Effect of acarbose on milk yield and composition in early-lactation dairy cattle fed a ration to induce subacute ruminal acidosis

Subacute ruminal acidosis reduces lactation performance in dairy cattle and most often occurs in animals fed a high concentrate:forage ration with large amounts of readily fermentable starch, which results in increased production of volatile fatty acids and lactic acid and a reduction in ruminal pH. Acarbose is commercially available (Glucobay, Bayer, Wuppertal, Germany) and indicated for the control of blood glucose in diabetic patients. In cattle, acarbose acts as an α-amylase and glucosidase inhibitor that slows the rate of degradation of starch to glucose, thereby reducing the rate of volatile fatty acid production and maintaining rumen pH at higher levels. The ability of acarbose to reverse the reduced feed intake and milk fat percentage and yield associated with a high concentrate:forage ration with a high risk of inducing subacute ruminal acidosis was evaluated in 2 experiments with lactating dairy cattle. In 2 preliminary experiments, the effects of a 70:30 concentrate:forage ration on ruminal pH and lactation were evaluated. Ruminal pH was monitored in 5 Holstein steers with ruminal cannulas every 10 min for 5 d. Ruminal pH was <5.5 for at least 4 h in 79% of the animal days. In dairy cows, the 70:30 concentrate:forage ration decreased feed intake 5%, milk fat percentage 7%, and milk fat yield 8% compared with a 50:50 concentrate:forage ration but did not affect milk yield. Early lactating dairy cattle were offered the 70:30 concentrate:forage ration with 0 or 0.75 g/d of acarbose added in a crossover design in 2 experiments. In the first experiment, acarbose increased dry matter feed intake (23.1 vs. 21.6 kg/d) and 3.5% fat-corrected milk yield (33.7 vs. 31.7 kg/d) because of an increase in percentage milk fat (3.33 vs. 3.04%) compared with control cows. In the second experiment, cows were fasted for 3 h before the morning feeding to induce consumption of a large meal to mimic conditions that might be associated with unplanned delayed feeding. In this experiment, acarbose also increased feed intake (22.5 vs. 21.8 kg/d) and 3.5% fat-corrected milk yield (36.9 vs. 33.9 kg/d) due to increased percentage milk fat (3.14 vs. 2.66%) compared with controls. Thus, acarbose reversed the decreased feed intake and low milk fat percentage and yield associated with feeding a high concentrate:forage ration shown to induce subacute ruminal acidosis in Holstein steers.     

Responses of milk fat composition to dietary fat or nonstructural carbohydrates in Holstein and Jersey cows

Milk fat from Jersey cows contains less oleic acid (cis-C18:1) and more short- and medium-chain fatty acids than does milk fat from Holstein cows. The objective of this experiment was to determine responses in milk fat composition when Jersey and Holstein cows were fed diets either high (37% of dry matter) or low (27% of dry matter) in content of nonstructural carbohydrates (NSC) and supplemented with either 0 or 2.5% (of dry matter) of a mostly saturated fat source. Four Holstein cows and four Jersey cows were used in a Latin square design with 28-d periods; diets were in a 2 x 2 factorial arrangement. Fat supplementation decreased contents of fatty acids synthesized de novo within the mammary gland and increased contents of C18:0 and cis-C18:1. Low-NSC diets tended to increase C16:0 and to decrease C18:0, cis-C18:1, and C18:3. Despite the differences in fatty acid composition between breeds, both breeds generally responded similarly to dietary treatments. An interaction of breed and fat indicated that the content of cis-C18:1 in milk fat was increased more by supplemental fat in Holsteins than in Jerseys. Interactions of breed x fat and breed x carbohydrate type showed that the ratio of cis-C18:1 to C18:0 decreased when Jerseys were supplemented with fat but increased for Holsteins, and decreased when Jerseys were fed the low-NSC diet but increased when Holsteins were fed low NSC. The data are consistent with the hypothesis (Beaulieu and Palmquist, 1995, J. Dairy Sci. 78:1336-1344) that mammary activity of stearoyl-coenzyme A desaturase is lower in Jerseys than in Holsteins.     

Factors Associated with Variation in Milk Fat Depression Resulting from High Grain Diets Fed to Dairy Cows

Thirty lactating Holstein cows were used in a crossover design with 4-wk periods to establish the relationship between chewing activity, molar proportions of ruminal volatile fatty acids, and milk fat depression resulting from feeding high grain-low forage diets. Milk production and dry matter intake were not affected by treatment. When cows were fed the high grain-low forage diet, milk fat decreased from 3.39 to 2.87%, ruminal acetate plus butyrate:propionate ratio decreased from 2.7 to 2.0, and total chewing time decreased from 659 min/24 h to 472 min/24 h. Percentage change in milk fat test between treatments was correlated to percentage change in the ruminal molar proportion of acetate, propionate, acetate plus butyrate:propionate ratio, and percentage change in total chewing time per kilogram neutral detergent fiber intake (n = 30, r = .38, −.50, .53, and −.30, respectively). More correlation coefficients were significant and correlations were higher if only cows that proceeded from control to high grain-low forage treatment were considered. As milk fat depression was increased by high grain feeding, magnitude of depression in chewing activity was decreased. Within treatment, time spent chewing increased as milk fat percentage decreased.     

Effect of Milk Pricing Systems on Income over Feed and Variable Costs of Dairy Cattle Breeds

An electronic spreadsheet program using a budgeting procedure was used to compare the effect of protein pricing differentials and cheese yield pricing systems on income over feed and variable costs of the six major dairy breeds. Increasing the protein differentials from $ .03 to .22/45.4 kg milk per .1 unit increase in protein percent above 3.2% decreased the difference in income over feed and variable costs between non-Holstein and Holstein breeds. With the prices and assumptions used, the income over feed and variable costs of non-Holstein breeds never equaled or surpassed that of Holsteins. With current milk, feed, and cheese prices, using a cheese pricing system caused a substantial decrease in income over feed costs for Holsteins and decreased the differences between Holsteins and non-Holsteins. Increased cheese prices, increased feed prices, and lowered milk prices also narrowed the differences in income over feed and variable costs between Holstein and non-Holstein breeds. Although changes in the milk pricing system make the non-Holstein breeds more competitive with Holsteins, non-Holstein breeds must produce between 224 and 1539 kg more milk with the various milk and feed price scenarios used for the income over feed and variable costs to equal that of Holsteins.     

Influence of Pecan Shells and Hulls as a Roughage Source on Milk Production,Rumen Fermentation,and Digestion in Ruminants,

In Experiment 1, 20 lambs (36 kg) were fed five diets containing 0, 5, or 10% pecan shells or hulls to evaluate digestion and nitrogen balance. Digestion was not depressed by diets containing 5% shells. Protein digestibility was not reduced and nitrogen balance was higher for lambs fed 5% hulls than for lambs in other groups. In Experiment 2, 8 Holstein cows (29.3 kg milk/d) were assigned to two diets: basal and basal with 5% shells in the grain mix. Cows fed diets containing shells produced the same amount of milk and milk fat as control cows. In Experiment 3, 12 Holstein cows (27.3 kg milk/d) were assigned to the same two diets used in Experiment 2 and a third treatment received 5% pecan hulls in the grain mix. Cows fed shells or hull diets reduced concentrate intake and milk production. In Experiment 4, 12 Hereford × Angus steers (474.5 kg) were fed diets used in Experiment 3 to examine rumen fermentation, digestion, and passage rates. Steers fed hulls had lower rumen ammonia N and higher rumen pH compared with steers fed the basal diet. Total rumen volatile fatty acid concentration was not different among treatments. Generally, rumen fluid from steers fed hulls had higher proportions of acetate and lower porportions of butyrate. Rumen fluid and particulate passage rates and digestion measurements were not affected by addition of shells or hulls.     

Effects of Feeding Synthetic Zeolite A and Sodium Bicarbonate on Milk Production Nutrient Digestion,and Rate of Digesta Passage in Dairy Cows

Four rumen-cannulated Holstein cows were fed synthetic zeolite A and NaHCO₃ to evaluate their affect on milk production, nutrient digestibility, rumen fermentation, and rate of digesta passage. Treatments were allocated in a 2 × 2 factorial arrangement within a 4 × 4 Latin-square design. Treatments consisted of control; 1.0% NaHCO₃; 2.0% zeolite; and 1.0% NaHCO₃ plus 2.0% zeolite. A total mixed ration with 50:50 concentrate to forage (80% corn silage, 20% haylage) DM was fed.Intake of DM was lower for cows receiving zeolite (18.7 vs. 20.7 kg/d). Decreases were noted in daily milk (26.3 vs. 28.9 kg/d). 4% FCM (23.6 vs. 25.6 kg/d); milk fat yield (.86 vs. .93 kg/d); milk protein yield (.85 vs. .95 kg/d); and milk protein percent (3.21 vs. 3.34) with zeolite. Digestibilities of DM, organic matter, and crude protein were also decreased by zeolite but ADF digestion was unaffected. Rumen pH was increased, ruminal propionate decreased, and acetate:propionate ratio increased by zeolite. All other VFA plus rumen NH₃ were not affected by treatment. Decreases due to zeolite were observed in liquid fractional rate of passage and liquid flow rate when measured by Cr-EDTA in the feces. No treatment differences were found in fractional rate of passage of feed particles. Addition of NaHCO₃ had no significant effects.     

Body composition and estimated tissue energy balance in Jersey and Holstein cows during early lactation

The rate and extent of estimated energy mobilization and the relationship between fat depth at the rib and thurl and body condition score (BCS) were investigated in Jersey and Holstein cows in early lactation. Twenty-six cows were paired by breed, parity, and calving date, and were individually fed a total mixed ration ad libitum from parturition through 120 d in milk. Feed intake and milk production were measured daily; body weight (BW), BCS, subcutaneous fat depth, milk composition, and concentration of plasma nonesterified fatty acids were measured every 2 wk. Estimated tissue energy balance (TEB) was calculated using 1989 NRC equations. Net energy intake was greater in early lactation for Holsteins compared with Jerseys, 37.8 and 28.2 Mcal/d, respectively. Milk energy was greater for Holsteins relative to Jerseys, 30.5 versus 21.2 Mcal/d. Fat depth and BCS did not differ between breeds. A positive relationship existed between fat depth and BCS for Jerseys; however, there was no significant relationship for Holsteins. The best-fit regression model for predicting TEB for Holsteins and Jerseys in early lactation included week of lactation, milk composition, and BCS. Jerseys remained in negative TEB for a shorter period of time relative to Holsteins. The TEB nadir was -6.19 and -12.9 Mcal/d, for Jerseys and Holsteins, respectively. Expressed as a proportion of metabolic BW (BW(0.75)), net energy intake did not differ between breeds, yet milk energy and estimated tissue energy loss were greater for Holsteins compared with Jerseys.     

Temporary alterations to postpartum milking frequency affect whole-lactation milk production and the energy status of pasture-grazed dairy cows

This study investigated the immediate and long-term effects of temporary alterations to postpartum milking frequency (MF) on milk production, body condition score (BCS), and indicators of energy status in pasture-grazed cows supplemented with concentrates. Multiparous Holstein-Friesian cows (n = 150) were randomly assigned to 1 of 5 groups at calving: milked twice daily (2×) throughout lactation (control), or milked either once daily (1×) or 3 times daily (3×) for 3 or 6 wk immediately postpartum, and then 2× for the remainder of lactation. During wk 1 to 3 postpartum, cows milked 1× produced 15% less milk and 17% less energy-corrected milk (ECM) than cows milked 2×. This immediate production loss increased to 20% less milk and 22% less ECM during wk 4 to 6 postpartum for cows that remained on 1× milking; these animals also produced less than 1× cows switched to 2× milking after 3 wk. During wk 8 to 32, when all cows were milked 2×, those previously milked 1× had sustained reductions in milk (−6%) and ECM (−8%) yields, which were not affected by the duration of reduced postpartum MF. In contrast, cows milked 3× postpartum had 7% greater milk yields during wk 1 to 6 compared with 2× controls, irrespective of the duration of increased MF. Milk yields also remained numerically greater (+5%) during wk 8 to 32 in cows previously milked 3×. Nevertheless, yields of ECM were not increased by 3× milking, because of lower milk fat and protein contents that persisted for the rest of lactation. In addition, indicators of cow energy status reflected an increasing state of negative energy balance with increasing MF. Cows milked 1× postpartum had greater plasma glucose and lower plasma nonesterified fatty acid concentrations during the reduced MF, and plasma glucose remained lower for 2 wk after cows had switched to 2× milking. Moreover, BCS was improved relative to 2× controls from wk 5 to 6. In contrast, cows milked 3× had lower plasma glucose concentrations, greater plasma nonesterified fatty acid concentrations, and greater BCS loss during wk 1 to 3; however, greater body fat mobilization was not sustained, indicating that additional energy supplements may be required to achieve better milk production responses. In conclusion, temporary 1× milking had lactation-long negative effects on milk and milk component yields but improved cow energy status and BCS, whereas temporary 3× milking immediately increased milk yield but did not improve milk fat and protein yields in pasture-grazed cows.     

Modeling of particle size distribution of sonicated coconut milk emulsion: Effect of emulsifiers and sonication time

Coconut milk was extracted from grated coconut meat with addition of water by a hydraulic press. This milk was mixed with emulsifiers (Gum Acacia and maltodextrin) at different ratios of emulsifier to fat (4, 2.75, and 1.5) and different maltodextrin (MD) to Gum Acacia (GA) ratio (0.67, 1.085, and 1.5). The emulsion was sonicated for different time durations (0.5–3.0 min). Particle size analysis of the sonicated coconut milk emulsion revealed that the number fraction of fat globules below 2 × 10⁻⁶ m increased as the emulsifier to fat ratio increased. However, at the highest ratio of emulsifier to fat this trend reversed even at higher sonication times. Similar slump in the increasing trend of globules below 2 × 10⁻⁶ m were observed at the highest value of ratio of MD to GA (1.5) studied. Modeling of particle size distribution by Rosin–Rambler–Sperling–Bennet relation was found to be a good tool for prediction of uniformity of distribution n and statistical average globule diameter M. The n values varied between 0.981 and 1.318 where as M values lied between 2.11 × 10⁻⁶ and 4.12 × 10⁻⁶ m. Linear regression fitting of n and M values as function of ratio of emulsifier to fat, ratio of MD to GA and the sonication time resulted in a good fit with relative deviation of 3.96% and 10.77%, respectively. These linear regression equations provided a suitable model to predict the sonication time required to achieve certain degree of size reduction with a relative deviation of 2.33%.     

Influence of Dietary Protein Concentration and Degradability on Milk Production,Composition, and Ruminal Protein Metabolism

Four groups of cows in early lactation, each group containing one mature cow and three cows in first lactation, were in a 4 × 4 Latin-square arrangement of treatments for us to study influences of altering quantity of undegraded dietary crude protein and quantity of crude protein on milk production and composition. Diets supplemented with protein sources were 1) soybean meal positive control (22.7% crude protein), 2) whole cottonseed-corn gluten meal (14.7% crude protein), 3) extruded whole soybean (14.5% crude protein), or 4) soybean meal supplemented (15.7% crude protein). Concentrate and sorghum silage were fed in a ratio of 62:38 dry matter. Dry matter intake was not influenced by dietary crude protein concentration or source. Cows consuming diet 2 produced less milk, milk protein, total solids, and solids-not-fat than cows receiving diets 1 and 4. Efficiency of conversion of dietary crude protein to milk protein was highest for cows receiving diet 3 and lowest for diet 1.Trial 2, a 4 × 4 Latin-square trial for collection of abomasal digesta, had four ruminal and abomasal cannulated steers and the four diets from the lactation trial; the trial was to determine the influence of source and concentrations of protein on quantity of protein reaching the abomasum daily. Crude protein intake by steers fed diet 1 was greater than for the other three diets. Percentages recovery of dietary crude protein were 122 and 130 for treatments 2 and 3, intermediate for treatment 4 (107%), and lowest for diet 1 (88.0%); crude protein digestibility in the total tract was highest for steers receiving diet 1.     

Response by Dairy Cows to Hay Supplement with Early Spring Grazing or to Delay in Turning to Pasture

Effects of moving cows from winter feeding to pasture at two stages of plant maturity and of supplementing long hay were observed. Holsteins were assigned to groups of seven as: A, moved to early pasture on May 2; B, same as A except supplemented with 2.7 kg long hay dry matter per cow daily; and C, retained on barn feeding until moved to mature pasture on May 23. Groups A and B were observed on pasture for 6 wk and group C for 3 wk. Concentrate was fed according to production. Dry matter intake as pasture was 16.6 and 15.8 kg per cow daily by groups A and B, respectively. Milk yield and milk protein percentage increased and milk fat percentage decreased when groups A and B went to pasture. Group C declined in milk yield and milk protein percentage compared with group A. Plasma stearic and linoleic acids were higher and oleic acid was lower in group B than in A. Plasma linolenic acid was lower in group C than in group A. There were no differences in rumen fluid composition or pH. The decline in milk fat content when cows were moved from indoor feeding to immature pasture appeared unrelated to inadequate dietary fiber or low ratio of acetate to propionate in rumen fluid.     

Effect of pH and level of concentrate in the diet on the production of biohydrogenation intermediates in a dual-flow continuous culture

Milk fat depression in cows fed high-grain diets has been related to an increase in the concentration of trans-10 C_18:1 and trans-10,cis-12 conjugated linoleic acid (CLA) in milk. These fatty acids (FA) are produced as a result of the alteration in rumen biohydrogenation of dietary unsaturated FA. Because a reduction in ruminal pH is usually observed when high-concentrate diets are fed, the main cause that determines the alteration in the biohydrogenation pathways is not clear. The effect of pH (6.4 vs. 5.6) and dietary forage to concentrate ratios (F:C; 70:30 F:C vs. 30:70 F:C) on rumen microbial fermentation, effluent FA profile, and DNA concentration of bacteria involved in lipolysis and biohydrogenation processes were investigated in a continuous culture trial. The dual-flow continuous culture consisted of 2 periods of 8 d (5 d for adaptation and 3 d for sampling), with a 2 × 2 factorial arrangement of treatments. Samples from solid and liquid mixed effluents were taken for determination of total N, ammonia-N, and volatile fatty acid concentrations, and the remainder of the sample was lyophilized. Dry samples were analyzed for dry matter, ash, neutral and acid detergent fiber, FA, and purine contents. The pH 5.6 reduced organic matter and fiber digestibility, ammonia-N concentration and flow, and crude protein degradation, and increased nonammonia and dietary N flows. The pH 5.6 decreased the flow of C_18:0, trans-11 C_18:1 and cis-9, trans-11 CLA, and increased the flow of trans-10 C_18:1, C_18:2n-6, C_18:3n-3, trans-11,cis-15 C_18:2 and trans-10,cis-12 CLA in the 1 h after feeding effluent. The pH 5.6 reduced Anaerovibrio lipolytica (32.7 vs. 72.1 pg/10 ng of total DNA) and Butyrivibrio fibrisolvens vaccenic acid subgroup (588 vs. 1,394 pg/10 ng of total DNA) DNA concentrations. The high-concentrate diet increased organic matter and fiber digestibility, nonammonia and bacterial N flows, and reduced ammonia-N concentration and flow. The high-concentrate diet reduced trans-11 C_18:1 and trans-10 C_18:1, and increased C_18:2n-6, C_18:3n-3 and trans-10,cis-12 CLA proportions in the 1 h after feeding effluent. The increase observed in trans-10,cis-12 CLA proportion in the 1 h after feeding effluent due to the high-concentrate diet was smaller that that observed at pH 5.6. Results indicate that the pH is the main cause of the accumulation of trans-10 C_18:1 and trans-10, cis-12 CLA in the effluent, but the trans-10,cis-12 CLA proportion can be also affected by high levels of concentrate in the diet.     

New human milk fat substitutes from butterfat to improve fat absorption

A new human milk fat substitute (HMFS) was produced from butterfat. A 2-week’s feeding experiment was performed using three groups of rats with 10 wt.% fat in their feed; the fat was either (1) butterfat-based HMFS + long-chain polyunsaturated fatty acids (LCPUFA), (2) the reference oil + LCPUFA, or (3) the reference oil without LCPUFA. The apparent fat absorption after intake of butterfat-based HMFS (95.9% ± 1.8%) was significantly higher than the other two groups, indicating that much less calcium soap was formed after feeding butterfat-based HMFS. Calcium contents in urines and faeces from the two groups fed LCPUFA in their diet were lower than those without supplementation of LCPUFA, suggesting that LCPUFA could improve calcium absorption by reducing the calcium excretion. It can thus be concluded that the butterfat-based HMFS improves fat absorption, and supplementation of LCPUFA in the formula improves calcium absorption.     

Milk Somatic Cells and Lactation in Small Ruminants

The milk somatic cell count (MSCC) is the basis for abnormal milk control programs. The current legal MSCC limit for bulk tank milk for goats and sheep in the United States is 1000 and 750 × 10³/ml, respectively. Milk somatic cell counts for goats are higher than MSCC for cows and sheep. The MSCC for goats free from intramammary infection (IMI) range from 270 to 2,000 × 10³/ml. Cell counts for sheep are similar to cows and range from 10 to 200 × 10³/ml. Neutro-phils comprise the major cell type in milk from uninfected goats and constitute 45 to 74% of the MSCC, compared with 2 to 28% for sheep and cows. The macrophage is the major cell type in milk from cows and sheep. Milk secretion in goats and sheep is largely apocrine in nature and cytoplasmic particles, similar in size to milk somatic cells, are normal constituents of their milk. Concentrations of cytoplasmic particles in sheep milk average 15 × 10³/ml, while goat milk averages 150 × 10³/ml. Therefore, to obtain accurate MSCC for goats, only cell counting procedures specific for DNA should be used. While IMI significantly increases MSCC for goats and sheep, noninfectious factors such as parity, stage of lactation, season and milk yield have been related to increased MSCC. An increase in MSCC for goats has been shown to decrease milk and fat yields. Intramammary infusion of antibiotics at dry-off and postmilking teat dipping in goats decreased the rate of new IMI and MSCC. Thus, mastitis control practices shown to be efficacious in cows are also effective in goats.     

Short communication: Temporal effect of feeding potassium carbonate sesquihydrate on milk fat in lactating dairy cows fed a fat-depressing diet

A lactation study with 10 multiparous dairy cows in early lactation, with an average of 64 days in milk (standard deviation = 37), were used to evaluate how quickly milk fat concentration would change when potassium carbonate sesquihydrate was abruptly added to the diet. The experiment had 3 periods. In period 1 (d 0 to 7) all cows were fed the same basal (control) diet with 1.8% soy oil, dry basis; in period 2 (d 8 to 28) 5 cows received the control diet, whereas the other 5 cows received the control diet plus 0.59% of added K with K carbonate sesquihydrate; and in period 3 (d 29 to 42) all 10 cows received the control diet. The control diet was formulated for a dietary cation-anion difference (DCAD), calculated as Na + K ? Cl ? S, of 37.7 mEq/100 g of dry matter (DM), 1.74% of DM as K, and 5.7% long-chain fatty acids (DM%), which included 1.8% of DM as soybean oil. Period 1 was used as a covariate. In period 2, d 8 to 28, 5 cows remained on the control diet whereas 5 cows were fed with the control diet plus K carbonate sesquihydrate (DCAD+ diet; DCAD of 54.3 mEq/100 g DM and 2.33% of DM as K). After feeding the DCAD+ diet, we noted a difference in milk fat concentration from 3.9 to 4.3% within 72 h. Over the 21 d of period 2, the DCAD+ diet resulted in significantly greater milk fat percentage from 4.0 to 4.3%, lactose from 4.74 to 4.82%, and fat efficiency in the form of fat in milk divided by fat in DMI from 1.27 to 1.49, without affecting dry matter intake (DMI), milk protein concentration, solids-not fat concentration, 3.5% fat-corrected milk, and protein efficiency in the form of protein in milk divided by protein in DMI. In period 3 (d 29–42), all cows were again fed the control diet, resulting in a tendency for greater milk fat concentration, significantly greater lactose concentration, and fat efficiency in the form of fat in milk divided by fat in DMI for the cows having received the DCAD+ diet during period 2. In conclusion, the abrupt addition of K carbonate sesquihydrate resulted in a greater milk fat concentration and tended to maintain the greater concentration after cessation of K carbonate sesquihydrate feeding.     

Effect of feeding extruded flaxseed with different grains on the performance of dairy cows and milk fatty acid profile

Sixteen Holsteins cows were used in a Latin square design experiment to determine the effects of extruded flaxseed (EF) supplementation and grain source (i.e., corn vs. barley) on performance of dairy cows. Extruded flaxseed diets contained 10% [dry matter (DM) basis] of an EF product that consisted of 75% flaxseed and 25% ground alfalfa meal. Four lactating Holsteins cows fitted with rumen fistulas were used to determine the effects of dietary treatments on ruminal fermentation. Intakes of DM (23.2 vs. 22.2 kg/d), crude protein (4.2 vs. 4.0 kg/d), and neutral detergent fiber (8.3 vs. 7.9 kg/d) were greater for cows fed EF diets than for cows fed diets without EF. Milk yield and composition were not affected by dietary treatments. However, 4% fat-corrected milk (30.5% vs. 29.6 kg/d) and solids-corrected milk (30.7 vs. 29.9 kg/d) were increased by EF supplementation. Ruminal pH and total volatile fatty acid concentration were not influenced by EF supplementation. However, feeding barley relative to corn increased molar proportions of acetate and butyrate and decreased that of propionate. Ruminal NH₃-N was lower for cows fed barley than for cows fed corn. Milk fatty acid composition was altered by both grain source and EF supplementation. Cows fed EF produced milk with higher polyunsaturated and lower saturated fatty acid concentrations than cows fed diets without EF. Feeding EF or corn increased the milk concentration of C18:0, whereas that of C16:0 was decreased by EF supplementation only. Extruded flaxseed supplementation increased milk fat α-linolenic acid content by 60% and conjugated linoleic acid content by 29%. Feeding corn relative to barley increased milk conjugated linoleic acid by 29% but had no effect on milk α-linolenic concentration. Differences in animal performance and milk fatty acid composition were mainly due to EF supplementation, whereas differences in ruminal fermentation were mostly due to grain source.     

Performance,carcass traits,muscle fatty acid composition and meat sensory properties of male Mahabadi goat kids fed palm oil,soybean oil or fish oil

This study examined the effect of palm, soybean or fish oils on the performance, muscle fatty acid composition and meat quality of goat kids. Twenty-four male Mahabadi kids (BW = 19.4 ± 1.2 kg) were divided into three groups according to liveweight and randomly allocated to one of three diets. Animals were fed ad libitum for 84 days. Different dietary fat sources had no effect on performance and/or carcass quality attributes. The soybean oil diet decreased 16:0 and 18:0 concentrations and increased 18:2 and 18:3 and the ratio of PUFA/SFA in the muscle compared with other treatments. Fish oil feeding increased 20:5 n-3 and 22:6 n-3 concentrations and decreased the ratio of n-6/n-3 in the muscle. The results demonstrate that the use of fish oil is a nutritional strategy to improve the health claimable long-chain omega-3 fatty acid content and n-6/n-3 ratio in goat meat without changing the sensory properties or colour of meat.     

Alkali-Treated Forage for Early Lactation Dairy Cows: Effect on Lactation Performance and Nutrient Digestibility

Our objective was to determine the effect of sodium hydroxide treatment (4 g NaOH/100 g forage DM) of an alfalfa-orchardgrass forage and its subsequent utilization by early lactation dairy cows. Forage was harvested as hay. Complete mixed diets consisted of 55% control or treated hay and 45% concentrate (DM basis) and were fed to eight early lactation Holstein cows in a crossover design. Chemical composition of hays and complete diets were similar. Intake of dry matter was greater when cows were fed treated hay (23.4 vs. 22.2 kg/d), as was milk yield (32.3 vs. 30.9 kg/d). Yield of 4% FCM, however, did not differ between diets (27.8 vs. 27.4 kg/d). Cows fed the treated hay diet had increased concentrations of total rumen volatile fatty acids and ruminal acetate, decreased ruminal isobutyrate concentration and pH, and increased apparent digestibility of NDF, ADF, hemicellulose, and lignin. Sodium hydroxide treatment also increased the proportion of potentially digestible DM and NDF compared with that of untreated forage. Alkali treatment improved the utilization of medium quality forage in the early lactation dairy cow.     

Protected Methionine and Heat-Treated Soybean Meal for High Producing Dairy Cows

Twenty-four high producing Holstein cows (14 primiparous and 10 multiparous) were fed concentrate mix containing heat-treated soybean meal without or with 15 g of added DL-methionine daily provided as 50 g of ruminally protected methionine product during wk 4 through 16 postpartum. The 15% crude protein mixed diets contained 30% (dry matter basis) corn silage, 15% alfalfa hay, and 55% concentrate mix. Covariant adjusted yields of milk (34.6 and 33.1 kg/d), 4% fat-corrected milk (28.4 and 27.6 kg/d), and solids-corrected milk (29.0 and 28.5 kg/d) were not increased by feeding supplemental methionine. Percentages of fat (2.81 and 2.92) and protein (2.88 and 2.92) were similar, whereas total solids (11.49 and 12.69) and solids-not-fat (8.68 and 8.77) were higher with supplemental methionine. Dry matter intakes (20.2 and 21.0 kg/d) were higher when cows were fed supplemental methionine. Ruminal pH, volatile fatty acids, and ammonia as well as blood serum urea and glucose were generally unaffected by methionine supplementation. Concentrations of methionine in arterial and venous plasma were elevated slightly when additional methionine was fed. The first-limiting amino acid for milk production, methionine, was calculated by several methods and was not changed by feeding supplemental ruminally protected methionine.     

The use of sedimentation field-flow fractionation in the size characterization of bovine milk fat globules as affected by heat treatment

Size distribution of fat globules affects the appearance, taste and stability of milk and milk-based products. Full-fat, semi-fat and chocolate bovine milk were subjected to heat treatment within a temperature range of 50–125 °C for 1 h. Sedimentation field-flow fractionation was employed to determine the changes in mean particle diameter of milk fat globules as affected by heat treatment. The mean particle diameter of fat droplets increased with increasing heating temperature for most samples. The particle size of fat globules increased on average 40 nm (4.65%) for full-fat and 72 nm (8.52%) for semi-fat milk following the heat treatment (50–125 °C). Chocolate milk exhibited considerable increase in particle size (104 nm, 12.53%) within a certain temperature range (50–110 °C), followed by a decrease in particle size when heated at 125 °C for 1 h. Heat-induced flocculation due to attractive interactions between hydrophobic sites on denatured protein molecules on different droplets was assumed to be mainly responsible for the increases in particle size observed in this study. Extensive heat-induced denaturation of milk proteins was also indicated by Native PAGE. Sedimentation field-flow fractionation proved to be a useful technique for adequately monitoring heat-induced changes in particle size distributions in milk.