RESUMO
Intermittent ethanol consumption changes the neuronal activity of the orbitofrontal cortex (OFC) in rodents, which has been attributed to important participation in the development of addiction, particularly alcoholism. The OFC participates in gustatory sensory integration. However, it is unknown whether this region can encode chemosensory elements of oral ethanol administration independently of the consumption movement (orofacial motor response) when administered for the first time (naïve mice). To answer this question, we used a sedated mouse model and a temporary analysis protocol to register extracellular neuronal responses during the oral administration of ethanol. Our results show an increase in neuronal frequency (in the first 500 ms) when low (0.6, 1, and 2.1 M) and high (3.2, 4.3, and 8.6 M) concentrations of ethanol are orally administered. The modulatory effect of ethanol was observed from low and high concentrations and differed from the tastants. There was consistent neuronal activity independent of the concentration of ethanol. Our results demonstrate a sensory representation of oral ethanol stimulation in the OFC neurons of naïve mice under sedation.
Assuntos
Alcoolismo , Etanol , Camundongos , Animais , Etanol/farmacologia , Córtex Pré-Frontal/fisiologia , Neurônios/fisiologia , SensaçãoRESUMO
A nanostructured matrix, consisting of titania, was designed in such a way that an antiepileptic drug could be encapsulated and released according to a well-defined time release schedule. The titania was synthesized by a sol-gel method in which titanium n-butoxide was used as the precursor for the formation of the sol. The synthesis was optimized to yield a homogeneous particle size with a high porosity and an anatase crystal structure. The antiepilectic drugs, phenytoine or valproic acid, were added during the gelation stage in order to obtain a homogeneous gel phase. The resulting nanostructured matrix including the drug showed only weak attractive forces, such as London forces, dipole-dipole coupling, and in some cases hydrogen bonds. The resulting assembly, referred to as a reservoir, was characterized using conventional FTIR and NMR spectroscopic techniques. Theoretical simulation studies were performed so as to obtain an understanding of the equilibrium electrostatic potential distribution and the relative charges on the titania and the anticonvulsants.
Assuntos
Anticonvulsivantes/administração & dosagem , Cápsulas , Sistemas de Liberação de Medicamentos , Espectroscopia de Ressonância Magnética , Titânio , Anticonvulsivantes/química , GéisRESUMO
The PetrifilmTM Aerobic Count Plate (ACP) developed by 3M laboratories, is a ready-to-use culture medium system, useful for the enumeration of aerobic bacteria in food. PetrifilmTMwas compared with a standard method in several different food products with satisfactory results. However, many studies showed that bacterial counts in PetrifilmTM were significantly lower than those obtained with conventional methods in fermented food. The purpose of this study was to compare the PetrifilmTM method for enumerating aerobic bacteria with a conventional method (PCA) in Crottin goat's cheese. Thirty samples were used for the colony count. The mean count and standard deviation were 7.18 ± 1.17 log CFU g-1 on PCA and 7.11 ± 1.05 log CFU g-1 on PetrifilmTM. Analysis of variance revealed no significant differences between both methods (t = 1.33, P = 0.193). The Pearson correlation coefficient (0.971, P=0.0001) indicated a strong linear relationship between the PetrifilmTM and the standard method. The results showed that PetrifilmTM is suitable and a convenient alternative to this standard method for the enumeration of aerobic flora in goat soft cheese.
PetrifilmTM Aerobic Count Plate (ACP) desarrollado por 3M es un sistema listo para usar, empleado para el recuento de bacterias aerobias en alimentos. PetrifilmTMfue comparado con los métodos estándar en diferentes productos alimenticios con resultados satisfactorios. Sin embargo, en alimentos fermentados, algunos estudios mostraron que el recuento de bacterias aerobias en PetrifilmTM fue significativamente menor que aquellos obtenidos con los métodos convencionales (PCA). El propósito de este estudio fue comparar el método PetrifilmTM para el recuento de bacterias aerobias con un método convencional en queso de cabra Crottin. Se usaron 30 muestras para el recuento de colonias. Las medias y desviaciones estándar fueron 7,18 ± 1,17 log UFC g-1 en PCA y 7,11 ± 1,05 log UFC g-1 en PetrifilmTM. El análisis de varianza mostró que no había diferencia significativa entre ambos métodos (t = 1,33, P = 0,193). El coeficiente de correlación fue 0,971 ( P = 0,0001) indicando una fuerte correlación lineal. Los resultados muestran a PetrifilmTM como un método apropiado y una alternativa conveniente a los métodos estándar para la cuantificación de flora aeróbica en queso blando de cabra.
Assuntos
Animais , Feminino , Técnicas Bacteriológicas , Bactérias Aeróbias/isolamento & purificação , Queijo/microbiologia , Microbiologia de Alimentos , Aerobiose , Bactérias Aeróbias/crescimento & desenvolvimento , Técnicas Bacteriológicas/instrumentação , Meios de Cultura , CabrasRESUMO
In order to evaluate the behavior of Yersinia enterocolitica and Salmonella typhimurium in Crottin goat's cheese, inoculated products stored at 5, 15 and 25 degrees C were analysed together with chemical and microbiological characteristics of the cheese. In general, low counts of microorganisms were detected. None of the samples showed the presence of Escherichia coli, Salmonella spp. or Y. enterocolitica. In the inoculation tests, Y. enterocolitica and S. typhimurium were inhibited during storage; nevertheless, these bacteria survived for extensive periods. The counts at the end of the experiments at 5 and 15 degrees C were high, indicating that contamination with high bacterial numbers represents a potential health hazard. The primary mathematical models used to analyse the behavior of Y. enterocolitica and S. typhimurium were the Vitalistic, Gompertz's empirical and Churchill's model. The mean square error was calculated for the three models in order to evaluate the goodness-of-fit of each one. For Y. enterocolitica, the Vitalistic model was the best at the three temperatures. For S. typhimurium, there was no significant difference between the three models at 5 and 15 degrees C; the Churchill model was clearly the best at 25 degrees C. These results confirm that, in order to predict the risk of transmission of pathogenic microorganisms in foods using mathematical models, it is essential to analyse their behavior in specific foods.
Assuntos
Queijo/microbiologia , Manipulação de Alimentos/métodos , Salmonella typhimurium/crescimento & desenvolvimento , Temperatura , Yersinia enterocolitica/crescimento & desenvolvimento , Animais , Contagem de Colônia Microbiana , Microbiologia de Alimentos , Cabras , Cinética , Matemática , Modelos BiológicosRESUMO
The Petrifilm Aerobic Count Plate (ACP) developed by 3M laboratories, is a ready-to-use culture medium system, useful for the enumeration of aerobic bacteria in food. Petrifilm was compared with a standard method in several different food products with satisfactory results. However, many studies showed that bacterial counts in Petrifilm were significantly lower than those obtained with conventional methods in fermented food. The purpose of this study was to compare the Petrifilm method for enumerating aerobic bacteria with a conventional method (PCA) in Crottin goat's cheese. Thirty samples were used for the colony count. The mean count and standard deviation were 7.18 +/- 1.17 log CFU g(-1) on PCA and 7.11 +/- 1.05 log CFU g(-1) on Petrifilm. Analysis of variance revealed no significant differences between both methods (t = 1.33, P = 0.193). The Pearson correlation coefficient (0.971, P = 0.0001) indicated a strong linear relationship between the Petrifilm and the standard method. The results showed that Petrifilm is suitable and a convenient alternative to this standard method for the enumeration of aerobic flora in goat soft cheese.
Assuntos
Bactérias Aeróbias/isolamento & purificação , Técnicas Bacteriológicas , Queijo/microbiologia , Microbiologia de Alimentos , Aerobiose , Animais , Bactérias Aeróbias/crescimento & desenvolvimento , Técnicas Bacteriológicas/instrumentação , Meios de Cultura , Feminino , CabrasRESUMO
The Petrifilm Aerobic Count Plate (ACP) developed by 3M laboratories, is a ready-to-use culture medium system, useful for the enumeration of aerobic bacteria in food. Petrifilm was compared with a standard method in several different food products with satisfactory results. However, many studies showed that bacterial counts in Petrifilm were significantly lower than those obtained with conventional methods in fermented food. The purpose of this study was to compare the Petrifilm method for enumerating aerobic bacteria with a conventional method (PCA) in Crottin goats cheese. Thirty samples were used for the colony count. The mean count and standard deviation were 7.18 +/- 1.17 log CFU g(-1) on PCA and 7.11 +/- 1.05 log CFU g(-1) on Petrifilm. Analysis of variance revealed no significant differences between both methods (t = 1.33, P = 0.193). The Pearson correlation coefficient (0.971, P = 0.0001) indicated a strong linear relationship between the Petrifilm and the standard method. The results showed that Petrifilm is suitable and a convenient alternative to this standard method for the enumeration of aerobic flora in goat soft cheese.
RESUMO
The relationship between indicator microorganism counts and the presence of Escherichia coli was determined in ready-to-eat food in food stores. Aerobic counts (CA), total coliforms (CT) and molds and yeast (ML) were registered in each food sample as well as the presence of E. coli in food, surface and hand samples. There was a high percentage of E. coli in cooked food (46% in 1 g), in raw food (31% in 0.1 g), in surfaces (37%) and in hands (21%). Significant correlations were found in CT, CA and ML in cooked food (P = 0.0001); no significant correlations were found in raw food (P > 0.01). The CT count in cooked food with E. coli was significantly higher than CT count in cooked food without E. coli (median 5.00 cfu/g and 1.54 cfu/g, respectively). Meanwhile, no significant differences were found in raw food.
Assuntos
Enterobacteriaceae/isolamento & purificação , Escherichia coli/isolamento & purificação , Contaminação de Alimentos , Microbiologia de Alimentos , Fungos/isolamento & purificação , Argentina , Manipulação de Alimentos , Mãos/microbiologia , Temperatura Alta , HumanosRESUMO
Se determinó la relación entre indicadores de contaminación y la presencia de Escherichia coli en alimentos listos para consumo en locales de venta directa al público, en Córdoba, Argentina. Se tomaron 60 muestras de alimentos, 16 de superficies y 14 de manos. Se determinaron bacterias mesófilas aerobias (CA), coliformes totales (CT), mohos y levaduras (ML) en alimentos y la presencia de E.coli en alimentos, superficies y manos. Se detecto E.coli en el 46 por ciento de los alimentos cocidos en 1 g de muestra y en el 31 por ciento de los alimentos crudos en 0,1 g de muestra. También se encontró E.coli en el 37 por ciento de las muestras de superficies y en el 21 por ciento de las provenientes de manos. Se encontraron correlaciones significativas al comparar de a pares CT, CA y ML en los alimentos cocidos (P=0,0001); en los crudos no se observaron correlaciones (P>0,01). El nivel de CT en alimentos cocidos que presentaban E.coli resultó significativamente más alto que el nivel de CT en los alimentos cocidos sin E.coli (mediana 5,00 ufc/g y 1,54 ufc/g, respectivamente). Los alimentos crudos con o sin presencia de E.coli no mostraron diferencias significativas en los niveles de CT. (AU)
Assuntos
Escherichia coli , Contaminação de Alimentos , Indicadores de Contaminação , Microbiologia de Alimentos , ArgentinaRESUMO
Se determinó la relación entre indicadores de contaminación y la presencia de Escherichia coli en alimentos listos para consumo en locales de venta directa al público, en Córdoba, Argentina. Se tomaron 60 muestras de alimentos, 16 de superficies y 14 de manos. Se determinaron bacterias mesófilas aerobias (CA), coliformes totales (CT), mohos y levaduras (ML) en alimentos y la presencia de E.coli en alimentos, superficies y manos. Se detecto E.coli en el 46 por ciento de los alimentos cocidos en 1 g de muestra y en el 31 por ciento de los alimentos crudos en 0,1 g de muestra. También se encontró E.coli en el 37 por ciento de las muestras de superficies y en el 21 por ciento de las provenientes de manos. Se encontraron correlaciones significativas al comparar de a pares CT, CA y ML en los alimentos cocidos (P=0,0001); en los crudos no se observaron correlaciones (P>0,01). El nivel de CT en alimentos cocidos que presentaban E.coli resultó significativamente más alto que el nivel de CT en los alimentos cocidos sin E.coli (mediana 5,00 ufc/g y 1,54 ufc/g, respectivamente). Los alimentos crudos con o sin presencia de E.coli no mostraron diferencias significativas en los niveles de CT.
Assuntos
Argentina , Escherichia coli , Contaminação de Alimentos , Microbiologia de Alimentos , Indicadores de ContaminaçãoRESUMO
The relationship between indicator microorganism counts and the presence of Escherichia coli was determined in ready-to-eat food in food stores. Aerobic counts (CA), total coliforms (CT) and molds and yeast (ML) were registered in each food sample as well as the presence of E. coli in food, surface and hand samples. There was a high percentage of E. coli in cooked food (46
in 1 g), in raw food (31
in 0.1 g), in surfaces (37
) and in hands (21
). Significant correlations were found in CT, CA and ML in cooked food (P = 0.0001); no significant correlations were found in raw food (P > 0.01). The CT count in cooked food with E. coli was significantly higher than CT count in cooked food without E. coli (median 5.00 cfu/g and 1.54 cfu/g, respectively). Meanwhile, no significant differences were found in raw food.
RESUMO
Testing for evidence of faecal contamination in river water has been traditionally accomplished by enumeration of thermotolerant coliform bacteria. In this work, deoxycholate lactose and m-Endo Agar LES media were evaluated using different techniques. The colony count methods were pour plate technique on Deoxycholate Agar (DCL pour plate), spread plating on m-Endo Agar LES (ELS spread), and membrane filtration on m-Endo Agar LES (ELF filtration). Typical thermotolerant coliform colonies were analysed by conventional biochemical tests. The three matched pairs showed statistically significant differences (P < 0.05) by the Wilcoxon signed rank test. One hundred and twenty three isolates obtained on m-Endo Agar LES (65%) were confirmed as E. coli. Likewise, one hundred and twenty isolates obtained on Deoxycholate Agar (71%) were confirmed as E. coli. The results of this study showed that the matched DCL-ELF presented the smaller statistically significant difference (P = 0.042) so, DCL could be used as alternative to ELF.
Assuntos
Técnicas Bacteriológicas/métodos , Meios de Cultura/farmacologia , Enterobacteriaceae/isolamento & purificação , Rios/microbiologia , Microbiologia da Água , Ágar/farmacologia , Argentina , Ácido Desoxicólico/farmacologia , Enterobacteriaceae/efeitos dos fármacos , Enterobacteriaceae/crescimento & desenvolvimento , Escherichia coli/efeitos dos fármacos , Escherichia coli/crescimento & desenvolvimento , Escherichia coli/isolamento & purificação , Fezes/microbiologia , Filtração , Temperatura Alta , Lactose/farmacologia , Poluição da ÁguaRESUMO
Bacteriological stability of water bottled in plastic containers and the growth kinetics of Pseudomonas aeruginosa were determined. Samples of water from the source, water to be bottled, finished product and sterile water bottled in non-returnable and returnable containers were analysed for aerobic colony count, coliforms, Escherichia coli and Ps. aeruginosa. The samples were examined for up to 30 d storage. Aerobic colony count increased 6 d after bottling to between 10(3) and 10(5) cfu ml-1. Coliforms and E. coli were not found in any sample. Pseudomonas aeruginosa was isolated from commercial products bottled in returnable plastic containers due to the contamination from the containers and the subsequent multiplication utilizing trace nutrients. The predominant Ps. aeruginosa strains showed high doubling time (26 h) due to competition from the accompanying flora. In the absence of competing flora Ps. aeruginosa reached higher density than the maximum reached by aerobic flora, with a doubling time of only 3.6 h. After 30 d storage, this micro-organism was predominant.
Assuntos
Águas Minerais/microbiologia , Pseudomonas aeruginosa/crescimento & desenvolvimento , Técnicas Bacteriológicas , Escherichia coli/crescimento & desenvolvimento , CinéticaRESUMO
A Moraxella bovis strain was isolated from a kerato-conjunctivities lesion of a calf in Villa Valeria (Córdoba); it was used to establish improved cultural conditions, such as nature and concentration of carbon and nitrogen sources, and pH control in shaken flasks. The selected conditions were assayed for biomass production in a bench-top fermentor. The strain is used by the pharmaceutical industry to produce vaccines and adjuvants. In the initial condition (48 h culture on blood agar) 0.019 g biomass/l.h-1 was obtained. With the use of liquid defined medium with pH control, productivity was increased to 0.153g/l.h-1, with optimum harvest time of 32 h.
Assuntos
Moraxella bovis/crescimento & desenvolvimento , Animais , Técnicas Bacteriológicas/instrumentação , Bovinos , Doenças dos Bovinos/microbiologia , Meios de Cultura , Fermentação , Ceratoconjuntivite Infecciosa/microbiologiaRESUMO
The indiscriminate use of extracorporeal shock waves in the treatment of urinary calculi has changed the place of percutaneous surgery in the treatment of renal lithiasis. The authors analyse current indications of PCN highlighting stone size. In their view, calculi greater than 2 cm warrant treatment by PCN since only 15-20% of patients are completely stone-free following a single session of ESWL. Attention is focussed on the staghorn calculus and the percutaneous approach. They describe the difficulty encountered in the fragmentation of the cystine calculus owing to its hardness and discuss the difficulties that may arise when using the percutaneous approach in patients with coexisting renoureteral conditions, in the treatment of lithiasis in children and in the obese patients.
Assuntos
Cálculos Renais/cirurgia , Nefrostomia Percutânea , Adulto , Fatores Etários , Criança , Contraindicações , Cistina , Humanos , Cálculos Renais/metabolismo , Cálculos Renais/patologia , Cálculos Renais/terapia , Litotripsia/efeitos adversos , Nefrostomia Percutânea/efeitos adversos , Obesidade , Obstrução Ureteral/cirurgiaRESUMO
En los últimos años el tratamiento de la Urolitiasis ha tenido importantes avances con la implementación de nuevas técnicas para la eliminación de cálculos de las vías urinarias, partiendo de la Cirugía convencional, la litotomía endoscópica y la nefrolitotomía percutánea; se han usado recientemente las ondas de choque extracorpóreas, con o sin inmersión para la desintegración de cálculos. La litotricia extracorpórea (LEC) aplicada actualmente en diversos centros del mundo para el tratamiento de la urolitiasis del adulto, ha demostrado su eficacia en el manejo de esta patología; sin embargo no existe suficientes reportes sobre la aplicación de esta modalidad terapéutica en Pediatría. Nosotros hemos venido utilizando esta técnica durante los últimos 16 meses para el tratamiento de niños con litiasis urinaria y entre Enero 1988 y Mayo 1989, 23 pacientes han sido sometidos a LEC con equipos Litotritor Electromagnético (LITHOSTAR) el cual posee una fuente de ondas de impulso ultracorto de baja potencia que asegura fragmentación del cálculo en finas partículas, las cuales son expulsadas espontáneamente por el niño y permiten su aplicación sin anestesia general y ambulatoriamente. De los 23 niños tratados 13 correspondieron al sexo femenino y 10 al masculino con rango de edad de 1.5 meses a 12 años (X 7.3 ñ 3.5) con predominio del grupo de 8 a 12 años (48%). Todos los pacientes presentaron clínica y radiología demostrativa de Urolitiasis. El tamaño de los cálculos osciló entre 5 y 6 mms a cálculos coraliformes (> 2 cms); 20 cálculos (87%) fueron de localización renal (2 bilaterales), 2 ureterales (9%) y 1 vesical (4%)..