Young male pigs consumed a diet of fatty minced beef, safflower oil, skim milk powder, sucrose, cornstarch and wheat bran. Starch provided 50% of total daily energy either as low amylose cornstarch, high amylose (amylomaize) cornstarch or as a 50/50 mixture of corn and high amylose starch. Neither feed intake nor body weight gain as affected by dietary starch. Final plasma cholesterol concentrations were significantly higher than initial values in pigs fed the 50/50 mixture of corn and high amylose starch. Biliary concentrations of lithocholate and deoxycholate were lower in pigs fed high amylose starch. Large bowel length correlated positively with the dietary content of high amylose starch. Concentrations of butyrate in portal venous plasma were significantly lower in pigs fed high amylose starch than in those fed cornstarch. Neither large bowel digesta mass nor the concentrations of total or individual volatile fatty acids were affected by diet. However, the pool of propionate in the proximal colon and the concentration of propionate in feces were higher in pigs fed amylose starch. Concentrations of starch were uniformly low along the large bowel and were unaffected by starch type. In pigs with cecal cannula, digesta starch concentrations were higher with high amylose starch than with cornstarch. Electron micrographic examination of high amylose starch granules from these animals showed etching patterns similar to those of granules obtained from human ileostomy effluent. It appears that high amylose starch contributes to large bowel bacterial fermentation in the pig but that its utilization may be relatively rapid.

Young male pigs were fed a diet formulated from human foods including either boiled white rice plus rice bran or heat-stabilized brown rice at equivalent levels of fiber for 3 wk. Stool and starch excretion were low in pigs fed white rice during the first 2 wk of the experiment. In pigs fed brown rice, their excretion was high during wk 1 but declined in wk 2 while short-chain fatty acid (SCFA) excretion was higher at both times. Large bowel digesta mass, measured during wk 3, was higher in pigs fed brown rice but only in the proximal colon. Large bowel and fecal starch concentrations were higher in pigs fed brown rice but the difference was insufficient to explain the increase in large bowel digesta mass. In pigs with a cecal cannula, digesta starch concentrations were equally higher when white or brown rice was fed compared with the corresponding rice which had been finely milled, indicating that particle size was a determinant of ileal digestibility. Concentrations and pools of total and individual SCFA were higher in all regions of the colon but not the cecum of pigs fed brown rice. Large bowel Ca(2+) concentrations were lower in pigs fed brown rice, suggesting greater absorption. The data confirm earlier findings that brown rice raises large bowel digesta mass and SCFA through greater fermentation of starch but show that starch itself makes a relatively small contribution to digesta and stool mass. Apparently, the rate of passage of digesta is a determinant of the concentrations and pools of SCFA in the distal colon and in feces.

Responses to exogenous growth hormone were measured in lactating dairy cows surgically prepared to allow measurement of nutrient exchanges across mammary and hind-limb muscle tissues. Cows were injected daily with either saline or growth hormone, at a dose of 0·1 mg/kg liveweight, over periods of 6 days.During administration of growth hormone milk yield, milk fat content and yields of milk fat protein and lactose increased. Arterial plasma concentrations of glucose and non-esterified fatty acids were increased, uptake of glucose by leg muscle tissue decreased, lactate release from leg muscle tended to increase, mammary uptake of non-esterified fatty acids increased, blood flow to leg muscle tended to increase and blood flow to mammary tissue increased during injection of growth hormone.The results show that growth hormone affects supply to and utilization of key nutrients by tissues, resulting in the supply to the mammary gland of additional precursors for milk synthesis.

The contribution of leg muscle, pregnant uterine tissue and lactating mammary gland to overall energy utilization was determined in Merino ewes. Ewes were offered one of three diets based on chaffed oaten hay (7 . 9 MJ metabolizable energy per kilogram dry matter); chaffed lucerne hay (8 . 6 MJ /kg); or a 50: 50 (w/w) mixture of chaffed oaten and lucerne hays (8·2 MJ/kg). Measurements were made during five different physiological states: dry (non-pregnant), at 94 and 125 days after mating, and at 20 and 50 days after lambing.Tissue energy use was calculated from oxygen uptake and carbon dioxide output obtained from measurement of blood flow and arteriovenous difference. Whole-body energy use was calculated from carbon dioxide energy rate. Energy use by leg muscle was 144 ± 8 (mean ± s.e.) kJ kg-I day-I, and unrelated to metabolizable energy intake, but leg energy use increased with ewe body weight. On the basis that leg muscle was representative of all muscle, total muscle energy use accounted for 26 ± 4% of whole-body energy expenditure in dry ewes. Uterine energy use per unit weight was respectively 348 ± 53 and 254 ± 23 kJ kg-I day-I at 94 and 125 days after mating.Milk production was highly correlated with weight of secretory tissue, and with blood flow to the mammary gland. The ratio of blood flow to milk produced was 473: 1 in ewes producing from 200 to 1000 ml of milk per day. The mammary gland used energy to produce milk with an efficiency of O· 90 ± 0 ·01, a value close .to the theoretical estimate ofO· 89. On the basis that metabolic rate does not increase during lactation, the efficiency of use of metabolizable energy for milk production was 0·51 ±0·05. Examination of energy use by different tissues indicated that energy use by muscle was related to weight, but energy use by remaining tissues (whole body less muscle, uterus and mammary gland) was related to metabolizable energy intake. The results reveal an increase in energy use by the remaining tissue in lactating ewes (8500 ± 569 kJ/day) compared with dry (5634 ± 216 kJ/day) and pregnant ewes (5815 ± 393 kJ/day).