A procedure was developed for the rapid analysis of titanium dioxide (TiO2) concentrations in feed and fecal samples. Samples were digested in concentrated H2SO4 for 2 h, followed by addition of 30% H2O2, and absorbance was measured at 410 nm. Standards were prepared by spiking blanks with increasing amounts of TiO2, resulting in a linear standard curve. Complete analysis using this procedure can typically be accomplished within 4.5 h. This procedure was compared to a previously published dry-ash procedure for the analysis of TiO2 in bovine fecal samples. Three sources of OM devoid of TiO2 (a forage sample, a bovine fecal sample without Cr2O3, and a bovine fecal sample containing Cr2O3) were spiked with graded amounts (0, 2, 4, 6, 8, or 10 mg) of TiO2. With our procedure, TiO2 recoveries averaged 96.7, 97.5, and 98.5%, for the three OM sources, respectively, vs. 74.3, 83.8, and 53.1% for the same samples analyzed using the dry-ash method. These results suggest that our procedure is a rapid and accurate alternative to dry-ash procedures for the determination of TiO2.

The objective of this study was to determine the forage:concentrate ratio that would provide the greatest duodenal flow of unsaturated fatty acids in ewes supplemented with soybean oil and to determine how diets differing in forage content affect flow of conjugated linoleic acid (CLA) and trans-vaccenic acid (18:1(trans-11)). Five mature ewes (66.5 +/- 12.8 kg) fitted with ruminal and duodenal cannulas were used in a 5 x 5 Latin square experiment. Diets were isonitrogenous and included bromegrass hay, cracked corn, corn gluten meal, urea, and limestone. Dietary fat was adjusted to 6% with soybean oil. Five ratios of forage:concentrate (18.4:81.6, 32.2:67.8, 45.8:54.2, 59.4:40.6, and 72.9:27.1) were fed at 1.3% of BW daily in equal allotments at 0630 and 1830. After 14 d, Cr2O3 (2.5 g) was dosed at each feeding for 7 d and ruminal, duodenal, and fecal collections were taken for the next 3 d. Duodenal flow of 18:0 increased linearly (P < 0.01) with dietary forage. Duodenal flow of 18:1(cis-9) and 18:2(cis-9,12) decreased (P < 0.001) but duodenal flow of 18:3(cis-9,12,15) increased (P < 0.01) with increased dietary forage. Biohydrogenation of dietary unsaturated fatty acids increased (P < 0.001) as dietary forage increased, which was concomitant with increased ruminal pH. Duodenal flow of 18:2(cis-9,trans-11) increased linearly (P < 0.01) with increased dietary forage but increased abruptly when forage was fed at 45.8%. Duodenal flow of the trans-10, cis-12 and cis-10, cis-12 CLA isomers decreased as dietary forage increased, but flow tended to increase on the highest-forage diet, resulting in both linear (P < 0.01) and quadratic (P < 0.01) effects. Duodenal flow of 18:1(trans-11) decreased from 8.28 g/d on the 18.4% forage diet to 5.47 g/d on the 59.4% forage diet then increased to 7.29 g/d on the highest-forage diet (quadratic, P < 0.1). Duodenal flow of 18:1(trans-11) was 27- to 69-fold greater than flow of CLA. We conclude that when ewes were fed a 6% crude fat diet duodenal flows of dietary fatty acids changed incrementally as dietary forage was increased, whereas changes in flows of CLA isomers seemed to be more abrupt. Biohydrogenation changes were gradual with diet, suggesting a gradual shift in ruminal microbial populations with increasing forage. Finally, the highest-concentrate diet supported the greatest duodenal flows of dietary unsaturated fatty acids, as well as the highest flow of 18:1(trans-11).

The purpose of this research was to examine the effects of various amounts of CP and RUP on AA flow to the small intestine and milk yield of lactating dairy cows. The first trial was a 5 x 5 Latin square design using five ruminally and duodenally cannulated multiparous cows. Diets contained chopped alfalfa hay, corn silage, high moisture corn, solvent-extracted soybean meal, and specially processed soybean meal (60.2% RUP). Soybean meal replaced high moisture corn to increase dietary CP from 14.5 to 16.5 or 18.5%, and specially processed soybean meal replaced solvent-extracted soybean meal in diets containing 16.5 or 18.5% CP to provide 6.2, 7.3, 6.7, and 8.3% RUP. Increasing dietary CP increased the flows of all AA to the duodenum. Increasing dietary RUP increased flows of Arg, His, Lys, Phe, Asp, and Glu to the duodenum. In a second trial, 36 cows were fed diets similar to those used in trial 1. Increased amounts of RUP in diets tended to increase milk yield because of improved protein status, improved intake of metabolizable energy, or both.

The effect of dilution rate (D) on carbohydrate, fibrous and nonfibrous, and protein fermentation by ruminal microorganisms was studied using a single-effluent continuous-culture system. The diets of fibrous carbohydrate, nonfibrous carbohydrate, or protein were formulated with soybean hulls (FC), ground corn (NFC), or isolated soy protein (PR) as the primary ingredient, respectively. Six dilution rates (.025, .050, .075, .10, .15, and .20/h of fermenter volume) were used. Digestibilities of DM, OM, and CP for the three diets and of NDF and ADF for the FC diet decreased (P<.001) as D increased, although the response of the digestibility to D varied with diet. Increasing D resulted in an increase in pH (P<.001) and a decrease (P<.001) in ammonia concentration. Daily volatile fatty acid production increased (quadratic; P<.01) for the FC and NFC diets, but decreased (quadratic; P<.001) for the PR diet. Increasing D quadratically increased (P<.001) the molar percentage of acetate and propionate, but quadratically decreased (P<.001) butyrate and valerate for the FC and NFC diets. For the PR diet, the molar percentage of propionate and valerate increased (quadratic; P<.01), whereas acetate and butyrate decreased (linear; P<.001) in response to increasing D. Molar percentage of isobutyrate and isovalerate decreased (P<.01) with increasing D for all three diets. As D increased, daily microbial N production showed quadratic responses with maximum values achieved at .126, .143, and .187/h D for the FC, NFC, and PR diet, respectively. There was a positive correlation between microbial growth efficiency (MOEFF) and D. A quadratic model fit the data of MOEFF as affected by D, and maximum MOEFF of 37.3, 59.6, and 71.4 g of bacterial N/kg OM truly fermented were calculated to be achieved at .177, .314, and .207/h D for the FC, NFC, and PR diet, respectively. Dilution rate significantly influenced the ruminal microbial fermentation of fibrous and nonfibrous carbohydrates and proteins, and was positively related to microbial yield and growth efficiency. In addition, microbial nitrogen composition, and therefore efficiency, was affected by substrate fermented.

One hundred twenty crossbred yearling steers (average weight = 445 +/- 32 kg) were used in an 84-d randomized complete block design experiment to determine the value of soybean hulls (SH) as a replacement for corn in concentrate diets formulated with or without added fat (lard). The steers were blocked by weight and alloted to one of eight treatments in a 4 x 2 factorial arrangement of treatments. The main factors were amount of SH (0, 20, 40, or 60% of diet DM) and amount of added fat (0 or 5% of diet DM). The basal diet without added fat or SH contained cracked corn (80%), a urea-based protein supplement (15%), and ground corn cobs (5%). Replacing corn with SH linearly (P = .03) decreased ADG, increased DMI (linear, P = .003; quadratic, P = .06), and linearly (P < .001) decreased gain efficiency. Fat addition tended (P = .08) to improve efficiency; ADG and DMI were unaffected (P > .05) by fat addition. Similar diets were fed to 16 wethers (average weight = 47 +/- 2.3 kg) in a randomized complete block design experiment to determine digestibility of NDF and dietary concentration of DE. Replacing corn with SH linearly increased DMI (P = .001) and NDF (P < .001) and linearly decreased (P < .001) the digestibility of DM. The digestibility of NDF tended to increase with increased SH. The digestibility of energy linearly (P = .0001) decreased with increased SH. The amount of fat had no effect (P > .05) on DMI or intake of NDF or digestibilities of these nutrients. The addition of fat tended (P = .07) to improve the intake of DE.(ABSTRACT TRUNCATED AT 250 WORDS)

No abstract

Twenty-four wether lambs (BW = 37.5 +/- 0.8 kg) were used in a 64-d randomized complete block design experiment to evaluate the effect of oscillating dietary CP with undegradable intake protein (UIP) on diet digestibility, N retention, and gastrointestinal (GI) organ mass. Four treatments consisted of a 13, 15, or 17% CP diet fed daily or a regimen in which dietary CP was oscillated between 13 and 17% on a 48-h basis (ACP). All diets consisted of 65% bromegrass hay (10.5% CP, 61.9% NDF, 37.2% ADF) and 35% corn-based supplement, and were formulated to contain the same amount of degradable intake protein (9.6% of dry matter), plus additional UIP (from SoyPLUS) to accomplish CP levels above 13%. Beginning on d 52, N balance collections were conducted for 8 d, after which lambs were killed on d 62 and 64 of the trial for measurement of GI organ mass. Because intake was restricted to 3.0% of initial body weight (dry matter basis), dry matter intake did not differ (P > or = 0.67) and no treatment effects (P > or = 0.36) on ADG, feed efficiency, or total tract DM digestibility were observed. Increasing dietary CP from 13 to 17% linearly increased (P = 0.0001) N digestibility, but lambs fed ACP had lower (P = 0.07) total tract N digestibility than those fed 15% CP daily. Although urinary N excretion increased linearly (P = 0.0001) with increasing CP, a linear increase (P = 0.07) was observed in N retention (g/d) with increasing dietary CP. Although the quantity of N retained by lambs fed ACP was not statistically different (g/d, P = 0.19; % of digested N, P = 0.23) from those fed 15% CP daily, N retention in lambs fed ACP was 42% lower than in those fed 15% CP daily (1.8 vs 3.1 g/d, respectively). Increasing CP linearly decreased (P < or = 0.09) weights of the reticulorumen, abomasum, and small intestine, but did not affect (P > or = 0.16) liver or omasum weights. Length of the small intestine was not affected (P > or = 0.45) by treatment, but lambs fed ACP had greater (P = 0.03) small intestine weights than those fed 15% CP daily. Increasing dietary CP linearly decreased (P = 0.03) total GI organ mass, and lambs fed ACP had a greater (P = 0.03) total GI organ mass than those fed 15% CP daily. Oscillating dietary CP may increase the weights of the GI organs, which may subsequently have negative effects on N and energy metabolism in the animal. Likewise, the potential for decreased GI organ mass in response to increased supply of CP with UIP deserves further investigation.

Two experiments were conducted to determine the effects of ruminal protein degradability, supplementation frequency, and increasing dietary protein on the expression and distribution of urea transporter-B (UT-B) in lambs fed low-quality forage (mature crested wheatgrass hay; 4.2 to 4.7% CP). In Exp. 1, 15 Dorset wether lambs (initial BW=45.8+/-1.3 kg) were blocked by initial BW and assigned to 1 of 3 treatments within a randomized complete block design for 28 d, with supplements fed to achieve 7, 10, or 13% total dietary CP. In Exp. 2, 13 Dorset wether lambs (initial BW=34+/-4 kg) were used in a completely randomized design and given 1 of 4 isonitrogenous supplements: 1) ruminally degradable protein (RDP) fed daily (n=3), 2) RDP fed on alternate days (n=3), 3) ruminally undegradable protein (RUP) fed on alternate days (n=3), or 4) a 50:50 mixture of RDP and RUP fed on alternate days (n=4) for 18 d. Alternate-day treatments were fed at twice that of daily supplementation. On the last day of both experiments, lambs were killed and samples taken for Western blot analyses for UT-B. Immunoblotting using a rabbit polyclonal antibody to UT-B confirmed the presence of distinct 32-kDa (consistent with a nonglycosylated UT-B protein) and 47-kDa (probable N-glycosylated form of UT-B) protein bands in all 9 tissues analyzed. In both experiments, the liver, dorsal rumen, reticulum, and ventral rumen displayed strong bands at 32 kDa and lighter bands at 47 kDa, whereas the cecum, large colon, spiral colon, and parotid salivary gland displayed slight 32-kDa bands and stronger, more visible bands at 47 kDa. Both protein bands were apparent in the kidney at similar visual intensities in Exp. 1, whereas the relative intensities of the 2 UT-B bands in the kidney were variable, and appeared somewhat reciprocal among animals in Exp. 2. Although the abundance of the 47-kDa UT-B band in the ventral rumen was greater (P=0.03) in lambs fed RDP daily in Exp. 2, no other treatment differences (P >or= 0.15 to 0.99) in the abundance of the 32- or 47-kDa UT-B proteins within tissues were observed in either experiment. Although protein supplementation strategy had little effect on UT-B expression in tissues other than the ventral rumen, differences in the degree of glycosylation of UT-B across tissues may provide insight into its regulation.