves displayed activity against Candida dubliniensis, C. albicans and C. krusei. However, the EtOAc fraction from that extract exhibited more significant activity than the ethanolic extract, showing antifungal activity for all fungi species investigated. The major compound 5,7,3'-trihydroxy-4'-methoxy-8-prenylisoflavone isolated from that EtOAc fraction was also active against C. parapsilosis and C. dubliniensis.
Acesso aberto (Open Access)
Novel anthraquinone derivatives produced by Pestalotiopsis guepinii, an endophytic of the medicinal plant Virola michelii (Myristicaceae)
(2011-05) OLIVEIRA, Marilene Nunes; SANTOS, Lourivaldo da Silva; GUILHON, Giselle Maria Skelding Pinheiro; SANTOS, Alberdan Silva; FERREIRA, Isabel Cristina Serrão; LOPES JÚNIOR, Manoel Leão; ARRUDA, Mara Silvia Pinheiro; MARINHO, Andrey Moacir do Rosário; SILVA, Milton Nascimento da; RODRIGUES FILHO, Edson; OLIVEIRA, Maria da Conceição Ferreira de
A new anthraquinone derivative, named guepinone (1), along with the known substances isosulochrin (2) and chloroisosulochrin (3), were isolated from a rice culture of Pestalotiopsis guepinii, an endophytic fungus of Virola michelii. The compounds were identified by analysis of 1D and 2D NMR and MS spectral data. The antimicrobial activity of these compounds was evaluated and chloroisosulchrin (3) was the most active.
Acesso aberto (Open Access)
Potencial herbicida da biomassa e de substâncias químicas produzidas pelo fungo endofítico Pestalotiopsis guepinii
(2008) SANTOS, Lourivaldo da Silva; OLIVEIRA, Marilene Nunes; GUILHON, Giselle Maria Skelding Pinheiro; SANTOS, Alberdan Silva; FERREIRA, Isabel Cristina Serrão; LOPES JÚNIOR, Manoel Leão; ARRUDA, Mara Silvia Pinheiro; SILVA, Milton Nascimento da; SOUZA FILHO, Antonio Pedro da Silva; RODRIGUES FILHO, Edson; OLIVEIRA, Maria da Conceição Ferreira de
Many of the chemical compounds found in nature that are produced by plants or microorganisms can offer new and efficient ways of controlling pests in agriculture and agricultural practice, with the help of fungi. The objective of this work is to characterize the inhibitory potential for seed germination and the plantlet development of two weed species using extracts and compounds obtained from biomass produced by Pestalotiopsis guepinii, an endophytic fungus of the species Virola michelii. The bioassays were developed under controlled conditions at 25 ºC and 12-hour photoperiod for germination, and at 25 ºC and 12-hour photoperiod for root and hypocotyl development. The crude extracts were analyzed at a concentration of 1.0% (m/v). The results showed that the more polar extracts (MeOH-1 and MeOH-2) have the highest inhibitory potential, although the hexane and ethyl acetate extract effects were important, especially for seed germination. Comparatively, weed seed germination was more sensitive to the effects than plantlet development. Mimosa pudica was more affected by the inhibitory effects of the extracts. However, for seed germination of Senna obtusifolia, the extract MeOH-1 showed 100% inhibition. The compounds ergosterol and ergosterol peroxide showed an inhibitory potential always below 35%, not showing the inhibitory potential of the hexane extract from which they were isolated. When these compounds were tested together, little increase was observed in the inhibitory activity.

Navegar

Navegando Artigos Científicos - ICEN por Autor "ARRUDA, Mara Silvia Pinheiro"