Animal performance and meat quality characteristics from feedlot-finished steers fed increasing levels of wet distillers grain.

One hundred forty-four steers were group-housed in 24 pens that were randomly assigned to one of four dietary treatments defined by the proportion of wet distiller grain plus solubles (WDGS; 0, 15, 30, or 45%) and fed for 84 d pre-slaughter. Animal performance was evaluated using the pen as the experimental unit. Whereas for carcass and meat quality characteristics, meat oxidative stability, and the consumer sensory quality of longissimus thoracis muscle one animal from each pen was randomly selected and used as the experimental unit. No differences (P > 0.05) were observed for subcutaneous fat thickness, rib eye area, marbling score or pH, color parameters, proximate composition, sarcomere length, Warner Bratzler shear force, and cooking loss. Feeding WDGS linearly increased total PUFA (P = 0.05), C18:2 n-6 (P = 0.004) proportions, and n-6/n-3 ratio (P < 0.01) but reduced C16:1 to C18:0 ratio (P < 0.01). Lipid oxidation was greater in beef from steers fed 30% and 45% WDGS (P = 0.05). Dietary WDGS linearly improved (P < 0.05) flavor and overall linking score in the consumer sensory panel.

Extubação paliativa em uma unidade de terapia intensiva cardiológica ­ um relato de caso / Palliative extubation in a cardiac intensive care unit ­ a case report

INTRODUÇÃO: A extubação paliativa é descrita como a retirada do tubo traqueal e da ventilação mecânica, quando todas as possibilidades de desmame ventilatório falharam ou o prognóstico do paciente é desfavorável. É um procedimento que evita prolongar a vida de maneira artificial e deve ser acordado juntamente com os familiares e a equipe. OBJETIVO: Relatar um caso de extubação paliativa numa unidade de terapia intensiva cardiológica. MÉTODO: Relato de caso RESULTADOS: Paciente do sexo feminino, portadora de Miocardiopatia Dilatada deu entrada no pronto-socorro em Insuficiência Cardíaca perfil C. Após a realização das medidas farmacológicas e o uso de ventilação não invasiva, não houve resposta satisfatória, evoluindo para intubação orotraqueal. A extubação ocorreu após 6 dias, porém em 24 horas houve falha de extubação, seguida de parada cardiorrespiratória (PCR) de 15 minutos. Foram realizadas todas as medidas pós PCR e mesmo a compensação clínica, não houve resposta neurológica favorável para progredir com uma nova extubação, desse modo, a equipe definiu os Cuidados Paliativos. O filho da paciente trouxe o relato de que ela não gostaria de viver de forma artificial e mesmo estando apreensivo com a possibilidade de óbito iminente após a extubação, visto que a mãe não tinha resposta favorável, ele não gostaria que mantivéssemos as medidas invasivas. Após uma conferência familiar com consenso entre a equipe e os familiares optou-se por realizar a extubação paliativa, para tal houve a suspensão de medicamentos não essenciais e foi otimizado as medicações para prevenir o estridor laríngeo. Para a extubação, foi realizado aspiração de alívio e o teste de respiração espontânea com resposta satisfatória e após 19 dias de intubação a paciente foi extubada, o procedimento ocorreu de maneira tranquila, não houve necessidade de aspiração ou suplementação com oxigênio, a paciente permaneceu com um Glasgow 6, eupneica em ar ambiente com uma fisionomia confortável, sem sinais de desconforto respiratório ou de dor. O atendimento fisioterapêutico foi mantido visando manter o conforto, a paciente teve o acompanhamento dos familiares com visita estendida e veio a falecer após 4 dias da extubação. CONCLUSÃO: A extubação paliativa ocorreu com o suporte da equipe e dos familiares, livre de dor ou desconforto e a paciente veio a falecer 4 dias após o procedimento. Esse relato de caso reforça a importância do alinhamento de condutas, da presença da família e a possibilidade de sobrevida após uma extubação paliativa.

Selenomethionine increases proliferation and reduces apoptosis in bovine mammary epithelial cells under oxidative stress.

The decline in mammary epithelial cell number as lactation progresses may be due, in part, to oxidative stress. Selenium is an integral component of several antioxidant enzymes. The present study was conducted to examine the effect of oxidative stress and selenomethionine (SeMet) on morphology, viability, apoptosis, and proliferation of bovine mammary epithelial cells (BMEC) in primary culture. Cells were isolated from mammary glands of lactating dairy cows and grown for 3 d in a low-serum gel system containing lactogenic hormones and 0 or 100 µM H2O2 with 0, 10, 20, or 50 nM SeMet. Hydrogen peroxide stress increased intracellular H2O2 to 3 times control concentrations and induced a loss of cuboidal morphology, cell-cell contact, and viability of BMEC by 25%. Apoptotic cell number more than doubled during oxidative stress, but proliferating cell number was not affected. Supplementation with SeMet increased glutathione peroxidase activity 2-fold and restored intracellular H2O2 to control levels with a concomitant return of morphology and viability to normal. Apoptotic BMEC number was decreased 76% below control levels by SeMet and proliferating cell number was increased 4.2-fold. These findings suggest that SeMet modulated apoptosis and proliferation independently of a selenoprotein-mediated reduction of H2O2. In conclusion, SeMet supplementation protects BMEC from H2O2-induced apoptosis and increased proliferation and cell viability under conditions of oxidative stress.

Selenomethionine stimulates expression of glutathione peroxidase 1 and 3 and growth of bovine mammary epithelial cells in primary culture.

This study examined the localization of cellular glutathione peroxidase (GPx1) and extracellular glutathione peroxidase (GPx3) in lactating mammary tissue and in primary cultures of bovine mammary epithelial cells (BMEC). The effect of selenium as selenomethionine (SeMet) on the growth and viability of BMEC and GPx protein expression and activity were also studied. Single mammary epithelial cells were recovered by serial collagenase/hyaluronidase digestion from lactating bovine mammary tissue and cultured in a low-serum collagen gel system enriched with lactogenic hormones and 0, 10, 20, or 50 nM SeMet. Positive immunostaining with anti-cytokeratin and bovine anti-casein confirmed the epithelial nature and differentiated state of BMEC. Addition of SeMet to media facilitated rapid confluence of BMEC and formation of dome structures. Immunohistochemical and immunocytochemical staining revealed that both GPx1 and GPx3 are synthesized by BMEC and localized in the cytoplasm and nucleus. Up to 50 nM SeMet linearly increased BMEC number and viability over 5 d of culture. Bovine mammary epithelial cells cultured in SeMet-supplemented medium also exhibited markedly elevated GPx activity and linear increases in abundance of GPx1 and GPx3 proteins. It is apparent that SeMet degradation to release Se for synthesis of selenoproteins is carried out by BMEC. Results indicate that bovine mammary epithelial cells express GPx1 and GPx3 in vivo and in vitro; SeMet enhances expression of these selenoproteins in vitro and the growth and viability of BMEC.