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1.
J. appl. oral sci ; 28: e20190519, 2020. tab, graf
Artículo en Inglés | LILACS, BBO | ID: biblio-1101254

RESUMEN

Abstract Natural products have emerged as a rich source of bioactive compounds for adjunctive treatments of many infectious and inflammatory conditions, including periodontitis. Among the monoterpenes with significant biological properties, there is the perillyl alcohol (POH), which can be found in several essential oils and has shown immunomodulatory properties in recent studies, which may be interesting in the treatment of non-neoplastic inflammatory disorders. Objective To determine the antibacterial and immune modulatory activities of the POH. Methodology The minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) of the POH for two significant Gram-negative periodontal pathogens were determined by macrodilution and subculture, respectively. Cell proliferation and cytotoxicity in RAW 264.7 macrophages were determined by Trypan Blue and mitochondrial enzymatic activity assay. The modulation of reactive oxygen species (ROS) was analyzed by flow cytometry and expression of TNF and arginase-1 by real-time PCR. Results The POH was effective against P. gingivalis (ATCC 33277) and F. nucleatum (ATCC 25586) with MIC= MBC=1600 μM. No cytotoxicity up to 100 µM was observed on macrophages. The cell proliferation was inhibited from 48 hours at 100 μM (p<0.05) and 250 μM (p<0.01). The POH increased ROS production at both 10 μM and 100 μM (p<0.05) in unstimulated cells. The PMA-induced ROS production was not affected by POH, whereas 100 μM significantly reduced lipopolysaccharide-induced (LPS-induced) ROS. The expression of TNF was not affected by POH in unstimulated cells or in cells polarized to M1 phenotype, whereas both concentrations of POH reduced (p<0.05) the expression of arginase-1 in M2-polarized macrophages. Conclusion The POH has antibacterial activity against periodontal pathogens and reduced proliferation of murine macrophages without significant cytotoxicity at concentrations up to 100 μM. In addition, the POH reduced the LPS-induced ROS and the expression of arginase-1 in M2-polarized macrophages.


Asunto(s)
Animales , Ratones , Fusobacterium nucleatum/efectos de los fármacos , Especies Reactivas de Oxígeno/análisis , Porphyromonas/efectos de los fármacos , Monoterpenos/farmacología , Macrófagos/efectos de los fármacos , Antibacterianos/farmacología , Arginasa/análisis , Factores de Tiempo , Productos Biológicos/farmacología , Pruebas de Sensibilidad Microbiana , Expresión Génica , Lipopolisacáridos/farmacología , Reproducibilidad de los Resultados , Factor de Necrosis Tumoral alfa/análisis , Fusobacterium nucleatum/crecimiento & desarrollo , Especies Reactivas de Oxígeno/metabolismo , Porphyromonas/crecimiento & desarrollo , Proliferación Celular/efectos de los fármacos , Reacción en Cadena en Tiempo Real de la Polimerasa , Citometría de Flujo , Células RAW 264.7 , Macrófagos/metabolismo
2.
Rev. méd. Chile ; 134(4): 465-468, abr. 2006. tab
Artículo en Español | LILACS | ID: lil-428546

RESUMEN

Background: Aspirative pleuropulmonary infections are usually caused by anaerobic flora of the mouth, mainly Prevotella, Fusobacterium and Peptostreptococcus spp. Penicillin in high doses is the traditional treatment for this type of infections but the rising resistance developed in recent years has induced the empiric use of clindamycin, increasing treatment costs. Aim: To study antimicrobial susceptibility of anaerobic bacteria isolated from pleuropulmonary infections. Material and methods: Thirty two strains obtained from bronchoalveolar lavage and 15 strains isolated from pleural effusions between 2000 and 2002, were studied. The phenotype of strains was identified using the semiautomated API 20 A method and their susceptibility to penicillin (PNC), clindamycin (CM) and chloramphenicol (CAF) was tested using the E test methods. Results: All the strains were susceptible to CAF, 95% to CM and 74.4% to PNC. The predominant genus was Prevotella, which also exhibited the higher resistance. Conclusions: As CM and CAF are active "in vitro", high rates of clinical response should be expected. In contrast, PNC is less effective, especially against pigmented Prevotella.


Asunto(s)
Humanos , Antibacterianos/farmacología , Bacterias Anaerobias/efectos de los fármacos , Infecciones Bacterianas/microbiología , Farmacorresistencia Bacteriana Múltiple , Neumonía Bacteriana/microbiología , Bacterias Anaerobias/aislamiento & purificación , Infecciones por Bacteroidaceae/microbiología , Resistencia al Cloranfenicol , Cloranfenicol/farmacología , Clindamicina/farmacología , Fusobacterium/efectos de los fármacos , Pruebas de Sensibilidad Microbiana , Penicilina G/farmacología , Porphyromonas/efectos de los fármacos , Prevotella/efectos de los fármacos
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