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1.
Toxicological Research ; : 99-106, 2013.
Artículo en Inglés | WPRIM | ID: wpr-59642

RESUMEN

Clostridium difficile infection (CDI) has become a significant threat to public health. Although broad-spectrum antibiotic therapy is the primary treatment option for CDI, its use has evident limitations. Probiotics have been proved to be effective in the treatment of CDI and are a promising therapeutic option for CDI. In this study, 4 strains of lactic acid bacteria (LAB), namely, Lactobacillus rhamnosus (LR5), Lactococ-cuslactis (SL3), Bifidobacterium breve (BR3), and Bifidobacterium lactis (BL3) were evaluated for their anti-C. difficile activity. Co-culture incubation of C. difficile (106 and 1010 CFU/ml) with each strain of LAB indicated that SL3 possessed the highest antimicrobial activity over a 24-hr period. The cell-free supernatants of the 4 LAB strains exhibited MIC50 values between 0.424 mg/ml (SL3) and 1.318 (BR3) mg/ml. These results may provide a basis for alternative therapies for the treatment of C. difficile-associated gut disorders.


Asunto(s)
Bacterias , Bifidobacterium , Clostridium , Clostridioides difficile , Técnicas de Cocultivo , Terapias Complementarias , Ácido Láctico , Lacticaseibacillus rhamnosus , Probióticos , Salud Pública , Piridinas , Esguinces y Distensiones , Tiazoles
2.
Journal of Veterinary Science ; : 165-167, 2009.
Artículo en Inglés | WPRIM | ID: wpr-54362

RESUMEN

The effect of extracellular beta-(1-->3), (1-->6)-glucan, produced by Paenibacillus polymyxa JB115, on nitric oxide (NO) production in RAW264.7 macrophages was investigated. beta-glucan induced the production of NO by RAW264.7 macrophages in a concentration- and time-dependent manner. Moreover, beta-glucan stimulation increased the mRNA expression of iNOS, COX-2 and IL-6 in RAW264.7 macrophages in a concentration-dependent manner.


Asunto(s)
Animales , Ratones , Bacillus/metabolismo , Línea Celular , Ciclooxigenasa 2/biosíntesis , Interleucina-6/biosíntesis , Lipopolisacáridos/farmacología , Macrófagos/efectos de los fármacos , Óxido Nítrico/biosíntesis , Óxido Nítrico Sintasa de Tipo II/biosíntesis , ARN Mensajero/biosíntesis , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , beta-Glucanos/metabolismo
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