Efeito da suplementação com colina protegida sobre parâmetros bioquímicos, produção e reprodução de vacas leiteiras no periparto / Effect of protected choline supplementation on biochemical parameters, production, and reproduction of dairy cows in peripartum

Avaliou-se o efeito da suplementação com colina protegida sobre o perfil energético, as enzimas hepáticas e a reprodução de vacas leiteiras no periparto. Quinze vacas leiteiras foram divididas em dois grupos experimentais: oito receberam 80 gramas de colina protegida por 21 dias no pré-parto e por 40 dias no pós-parto e sete foram consideradas controle. Amostras de sangue foram coletadas nos dias 10, 20, 30 e 60 pós-parto para avaliação dos perfis energético e hepático. Aos 60 dias pós-parto, realizou-se exame ginecológico dos animais para avaliação da saúde reprodutiva. A suplementação com colina protegida não alterou os níveis de beta-hidroxibutirato (BHBA), ácidos graxos não esterificados (AGNE), frutosamina, fator de crescimento semelhante a glicose I (IGF-I), status oxidante total (TOS), aspartato aminotransferase (AST) e gamaglutamiltransferase (GGT) no pós-parto. Não houve diferença também quanto à produção de leite. Aos 60 dias pós-parto, vacas suplementadas com colina protegida apresentaram menor número de casos de endometrite que vacas do grupo controle. A suplementação de colina protegida não alterou o perfil bioquímico e a produção de leite, mas reduziu o número de casos de endometrite no pós-parto de vacas leiteiras.(AU)

The study aimed to evaluate the effect of supplementation with protected choline on the energy profile, liver enzymes and reproduction in dairy cows in peripartum. Fifteen cows were divided into two groups: 8 received 80 grams of protected choline for 21 days pre-partum and 40 days postpartum, and 7 were considered control. Blood samples were collected on days 10, 20, 30, and 60 postpartum to evaluate the energy and hepatic profiles. After 60 days postpartum a gynecological examination of animals for evaluation of reproductive health was done. The supplementation with choline protected did not alter the beta-hydroxybutyrate levels (BHBA), non-esterified fatty acids (NEFA), fructosamine, like growth factor glucose (IGF-I), total oxidant status (TOS), aspartate aminotransferase (AST) and glutamiltrasferase range (GGT) postpartum. There was no difference in milk production. After 60 days postpartum, cows fed protected choline had fewer cases of endometritis that cows in the control group. The protected choline supplementation did not alter the biochemical profile and milk production, but reduced the number of endometritis cases in postpartum dairy cows.(AU)

Farelo de tungue in natura ou detoxificado na alimentação de carpa húngara (Cyprinus carpio) / In natura or detoxified tung meal in feeding Hungarian carp (Cyprinus carpio)

Este estudo avaliou a substituição parcial de farinhas de origem animal pelo farelo de tungue como fonte proteica no arraçoamento de carpa húngara. Os tratamentos compreenderam a inclusão de farelo de tungue in natura ou detoxificado (obtido após aplicação de tratamento químico ao farelo), e o tratamento referência consistiu de base proteica composta por farinha de carne e ossos suína e farinha de peixe. O período de alimentação foi de 63 dias. No decorrer de 30 dias experimentais não foi observada diferença em indicadores de crescimento entre os animais que consumiram as rações controle e com farelo de tungue tratado quimicamente, porém o consumo da ração com farelo de tungue in natura provocou redução no desempenho até o final do período experimental. Após 63 dias de arraçoamento, alguns indicadores de crescimento mostraram-se inferiores também para o tratamento que continha farelo de tungue tratado em relação ao controle. A análise bioquímica no plasma e no fígado revelou aumento de triglicerídeos, glicogênio, glicose e a utilização de outras fontes, possivelmente aminoácidos, como precursores energéticos na produção de energia quando os animais consumiram a dieta com farelo de tungue in natura em relação às demais, o que refletiu na menor concentração de proteína e na maior deposição de gordura na carcaça. Em relação à atividade de enzimas digestivas, tripsina apresentou atividade aumentada no tratamento com farelo de tungue in natura e protease ácida, quimotripsina, amilase e lipase não foram alteradas em nenhum dos tratamentos avaliados...

This study evaluated the partial replacement of animal meal by tung meal as protein source in feeding Hungarian carp. The treatments consisted of the inclusion of in natura or detoxified tung meal (obtained after chemical treatment applied to tung meal) as well as the reference treatment in which the protein basis was composed of meat and bone pork meal and fish meal. The feeding period was 63 days. During 30 experimental days no difference was observed in growth indicators among animals fed the control diet or with chemically treated tung meal, however, the consumption of diets with in natura tung meal caused reduced performance until the end of the experimental period. After 63 days of feeding, some growth indicators were also are lower for the treatment containing treated tung meal compared to control. Biochemical analysis in plasma and liver revealed increased triglycerides, glycogen, glucose and use of other sources, possibly amino acids, as precursors in the production of energy when animals consumed the diet with in nature tung meal in relation to others, which reflected in lower levels of protein and higher fat deposition in the carcass. Regarding the activity of digestive enzymes, trypsin showed increased activity in the treatment with in natura tung meal and acid protease, chymotrypsin, amylase and lipase were not changed in any of the treatments...

Exposure to sublethal concentrations of Zn(II) and Cu(II) changes biochemical parameters in Leporinus obtusidens.

The aim of the present study was to assess the effect of the exposure of Leporinus obtusidens (Piava) to zinc and copper on catalase activity in the liver, delta-aminolevulinate dehidratase (delta-ALA-D) activity in liver, muscle, brain and kidney, and thiobarbituric reactive species (TBARS) in brain, muscle and liver. In addition, hematological parameters were measured in blood. The fish were exposed to 10% and 20% of the derived LC(50) values, 2.3 and 4.6 mg Zn l(-1) and 0.02 and 0.04 mg Cu l(-1), and sampled on days 30 and 45. Exposure to Zn(II) and Cu(II) decreased hematological parameters and also delta-ALA-D activity mainly in liver and kidney at all concentrations tested. Liver catalase activity increased after zinc or copper exposure at all concentrations and exposure times tested. Thiobarbituric reactive substances (TBARS) increased in the brain and liver of the fish exposed to zinc(II) for 45 days at both metal concentrations. In muscle, zinc(II) increased TBARS production at both exposure times and concentrations tested. Copper(II) exposure reduced the TBARS levels in liver at both concentrations and times tested. In brain, there was a decrease in TBARS levels only after 45 days of exposure. In muscle, this decrease was observed after 30 days of exposure at both concentrations. Although zinc and copper are required as microelements in the cells, our results showed that the sublethal concentrations of these metals can change biochemical parameters which may alter normal cellular function. These results pointed out the differential sensitivity of fish tissues to essential, but also toxic and environmentally relevant metals. The alterations of distinct biochemical parameters in fish tissues certainly contribute to the toxicity of Zn and Cu, and are of importance for an area that has been growing and has still been poorly explored in the literature.

Colorimetric determination of formaldehyde in air using a hanging drop of chromotropic acid.

A simple and sensitive method to determine parts per billion (ppb) of atmospheric formaldehyde in situ, using chromotropic acid, is described. A colorimetric sensor, coupled to a droplet of 15.5 microL chromotropic acid, was constructed and used to sample and quantify formaldehyde. The sensor was set up with two optical fibers, a light emitting diode (LED) and two photodiodes. The reference and transmitted light were measured by a photodetection arrangement that converts the signals into units of absorbance. Air was sampled around the chromotropic acid droplet. A purple product was formed and measured after the sampling terminated (typically 7 min). The response is proportional to the sampling period, analyte concentration and sample flow rate. The detection limit is approximately 2 ppb and can be improved by using longer sampling times and/or a sampling flow rate higher than that used in this work, 200 mL min-1. The present technique affords a simple, inexpensive near real-time measurement with very little reagent consumption. The method is selective and highly sensitive. This sensor could be used either for outdoor or indoor atmospheres.