To investigate the impact of rumen microbial sequestration of VFA carbon on
estimates of acetate availability based on intraruminal infusion of [2-C-1
3] acetate, three nonlactating or low-yielding dairy cows were continuously
intraruminally infused with [2-C-13] acetate for 26 h. The C-13 content of
ruminal VFA, duodenal carbon, and fatty acids (FA) and AA isolated from li
quid-associated ruminal microbes and duodenal DM was measured by an isotope
ratio mass spectrometer interfaced to an elemental analyzer or a gas-liqui
d chromatograph. The ruminal gross production of acetate was 38 +/- 4 mol/d
and could account for about 38% of the DE intake. Of the intraruminally in
fused C-13 in [2-C-13]acetate, 7.6 +/- 0.9% was recovered at the duodenum.
The C-13 content of ruminal propionate, butyrate, and valerate increased (P
< 0.05) with intraruminal infusion of [2-C-13] acetate. It was estimated t
hat about 28% of the C-13 intraruminally infused in [2-C-13]acetate could b
e accounted for by duodenal C-13 flow and absorption of non-acetate VFA. A
number of FA isolated from liquid-associated ruminal microbes (C-6, C-12, C
-14, ante-iso C-15, and iso C-15) were enriched with C-13 (P < 0.05) at a l
evel comparable to the enrichment of ruminal butyrate. Any absorption of th
ese FA from the rumen would further contribute to non-acetate C-13 uptake.
A maximum of 72% of the ruminal gross production of acetate represented ace
tate absorption from the rumen in the present study. Consequently, previous
ly used models using intraruminal isotope dilution techniques seem not to b
e appropriate for measuring acetate availability in ruminants. The number o
f metabolites exchanging carbon with acetate was found to be so high that a
ssessments of the entire range of inter conversions seem to be practically
impossible. Portal absorption studies are discussed as an alternative metho
d of estimating VFA availability to the metabolism in ruminants.