Capacidad antimicrobiana de propoleo en terapia pulpar / Antimicrobial capacity of propolis in pulp therapy

Introducción: La terapia con pulpotomía es un tratamiento comúnmente llevado a cabo en pacientes pediátricos para contrarrestar la infección presente, frecuentemente se utilizan agentes químicos como antimicrobianos siendo algo contradictorios en cuanto a sus efectos. Objetivo: Evaluar la acción antimicrobiana del extracto etanólico de propóleo al 10% en terapia pulpar de órganos dentarios primarios. Materiales y Metodos: En este estudio se utilizó el Extracto Etanólico de Propóleo (EEP) al 10% de origen natural para el tratamiento de pulpotomías, su acción antimicrobiana fue evaluada mediantela recolección de muestras microbiológicas antes de la colocación de EEP muestra (S1) y después de su colocación muestra (S2). Se evaluó el grado de desarrollo microbiano en Unidades McFarland y por conteo de UFC en dos tiempos inicial y 24 hrs. Resultados: El propóleo mostró capacidad antimicrobiana ya que los resultados presentan una disminución promedio del crecimiento bacteriano entre las 20 muestras, siendo de 8, 30 a 8,10 en S1 y S2, así como de 9,18 a 8,96 en S1a y S2a. Los resultados muestran un efecto antimicrobiano, obteniendo diferencias entre S1 y S2, resultados que favorecen la capacidad antimicrobiana del propóleo. Conclusiones: El uso de extractos de plantas o derivados naturales como puede ser el propóleo para el tratamiento de terapias pulpares como son las pulpotomías en dientes temporales es prometedor como alternativa del formocresol.

Propolis cinnamic acid derivatives induce apoptosis through both extrinsic and intrinsic apoptosis signaling pathways and modulate of miRNA expression.

Propolis cinnamic acid derivatives have a number of biological activities including anti-oxidant and anti-cancer ones. In this study, we aimed to elucidate the mechanism of the anti-cancer activity of 3 representative propolis cinnamic acid derivatives, i.e., Artepilin C, Baccharin and Drupanin in human colon cancer cell lines. Our study demonstrated that these compounds had a potent apoptosis-inductive effect even on drug-resistant colon cancer cells. Combination treatment of human colon cancer DLD-1 cells with 2 of these compounds, each at its IC20 concentration, induced apoptosis by stimulating both intrinsic and extrinsic apoptosis signaling pathways. Especially, Baccharin plus Drupanin exhibited a synergistic growth-inhibitory effect by strengthening both intrinsic and extrinsic apoptotic signaling transduction through TRAIL/DR4/5 and/or FasL/Fas death-signaling loops and by increasing the expression level of miR-143, resulting in decreased expression levels of the target gene MAPK/Erk5 and its downstream target c-Myc. These data suggest that the supplemental intake of these compounds found in propolis has enormous significance with respect to cancer prevention.

Verificação da interferência do solvente propilenoglicol sobre o efeito da própolis na produção de lagartas de Bombyx mori L. (Lepidoptera: bombicidae) comparado ao extrato alcoólico de própolis / Interference of propyleneglycol solvent on the effect of propolis in the production of silkworm Bombyx mori L. (Lepidoptera: bombicidae) compared to propolis alcoholic extract / Verificación de la interferencia del solvente propilenoglicol sobre el efecto de propóleos en la producción de gusano de seda Bombyx mori L. (lepidoptera: bombicidae) comparado al extracto alcohólico de propóleos

Este experimento foi realizado no Laboratório de Sericicultura, no Campus Sede da Universidade Paranaense (UNIPAR) de Umuarama, no período de fevereiro a outubro de 2011, com o objetivo de verificar o efeito da própolis em diferentes dosagens na alimentação durante o desenvolvimento biológico do bicho-da-seda (Bombxy mori L.). O método empregado na parte experimental foi a pulverização do extrato glicólico de própolis, diluído em 500mL de água destilada nas folhas de amoreira, nas seguintes dosagens, água-controle, 25mL, 30mL, 35mL e 40mL compondo os tratamentos: controle, T1 , T2 , T3 e T4 respectivamente. As folhas de amoreira foram fornecidas cinco vezes ao dia, durante o manejo alimentar. Verificou-se, pelos resultados obtidos, que as diferentes dosagens de própolis utilizadas não interferiram no ganho de peso das lagartas, no peso dos casulos verdes, no peso da casca sérica e crisálidas, quando comparado ao tratamento controle, mas quando se compara o Controle e T4 do ensaio da primavera, respectivamente, para os teores de seda bruto e líquido, há resultados significativos. Portanto, verificou-se que o extrato glicólico de própolis, em dosagens de 40mL, pode prejudicar o teor líquido de seda em uma produção de casulos, trazendo resultados pouco apreciados dentro da sericicultura...

This experiment was performed at the Laboratory of Sericulture, at the main campus of University Paranaense (UNIPAR), in the city of Umuarama, from February to October 2011, in order to verify the effect of different doses of propolis in feeding during the biological development of silkworm (Bombyx mori L.). The method used in the experiment was the spraying of propolis glycolic extract dissolved in 500-mL distilled water on the mulberry leaves in the following water- -control dosages: 25mL, 30mL, 35mL and 40mL related to the treatment controls T1, T2, T3 and T4, respectively. Mulberry leaves were provided five times a day for feeding management. The results obtained showed that the different dosages of propolis used did not affect the weight gain of the larvae, the weight of green cocoons, shells and pupae when compared to the control treatment. However, when comparing the control and T4 from the Spring assay, respectively, to the levels of crude and net silk, significant results were noted. Thus, it can be concluded that propolis glycolic extract in 40-ml dosages may impair the net silk content in a cocoon production, presenting negative results in sericulture...

: Este experimento se llevó a cabo en el Laboratorio de Sericultura, Campus Sede de la Universidad Paranaense (UNIPAR) de Umuarama, en el período de febrero a octubre de 2011, con el fin de verificar el efecto de propóleos en diferentes concentraciones en la alimentación durante el desarrollo biológico del gusano de seda (Bombyx mori L.). El método utilizado en el experimento fue la pulverización de extracto glicólico de propóleos, disuelto en 500 ml de agua destilada en las hojas de morera, en las siguientes dosis, agua control, 25 mL, 30mL, 35 mL, y 40 mL componiendo los tratamientos: control T1 , T2 , T3 e T4 respectivamente. A las hojas de morera se les han dado cinco veces al día, durante el manejo alimentar. Se verificó, por los resultados obtenidos, que las diferentes dosis de propóleos utilizados no afectaron en la ganancia de peso de los gusanos, en el peso de los capullos verdes, en el peso de la cáscara sérica y crisálidas, en comparación con el tratamiento de control, pero cuando se compara el Control y T4 del ensayo de la primavera, respectivamente, para los niveles de seda cruda y líquida, hay resultados significativos. Por lo tanto, se encontró que el extracto glicólico de propóleos, en dosis de 40 mL, puede perjudicar la concentración líquida de seda en una producción de capullos, trayendo resultados poco apreciados dentro de la sericultura...

Preparation and characterisation of ethylcellulose microparticles containing propolis

Ethylcellulose microparticles containing propolis ethanolic extract (PE) were prepared by the emulsification and solvent evaporation method. Three ratios of ethylcellulose to PE dry residue value (DR) weretested (1:0.25, 1:4 and 1:10). Moreover, polysorbate 80 was used as emulsifier in the external phase (1.0 or 1.5% w/w). Regular particle morphology without amorphous and/or sticking characteristics was achieved only when an ethylcellulose: DR ratio of 1:0.25 and 1.0% polysorbate 80 were used. Microparticles had a mean diameter of 85.83 mium. The entrapment efficiency forpropolis of the microparticles was 62.99 more or less 0.52%. These ethylcellulose microparticles containing propolis would be useful for developing propolis aqueous dosage forms without the strong and unpleasant taste, aromatic odour and high ethanol concentration of PE.

Water extract of propolis and its main constituents, caffeoylquinic acid derivatives, exert neuroprotective effects via antioxidant actions.

We investigated whether water extract of Brazilian green propolis (WEP) and its main constituents [caffeoylquinic acid derivatives (3,4-di-O-caffeoylquinic acid, 3,5-di-O-caffeoylquinic acid, chlorogenic acid) and cinnamic acid derivatives (p-coumaric acid, artepillin C, drupanin, baccharin)] exert neuroprotective effects against the retinal damage induced by oxidative stress. Additionally, their neuroprotective effects were compared with their antioxidant effects. WEP, 3,4-di-O-caffeoylquinic acid, 3,5-di-O-caffeoylquinic acid, chlorogenic acid, and p-coumaric acid (but not artepillin C, baccharin, or drupanin) concentration-dependently inhibited oxidative stress-induced neurotoxicity [achieved using L-buthionine-(S,R)-sulfoximine (BSO) to deplete glutathione in combination with glutamate to inhibit cystine uptake] in cultured retinal ganglion cells (RGC-5, a rat ganglion cell line transformed using E1A virus). At their effective concentrations against oxidative stress-induced retinal damage, WEP, 3,4-di-caffeoylquinic acid, 3,5-di-caffeoylquinic acid, and chlorogenic acid (but not cinnamic acid derivatives) inhibited lipid peroxidation (LPO) in mouse forebrain homogenates. Thus, the neuroprotective effects of WEP and caffeoylquinic acid derivatives paralleled those against LPO. These findings indicate that WEP and caffeoylquinic acid derivatives have neuroprotective effects against retinal damage in vitro, and that these effects may be partly mediated via antioxidant effects.

Peroral application of water-soluble derivative of propolis (WSDP) and its related polyphenolic compounds and their influence on immunological and antitumour activity.

Polyphenolic compounds are widely distributed in the plant kingdom and display a variety of biological activities, including chemoprevention and growth inhibition of tumours. Propolis contains a conglomerate of polyphenolic compounds. We investigated the effect of propolis and polyphenolic compounds, components of propolis, on the growth and metastatic potential of a transplantable mammary carcinoma (MCa) of the mouse. Metastases in the lung were generated by 2 x 10(5) tumour cells injected intravenously (i.v.). A water-soluble derivative of propolis (WSDP) and the polyphenolic compounds (caffeic acid (CA) and caffeic acid phenethyl ester (CAPE)) were given to mice perorally before or after tumour cell inoculation. WSDP, CA and CAPE reduced the number of metastases in the lung. This implies that the antitumour activities of the compounds used in these studies are mostly related to the immunomodulatory properties of the compounds, their cytotoxicity to tumour cells, and their ability to induce apoptosis and/or necrosis.

Caffeic acid phenethyl ester (CAPE) analogues: potent nitric oxide inhibitors from the Netherlands propolis.

The MeOH and water extracts of the Netherlands propolis were tested for their inhibitory activity toward nitric oxide (NO) production in lipopolysaccharide (LPS)-activated murine macrophage-like J774.1 cells. Both of the extract possessed significant NO inhibitory activity with IC(50) values of 23.8 and 51.5 microg/ml, respectively. Then 13 phenolic compounds obtained from the MeOH extract showing stronger NO inhibition were examined on their NO inhibitory activities. Caffeic acid phenethyl ester (CAPE) analogues, i.e., benzyl caffeate, CAPE and cinnamyl caffeate, possessed most potent NO inhibitory activities with IC(50) values of 13.8, 7.64 and 9.53 microM, respectively, which were two- to four-fold stronger than the positive control N(G)-monomethyl-L-arginine (L-NMMA; IC(50), 32.9 microM). Further study on the synthetic analogues of CAPE revealed that both of 3-phenylpropyl caffeate (18; IC(50), 7.34 microM) and 4-phenylbutyl caffeate (19; IC(50), 6.77 microM) possessed stronger NO inhibitory activity than CAPE (10) and that elongation of alkyl side chain of alcoholic parts of caffeic acid esters enhance the NO inhibitory activity. In addition, it was found that CAPE analogues having longer carbon chain (>C(5)) in alcoholic part showed toxic effects toward J774.1 cells. This NO inhibitory effect may directly correlate with antiinflammatory properties of the Netherlands propolis.

Immunomodulation by water-soluble derivative of propolis: a factor of antitumor reactivity.

The antimetastatic efficacy of a water-soluble derivative of propolis (WSDP) was studied. Tumor was a transplantable mammary carcinoma of CBA mouse. Metastases in the lung were generated by 2 x 10(5) viable tumor cells i.v. WSDP was given intraperitoneally at doses of 50 or 150 mg/kg before or after tumor cell inoculation. Therapies reduced the number of metastases in the lung and tumor growth was suppressed significantly by WSDP. It is likely that antimetastatic activity of the WSDP is mainly mediated by immunomodulatory activity. Changes in several immunological parameters such as production of lymphocyte activating factor by peritoneal macrophages and the efficacy of those macrophages to kill tumor cell in vitro, responses of lymphocytes to mitogen, and weight and cellularity of spleen, respectively, correlated well with antimetastatic properties of the WSDP. Based on results we postulate that the antimetastatic activity of propolis includes a pronounced immunomodulatory activity mainly toward augmentation of nonspecific antitumor resistance in mice via macrophage activation.