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1.
J Dairy Sci ; 101(2): 1227-1233, 2018 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-29174150

RESUMEN

Utilization of nutrients to improve overall heifer health is of interest because of the importance of replacement heifers to the dairy industry. The objective of our study was to compare the effect of supplementation of dietary n-3 and n-6 fatty acids (FA) on FA concentrations in peripheral blood mononuclear cells (PBMC) of Holstein calves. Twenty-seven Holstein heifer calves (107 ± 2.6 d of age; 142.6 ± 6.5 kg of body weight) from the university research and teaching herd were randomly assigned to a common TMR supplemented with 1 of 3 treatments: Ca salts of flaxseed FA (Virtus Nutrition, Corcoran, CA) containing 35% 18:3 n-3 (N3), Ca salts of soybean FA (Virtus Nutrition) containing 50% 18:2 n-6 (N6), or a 50:50 mix of N3 and N6. Treatments were supplemented with FA at 4% of dietary dry matter and fed for 30 d. Feed intake was recorded daily, and body weight, wither height, and body condition score were measured weekly throughout the study. On d 28 heifers were vaccinated with a Pasteurella vaccine and the temperature response to the vaccine was recorded. Blood was collected on d 0 and 28 for PBMC isolation. After total lipid extraction and FA methyl ester preparation, FA composition of PBMC was measured. We observed no effect of treatment on body weight gain, body condition score change, or wither height change. Heifers receiving the N3 diet had a lower temperature response to Pasteurella challenge compared with both the mix and N6 diets. Heifers consuming the N3 diet had a greater content of total n-3 FA, α-linolenic acid, and eicosapentaenoic acid in PBMC compared with heifers fed the N6 and mix diets. Heifers receiving the N3 diet also had a lower content of total n-6 FA, linoleic acid, and arachidonic acid in PBMC than heifers fed the N6 and mix diets. In conclusion, our study determined that feeding weaned female Holstein heifers a diet high in n-3 FA increased concentrations of n-3 FA in PBMC.


Asunto(s)
Alimentación Animal/análisis , Bovinos/metabolismo , Ácidos Grasos Omega-3/metabolismo , Ácidos Grasos Omega-6/metabolismo , Leucocitos Mononucleares/metabolismo , Animales , Peso Corporal , Bovinos/crecimiento & desarrollo , Dieta/veterinaria , Suplementos Dietéticos/análisis , Ácidos Grasos Omega-3/análisis , Ácidos Grasos Omega-6/análisis , Femenino , Leucocitos Mononucleares/química , Destete , Aumento de Peso
2.
Neuron ; 31(6): 973-85, 2001 Sep 27.
Artículo en Inglés | MEDLINE | ID: mdl-11580897

RESUMEN

Among the most intriguing forms of Ca(2+) channel modulation is the regulation of L-type and P/Q-type channels by intracellular Ca(2+), acting via unconventional channel-calmodulin (CaM) interactions. In particular, overexpressing Ca(2+)-insensitive mutant CaM abolishes Ca(2+)-dependent modulation, hinting that Ca(2+)-free CaM may "preassociate" with these channels to enhance detection of local Ca(2+). Despite the far-reaching consequences of this proposal, in vitro experiments testing for preassociation provide conflicting results. Here, we develop a three filter-cube fluorescence resonance energy transfer method (three-cube FRET) to directly probe for constitutive associations between channel subunits and CaM in single living cells. This FRET assay detects Ca(2+)-independent associations between CaM and the pore-forming alpha(1) subunit of L-type, P/Q-type, and, surprisingly, R-type channels. These results now definitively demonstrate channel-CaM preassociation in resting cells and underscore the potential of three-cube FRET for probing protein-protein interactions.


Asunto(s)
Canales de Calcio Tipo L/metabolismo , Canales de Calcio Tipo N/metabolismo , Canales de Calcio Tipo R/metabolismo , Calcio/metabolismo , Calmodulina/metabolismo , Espectrometría de Fluorescencia/métodos , Canales de Calcio Tipo L/química , Canales de Calcio Tipo N/química , Canales de Calcio Tipo R/química , Calmodulina/química , Línea Celular , Transferencia de Energía , Retroalimentación , Genes Reporteros , Proteínas Fluorescentes Verdes , Humanos , Activación del Canal Iónico , Proteínas Luminiscentes/análisis , Sustancias Macromoleculares , Técnicas de Placa-Clamp , Unión Proteica , Estructura Terciaria de Proteína , Proteínas Recombinantes de Fusión/análisis , Sensibilidad y Especificidad , Espectrometría de Fluorescencia/instrumentación , Transfección
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