Sheep (Flemish female x Texel male, 55 kg BW), fitted with a PVC cannula in
the dorsal rumen and single T-shaped PVC cannulas in the proximal duodenum
, distal duodenum, mid-jejunum and terminal ileum were fed hay or hay-conce
ntrate diets at various levels of nitrogen and cell walls (NDF) (22 to 32 g
N/d; 150 to 699 g NDF/d). Co-EDTA and Cr-NDF were used as markers to measu
re the flow rate of digesta. Ribonucleic acid (RNA) in intestinal digesta a
nd in rumen bacteria was determined with orcinol after extraction with sodi
um chloride, precipitation with tungstophosphoric acid and alkaline hydroly
sis.
The RNA:total N ratio in bacteria, harvested from the rumen, amounted to 0.
70 (CV 4.4%). The apparent digestibility of RNA in different sections of th
e intestine was higher than of total N. About 6% of RNA entering the duoden
um disappeared between the proximal and distal duodenum. At jejunum, the ne
t disappearance of RNA amounted to 68% of the quantity which entered the pr
oximal duodenum. A higher result of 71% was obtained at the ileum. Total ne
t disappearance of RNA between the proximal duodenum and rectum averaged 75
%. Sixteen percent of RNA leaving the ileum was apparently digested in the
large intestine.
The true digestibility of RNA between the proximal duodenum and the termina
l ileum. as estimated by multiple regression analysis, amounted to 78%. Of
the amount of RNA entering the ileum, 24% was of endogenous origin. At ileu
m, the RNA pas:;age was positively related to the ileal flow of NDF (R-2 =
0.67) and N (R-2 = 0.94). The passage of RNA increased by 3 mg RNA per g il
eal indigestible NDF. Ileal endogenous N consisting of approximately 2% of
endogenous RNA-N.
In conclusion, the digestion capacity in the first part of the small intest
ine is high. Rising flows of indigestible cell walls and nitrogen increase
the loss of ileal RNA. Further, using RNA as a microbial marker to assess t
he amount of microbial protein entering the duodenum of ruminants, digesta
samples should be collected immediately post pylorus at the proximal duoden
um, in order to avoid underestimation of the microbial protein synthesis in
the rumen.