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1.
Molecules ; 24(14)2019 Jul 10.
Artigo em Inglês | MEDLINE | ID: mdl-31295880

RESUMO

The difficulties encountered and the numerous side effects present in the treatment of cutaneous leishmaniasis have encouraged the research for new compounds that can complement or replace existing treatment. The growing scientific interest in the study of plants, which are already used in folk remedies, has led our group to test Endlicheria bracteolata essential oil against Leishmania amazonensis. Several species of the Lauraceae family, or their compounds, have relevant antiprotozoal activities Therefore, the biological potential on L. amazonensis forms from the essential oil of Endlicheria bracteolata leaves was verified for the first time in that work. The antileishmanial activity was evaluated against promastigotes and intracellular amastigotes, and cytotoxicity were performed with J774.G8, which were incubated with different concentrations of E. bracteolata essential oil. Transmission electron microscopy and flow cytometry were performed with E. bracteolata essential oil IC50. Promastigote forms showed E. bracteolata essential oil IC50 of 7.945 ± 1.285 µg/mL (24 h) and 6.186 ± 1.226 µg/mL (48 h), while for intracellular amastigote forms it was 3.546 ± 1.184 µg/mL (24 h). The CC50 was 15.14 ± 0.090 µg/mL showing that E. bracteolata essential oil is less toxic to macrophages than to parasites. Transmission electron microscopy showed that E. bracteolata essential oil treatment is capable of inducing mitochondrial damage to promastigote and intracellular amastigote forms, while flow cytometry showed ΔÑ°m disruption in treated parasites. These results could bring about new possibilities to develop products based on E. bracteolata essential oil to treat cutaneous leishmaniasis, especially for people who cannot receive the conventional therapy.


Assuntos
Antiprotozoários/farmacologia , Leishmania mexicana/química , Leishmania/efeitos dos fármacos , Óleos Voláteis/farmacologia , Animais , Antiprotozoários/química , Cromatografia Gasosa-Espectrometria de Massas , Macrófagos/efeitos dos fármacos , Macrófagos/parasitologia , Macrófagos/patologia , Macrófagos/ultraestrutura , Camundongos , Óleos Voláteis/química , Testes de Sensibilidade Parasitária
2.
PLoS One ; 12(10): e0187380, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29088304

RESUMO

Copaifera oleoresin is one of the most used natural products in popular medicine all over the world. Among other effects (i.e., anti-inflammatory, antinociceptive, microbicidal) one of the most well-known is its wound healing capacity. However, the mechanism by which the oleoresin presents its effect is still not clear. In this study, our aim was to evaluate the wound healing capacity of oleoresin obtained from Copaifera paupera, its mechanism of action and identify its major components. For these purposes, diabetic Swiss Webster mice were topically treated with oleoresin (100, 150 or 200 mg/kg) for 14 consecutive days after an excision was performed in the back of the mice. Cytokines, wound retraction and histological evaluation were conducted at 3, 7 and 10 days (for cytokines); 0, 3, 7, 10 and 14 days (for wound retraction); and 7 and 14 days (for histological evaluation). Our data indicate that oleoresin significantly reduced production of MCP-1 and TNF-α at days 7 and 10 post-excision and increased IL-10 production at both days. All treatments demonstrated an effect similar or higher to that in collagenase-treated mice. Histological evaluations demonstrated that higher dose treatment resulted in better resolution and closure of the wound and higher levels of collagen deposition and indexes of re-epithelialization even when compared with the collagenase-treated group. The treatment with oleoresin from Copaifera paupera demonstrated that it is even better than an ointment routinely used for improvement of wound healing, suggesting this oleoresin as an option for use in diabetic patients.


Assuntos
Fabaceae/química , Extratos Vegetais/farmacologia , Cicatrização/efeitos dos fármacos , Animais , Quimiocina CCL2/metabolismo , Cromatografia Gasosa-Espectrometria de Massas , Masculino , Camundongos , Fator de Necrose Tumoral alfa/metabolismo
3.
Acta sci., Biol. sci ; 38(2): 215-220, abr.-jun. 2016.
Artigo em Inglês | LILACS | ID: biblio-2534

RESUMO

Leaves surfaces, which represent an interface with plants and the environment, have several structures with specific functions. Some foliar properties, including wettability and mechanical containment, are inferred in terms of cellular adaptation and the presence or absence of cuticular wax. Various morphological parameters, ranging from macro- to nano scales, are analyzed and contribute to the study of taxonomy, pharmacognosy, and ecology of plants. The aim of this paper was to analyze the effect and influence of epicuticular wax granules on the hydrophobicity of Anacardium occidentale L. leaf surfaces. Leaf specimens were directly examined with an environmental scanning electron microscope without metal coating. Images revealed epidermis ornament, stomata type, was, and trichomes. Static contact angle between water and the surface was also measured on both sides. On the adaxial side, an angle of 104.09° ± 0.95° was found, suggesting that adaxial surface is hydrophobic. On the abaxial side, the angle was 62.20° ± 1.60°, which indicates a hydrophilic nature, probably because of the greater amount of epicuticular wax on the adaxial leaf surface. The present investigation provided an important contribution to morphological and ultrastructural characterization of leaves of cashew tree, which is a plant of great medicinal and economic importance.


Superfícies de folhas têm diversas estruturas com funções específicas e contribuem para a relação delas com o meio ambiente. Algumas propriedades foliares, incluindo molhabilidade e contenção mecânica, são inferidas em termos de adaptação celular e da presença ou ausência de cera cuticular. Diversos parâmetros morfológicos, variando da macroescala até a nanoescala, são analisados e contribuem para o estudo de taxonomia, farmacognosia e ecologia de plantas. O objetivo deste trabalho foi analisar o efeito e a influência de grãos de cera epicuticular na hidrofobicidade da superfície de folhas de Anacardium occidentale L. Amostras de folha foram examinadas com um microscópio eletrônico de varredura ambiental sem recobrimento metálico. As imagens evidenciaram algumas características (epiderme, tipo de estômato, cera e tricomas). O ângulo de contato estático entre a água e a superfície também foi medido em ambos os lados. No lado adaxial, foi encontrado um ângulo de 104,09° ± 0,95°, sugerindo que esta é hidrofóbica. No lado abaxial, o ângulo foi de 62,20° ± 1,60°, que indica uma natureza hidrofílica, provavelmente devido à grande quantidade de cera epicuticular na superfície abaxial da folha. A presente investigação forneceu uma contribuição importante para a caracterização morfológica e ultra-estrutural de folhas de cajueiro, que é uma planta de grande importância econômica.


Assuntos
Molhabilidade , Anacardium , Microscopia Eletrônica , Ecossistema Amazônico
4.
Braz. j. microbiol ; 46(1): 261-264, 05/2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-748265

RESUMO

The monoterpenoid 1,8-cineole is obtained from the leaves of Eucalyptus globulus and it has important biological activities. It is a cheap natural substrate because it is a by-product of the Eucalyptus cultivation for wood and pulp production. In this study, it was evaluated the potential of three filamentous fungi in the biotransformation of 1,8-cineole. The study was divided in two steps: first, reactions were carried out with 1,8-cineole at 1 g/L for 24 h; afterwards, reactions were carried out with substrate at 5 g/L for 5 days. The substrate was hydroxylated into 2-exo-hydroxy-1,8-cineole and 3-exo-hydroxy-1,8-cineole by fungi Mucor ramannianus and Aspergillus niger with high stereoselectivity. Trichoderma harzianum was also tested but no transformation was detected. M. ramannianus led to higher than 99% of conversion within 24 h with a starting high substrate concentration (1 g/L). When substrate was added at 5 g/L, only M. ramannianus was able to catalyze the reaction, but the conversion level was 21.7% after 5 days. Both products have defined stereochemistry and could be used as chiral synthons. Furthermore, biological activity has been described for 3-exo-hydroxy-1,8-cineol. To the best of our knowledge, this is the first report on the use of M. ramannianus in this reaction.


Assuntos
Aspergillus niger/metabolismo , Cicloexanóis/metabolismo , Eucalyptus/química , Monoterpenos/metabolismo , Mucorales/metabolismo , Hidroxilação , Fatores de Tempo , Trichoderma/metabolismo
5.
Rev Bras Parasitol Vet ; 24(1): 36-44, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25909251

RESUMO

Essential oil of Cymbopogon citratus collected from Brazil and Cuba was tested to a chemical characterization and then was tested on the post-embryonic development of Musca domestica. The chemical composition analysis by GC-MS of the oils from Brazil/Cuba allowed the identification of 13 and 12 major constituents respectively; nine of them common to both. In the both oils, the main components were the isomers geranial and neral, which together form the compound citral. This corresponds to a total of 97.92%/Brazil and 97.69%/Cuba of the compounds identified. The monoterpene myrcene, observed only in the sample of Cuba, presented a large relative abundance (6.52%). The essential oil of C. citratus (Brazil/Cuba) was dissolved in DMSO and tested at concentrations of 5, 10, 25, 50, 75 and 100% and citral was prepared by mixing 16.8 mg with 960 µL DMSO. Both essential oils and monoterpene citral were applied topically to newly-hatched larvae (1µL/larva). The results showed a lethal concentration (LC50) of 4.25 and 3.24% for the Brazilian and Cuban essential oils, respectively. Mortalities of larval and newly-hatched larvae to adult periods were dose-dependent for the two both oils as for monoterpene citral, reaching 90%. Both essential oils and citral caused morphological changes in adult specimens.


Assuntos
Cymbopogon , Moscas Domésticas/efeitos dos fármacos , Inseticidas , Óleos Voláteis/química , Óleos Voláteis/farmacologia , Animais , Brasil , Cuba
6.
Rev. bras. parasitol. vet ; 24(1): 36-44, Jan-Mar/2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-744658

RESUMO

Essential oil of Cymbopogon citratus collected from Brazil and Cuba was tested to a chemical characterization and then was tested on the post-embryonic development of Musca domestica. The chemical composition analysis by GC-MS of the oils from Brazil/Cuba allowed the identification of 13 and 12 major constituents respectively; nine of them common to both. In the both oils, the main components were the isomers geranial and neral, which together form the compound citral. This corresponds to a total of 97.92%/Brazil and 97.69%/Cuba of the compounds identified. The monoterpene myrcene, observed only in the sample of Cuba, presented a large relative abundance (6.52%). The essential oil of C. citratus (Brazil/Cuba) was dissolved in DMSO and tested at concentrations of 5, 10, 25, 50, 75 and 100% and citral was prepared by mixing 16.8 mg with 960 µL DMSO. Both essential oils and monoterpene citral were applied topically to newly-hatched larvae (1µL/larva). The results showed a lethal concentration (LC50) of 4.25 and 3.24% for the Brazilian and Cuban essential oils, respectively. Mortalities of larval and newly-hatched larvae to adult periods were dose-dependent for the two both oils as for monoterpene citral, reaching 90%. Both essential oils and citral caused morphological changes in adult specimens.


O óleo essencial de Cymbopogon citratus, coletado no Brasil e em Cuba, foi caracterizado quimicamente e testado no desenvolvimento pós-embrionário de Musca domestica. A análise da composição química dos óleos essenciais (Brasil/Cuba), por Cromatografia Gasosa acoplada ao espectrômetro de massa (GC-EM), permitiu a identificação de 13 e 12 componentes principais, respectivamente; nove deles comuns aos dois. Em ambos os óleos, os principais componentes foram os isômeros geranial e neral, que, juntos, formam o composto citral. Esse corresponde a um total de 97,92%/Brasil e 97,69%/Cuba dos compostos identificados. O monoterpeno mirceno, observado na amostra cubana, apresentou grande abundância relativa (6,52%). O óleo de C. citratus (Brasil/Cuba) foi dissolvido em DMSO, obtendo–se as concentrações de 5, 10, 25, 75 e 100%; e o citral (16,8 mg) foi misturando com 960mL de DMSO. Tanto o óleo essencial como o monoterpeno citral foram aplicados topicamente nas neolarvas (1µL/larva). Os resultados mostraram uma concentração letal (CL50) de 4,25% e 3,24% para o óleo essencial brasileiro e cubano, respectivamente. As mortalidades do período larval e o de neo-larva a adulto foram dose-dependentes, tanto para os óleos como para o monoterpeno citral, podendo chegar a 90%. Ambos os óleos essenciais e citral causaram alterações morfológicas nos espécimes adultos.


Assuntos
Animais , Óleos Voláteis/farmacologia , Óleos Voláteis/química , Cymbopogon , Moscas Domésticas/efeitos dos fármacos , Inseticidas , Brasil , Cuba
7.
Exp Parasitol ; 148: 66-72, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25448354

RESUMO

Current treatments for leishmaniasis present some difficulties due to their toxicity, the use of the intravenous route for administration and therapy duration, which may lead to treatment discontinuation. The aim of this study is to investigate new treatment alternatives to improve patients well being. Therefore, we evaluated the inhibitory effect of (-)α-bisabolol, a sesquiterpene alcohol found in various essential oils of different plant species, against the promastigotes and intracellular amastigotes forms of Leishmania amazonensis, as well as the cytotoxic, morphological and ultrastructural alterations of treated cells. Promastigotes forms of L. amazonensis were incubated with (-)α-bisabolol to determine the antileishmanial activity of this compound. The cytotoxicity effect was evaluated by testing against J774.G8 cells. After these tests, the infected and uninfected cells with L. amazonensis were used to determine if the (-)α-bisabolol was able to kill intracellular parasites and to cause some morphological changes in the cells. The (-)α-bisabolol compound showed significant antileishmanial activity against promastigotes with a 50% effective concentration of 8.07 µg/ml (24 h) and 4.26 µg/ml (48 h). Against intracellular amastigotes the IC50 (inhibitory concentration) of (-)α-bisabolol (24 h) was 4.15 µg/ml. The (-)α-bisabolol also showed a cytotoxic effect against the macrophage strain J774.G8. The value of 50% cytotoxic concentration was 14.82 µg/ml showing that (-)α-bisabolol is less toxic to macrophages than to the parasite. Ultrastructural studies of treated promastigotes and amastigotes showed several alterations, such as loss of cytoplasmic organelles, including the nucleus, and the presence of lipid inclusions. This study showed that (-)α-bisabolol has promising antileishmanial properties, as it can act against the promastigote forms and is able to penetrate the cell, and is also active against the amastigote forms. About 69% of the promastigotes forms suffered mitochondrial membrane damage after treatment with IC50 of (-)α-bisabolol, suggesting inhibition of the metabolic activity of parasites. These results open new prospects for research that can contribute to the development of products based on essential oils or isolated compounds from plants for the treatment of cutaneous leishmaniasis.


Assuntos
Antiprotozoários/farmacologia , Leishmania mexicana/efeitos dos fármacos , Sesquiterpenos/farmacologia , Animais , Antiprotozoários/toxicidade , Linhagem Celular , Citometria de Fluxo , Humanos , Concentração Inibidora 50 , Leishmania mexicana/crescimento & desenvolvimento , Leishmania mexicana/ultraestrutura , Macrófagos/efeitos dos fármacos , Camundongos , Camundongos Endogâmicos BALB C , Microscopia Eletrônica de Transmissão , Sesquiterpenos Monocíclicos , Sesquiterpenos/toxicidade
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