Torta de mamona não destoxificada na indução da muda forçada em poedeiras comerciais / Non-detoxified castor bean for molt induction in laying hens

Avaliou-se o uso de dietas com diferentes porcentagens de torta de mamona não destoxificada (TM) na indução da muda forçada, sendo utilizadas 120 poedeiras Lohman LSL de 81 semanas, distribuídas ao acaso em quatro tratamentos, com cinco repetições de seis aves. Um dos tratamentos consistiu na indução da muda pelo método do jejum por 11 dias, e os demais no uso de dietas de muda, compostas pela mistura de dieta de postura e TM nas quantidades de 20, 30 e 40 por cento, por até 21 dias ou até quando as aves atingissem 23 por cento de perda do peso. Diferenças significativas foram observadas nos eritrócitos, no hematócrito, na concentração média de hemoglobina globular, na proteína total do plasma, nos leucócitos e na alanina aminotransferase, medidos durante a indução da muda, bem como no desempenho das aves após a muda, no que diz respeito ao consumo de ração, à porcentagem de postura, ao peso do ovo, à massa do ovo e à conversão alimentar. A qualidade dos ovos não variou estatisticamente entre os métodos avaliados. A utilização da dieta de muda forçada contendo 40 por cento de TM promoveu resultados semelhantes aos obtidos com o método do jejum, tanto para consumo de ração, porcentagem de postura, peso do ovo, massa do ovo, e conversão alimentar, como inerentes à qualidade dos ovos, quanto para densidade específica, unidade Haugh, porcentagens de gema, casca e albúmen. No entanto, menores alterações nos valores de eritrócitos, hematócrito e alanina aminotransferase foram observadas nesse método supracitado. O uso da dieta de muda contendo 40 por cento de TM mostrou-se uma alternativa viável ao uso do método do jejum...

We evaluated diets with different percentages of non-detoxified castor bean (TM) in the induction of molt, with 120 Lohman LSL hens at 81 weeks of age being used, randomly allotted to four treatments with five replicates of six birds each. One of the treatments consisted in the induction of changes by the method of fasting for 11 days, and the others used diet switches, composed by mixing posture and TM diet in the amounts of 20, 30 and 40 percent for up to 21 days or until when the birds reach 23 percent weight loss. Significant differences were observed in erythrocytes, hematocrit, mean concentration of corpuscular hemoglobin, total protein in plasma, leukocytes and alanine aminotransferase measured during induction of changes, and the performance of birds after moulting, such as feed intake, percentage of laying, egg weight, egg mass and feed conversion. The quality of the eggs did not vary significantly among the methods evaluated. The use of forced molting diet containing 40 percent of TM promoted results similar to those obtained with the method of fasting, both feed intake and the percentage of egg, egg weight, egg mass, and feed conversion, as inherent quality of eggs, as the specific gravity, Haugh unit, yolk percentage, albumen and shell. However, minor changes in the values of erythrocytes, hematocrit and alanine aminotransferase were observed in the method above. The use of diets containing 40 percent change TM proved to be a viable alternative to the use of the fasting method...

In vitro penetration of bleaching agents into the pulp chamber.

AIM: To investigate pulp chamber penetration of bleaching agents in teeth following restorative procedures. METHODOLOGY: Bovine lateral incisors were sectioned 3 mm apical to the cemento-enamel junction and the coronal pulpal tissue was removed. Teeth were divided into six groups (n = 10): G1, G2 and G3 were not submitted to any restorative procedure, while G4, G5 and G6 were submitted to Class V preparations and restored with composite resin. Acetate buffer was placed in the pulp chamber and treatment agents were applied for 60 min at 37 degrees C as follows: G1 and G4, immersion into distilled water; G2 and G5, 10% carbamide peroxide (CP) exposure; G3 and G6, 35% CP bleaching. The buffer solution was removed and transferred to a glass tube where leuco crystal violet and horseradish peroxidase were added, producing a blue solution. The optical density of the blue solution was determined spectrophotometrically at 596 nm. A standard curve made with known amounts of hydrogen peroxide was used to convert the optical density values of the coloured samples into microgram equivalents of hydrogen peroxide. Data were submitted to anova and Tukey's test (5%). RESULTS: Amounts of hydrogen peroxide found in the pulp chamber of G2 and G5 specimens (0.1833 +/- 0.2003 micro g) were significantly lower (P = 0.001) when compared to G3 and G6 specimens (0.4604 +/- 0.3981 micro g). Restored teeth held significantly higher (P = 0.001) hydrogen peroxide concentrations in the pulp chamber than intact teeth. CONCLUSION: Higher concentrations of the bleaching agent produced higher levels of hydrogen peroxide in the pulp chamber, especially in restored teeth.