Starch is the major energy component of grains. Wheat contains 77% of DM as starch, corn and sorghum contain 72%, and barley and oats contain 57 to 58%. In vitro systems have provided valuable data on kinetic aspects of starch digestion. Molecular biological techniques have provided a clearer picture of the ruminal microbial milieu. Proportions of starch fermented in the rumen can be predicted satisfactorily for a variety of grains and processing methods. Compared with dry rolling, steam processing (flaking or rolling) increases ruminal digestibility of starch (percentage of intake) from 52 to 78% for sorghum, from 75 to 85% for corn, and six percentage units or less for other grains. Recent research provides new insight into pancreatic function and intestinal glucose transport systems. The capacity to digest starch in the intestine ranges from 45 to 85% of starch entering the duodenum, with that capacity apparently limited by the supply of pancreatic amylase. There is evidence that amylase secretion may be enhanced by increasing duodenal entry of protein. Capacity for active transport of glucose across of gut wall does not seem to limit the amount of starch digested that is absorbed as glucose. For ruminants eating medium- to high-concentrate diets, about 30% of their total glucose need comes from glucose absorption, 50% from organic acid absorption (substrates for hepatic gluconeogenesis), and 20% from other sources. When glucose absorption from the gut increases, ruminants generally adjust (decrease) gluconeogenesis to meet their need; that need is directly linked to DE intake. In terms of overall ME yield, grain starch is best used when it is fermented in the rumen. However, close coordination of protein and starch supply to the duodenum may improve capture of starch in the form of glucose.

Growing cattle in the United States consume up to 6 kg of starch daily, mainly from corn or sorghum grain. Total tract apparent digestibility of starch usually ranges from 90 to 100% of starch intake. Ruminal starch digestion ranges from 75 to 80% of starch intake and is not greatly affected by intake over a range of 1 to 5 kg of starch/d. Starch apparently digested in the small intestine decreases from 80 to 34% as starch entering the small intestine increases from 0.2 to 2 kg/d. Starch apparently digested in the large intestine ranges from 44 to 46% of starch entering the large intestine. Approximately 70% of starch digested in the small intestine appears as glucose in the bloodstream. Within the range of starch intakes that do not cause rumen upsets, increasing starch (and energy) intake increases the amount of starch digested in the rumen, increases the supply of starch to the small intestine, increases starch digested in small intestine (albeit at reduced efficiency), and increases starch digested in the large intestine, such that total tract digestibility remains relatively constant. With increased starch intake, most of the starch is still digested in the rumen, but increasing amounts of starch escape ruminal and intestinal digestion, and disappear distal to the ileocecal junction. Again, within the range of starch intakes that do not cause rumen upsets, as starch intake increases, hepatic gluconeogenesis increases, glucose entry increases, and glucose irreversible loss increases, with a significant portion lost as CO2. The ability to increase use of dietary starch to support greater weight gains or improved marbling could come from increasing starch digestion in a healthy rumen or in the small intestine, but we conclude that the main limit to use of dietary starch to support live weight gain is digestion and absorption from the small intestine. Increased oxidation of glucose at greater starch intakes may alter energetic efficiency by sparing other oxidizable substrates, like amino acids.

Daily grab samples of feed were composited weekly, then ground (l mm). Dry matter was determined gravimetrically (24 h, 100'C), and N content of samples was determined using Kjeldahl procedures. Steers were weighed biweekly.

A useful approach of the study of nutrient absorption and metabolism is in vivo measurement of blood flow across portal-drained viscera and liver, and flux of bloodborne metabolites, successful application of the approach requires correct placement of chronic catheters in appropriate blood vessels. Additionally, catheters must stay patent long enough to allow the animal to recover from surgery and to complete an experimental protocol. This paper describes surgical techniques to install chronic catheters in mesenteric veins, the hepatic portal vein, and an hepatic vein of cattle. Techniques for access to arterial blood are described also. Materials, equipment, and supplies required for surgery, blood sampling, and blood flow determination are described. Commercial sources of supplies are suggested. Blood flow is measured by downstream dilution of para-aminohippurate, which is infused into a mesenteric vein. Examples of blood flow data for three types of cattle are provided.