This study examined the impact of leucine (Leu) derived from complete meals on stimulation of skeletal muscle protein synthesis (MPS). Expt. 1 examined time course changes in translation initiation and MPS after a meal. Male rats ( approximately 300 g) were trained for 5 d to eat 3 meals/d providing 20, 50, and 30% of energy from whey protein, carbohydrates, and fats, respectively. Plasma and skeletal muscle were collected at time 0 (baseline) after 12 h of food deprivation and then at 45, 90, 135, 180, and 300 min after a 4-g meal. Plasma Leu increased at 45 min and remained elevated through 180 min. MPS peaked at 45-90 min and returned to baseline by 180 min. Plasma Leu correlated with phosphorylation of ribosomal protein p70 S6 kinase (r = 0.723; P < 0.05), eukaryotic initiation factor 4E binding protein-1 (r = 0.773; P < 0.05), and MPS (r = 0.608; P < 0.05) over time. Expt. 2 examined 3 levels of protein intake (10, 20, and 30% of energy) from 2 sources (wheat and whey) with different Leu contents ( approximately 6.8 and approximately 10.9%, respectively) on stimulation of initiation and MPS. Rats were trained to eat 3 meals/d providing 14, 56, and 30% of energy from protein, carbohydrates, and fats. On d 6, MPS was evaluated at 90 min after rats consumed 1 of the 6 test meals. Whey protein stimulated initiation and MPS more than wheat and the differential response related to greater plasma Leu responses in the whey groups. These studies demonstrate that peak activation but not duration of MPS is proportional to the Leu content of a meal.

To compare the effectiveness of 2 phytase enzymes (Phyzyme and Natuphos), growth performance, fibula ash, and Ca and P digestibilities were evaluated in 4 studies. The first 3 studies used 832 pigs (i.e., 288 in the nursery phase, initial BW 8.1 kg; 288 in the grower phase, initial BW 24.2 kg; and 256 in the finisher phase, initial BW 57.8 kg) and were carried out over periods of 28, 42, and 60 d, respectively. Dietary treatments in each study consisted of a positive control [available P (aP) at requirement level]; negative control (Ca remained as in the positive control, and aP at 66, 56, and 40% of the requirement for the nursery, grower, and finisher studies, respectively); negative control plus graded levels of Phyzyme [250, 500, 750, or 1,000; measured as phytase units (FTU)/kg] or Natuphos (250 and 500 FTU/kg for the nursery and grower studies, or 500 and 1,000 FTU/kg for the finisher study) plus a very high dose of Phyzyme (tolerance level, at 10,000 FTU/kg) in the nursery and grower experiments. Across the 3 studies, there was no effect of any dietary treatment on ADFI, but the negative control reduced ADG (10%), G:F (7%), and bone ash (8%) compared with the positive control. In the nursery study, phytase addition increased G:F and bone ash linearly (P < 0.01). In the grower study, phytase increased ADG, G:F, and bone ash linearly (P < 0.01). In the finisher study, phytase addition increased ADG and bone ash linearly (P < 0.01) and increased G:F quadratically (P < 0.05); G:F was, on average, 5% greater (P < 0.05) with Phyzyme than with Natuphos. The fourth study was conducted to investigate the P-releasing efficacy of the 2 phytases. The apparent fecal digestibility of P, measured with chromic oxide as an external marker in 35 pigs (55.9 kg of BW), showed that aP increased (P < 0.001) by 0.17 and 0.06 g (+/- 0.023) per 100 FTU consumed for Phyzyme and Natuphos, respectively. Also, Phyzyme at 10,000 FTU/kg was not detrimental to animal health or growth performance. At doses intended for commercial conditions, Phyzyme proved to be effective in releasing phytate bound P from diets, with an efficacy superior to a commercially available enzyme.

This study evaluated the effects of gender and feeding of ractopamine on growth performance, carcass, and meat quality characteristics of pigs reared under commercial conditions. The study was performed as a randomized complete block design (blocking factor date of start on test) with a 3 × 2 factorial arrangement of treatments: 1) gender [gilt vs. surgical castrate vs. intact males immunocastrated] and 2) ractopamine level (0 vs. 5 g/ton). The study was conducted out over a fixed duration (126 d) from 1 wk after weaning (28 d of age; 8.04 ± 1.31 kg BW) to 154 d of age (111.44 ± 4.67 kg BW) in 3 growth periods: nursery (d 0 to 35 of the study), growing (d 35 to 70), and finishing (d 70 to 126). Ractopamine was fed for the final 28 d of the study (d 98 to 126). Pigs were kept in groups of 10 or 11 in the nursery phase and then moved to the growing-finishing facility where they were kept in groups of 22 to the end of the study. At the end of the growth study, pigs were harvested and carcass and pork quality were evaluated, including consumer evaluation of eating quality. During the nursery, there was no effect of gender (P > 0.05) on G:F, but surgical castrates grew faster (P < 0.05) than intact males and gilts and had greater (P < 0.05) ADFI than intact males. There was no effect of gender (P > 0.05) on ADG in the growing period; however, immunocastrated males had lower ADFI than surgical castrates and greater G:F than surgical castrates and gilts. In finishing, immunocastrated males and surgical castrates had similar ADG but grew faster than gilts; G:F was greater for immunocastrated males than the other genders. Feeding 5 compared to 0 g/ton ractopamine increased ADG and G:F but had no effect (P > 0.05) on carcass yield or fresh meat quality. Carcass yield was lower but percentage lean cut yield was greater for immunocastrated males than for surgical castrates. Longissimus muscle drip loss was greater (P = 0.05) for immunocastrated males than surgical castrates. Gender had no effect (P > 0.05) on consumer panel evaluation. Feeding ractopamine had no effect on pork flavor and tenderness but improved juiciness scores. Odor scores were similar (P > 0.05) for surgical castrates and immunocastrated males that were fed ractopamine. Consumers gave lower liking scores for odor for immunocastrated males than surgical castrates that were not fed ractopamine. This study highlights the feed efficiency and lean cut yield advantage for immunocastrated males compared to surgical castrates and suggests a similar growth response to feeding ractopamine in these genders. Although immunocastrated males had a lower carcass yield and higher drip loss, panelists were not able to detect differences in pork juiciness, flavor, and tenderness when compared to surgical castrate pigs.

The effects of dietary energy source and feed withdrawal on muscle glycolytic potential (GP) and blood acid-base responses to handling were investigated in slaughter-weight pigs (initial BW 94.7 ± 1.01 kg). Crossbred pigs (n = 96; 48 barrows, 48 gilts) were used in a randomized complete block design with a 4 × 2 × 2 factorial arrangement of treatments: l) diet [control, high fat (10% supplemental fat), low-digestible carbohydrate (20% total starch), and high-fat/low-digestible carbohydrate (10% supplemental fat and 20% total starch)]; 2) feed withdrawal (0 and 36 h); and 3) sex (barrow and gilt). Diets were fed for 28 d before the feed withdrawal treatment was applied, at the end of which all pigs were individually moved through a 12.20-m-long × 0.91-m-wide passageway for 16 laps (195 m total distance), with the assistance of an electric goad (2 times per lap). Longissimus muscle biopsies were collected at the beginning of the feeding and feed withdrawal periods and immediately after and 4 h after the handling procedure. Venous blood was collected 2 h before and immediately after the handling procedure to measure acid-base responses. At the end of the feeding period, pigs fed the control and high-fat diets were heavier (P < 0.001) than those on the low-digestible carbohydrate and the high-fat/low-digestible carbohydrate diets (129.8, 130.9, 114.0, and 122.1 kg, respectively; SEM 1.91). Diet, feed withdrawal, and sex did not affect (P > 0.05) blood acid-base responses to handling. Muscle GP at the end of the feeding period and 4 h posthandling was least (P < 0.05) for pigs fed the high-fat diet and similar for the other 3 diet treatments. Pigs subjected to 36 h compared with 0 h of feed withdrawal had less GP (P < 0.05) immediately after and 4 h after the handling procedure. There was an interaction between diet and feed withdrawal treatments for changes in GP from the start of feed withdrawal to 4 h posthandling. The reduction in GP was greater (P < 0.05) for fasted than for fed pigs receiving the control and high-fat diets, but was similar (P > 0.05) for fasted and fed pigs receiving the 2 low-digestible carbohydrate diets. In conclusion, neither dietary energy source nor fasting affected blood acid-base responses to handling; however, fasting-induced changes in LM GP were diet dependent.