Avaliação do quadro clínico e perfil bioquímico de bovinos durante indução e tratamento de hipocalcemia

O presente trabalho objetivou estudar o quadro sintomatológico, algumas variáveis bioquímicas e a resposta ao tratamento com cálcio de bovinos com hipocalcemia induzida experimentalmente. Foram utilizadas 12 novilhas distribuídas nos grupos controle (n = 5) e tratado (n = 7). Foi infundida solução de EDTA a 5% até o animal apresentar sinais clínicos de hipocalcemia, quando então era iniciado o tratamento com solução contendo cálcio, fósforo, magnésio e glicose, na dose de 1 mL/kg/PV, em 30 minutos, enquanto que o grupo controle recebia apenas solução fisiológica na mesma dose. Exame clínico e coleta de amostras sanguíneas foram realizados nos tempos T0 (basal), T1 (Fase I, caracterizada por tremores musculares), T2 (ao final da infusão com EDTA), T3 (ao final do tratamento) e T4 (24 horas após o término do experimento). Todas as novilhas mostraram diminuição temporária da concentração de cálcio total e livre, fósforo, e apresentaram quadro clássico de hipocalcemia. A taquicardia, a hipofonese e a atonia ruminal desapareceram no decorrer do tratamento, sendo observado aumento no cálcio livre e total e fósforo. O medicamento usado no tratamento dos animais foi eficaz na recuperação do quadro clínico de hipocalcemia dentro de 30 minutos, promovendo retorno das principais variáveis do perfil bioquímico aos valores basais.The present work aims to study the clinical picture, biochemical profile and treatment response in cattle with induced hypocalcaemia. Were utilized 12 heifers randomly distributed in treated (n = 7) and control (n = 5) groups. The induction model was carried on by continuous EDTA infusion into jugular vein until the animals present clinical signs of hypocalcaemia. After that, the treated group received a calcium (Ca) solution enriched with phosphorus, magnesium and glucose with a dose of 1 mL/kg/BW in 30 minutes, meanwhile, the control group was treated with the same dose of physiologic solution. Clinical examination were performed and blood samples were obtained in times T0 (basal time), T1 (beginning of hypocalcaemia); T2 (end of EDTA infusion); T3 (end of treatment) and T4 (24 hours after the induction). All the heifers present temporary blood calcium and phosphorus reduction and demonstrated classical clinical picture of hypocalcaemia. The treated group present full clinical recovery and blood calcium and phosphorus increase. Most evident clinical signs were increasing heart beat, hypophonesis and rumenal atony. Those symptoms were reversed after calcium treatment. The solution used for treatment was efficient on clinical recovery within thirty minutes, promoting the return to basal levels of the most of biochemical's variables

Prevention of acute ruminal lactic acidosis in sheep by probiotic or monensin supplementation: clinical aspects

The aim of this study was to evaluate the effects of two additives (probiotic and monensin) over clinical parameters of sheep submitted to acute ruminal lactic acidosis (ARLA). Eighteen sheeps were divided into three groups of six animals each as follows: probiotic group, supplemented with 4×109 CFU/animal/day of Saccharomyces cerevisiae; monensin group, supplemented with 33 mg of monensin sodium per kg of diet; and control group, without any supplementation. After 30 days of diet (75% of Coast-cross hay and 25% concentrate with 14% of crude protein) and additive intake, ARLA was induced in the all animals by intraruminal administration of 15g of sucrose per kilogram (kg) of body weight. Complete physical examinations to assess the vital signs of the animals were conducted at the following times: baseline (T0), six (T6h), 12 (T12h), 18 (T18h), 24 (T24h), 36 (T36h), and 48 (T48h) hours after ARLA induction. At those times, blood samples were obtained to determine the plasma volume deficit (PVD) and ruminal content for pH measurement. All animals experienced clinical signs of ARLA with ruminal pH lower than 4.9 at T24h. The heart rate and PVD were lower (P < 0.05) in the probiotic group at T36h. Compared to the control and monensin groups, the probiotic group experienced milder ARLA characterized by lower degrees of dehydration and fewer clinical symptoms