Five multiparous Saanen goats in late lactation were infused with S-35-cyst
eine into the mammary gland via the external pudic artery. A further 2 goat
s were infused with S-35-methionine via the same artery and later with S-35
-methionine into the jugular vein. Total uptake of cysteine from the arteri
al blood supply by the mammary gland was approximately 6% of the S-35-cyste
ine flux past the gland, whereas uptake of methionine was 30-40%. Total mam
mary uptake of cysteine was also lower than that of methionine when express
ed as a percentage of whole body utilisation (6.5 and 14%, respectively). T
he uptake from the blood did not account for output in the milk for either
cysteine or methionine. Both amino acids were highly conserved by the gland
as shown by little release of any degraded constitutive protein amino acid
s and no evidence of oxidation products of either cysteine or methionine be
ing released into the blood. Comparison of S-35 activity in the milk from t
he infused and non-infused sides of the gland showed up to 10% trans-sulfur
ation of methionine to cysteine within the gland, none of which was exporte
d in the venous drainage. Total ATP production by one side of the gland was
12.1 mol/day or 13 mmol/min.kg mammary tissue, of which 15% was required f
or gland protein synthesis. The experimental measurements from both the cys
teine and methionine infusions were used to solve a model of gland amino ac
id uptake and partitioning. Modelling radioactivity of both amino acids in
the blood, intracellular free pool, and milk protein suggested that a singl
e intracellular pool cannot be the only source of amino acid for protein sy
nthesis. The model also provides support for the hypothesis that a signific
ant proportion of the uptake of at least some amino acids by the mammary gl
and is from intracellular hydrolysis of extracellularly derived peptides.