G. Rychen et al., INCORPORATION OF [C-14] IN MILK-PROTEINS AFTER A RUMINAL INFUSION OF D-[U-C-14]GLUCOSE IN DAIRY GOATS, Small ruminant research, 27(3), 1998, pp. 251-256
Three rumen cannulated lactating goats fitted with a temporary polyvin
yl intravenous catheter were used to study [C-14] incorporation in mil
k proteins (casein (CN), whey proteins (WP)) in comparison with incorp
oration in lactose (LAC) and in milk fat (MF) after a single ruminal s
upply of D-[U-C-14]glucose ([C-14]GLU) (9.2 MBq/goat). Rumen fluid and
venous blood samples were collected at 0.5 h, 1 h, 1.5 h, 2 h, 3 h, 6
h, 8 h, 10 h, 12 h, 24 h, 36 h, 48 h, 60 h, 72 h, and 84 h; and milk
samples were taken at 6 h, 12 h, 24 h, 36 h, 48 h, 60 h, 72 h, and 84
h after the tracer administration. As expected, radioactivity followed
a logarithmic decline in total rumen fluid. In plasma and in milk, hi
ghest [C-14] labelling was observed at 0.5 h and 6 h, respectively. [C
-14]-enrichment curves in CN, in WP, in LAC and in MF were similar and
the measured radioactivity levels were in the same range. [C-14]-labe
lling peak was observed either at the first milking for LAC (3750 mBq/
mg C), for CN (2048 mBq/mg C) and for WP (1334 mBq/mg C), or at the se
cond milking for MF (2101 mBq/mg C). Approximately 1% of the ruminal-a
dministered radioactivity was found in milk proteins. Recovery in milk
proteins was similar to recovery in MF and represented about 30% of r
adioactivity obtained in LAG. Thus, end products of glucose metabolism
in the rumen are used in relatively high amounts for protein synthesi
s. Further experiments should now be carried out to specify the associ
ated biochemical pathways. (C) 1998 Elsevier Science B.V.