Effects of altering dietary cation-anion difference on calcium and energy metabolism in peripartum cows.

Our objective was to determine the effects of varying dietary cation-anion differences (DCAD: meq[(Na + K) - (Cl + S)]/100 g of dry matter) in prepartum diets on Ca, energy, and endocrine status prepartum and postpartum. Holstein cows (n = 21) and heifers (n = 34) were fed diets with varying amounts of CaCl2, CaSO4, and MgSO4 to achieve a DCAD of +15 (control), 0, or -15 meq/100 g of dry matter for the last 24 d before expected calving. Dietary Ca concentration was increased (by CaCO3 supplementation) with decreasing DCAD. Plasma ionized Ca concentrations prepartum and at calving in both cows and heifers increased with reduced DCAD in the diet. At calving, plasma ionized Ca concentration was 3.67, 3.85, and 4.35 for cows and 4.44, 4.57, and 4.62 mg/dl for heifers fed diets containing +15, 0, and -15 DCAD, respectively. All heifers had normal concentrations of plasma ionized Ca (>4 mg/dl) at calving. Also at calving, plasma concentrations ofparathyroid hormone and calcitriol were less in cows and heifers fed diets containing reduced DCAD, but the plasma concentration of hydroxyproline was not affected by diet. Prepartum dry matter intake, energy balance, and body weight gains were lower and concentration of liver triglyceride was higher for heifers but not cows fed the -15 DCAD diet. Also, nonesterified fatty acids the last week prepartum were positively correlated with liver triglyceride for heifers but not cows. Feeding of anionic salts plus CaCO3 to reduce DCAD to -15 and increase Ca in prepartum diets prevents hypocalcemia at calving in cows, but decreases prepartum dry matter intake and increases the concentration of liver triglyceride in heifers. That heifers maintained calcium homeostasis at calving regardless of diet but ate less when fed the -15 DCAD diet suggests that they should not be fed anionic salts before calving.

Nutrient requirements for dairy cattle of the National Research Council versus some commonly used ration software.

The first edition of the Nutrient Requirements of Dairy Cattle was published by the National Research Council (NRC) in 1945. The current document is the sixth revised edition, published in 1989, and it appears that we are a few years from another edition being in print. Software designed to evaluate and formulate rations for dairy cattle commonly determine nutrient requirements using the NRC as a standard. However, the generation of new knowledge in dairy nutrition occurs more rapidly than the release of the NRC publication, and the developers of the software often modify the requirements based on more recently published research, geographical peculiarities, or factors not explicitly considered by NRC. The first step in evaluating or formulating rations is the prediction of dry matter intake (DMI). The primary variables used by NRC to predict DMI are body weight (BW) and fat-corrected milk (FCM) yield; however, developers of software programs often use different equations based on personal preference, availability of research data with given equations, and incorporation of other factors in addition to BW and FCM yield. The additional factors are included to provide a more dynamic estimation of DMI and, therefore, reduce the difference between predicted and actual DMI. Nutrients required for maintenance, lactation, and growth must be consumed in adequate quantities (e.g., kilograms or calories), but the dietary concentration of nutrients for a given animal group may differ because of DMI. Even when nutrients are fed above the requirements, dietary concentrations of nutrients may be important in some situations to minimize the risk of underfeeding caused by variability in the nutrient composition of feedstuffs and to account for interactions of certain nutrients (e.g., minerals). New research discoveries need to be incorporated into ration formulation strategies promptly, and the strategies used for ration formulation need to be dynamic.

Dry cow diet, management, and energy balance as risk factors for displaced abomasum in high producing dairy herds.

The objective of this study was to determine prepartum risk factors for displaced abomasum. The design was a prospective study of 1170 multiparous Holstein cows from 67 high producing dairy herds in Michigan. Each farm was visited four times within a 6-wk period. At each visit, data on nutrition and management were collected. All multiparous cows within 35 d of projected calving were assigned a body condition score, and blood was sampled to determine the concentration of nonesterified fatty acids in plasma. A multivariable linear regression model was used to determine risk factors associated with the incidence of displaced abomasum during lactation on a herd basis. A multivariable logistic regression model with random effect was used to determine risk factors for displaced abomasum on an individual cow basis. Significant risk factors for displaced abomasum included a negative energy balance prepartum (as estimated from plasma nonesterified fatty acids), a high body condition score, suboptimal feed bunk management prepartum, prepartum diets containing > 1.65 Mcal of net energy for lactation/kg of dry matter, winter and summer seasons, high genetic merit, and low parity.

Ammonia versus urea-treated silages with varying urea in concentrate.

In four factorial experiments, 96 lactating Holstein cows averaging 100 days postpartum were fed corn silage (21 to 31% dry matter) ad libitum treated with aqueous ammonia (.3 to .4%) or urea (.5 to .7%). Concentrates fed at 1 kg/3 kg milk contained 0, .7, or 1.4% urea in Experiment 1 and 0 or 1.4% in Experiments 2, 3, and 4. Following 14-day pretreatment, experimental rations were fed for 65 days in Experiment 1 and 84 days in Experiments 2, 3, and 4. Urea in grain and urea in silage depressed intakes of silage and total dry matter. Milk persistences were lowered only by the diet containing urea in both grain and silage. Bodyweight changes, percent milk fat, and feed efficiencies were not altered significantly by treatments.

Microbial phospholipid synthesis as a marker for microbial protein synthesis in the rumen.

Phosphate uptake into intracellular inorganic phosphorus and cellular phospholipids and the relationship between cell growth and phospholipid synthesis were studied with suspensions of washed ruminal bacteria in vitro with (33)P-phosphorus. It was shown that ruminal bacteria accumulated inorganic phosphate at a low rate when incubated without substrate. Upon the addition of substrate, the rate of inorganic phosphorus uptake into the cells increased markedly, and phospholipid synthesis and cell growth commenced. There was a highly significant relationship (r = 0.98; P < 0.01) between phospholipid synthesis and cell growth. The specific activity of the intracellular inorganic phosphorus did not equilibrate with phosphorus medium. When ruminal contents from sheep fed a high or low protein diet were incubated in vitro, the rate of (33)P incorporation into microbial phospholipids was higher for the high protein diet. Since there was a high relationship between phospholipid synthesis and growth, rumen contents were collected before and various times after feeding and incubated with (33)P-phosphorus in vitro. The short-term, zero time approach was used to measure the rate of microbial phospholipid synthesis in whole rumen contents. In these studies the average specific activity of the intracellular inorganic phosphorus was used to represent the precursor pool specific activity. Microbial phospholipid synthesis was then related to protein (N x 6.25) synthesis with appropriate nitrogen-to-phospholipid phosphorus ratios. Daily true protein synthesis in a 4-liter rumen was 185 g. This represents a rate of 22 g of protein synthesized per 100 g of organic matter digested. These data were also corrected for ruminal turnover. On this basis the rate of true protein synthesis in a 4-liter rumen was 16.1 g of protein per 100 g of organic matter digested. This value represents a 30-g digestible protein-to-Mcal digestible energy ratio which is adequate for growing calves and lambs.