Effects of increasing ruminally degraded nitrogen and abomasal casein infusion on net portal flux of nutrients in yearling heifers consuming a high-grain diet
Cr. Krehbiel et Cl. Ferrell, Effects of increasing ruminally degraded nitrogen and abomasal casein infusion on net portal flux of nutrients in yearling heifers consuming a high-grain diet, J ANIM SCI, 77(5), 1999, pp. 1295-1305
Seven Meat Animal Research Center (MARC) III heifers (410 +/- 25 kg) fitted
with hepatic portal, mesenteric venous, carotid catheters, and an abomasal
cannula were used in a 7 x 5 incomplete Latin square design experiment. Th
e objective was to evaluate the effects of increasing levels of ruminally d
egradable N (RDN) with or without the addition of abomasally infused casein
on portal-drained visceral (PDV) flux of nutrients. Treatments consisted o
f dietary CP percentage levels of 9.5 (control), control plus .72% dietary
urea (11.5U), control plus 1.44% dietary urea (13.5U), control plus abomasa
lly infused casein (250 g/d; 11.5C), or control plus .72% dietary urea and
abomasally infused casein (250 g/d; 13.5UC). All diets contained (DM basis)
80% ground corn, 15% corn silage, and 5% dry supplement and were provided
for ad libitum consumption. Nitrogen intake increased (linear, P < .001) as
CP increased from 9.5 to 13.5%. Portal-drained visceral release of ammonia
N increased (linear, P < .10) as RDN increased, and was greater (P < .05)
when protein was fed compared with heifers fed control (P < .10). Urea N re
moval by PDV was not affected (P > .10) by level of RDN but was greatest wh
en 11.5C was fed and least when 13.5UC was fed. Net or-amino N (AAN) releas
e by PDV was greatest when 13.5UC was fed (309 mmol/h), least when 9.5% CP
was fed (112 mmol/h), and intermediate for the other groups (205 to 252 mmo
l/h). These data suggest that removal of N by the PDV may promote microbial
protein synthesis when dietary RDN is low. When RDN needs have been met an
d amino acids are deficient for the host, escape protein should be fed to i
ncrease amino acid absorption.