RESUMO
The incidence of canine obesity appears to be increasing dramatically and understanding factors impacting the amount of food pet owners provide their dogs may improve weight management. Human research has shown the size of food bowls, plates and utensils can significantly impact the amount of food portioned and consumed. This effect can be attributed to both the Delboeuf optical illusion and the Ebbinghaus-Titchener size-contrast illusion. To investigate the existence of a similar effect with dog owners, 54 dogs and their owners were recruited for a four treatment randomized prospective trial. Owners scooped out a normal kibble-based meal using a small bowl and small scoop, small bowl and large scoop, large bowl and small scoop or a large bowl and large scoop. Each treatment was used once per owner over four visits. Repeated measures anova revealed the mean amount of food portioned using the small bowl and small scoop was significantly less than all other bowl and scoop combinations (150.7 g vs. 171.5 g vs. 172.7 g vs. 184.5 g, p < 0.05). The small bowl and large scoop combination did not differ from large bowl and small scoop (171.5 g vs. 172.7 g, p > 0.05). Owners were more likely to portion a larger amount of food with a large bowl and large scoop. Results are consistent with human data and emphasize the need for owners to use standard measuring cups. Results also suggest owner compliance during weight loss programs may be improved with smaller bowls and serving scoops.
Assuntos
Ração Animal , Criação de Animais Domésticos/métodos , Doenças do Cão/etiologia , Utensílios Domésticos , Obesidade/veterinária , Animais , Cães , Humanos , Obesidade/etiologia , Ilusões Ópticas , Percepção VisualRESUMO
Crude extracts from maize plants treated with varying concentrations of AAtrex, an s-triazine herbicide, were tested for the induction of gene conversion in a diploid strain of Saccharomyces cerevisiae heteroallelic at two loci. These extracts were then subjected to analysis by higher pressure liquid chromatography (HPLC), and the fractions collected in water, 50% methanol, and 100% methanol were similarly tested. Dose-dependent convertogenic activity observed in the 50% methanol fractions suggested that the mutagen(s) is recovered in this fraction.
Assuntos
Atrazina/metabolismo , Mutagênicos/isolamento & purificação , Extratos Vegetais/toxicidade , Zea mays/metabolismo , Cromatografia Líquida de Alta Pressão , DNA/metabolismo , Conversão Gênica/efeitos dos fármacos , Genes/efeitos dos fármacos , RNA/metabolismo , Zea mays/toxicidadeAssuntos
Benzopirenos/farmacologia , Reparo do DNA/efeitos dos fármacos , DNA de Neoplasias/metabolismo , Compostos de Epóxi/farmacologia , Éteres Cíclicos/farmacologia , Neoplasias Pulmonares/metabolismo , Benzopirenos/metabolismo , Células Cultivadas , Compostos de Epóxi/metabolismo , Humanos , Cinética , Neoplasias Pulmonares/induzido quimicamente , Neoplasias Experimentais/metabolismoRESUMO
A protocol is described for cytogenetic assays of chemical mutagens using mammalian cells in vitro. The system employs continuous drug treatment (3 concentrations) for up to 8 h and recovery-cell populations after pulse treatments with a high dose. Both direct fixation (for recording spindle anomalies in anaphase) and colcemid-hypotonic fixation (for reading metaphase chromosome aberrations) are used in order to estimate the effects of an agent as a mitotic poison and as a clastogen respectively. Some DNA intercalating dyes (acridine orange, quinacrine mustard, neutral red) were found to be highly clastogenic whereas others (quinacrine dihydrochloride, 33258 Hoechst) are not.
Assuntos
Técnicas Genéticas , Mutagênicos , Linhagem Celular , Cromossomos/efeitos dos fármacos , Técnicas CitológicasRESUMO
We report a procedure for combining sister chromatid differential staining and G banding in the same metaphase plate. Mammalian cells in culture are grown in medium containing 5-bromodeoxyuridine for two cell cycles, and conventional air-dried preparations are made. The slides are treated with a trypsin or a urea solution the same way as for regular G banding. This method is simple and fast and provides additional information for cytogeneticists.