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Two unusual phorbol esters, namely 20-deoxyphorbol-3,4,12-triacetate-13-phenylacetate (1) and phorbol-3,4,12,13-tetraacetate-20-phenylacetate (2) plus ingol-3,8,12-triacetate-7-phenylacetate (3) were isolated from the latex of Euphorbia umbellata and identified by HRESIMS and 2D NMR. Compound 1 is herein described for the first time. Assignment of the phenylacetyl group at C-7 in compound 3 was suggested by the HMBC and NOESY spectra obtained in pyridine-d5. In addition to the latex and its distinct terpenoid fractions, the isolated compounds were tested as latent reversal agents against HIV-1-infected J-Lat cells, with reference to phorbol-12-myristate-13-acetate and ingenol-B. Compound 2 reverted 75-80% the viral latency on the GFP-positive cells, resulting EC50 3.70 µg/mL (SI 6.7), while 1 induced 34-40% reactivation at the same concentration range (4-20 µg/mL). The ingol derivative 3 was ineffective. Phorbol esters were confirmed as effective constituents in the latex since the fraction containing them was 2.4-fold more active than the lyophilised latex at the lowest concentration assayed.

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Rhizophora extracts have several potential biological activities, and their metabolites can be used in the pharmaceutical industry. Extracts of Rhizophora species obtained from mangroves have shown prospective activity against Staphylococcus aureus. This study aimed to investigate the chemical profile of Rhizophora mangle leaves from fringe, basin, and transition mangrove zones and their bactericidal/bacteriostatic potential against S. aureus. R. mangle leaves were collected monthly in 2018 from litterfall in three different zones of the mangrove of Guaratiba State Reserve: fringe, basin, and transition. Extracts were prepared from the material collected in October and December for LC-HRMS/MS analysis, and dereplication was performed using a molecular library search and the classical molecular networking GNPS platform. The minimum inhibitory concentrations (MICs) of the aqueous extract of R. mangle against S. aureus were determined. No S. aureus growth was observed compared to the control for extracts collected from September to December. Different compounds were annotated in each region, yet a marked presence of phenolic compounds was noted, among them glycosylated flavonoid derivatives of quercetin and kaempferol. The results suggest bactericidal/bacteriostatic activity for extracts of R. mangle leaves collected in 2018 from three mangrove forest zones.

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Resumen El presente estudio evaluó la actividad antimicrobiana de extractos y aceites esenciales de Lippia graveolens y Lippia alba, frente a nueve cepas de Aeromonas spp., aisladas de Oreochromis niloticus. Los extractos crudos se obtuvieron por la técnica de percolación y a través de la extracción de CO2 supercrítico, mientras que los aceites esenciales se realizaron mediante la técnica de hidrodestilación empleando un equipo Clevenger. La actividad antimicrobiana para cada extracto y aceite esencial se verificó mediante el método de difusión en disco a las 24 horas. El aceite esencial de L. graveolens mostró mayor efectividad para inhibir patógenos bacterianos de peces (100%), en comparación con los extractos. Se obtuvo un diámetro de inhibición que osciló entre 25,20 a 36,94 mm. Los extractos de fluido supercrítico y de la técnica de percolación con acetato de etilo y ciclohexano presentaron la misma efectividad (77,78%). El extracto crudo obtenido con etanol al 95% mostró efecto antimicrobiano limitado (22,22%), presentando el menor halo de inhibición (8,34 y 9,57 mm). Por otro parte, L. alba mostró menor actividad antibacteriana. El aceite esencial inhibió únicamente el 66,67% de las bacterias patógenas, presentando un halo de inhibición que oscila entre 10,68 a 16,29 mm. El resultado de este estudio indica que los aceites esenciales de L. graveolens y L. alba son una alternativa prometedora para el control del crecimiento de Aeromonas spp.

Abstract This study evaluated the antimicrobial activity of Lippia graveolens and Lippia alba extracts and essential oils against nine strains of Aeromonas spp., isolated from Oreochromis niloticus. The crude extracts were obtained by percolation technique and CO2 supercritical fluid extraction, while the essential oils by applying hydro-distillation technique using a Clevenger apparatus. The antimicrobial activity for each extract and essential oils was verified through the disc diffusion method at 24 hours. The essential oil of L. graveolens showed higher effectiveness to inhibit fish bacterial pathogens (100%) than the extracts, revealing an inhibition zone diameter that ranged from 25.20 - 36.94 mm. The extracts from supercritical fluid and from the percolation technique with ethyl acetate and cyclohexane presented the same effectiveness (77.78%). The crude extract obtained with ethanol 95% showed limited antimicrobial effect (22.22%), presenting the smallest inhibition zone (ranged from 8.34 to 9.57 mm). On the other hand, L. alba displayed a lower antibacterial activity, being the essential oil 66.67% effective, presenting an inhibition zone ranging between 10.68 to 16.29 mm. The result of this study indicates that essential oils from both L. graveolens and L. alba offer a promising alternative for the control of Aeromonas spp. growth.

Resumo Neste estudo avaliou-se a atividade antimicrobiana de extratos e óleos essenciais de Lippia graveolens e Lippia alba, contra nove cepas de Aeromonas spp., isoladas de Oreochromis niloticus. Os extratos brutos foram obtidos pela técnica de percolação e por extração supercrítica com CO2, enquanto os óleos essenciais foram obtidos por hidrodestilação em aparelho tipo Clevenger. A atividade antimicrobiana para cada extrato e óleo essencial foi verificada pelo método de disco-difusão em 24 horas. O óleo essencial de L. graveolens apresentou maior eficácia na inibição de patógenos bacterianos em peixes (100%), comparado aos extratos. Obteve-se um diâmetro de halo de inibição que variou entre 25,20 e 36,94 mm. Os extratos do fluido supercrítico e da percolação com acetato de etila e ciclohexano apresentaram a mesma eficácia (77,78%). O extrato bruto obtido com etanol 95% apresentou efeito antimicrobiano limitado (22,22%), apresentando o menor diámetro de halo de inibição (8,34 e 9,57 mm). Por outro lado, L. alba apresentou menor atividade antibacteriana. O óleo essencial inibiu apenas 66,67% das bactérias patogênicas, apresentando um halo de inibição que varia de 10,68 a 16,29 mm de diámetro. Os resultados deste estudo indica que os óleos essenciais de L. graveolens e L. alba são uma alternativa promissora para o controle do crescimento de Aeromonas spp.

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Euterpe oleracea Mart. (Arecaceae) is an endogenous palm tree from the Amazon region. Its seeds correspond to 85% of the fruit's weight, a primary solid residue generated from pulp production, the accumulation of which represents a potential source of pollution and environmental problems. As such, this work aimed to quantify and determine the phytochemical composition of E. oleracea Mart. seeds from purple, white, and BRS-Pará açaí varieties using established analytical methods and also to evaluate it as an eco-friendly corrosion inhibitor. The proanthocyanidin quantification (n-butanol/hydrochloric acid assay) between varieties was 6.4-22.4 (w/w)/dry matter. Extract characterization showed that all varieties are composed of B-type procyanidin with a high mean degree of polymerization (mDP ≥ 10) by different analytical methodologies to ensure the results. The purple açaí extract, which presented 22.4% (w/w) proanthocyanidins/dry matter, was tested against corrosion of carbon steel AISI 1020 in neutral pH. The crude extract (1.0 g/L) was effective in controlling corrosion on the metal surface for 24 h. Our results demonstrated that the extracts rich in polymeric procyanidins obtained from industrial açaí waste could be used to inhibit carbon steel AISI 1020 in neutral pH as an abundant, inexpensive, and green source of corrosion inhibitor.

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Three known compounds, 20-deoxyphorbol-5ß-hydroxy-12-tiglate-13-isobutyrate (1), 20-deoxyphorbol-5ß-hydroxy-12-tiglate-13-phenylacetate (2), and 4-deoxy-4ß-phorbol-12-tiglate-13-phenylacetate (3), were reisolated from the latex of Euphorbia umbellata through a bioguided fractionation process to target HIV-1 latency reactivation. The in vitro bioassay using infected T-cell lymphoblasts (J-Lat 10.6), complemented with surface CD4 receptor downregulation assessment, led to isolation of the compounds as a highly active ternary mixture. Effective purification of the individual compounds was achieved by first subjecting a phorbol-enriched fraction (previously prepared from crude latex) to MPLC, followed by semipreparative HPLC and characterization by 1D and 2D NMR spectroscopy and (+)-HRESIMS. Compared with a positive control, the isolated compounds were effective in reactivating 68-75% of the virus latency in the range of 9.7-0.097 µM for compound 1, 8.85-0.088 µM for compound 2, and 9.1-0.091 µM for compound 3, with the latter maintaining steady effectiveness down to a 10-5 dilution. Accordingly, compound 3 may serve as a promising lead compound for the development of anti-HIV drugs based on latency reactivation therapy.

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Anomalocalyx uleanus (Pax & K. Hoffm.) Ducke (Euphorbiaceae) is a singular species in the genus and is restricted and exclusive to the Brazilian Amazon. A phytochemical study of A. uleanus leaves was performed, yielding the isolation of five major compounds: catechin/epicatechin, afzelin, quercetin 3-O-α-L-rhamnopyranoside, and astilbin. The phytochemical compositions of the methanolic extracts of leaves, roots, bark, and stem bark were determined using a dereplication approach. Forty-six compounds were annotated from the liquid chromatography-mass spectrometry (LC-MS/MS) data, while four lipids were identified using gas chromatography-mass spectrometry (GC-MS). In total, fifty compounds were detected, and they belonged to the primary metabolism and several classes of natural products such as flavonoids, flavonoids O-glycosides, flavonoids C-glycosides, biflavonoids, procyanidin, triterpene, triterpenes esterified with phenylpropanoids, phenylpropanoid derivatives, flavonolignans, coumarins, quinic acid derivatives, and benzoic acid derivatives. This is the first report on the phytochemical data of the genus Anomalocalyx, and the results of this study will contribute to the chemosystematic knowledge of the Euphorbiaceae family and justify the need for investigation of the pharmacological potential of the species A. uleanus.

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Background: Pimenta dioica is a native tree of Central America, Southern Mexico, and the Caribbean used in traditional medicine. It grows in wet forests in the Guatemalan departments of Petén and Izabal. Since the plant is not being economically exploited in Guatemala, this study was aimed at determining the composition of the essential oil of P. dioica leaves and fruits and the antibacterial activity of the leaves in order to evaluate its possible use in health products. The essential oils of fruits and leaves are used as rubefacient, anti-inflammatory, carminative, antioxidant, and antiflatulent in different countries. Fruits and leaves of P. dioica from Izabal Department were collected in April 2014 and extracted by hydrodistillation method. The oils were analyzed by gas chromatography coupled with mass spectrometry (GC/MS). Yields of 1.02 ± 0.11% for dried leaves and 1.51 ± 0.26% for fruits were obtained. Eugenol was the main component (65.9-71.4%). The leaf oil showed growth inhibition against two Gram-positive and two Gram-negative bacteria. The authors consider that the tree's leaves can be evaluated as a source of ingredients for antiseptic products, and that it is important to evaluate other types of properties such as anti-inflammatory activity.

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The composition and the antinociceptive activity of the essential oil of Stevia serrata Cav. from a population located in the west highlands of Guatemala were evaluated. A yield of 0.2% (w/w) of essential oil was obtained by hydrodistillation of the dried aerial parts of the plant. The essential oil analysed by GC-FID and GC-MS showed a high content of sesquiterpenoids, with chamazulene (60.1%) as the major component and 91.5% of the essential oil composition was identified. To evaluate antinociceptive activity in mice, the essential oil of S. serrata Cav. was administered as gavage, using three different doses. In the formalin test, the animals were pre-treated with oral doses of the essential oil before the administration of formalin. Oral administration of S. serrata Cav. essential oil produced a marked antinociceptive activity. Therefore, the plant could be domesticated as a source of essential oil rich in chamazulene for developing medicinal products.

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This is the first report investigating the effects of cultivation, growth under full sunlight (MSL) or shade (MS), and processing (drying, sapeco and roasting) on the composition and antioxidant potential of maté. Samples were roasted (180 °C, 200 °C, 220 °C or 240 °C) for a fixed time (10 min) or roasted (10, 20, 30 or 40 min) at a fixed temperature (200 °C). HPLC/UV/MS analysis and measures of total phenolic content (TPC) and antioxidant activity (2,2-diphenyl-1-picrylhydrazyl (DPPH) inhibition and soybean oil oxidation) were used to analyse phytochemicals. There were significant differences (p < 0.05, ANOVA/Tukey) in phenolics between MS and MSL samples following certain processing steps, but Principal Component Analysis (PCA) indicated no distinction between MS and MSL samples, suggesting that light intensity had no effect on phenolics. Caffeine increased significantly (p < 0.05) in MS samples. Temperature was more important than time, since pyrolysis of phenolics was more intense at 240 °C.

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The culture of sunflower (Helianthus annuus L.) has been consolidated in different regions of Brazil, and presents interesting characteristics on agronomic aspects, oil composition and protein quality. The defatted sunflower meal has been used to feed, but browning limits its use for human consumption. Sunflower meal contains chlorogenic acid, a potent antioxidant, which in turn is oxidized by polyphenol oxidase, producing compounds that darken the meal and reduce the nutritional quality of protein. In this research chlorogenic acid extracts were obtained from defatted sunflower meal, using methanol or ethanol as solvent, at temperatures of 25, 40 and 60°C and contact times of 30 and 60 minutes in a three classification criteria experiments. There were significant differences between solvent, time and temperature (P 0.05). The highest removal efficiency of chlorogenic acid was of 40%, when methanol was used. Chlorogenic acid extracts obtained have potential for use as antioxidant.

A cultura de girassol (Helianthus annuus L.) vem se consolidando no Brasil, pois se adapta a diversas regiões do país e apresenta características interessantes tanto do ponto de vista agronômico, quanto em relação à composição do óleo e à qualidade de sua proteína. O farelo desengordurado de girassol tem sido utilizado para ração, mas seu escurecimento limita o uso para consumo humano. O farelo contém ácido clorogênico, um potente antioxidante, que quando oxidado pela polifenoloxidase gera compostos que causam o escurecimento e reduzem a qualidade nutricional da proteína. Neste trabalho, foram obtidos extratos de ácido clorogênico, a partir do farelo desengordurado de girassol, utilizando-se metanol ou etanol como solvente, nas temperaturas de 25, 40 e 60°C e tempos de contato de 30 e 60 minutos, constituindo um experimento a três critérios de classificação. Houve diferença significativa entre solventes, tempo e temperaturas (P 0,05). A maior eficiência de remoção de ácido clorogênico foi de 40%, quando o metanol foi utilizado. Os extratos de ácido clorogênico obtidos têm potencial de uso como antioxidante.

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The culture of sunflower (Helianthus annuus L.) has been consolidated in different regions of Brazil, and presents interesting characteristics on agronomic aspects, oil composition and protein quality. The defatted sunflower meal has been used to feed, but browning limits its use for human consumption. Sunflower meal contains chlorogenic acid, a potent antioxidant, which in turn is oxidized by polyphenol oxidase, producing compounds that darken the meal and reduce the nutritional quality of protein. In this research chlorogenic acid extracts were obtained from defatted sunflower meal, using methanol or ethanol as solvent, at temperatures of 25, 40 and 60°C and contact times of 30 and 60 minutes in a three classification criteria experiments. There were significant differences between solvent, time and temperature (P 0.05). The highest removal efficiency of chlorogenic acid was of 40%, when methanol was used. Chlorogenic acid extracts obtained have potential for use as antioxidant.

A cultura de girassol (Helianthus annuus L.) vem se consolidando no Brasil, pois se adapta a diversas regiões do país e apresenta características interessantes tanto do ponto de vista agronômico, quanto em relação à composição do óleo e à qualidade de sua proteína. O farelo desengordurado de girassol tem sido utilizado para ração, mas seu escurecimento limita o uso para consumo humano. O farelo contém ácido clorogênico, um potente antioxidante, que quando oxidado pela polifenoloxidase gera compostos que causam o escurecimento e reduzem a qualidade nutricional da proteína. Neste trabalho, foram obtidos extratos de ácido clorogênico, a partir do farelo desengordurado de girassol, utilizando-se metanol ou etanol como solvente, nas temperaturas de 25, 40 e 60°C e tempos de contato de 30 e 60 minutos, constituindo um experimento a três critérios de classificação. Houve diferença significativa entre solventes, tempo e temperaturas (P 0,05). A maior eficiência de remoção de ácido clorogênico foi de 40%, quando o metanol foi utilizado. Os extratos de ácido clorogênico obtidos têm potencial de uso como antioxidante.

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The culture of sunflower (Helianthus annuus L.) has been consolidated in different regions of Brazil, and presents interesting characteristics on agronomic aspects, oil composition and protein quality. The defatted sunflower meal has been used to feed, but browning limits its use for human consumption. Sunflower meal contains chlorogenic acid, a potent antioxidant, which in turn is oxidized by polyphenol oxidase, producing compounds that darken the meal and reduce the nutritional quality of protein. In this research chlorogenic acid extracts were obtained from defatted sunflower meal, using methanol or ethanol as solvent, at temperatures of 25, 40 and 60°C and contact times of 30 and 60 minutes in a three classification criteria experiments. There were significant differences between solvent, time and temperature (P 0.05). The highest removal efficiency of chlorogenic acid was of 40%, when methanol was used. Chlorogenic acid extracts obtained have potential for use as antioxidant.

A cultura de girassol (Helianthus annuus L.) vem se consolidando no Brasil, pois se adapta a diversas regiões do país e apresenta características interessantes tanto do ponto de vista agronômico, quanto em relação à composição do óleo e à qualidade de sua proteína. O farelo desengordurado de girassol tem sido utilizado para ração, mas seu escurecimento limita o uso para consumo humano. O farelo contém ácido clorogênico, um potente antioxidante, que quando oxidado pela polifenoloxidase gera compostos que causam o escurecimento e reduzem a qualidade nutricional da proteína. Neste trabalho, foram obtidos extratos de ácido clorogênico, a partir do farelo desengordurado de girassol, utilizando-se metanol ou etanol como solvente, nas temperaturas de 25, 40 e 60°C e tempos de contato de 30 e 60 minutos, constituindo um experimento a três critérios de classificação. Houve diferença significativa entre solventes, tempo e temperaturas (P 0,05). A maior eficiência de remoção de ácido clorogênico foi de 40%, quando o metanol foi utilizado. Os extratos de ácido clorogênico obtidos têm potencial de uso como antioxidante.

RESUMO

Leaf and stem explants of Cleome rosea formed calluses when cultured on MS medium supplemented with different concentrations of 2,4-dichlorophenoxyacetic acid (2,4-D) or 4-amino-3,5,6-trichloropicolinic acid (PIC). The highest biomass accumulation was obtained in the callus cultures initiated from stem explants on medium supplemented with 0.90 microM 2,4-D. Reddish-pink regions were observed on callus surface after 6-7 months in culture and these pigments were identified as anthocyanins. Anthocyanins production was enhanced by reducing temperature and increasing light irradiation. Pigmented calluses transferred to MS1/2 with a 1:4 ratio NH(4)(+)/NO(3)(-), 70 g L(-1) sucrose and supplementation with 0.90 microM 2,4-D maintained a high biomass accumulation and showed an increase of 150% on anthocyanin production as compared with the initial culture conditions. Qualitative analysis of calluses was performed by high performance liquid chromatography coupled to diode array detector and electrospray ionization mass spectrometry (HPLC-DAD/ESIMS). Eleven anthocyanins were characterized and the majority of them were identified as acylated cyanidins, although two peonidins were also detected. The major peak was composed by two anthocyanins, whose proposed identity were cyanidin 3-(p-coumaroyl) diglucoside-5-glucoside and cyanidin 3-(feruloyl) diglucoside-5-glucoside.

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Em 65 baços (50 formolizados, cujos pedículos arteriais foram dissecados, e 15 de necrópsias, para a arteriografia lienal) foi estudado o modo de divisäo terminal da artéria lienal e seus ramos extra-hilares dirigidos às extremidades do órgäo (artérias polares). Verificou-se bifurcaçäo da artéria lienal em 46/50 casos; artéria polar do tipo I, longa e relativamente calibrosa, com origem direta na artéria lienal, anteriormente à sua divisäo terminal, em 4/50 casos; artéria polar do tipo II, ramo de um ramo primário ou secundário da divisäo terminal da artéria lineal, curta, menos calibrosa e presente em até três ramos para um mesmo pólo, em 13/50 casos. O estudo estatístico da distância desses ramos arteriais à face visceral do baço indica os valores médios de: 2,88 cm (divisäo terminal), 5,10 cm (artéria polar I) e 1,70 cm (artéria polar II). É discutida a aplicaçäo desse conhecimento à esplenectomia parcial

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