|
|
||||||||



* Département des sciences animales, Pavillon Paul-Comtois, Université Laval, Sainte-Foy, QC, Canada, G1K 7P4
Dairy and Swine Research and Development Centre, Agriculture and Agri-Food Canada, Lennoxville, QC, Canada, J1M 1Z3
Faculté de médecine vétérinaire, Université de Montréal, St-Hyacinthe, QC, Canada, J2S 7C6
Corresponding author:
H. LaPierre; e-mail:
lapierreh{at}em.agr.ca.
To define the temporal variations of whole body and mammary leucine kinetics over a 12-h period between two milkings, we used two groups of four Holstein cows, one in their second and the other in their third or fourth lactation. Cows were infused with L-[1-13C]leucine during the 12-h interval between two milkings. Blood was sampled every 30 min during that period from arterial and mammary sources. Time after milking did not affect whole body irreversible loss rate of leucine but affected whole body leucine oxidation, which broadly followed variations in arterial plasma leucine concentration. Similarly, mammary leucine irreversible loss rate and leucine used for protein synthesis were not affected by time after milking. Leucine oxidation by the mammary gland was, however, affected by time after milking. It increased by 15% from the first 2-h period to the following 4-h period and then decreased by 13% over the following 2-h period. A 21% increase in leucine oxidation was observed from 8 to 10 h after milking, and then it decreased by 26% over the last 2-h period. Protein degradation expressed as percentage of mammary leucine flux followed a similar temporal pattern. Leucine used for protein synthesis by the mammary gland was unaltered over time after milking, suggesting that the increased availability of leucine resulting from mammary protein breakdown would increase intracellular concentrations of leucine, which would have favored its catabolism. Overall, these results confirm the high metabolic activity of the mammary gland, as protein synthesis by the mammary gland averaged 43% of whole body protein synthesis.
Key Words: dairy cow kinetics protein metabolism
Abbreviation key: APE = atom percent excess, IE = isotopic enrichment, FIL = feedback inhibitor of lactation, IE = isotopic enrichment, ILR = irreversible loss rate, MOP = 4-methyl 2-oxopentanoate
This article has been cited by other articles:
![]() |
A.-A. Gingras, P. J. White, P. Y. Chouinard, P. Julien, T. A. Davis, L. Dombrowski, Y. Couture, P. Dubreuil, A. Myre, K. Bergeron, et al. Long-chain omega-3 fatty acids regulate bovine whole-body protein metabolism by promoting muscle insulin signalling to the Akt-mTOR-S6K1 pathway and insulin sensitivity J. Physiol., February 15, 2007; 579(1): 269 - 284. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |