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1.
J Dairy Sci ; 103(6): 5061-5069, 2020 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-32229126

RESUMEN

The rates of development of 2 tissues in mammary glands, parenchyma (PAR) and the mammary fat pad (MFP), in response to nutrition in early life might have a major bearing on lifetime milk production. Historical studies reported that feeding greater amounts of dietary nutrients from postweaning to puberty increased growth rates of heifers and stimulated the growth of MFP at the expense of PAR, which might suggest compromised mammary development and future milk production. The current study sought to determine if a higher volume of whole milk (8 vs. 4 L/d) offered to calves would increase rates of growth and development of PAR in mammary glands at weaning (1 to 12 wk). To measure these tissues, we developed 2 simple methods to assess the size of PAR and MFP at the time of screening using ultrasound. We report that calves offered 8 L/d of whole milk had greater rates of growth until weaning (0.86 ± 0.06 vs. 0.81 ± 0.09 kg/d), compared with calves offered 4 L/d. Ultrasonography showed that despite the faster rates of growth in calves offered 8 L/d of milk/d, the ratio of PAR:MFP depth was 40% less at weaning in the front glands (34%) compared with calves offered 4 L of milk/d. Rear glands were less impaired. The ultrasound methods developed here might be useful to monitor the development of mammary glands in response to different nutritional regimens during the preweaning period.


Asunto(s)
Alimentación Animal , Bovinos/crecimiento & desarrollo , Glándulas Mamarias Animales/crecimiento & desarrollo , Leche , Tejido Adiposo/crecimiento & desarrollo , Alimentación Animal/análisis , Animales , Peso Corporal , Dieta/veterinaria , Femenino , Estado Nutricional , Destete
2.
N Z Vet J ; 54(6): 323-8, 2006 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17151732

RESUMEN

AIM: To gather information on the repeatability of a faecal nematode egg count (FEC) reduction (FECR) test (FECRT), evaluating both different methods of calculating efficacy and variations within a method, in order to supply veterinarians and other advisors with sufficient information to apply some level of confidence around a diagnosis of anthelmintic resistance based on FECRT results. METHODS: Two commercial sheep farms were selected on the basis of having previously recorded FECR <95% after treatment with ivermectin (Farm 1) or albendazole (Farm 2). On each farm at least 250 lambs, managed as a single mob, were individually ear-tagged and sampled for FEC. The resulting counts were used, 3-4 days later, to sort the lambs into 24 groups of 10. First, the animals were split into three groups of 80, having high, medium or low FEC. Second, within each of these groups the 80 animals were further divided into four replicate mobs of 20 (each with the same mean count). Third, each of these replicates was further split into two groups of 10: those that would be drenched and those that would remain as untreated controls. All animals were again faecal-sampled and those in the drenched groups were dosed, using a syringe, to their individual liveweight, with ivermectin (Farm 1) or albendazole (Farm 2). Ten days after treatment all animals were individually faecal sampled again. FEC and larval cultures were undertaken for all 24 groups from both pre- and post-treatment samples. Efficacy (FECR) of the undifferentiated FECRT was calculated using three different equations, and efficacy by genus was also calculated. RESULTS: Calculated efficacies differed between equations, and the equation which did not utilise an untreated control yielded significantly lower efficacy estimates on both farms. Faecal cultures varied considerably in the proportions of parasite genera recovered. In general, this did not differ between FEC groups, except on Farm 1 where Haemonchus spp were more common and Cooperia spp less common in high-FEC samples. Estimated efficacies against individual genera varied considerably or very little, depending on the level of resistance. On both farms, differing proportions of tests against some genera passed or failed FECRTs based on a threshold pass mark of > or =95% FECR. CONCLUSION: There was considerable variability in the outcomes of FECRTs and in larval culture results. Caution is warranted in interpreting the results of FECRTs when efficacy values fall into the 90-95% range. Further, the possibility of a test returning a false-negative result is raised, indicating that even an efficacy estimated > or =95% may not guarantee the absence of resistant parasites.


Asunto(s)
Antihelmínticos/uso terapéutico , Resistencia a Medicamentos , Heces/parasitología , Infecciones por Nematodos/veterinaria , Recuento de Huevos de Parásitos/veterinaria , Enfermedades de las Ovejas/tratamiento farmacológico , Albendazol/uso terapéutico , Análisis de Varianza , Animales , Relación Dosis-Respuesta a Droga , Ivermectina/uso terapéutico , Nematodos/efectos de los fármacos , Nematodos/aislamiento & purificación , Infecciones por Nematodos/diagnóstico , Infecciones por Nematodos/tratamiento farmacológico , Recuento de Huevos de Parásitos/métodos , Recuento de Huevos de Parásitos/normas , Distribución Aleatoria , Reproducibilidad de los Resultados , Sensibilidad y Especificidad , Ovinos , Enfermedades de las Ovejas/diagnóstico , Resultado del Tratamiento
3.
N Z Vet J ; 39(4): 145-6, 1991 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-16031642

RESUMEN

Six Friesian calves from a pedigree herd died or were killed within 1 week of birth because of progressive central nervous disease in which the only consistent lesion was cerebral oedema. The cause was citrullinaemia, resulting from an autosomally inherited dysfunction of the urea cycle enzyme arginosuccinate synthetase. Citrullinaemia was diagnosed by demonstrating markedly elevated concentrations of citrulline in the blood of one calf and in the cerebral spinal fluid of another. One of two sires used in the herd was a heterozygous carrier of the disease. Heterozygocity was demonstrated using a polymerase chain reaction/restriction endonuclease test designed to detect the genetic mutation that causes citrullinaemia in cattle.

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