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1.
Food Res Int ; 99(Pt 1): 495-500, 2017 09.
Artículo en Inglés | MEDLINE | ID: mdl-28784510

RESUMEN

This study aimed to investigate the effect of a synbiotic beverage made from soy and yacon (Smallanthus sonchifolius) extracts containing Bifidobacterium animalis ssp. lactis BB-12 on healthy elderly individuals' intestinal polyamine concentrations. A randomized, double-blinded, placebo-controlled trial has been conducted with twenty-nine volunteers (over 65years of age) who either had a daily intake of 150mL of synbiotic (synbiotic group - S) or placebo (placebo group - P) beverages. Both had the same nutrient composition, except that a probiotic culture was added to the synbiotic beverage. Total experiment time was 8weeks, which was divided into 3 consecutive phases: a prefeeding period (2weeks), followed by a feeding period (4weeks) and a postfeeding period (2weeks). Stool samples were collected at 3 time periods. Fecal concentrations of polyamines, putrescine (PUT), cadaverine (CAD) and spermidine (SPD) that were obtained during the synbiotic and placebo consumption period were significantly higher (p<0.05) than those found during the pre-consumption baseline level period. No significant differences in the number of bifidobacteria, clostridia, or enterobacteria were observed in any of the two groups at the three time periods. Similarly, no significant effect on the production of proinflammatory cytokines tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6) and anti-inflammatory interleukin-10 (IL-10) was induced by the synbiotic or placebo beverages consumption. The results herein indicate that both the synbiotic and the placebo beverage consumption have increased polyamines levels, which are often reduced in elderly individuals, without influencing inflammatory responses. In addition, both placebo and synbiotic beverages seems to contribute by maintaining increased polyamines levels.


Asunto(s)
Asteraceae , Bebidas/microbiología , Bifidobacterium animalis/metabolismo , Microbioma Gastrointestinal , Extractos Vegetales/administración & dosificación , Poliaminas/metabolismo , Alimentos de Soja , Simbióticos/administración & dosificación , Factores de Edad , Anciano , Animales , Brasil , Línea Celular , Citocinas/metabolismo , Método Doble Ciego , Heces/química , Heces/microbiología , Femenino , Humanos , Mediadores de Inflamación/metabolismo , Macrófagos/metabolismo , Macrófagos/microbiología , Masculino , Ratones , Factores de Tiempo , Regulación hacia Arriba
2.
Int J Nanomedicine ; 10: 585-94, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25609963

RESUMEN

Methyl dihydrojasmonate (MJ) has been studied because of its application as an antitumor drug compound. However, as MJ is a poorly water-soluble compound, a suitable oil-in-water microemulsion (ME) has been studied in order to provide its solubilization in an aqueous media and to allow its administration by the parenteral route. The ME used in this work was characterized on the pseudo-ternary phase diagram by dynamic light scattering and rheological measurements. Regardless of the drug presence, the droplet size was directly dependent on the oil/surfactant (O/S) ratio. Furthermore, the drug incorporation into the ME significantly increased the ME diameter, mainly at low O/S ratios. The rheological evaluation of the systems showed that in the absence of drug a Newtonian behavior was observed. On the other hand, in the presence of MJ the ME systems revealed pseudoplastic behavior, independently of the O/S ratio. The in vivo studies demonstrated that not only was the effect on the tumor inhibition inversely dependent on the MJ-loaded ME administered dose, but also it was slightly higher than the doxorubicin alone, which was used as the positive control. Additionally, a small antiangiogenic effect for MJ-loaded ME was found at doses in which it possesses antitumor activity. MJ revealed to be nontoxic at doses higher than 350 mg/kg, which was higher than the dose that provides tumor-inhibition effect in this study. Because the MJ-loaded ME was shown to have anticancer activity comparable to doxorubicin, the ME described here may be considered a suitable vehicle for parenteral administration of MJ.


Asunto(s)
Antineoplásicos , Materiales Biocompatibles , Ciclopentanos , Portadores de Fármacos , Emulsiones , Animales , Antineoplásicos/química , Antineoplásicos/toxicidad , Materiales Biocompatibles/química , Materiales Biocompatibles/toxicidad , Ciclopentanos/química , Ciclopentanos/toxicidad , Portadores de Fármacos/química , Portadores de Fármacos/toxicidad , Emulsiones/química , Emulsiones/toxicidad , Femenino , Masculino , Ratones , Ratones Endogámicos BALB C
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