No abstract

Rumen passage kinetics of forage and concentrate fiber were analyzed to determine intrinsic feed effects and extrinsic ration effects on the retention time of fiber in the rumen. Sixteen Danish Holstein cows (557 ± 37 kg of body weight, 120 ± 21 d in milk, mean ± SD), 8 fitted with ruminal cannulas, were used in a completely randomized block experiment. Treatments differed in forage type (corn silage vs. grass silage) and forage:concentrate ratio (50:50 vs. 75:25 on organic matter basis). Fiber passage kinetics were studied based on rumen evacuations and on marker excretion profiles in feces fitted to 1 and 2 pool models. Each cow received ytterbium (Yb)-labeled fiber of the forage fed in the ration, samarium (Sm)-labeled fiber of the forage not fed in the ration, and concentrate fiber labeled with lanthanum (La), all as a single pulse dose. Nineteen fecal grab samples were taken per cow. Rumen liquid passage was studied using chromium-EDTA dosed as a single pulse into the rumen, followed by sampling of rumen liquid from both the ventral and medial rumen. Rumen mean retention time did not differ between forages when based on Yb-excretion profiles but was numerically longer for grass silage- than for corn silage-based rations using rumen evacuation data. Liquid rate of passage did not differ when calculated from medial or ventral rumen liquid samples, indicating that estimates for the probability of rumen liquid escape were independent of rumen sampling site. Total mean retention time decreased from forage fiber to concentrate fiber to liquid. The forage type itself (corn silage or grass silage) rather than the ration composition seemed to determine the total-tract retention time of forage fiber.

Particle size alterations during neutral detergent fiber (NDF) determination and in situ rumen incubation were analyzed by dry sieving and image analysis to evaluate the in situ procedure for estimation of NDF degradation parameters and indigestible NDF concentration in terms of particle size. Early-cut and late-cut grass silages, corn silage, alfalfa silage, rapeseed meal, and dried distillers grains were examined. Treatments were (1) drying and grinding of forage samples and grinding of concentrates; (2) neutral detergent-soluble (NDS) extraction; (3) machine washing and NDS extraction; (4) 24-h rumen incubation, machine washing, and NDS extraction; and (5) 288-h rumen incubation, machine washing, and NDS extraction. Degradation profiles for potentially degradable NDF were determined and image analysis was used to estimate particle size profiles and thereby the risk for particle loss. Particle dimensions changed during NDF determination and in situ rumen incubation and variations depended on feedstuff and treatment. Corn silage and late-cut grass silage varied most in particle area among feedstuffs, with an increase of 139% between 0 and 24h and a decrease of 77% between 24 and 288 h for corn silage and a decrease of 74% for late-cut grass silage between 24- and 288-h in situ rumen incubation. Especially for late-cut grass silage residues after 288 h in situ rumen incubation, a high mass proportion in the critical zone for escape was found. Particle area decreased linearly with increasing incubation time. Particle loss during in situ rumen incubation cannot be excluded and is likely to vary among feedstuffs.

A multicatheter sow model was established to study the effects of dietary β-hydroxy β-methyl butyrate (HMB) supplementation on net portal flux (NPF) and net hepatic flux (NHF) of HMB, glucose, and the AA Ala, Gly, Ile, Leu, Phe, Tyr, and Val. Eight second parity sows were fitted with permanent indwelling catheters in an artery and in the portal, hepatic, and mesenteric veins. Eight hourly sets of blood samples were taken starting 30 min before the morning meal on day -3 and day 3 relative to parturition. Four control (CON) sows were fed a standard lactation diet from day -15 and throughout the experiment, and 4 HMB sows were fed the control diet supplemented with 15 mg Ca(HMB)(2)/kg BW mixed in one third of the morning meal from day -10 until parturition. Net portal flux of HMB was affected by treatment (Trt; P < 0.01) and peaked in the HMB sows at 6.9 mmol/h 30 min after the morning meal and then decreased towards preprandial level (0.0 mmol/h) 3.5 h after the meal, revealing that dietary HMB was rapidly absorbed from the intestine. The NHF of HMB tended to be affected by Trt (P = 0.06) showing a small hepatic uptake of HMB (1.1 mmol/h) in HMB sows. Net portal flux of glucose and all measured AA, except for Gly and Tyr, were affected the Trt × time interaction (P < 0.01). The NPF was positive for all nutrients, indicating absorption from the intestine to the portal blood. Absorption rates appeared to be more stable for HMB than for CON sows. Net hepatic flux of glucose was not affected by Trt. It was negative from 1.5 to 2.5 h after the meal, indicating hepatic uptake, but positive before and after, indicating net hepatic release of glucose. Net hepatic fluxes of AA were negative and were not affected by Trt (P > 0.10), except for Phe (P < 0.05). In conclusion, HMB reduced the variation in net portal flux of glucose and AA during 8 h of blood sampling and suggest that the improved sow productivity observed by others may be due to a more uniform nutrient absorption pattern into portal blood.