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Biomedical subjects

R L Preston

Publications and source records attributed to R L Preston.

At least 37 records · Page 2Linked to original sources

Improved enzymatic method to measure processing effects and starch availability in sorghum grain.

A modified enzymatic method to measure processing effects and starch availability in steam-flaked sorghum grain (SFSG) was developed. To establish the method, experiments were conducted to determine the required enzyme concentration, color reagents, precipitants, sample particle size, shaking frequency and buffer pH. Glucose release at different incubation times (0 to 48 h) from uncooked (UNC) or fully cooked (CK, 100% gelatinized) ground sorghum grain, a 50:50 mixture of UNC and CK (C50) and SFSG was determined. Glucose release from UNC, CK and SFSG was expressed as one-component equations with rate constant k and r2 of .119 and .98, 1.781 and .98, and .368 and .99, respectively; C50 was characterized by having two starch components, one with a fast rate constant, 2.624/h, and one with a slow rate constant, .066/h (R2 = .99). Different degrees of gelatinization were obtained by mixing different proportions of CK and UNC. Glucose release from these samples was highly correlated with starch gelatinization (r2 = .99). By adjusting the tension between mill rollers, five SFSG samples with bulk densities ranging from 476 to 283 g/liter (37 to 22 lb/bu) were produced; respective roller mill electrical load ranged from 21 to 51.5 amps. Enzymatic determination of glucose release resulted in values of 422, 512, 588, 618 and 678 mg/g, which were more closely related to bulk density than birefringence measurements. The modified method for starch availability determination was found to be relatively simple, fast and sensitive, and is recommended.

Animal Feed↗

Estimating starch availability and protein degradation of steam-flaked and reconstituted sorghum grain through a gas production technique.

Five steam-flaked sorghum grain (SFSG) samples with bulk densities of 476, 412, 347, 309 and 283 g/liter made by adjusting tension between mill rollers and three reconstituted sorghum grain (RSG) samples with reconstitution times of 10, 20 and 30 d and a control sample were analyzed for gas production kinetics (rumen liquor fermentation) and enzymatic glucose release (amyloglucosidase). Protein degradation was estimated from 6-h gas production and residual ammonia in the liquid. Gas production followed first-order kinetics (r2 greater than .98; P less than .01) and was used to describe rate and extent of digestion kinetics. Rate of gas production increased as processing degree increased. The magnitude of increase in gas production, however, was much less for RSG than for SFSG. Linear relationships were observed between enzymatic glucose release and the gas production rate constant k as well as gas production at 4,6 and 8 h (r2 greater than .98; P less than .01). Protein degradation decreased with processing degree of SFSG but increased with reconstitution time. A technique based on 6-h gas production and residual ammonia in the liquid is proposed to estimate both ruminal starch availability and ruminal protein degradability for processed sorghum grain.

Animal Feed↗

Titration of the recombinant bovine somatotropin dosage that maximizes the anabolic response in feedlot steers.

The objective of this study was to determine the minimum dosage of recombinant bovine somatotropin (bST) required to elicit maximum depression in plasma urea nitrogen (PUN), an indicator of anabolic activity. Twenty-four steers (389 kg) were blocked by weight into six pens. Six steers were placed on each of the following bST doses: 0, 8, 16 and 32 mg bST/d. Treatments were administered once daily via subcutaneous injections for 21 d. Steers were weighed and jugular blood samples were taken on d 0, 1, 4, 7, 10, 13, 16 and 21 at 1400, approximately 4 h after feeding. Delta PUN (DPUN) was calculated as PUN - d 0 PUN. There was no dose x time interaction (P = .94) in DPUN. Maximum reduction in DPUN with bST occurred by d 7 (P less than .05). Linear (P less than .01) and quadratic (P less than .05) orthogonal contrasts indicated that DPUN depression increased with bST administration, with maximal reduction calculated to occur with 23 mg (59 micrograms/kg) bST/d. There was no further decrease in DPUN with 32 than with 16 mg bST, indicating that the minimum daily dose is at least 16 mg but no more than 23 mg. A similar dose response was observed in daily gain. Results from this study indicate that bST reduced PUN in a dose-dependent manner and that 41 to 64 micrograms/kg body weight maximized the anabolic effect of bST in growing steers.

Animals↗

Digestibility of cotton plant by-product diets for sheep at two levels of intake.

Crossbred wethers (n = 48) were assigned randomly to 1 of 12 experimental diets, arranged in a 3 X 2 X 2 split plot to evaluate three levels of cotton plant by-product (25, 50 and 75% CPB), two levels of NaOH treatment of CPB (0 and 4%) and two levels of monensin supplementation (0 and 30 ppm, DM basis) at two intake levels (70 and 90% of ad libitum). Intake was a within-lamb variable. Ad libitum intake was established over an initial 17-d adjustment period. Feed intake and fecal output were recorded during collection periods with aliquots retained for laboratory analysis. Intake was affected by a linear CPB X monensin interaction (P less than .06) with monensin depressing intake more at higher CPB levels. Neutral detergent fiber (NDF) digestibility decreased linearly (P less than .001) as the dietary level of CPB increased. NaOH treatment of CPB improved (P less than .001) the digestibility of organic matter (OM) and NDF. The supplementation of 30 ppm monensin resulted in greater (P less than .004) apparent digestibilities of NDF and hemicellulose (HC). Increasing daily feed intake from 70 to 90% of ad libitum decreased (P less than .004) digestibility of NDF, HC and ADF.

Analysis of Variance↗

Effects of ruminal escape proteins and canola meal on nitrogen utilization by growing lambs.

The effects of ruminal escape proteins and canola meal (CM) on N utilization by growing lambs were evaluated in two experiments. In both experiments, seven supplemental dietary protein treatments were fed. For each of these protein treatments a 3 x 3 Latin square metabolism trial was conducted, using two sets of three lambs and three periods. Within square treatments were 1.4, 1.7 and 2.0 times maintenance intake levels. In Exp. 1, protein treatments were control (7.0% CP, DM basis), urea fed at 9.5 or 12% dietary CP, CM fed at 9.5 or 12% dietary CP and a 50:50 (N basis) mixture of blood meal/corn gluten meal (BC) fed at 9.5 or 12% dietary CP. In Exp. 2, protein treatments were urea, 64% urea and 36% BC (all mixtures on a N basis), 36% urea and 64% BC, BC, 50% CM and 50% BC (CM/BC), CM and soybean meal (SBM), all at 10.5% CP. In Exp. 1, apparent N digestibility (AND) was lower for CM diets than for urea (P = .13) and BC (P less than .05) diets (49.0 vs 50.6 and 51.3%, respectively). Absorbed N was utilized with similar efficiencies for all supplemental protein sources. Dietary CP and digestible protein (DP) were closely related (DP = .879[CP%] -3.66; r2 = .91), indicating that for urea, CM and BC total tract N digestibility was not influenced by theoretical ruminal degradability. In Exp. 2, N balance and N utilization efficiency indicated that the optimal extent of ruminal protein degradation was about 50%. Nitrogen balance was similar for the CM, CM/BC and SBM treatments.(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Feed↗

The role of glucose infusion on the metabolism of nitrogen in ruminants.

This work determined the time necessary to stabilize the decrease in urinary N excretion after initiating continuous i.v. glucose infusion and the quantity of glucose required to maximize N balance in growing wether lambs fed a high-protein diet (21.1% CP, DM basis). In the first experiment, six wethers (30 kg) were used in a 10-d crossover design comparing jugular infusion of glucose (600 kcal gross energy/d) plus saline with saline alone. The second infusion experiment was carried out with six wethers (31 kg) assigned to two 3 x 3 plus extra period latin squares, with glucose infusion rates of 0, 300 and 600, and 0, 450 and 900 kcal/d, respectively. Urinary N decreased (P less than .02) by d 2 of glucose infusion, remained stable to the end of the 10-d infusion period, and returned to the preinfusion level within 2 d after glucose infusion was discontinued. Urinary N decreased (P less than .01) and N balance increased (P less than .005) with an increasing level of glucose infusion through 600 kcal/d. Plasma glucose and insulin were elevated (P less than .05) only by infusion of 900 kcal/d of glucose. Glucose was present in the urine of wethers infused with 900 kcal/d of glucose. Glucose infusion had no effect on diet digestibility, hematocrit or plasma urea N. The level of glucose infused into growing wether lambs that maximized reduction of urinary N and was fully utilized for protein deposition without increasing plasma glucose and insulin was about 12 g.Wk-.75.d-1.

Animals↗

Dose-response relationship of the ionophore tetronasin in growing-finishing cattle.

The dose-response relationship of the ionophore tetronasin was defined in growing-finishing cattle (84 heifers and 84 steers). Cattle were allotted by sex and weight replication (light and heavy) to 24 pens. Six dosages (D) of tetronasin (0, 3.7, 7.3, 11.0, 14.7 and 18.3 mg/kg, dry matter [DM] basis) were fed. Diets containing 40, 25 and 10% roughage were fed for 84, 56 and either 56 (heavy replication) or 91 d (light replication), respectively. Average starting weights were 242 and 270 kg and ending weights were 433 and 480 kg for heifers and steers, respectively. No interactions existed for ionophore with sex (P greater than .2) over the trial. Ionophore treatment did not affect overall average daily gain (.94 kg/d; P greater than .2). Daily DM intake (kg/d) decreased linearly as the level of tetronasin increased (8.4-.042D (dosage), r2 = .83, P less than .001). Gain efficiency (gain/feed, kg/100 kg DM) increased curvilinearly as ionophore dosage increased (11 + .16D - .0058D2, r2 = .77, P less than .001). Solving the first derivative indicated an optimum dose for gain efficiency improvement of 13.8 mg/kg. The gain efficiency response was greatest the first 84 d, less the next 56 d and minimal the last 56 or 91 d (20, 7 and 2% improvement for D = 14.7 mg/kg, respectively). Tetronasin was found to improve gain efficiency by about 10% over control at an optimum dosage of 13.8 mg/kg.

Animals↗

Procedural and mathematical considerations in urea dilution estimation of body composition in lambs.

Two experiments (n = 46 and 56, respectively) were conducted to evaluate urea dilution as an estimator of body composition in lambs and to address certain procedural and mathematical considerations in this technique. In Exp. 1, 14 blood samples were taken over 240 min after urea infusion. The equation describing the urea clearance curve was: delta PUN = 9.7e-.1727(min) + 10.4e-.0021(min), pools 1 and 2, respectively (r2 = .99, P less than .001; individual lamb effects removed). In the combined experiments, urea space (US) was related to percentage of empty body water (PEBH2O) by the equation 31.7 + .471 US (empty body weight basis; r2 = .56, P less than .001). The regression equation indicates that the US-PEBH2O relationship in lambs is different from that reported in cattle, even though urea clearance kinetics are similar. Although the prediction equations appeared to be biologically valid, considerable error was associated with the composition estimates. The PEBH2O was predicted as well by live weight (r2 = .69; SEy.x = 3.0) as by US in these experiments. The two-sample method (T12 minus T0) to determine the change in marker concentration was shown to be related more closely (r2 = .56) to PEBH2O than the standard multisample extrapolation to T0 method (r2 = .0 and .38 for pools 1 and 2, respectively). An equilibration time of 9 to 12 min provided the best estimate of body composition in lambs.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Influence of sarsaponin on growth, feed and nitrogen utilization in growing male rats fed diets with added urea or protein.

Two experiments were conducted with growing male rats to determine the effects of 120 ppm of dietary sarsaponin (S) on nitrogen (N) metabolism when urea or protein are added to the diet. Growth, feed efficiency, N digestibility and balance, urinary N and ammonia-N (NH3-N), and cecal urease and NH3-N were measured. Growth and feed utilization were unaffected by dietary S. Adding urea or protein to the diet increased apparent N digestibility and increased urinary-N excretion. Urea did not affect N balance, whereas growth, feed utilization and N balance were maximized with 22% compared with either 16 or 28% dietary protein. Urinary NH3-N excretion was decreased by S when urea was added to the diet but was not affected when fed with increasing dietary protein. Cecal urease was decreased by S when urea was added or when the protein level was increased in the diet; effects on cecal NH3-N varied between the two experiments. Plasma urea-N was decreased by S. It is concluded that S has minor effects on N metabolism in rats and that NH3-N formation or excretion is only marginally affected by dietary S. If S decreases NH3-N level in confinement facilities, it is concluded that the effect is after the waste material is excreted by the animal, perhaps through reduced urease activity.

Animals↗

Plasma, rumen and urine pools in urea dilution determination of body composition in cattle.

To determine if urea diffuses into reticulo-ruminal water (RRW) during urea dilution estimation of body composition, four 450-kg heifers were infused intravenously with a solution containing 65.05 g urea plus .95 g 15N-urea, after a 20-h removal of feed. Blood, urine and rumen fluid were collected before infusion and at various times for 120 min after infusion. Plasma 15N clearance was described by a two-pool model. Plasma and urine 15N levels equilibrated within 12 min post-infusion and then declined at similar rates, suggesting that renal clearance is a major component of the second pool. Rumen fluid contained no urea and rumen NH3-N did not increase during the study. Rumen fluid and plasma 15N did not equilibrate over the time studied (rumen fluid 15N/plasma 15N = .07 and .17 at 12 and 120 min after infusion, respectively). Therefore, urea dilution at 12 min overestimates empty body water only by the volume of urine produced during this time; RRW influences urea dilution estimation of body composition only as a component of live weight.

Animals↗

Feedlot performance and carcass characteristics of steers fed diets containing ammonium salts of the branched-chain fatty acids and valeric acid.

Two trials were conducted to study the effects of feeding a mixture of ammonium salts of isovaleric, 2-methylbutyric, isobutyric and valeric acids (AS-VFA) on feedlot performance and carcass characteristics of growing and finishing Angus, Hereford and Angus X Hereford steers. In trial 1,192 steers (8 steers/pen, 6 pen/treatment) averaging 251 kg body weight and in trial 2, 240 steers (8 steer/pen, 7 pens/treatment, 9 pens/control treatment) averaging 216 kg body weight were randomly assigned to four anhydrous ammonium salt-volatile fatty acid (AS-VFA) treatment levels: 0 (control), .14, .28 and .42% of the diet dry matter (DM). In each trial, the growing and finishing diets were isocaloric, isonitrogenous and supplemented with monensin (26 mg/kg diet). In both trials, steers received implants of 200 mg progesterone and 20 mg estradiol benzoate. Combined data from the trials confirmed the absence of average daily gain and feed conversion responses during the growing period. During the finishing period, the combined data for gain and feed conversion for the control steers and the steers fed .14, .28 and .42% AS-VFA were 1.43, 7.09; 1.43, 6.99; 1.48, 6.67 and 1.45, 6.80, respectively. Gains increased 3.5% (P less than .10) and feed conversion improved 5.9% (P less than .07) in steers fed .28% AS-VFA compared with gain and feed conversion of the control steers. At the end of the growing period in the first trial, a urea dilution technique was used to estimate the body composition of 12 steers from each treatment. Estimates of percent body fat and percent body protein were similar (P greater than .20) for all steers, irrespective of treatment. At the end of the trials, carcass yield grades for the combined data were 2.6 and 2.8 (P less than .10) for steers fed .28% AS-VFA and for the control steers, respectively. Carcass weight, dressing percentage and marbling score were lower (P less than .10) in steers fed AS-VFA than for steers fed the control. However, in general, carcass characteristics were not greatly influenced by AS-VFA. A possible use for a supplement containing branched-chain fatty acids and valeric acid in finishing steer diets is suggested by the improvement in feedlot performance and by the slight increase in carcass yield.

Animals↗

Effect of energy intake on the postpartum interval in beef cows and the adequacy of the cow's milk production for calf growth.

Lactating Hereford and Hereford X Angus cows, 2 to 6 yr old, and their calves were used in two trials to study the effects of energy intake on the postpartum interval (PPI) and the adequacy of the cow's milk production for calf growth. In trial 1, 23 cows were fed either 120 (high energy, HE) or 100% (adequate energy, AE) of National Research Council energy recommendations. Cow weights, calf weights and milk production were determined 1 wk after calving and every 2 wk until 17 wk postcalving . One-half of the calves received creep feed from the start of the study, whereas the other half did not receive creep feed until their average daily gain was below .23 kg/d. In trail 2, 19 cows were fed energy levels of 100 (AE) or 85% (low energy, LE). Estimated percentage body fat ( EPBF ) was estimated twice during the study; other variables were determined as in trial 1. In trial 1, the HE cows gained more weight (P less than .01) and produced more milk (P less than .01). In trial 2, the AE cows gained more weight (P less than .01) and produced calves 17 kg heavier (P less than .01) at the end of the study than did the LE cows. Milk production was not influenced by energy treatment (P greater than .2). It required 7.5 kg of milk and 2.3 kg of creep feed to produce 1 kg of calf gain in trial 1.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Transport of amino acids for glutathione biosynthesis in human and dog red cells.

Cysteine and glycine for glutathione biosynthesis in human red cells enter via specific amino acid transport systems, principally system ASC and gly respectively. In contrast, human red cells are impermeable to glutamate, but glutamine enters via a Na-dependent, saturable pathway, which apparently obeys Michaelis-Menten kinetics with appKm and Vmax values of 90-160 microM and 140-240 mumol/1.cells/h respectively. Dog red cells however, do show a Na-dependent glutamate uptake which apparently obeys Michaelis-Menten kinetics with appKm and Vmax values of 4-6 microM and 70-110 mumol/1.cells/h respectively.

Animals↗

Effects of unstirred layers on the kinetics of carrier-mediated solute transport by two systems.

Equations describing the effect of unstirred layers on the simultaneous transport of a solute via two mediated systems have been derived. It has been previously established that unstirred layers cause convex curvature of Eadie-Hofstee transformations of kinetic data for single mediated transport systems. On the other hand, multiple transport systems produce concave curvature in this plot. A numerical example is presented which illustrates the fact that under some circumstances the opposing effects can nearly cancel out, producing an erroneous apparently linear relation. Furthermore, statistical analysis of these curves suggests that the normal error encountered in physiological transport measurements can readily obscure evidence of unstirred layers. It is suggested that kinetic analysis of transport, particularly in epithelial tissues, should whenever possible, include independent measurements of unstirred layers, employ a broad range of substrate concentrations, and vary the stirring rate of the medium. Evaluation of the 'true' kinetic constants can then be made with the relations derived here. In addition, several limiting cases have been discussed which reduce to simpler kinetic descriptions published earlier.

Biological Transport↗

Variation of inorganic phosphorus in blood plasma and milk of lactating cows.

Diurnal changes in percents of inorganic phosphorus in plasma were measured in three Holstein cows fitted with indwelling jugular catheters. Blood was sampled 34 times over 48 h. Changes of inorganic phosphorus of blood plasma appeared to be related to patterns of feed consumption. In a second experiment, effects of diet, season of calving, stage of lactation, lactation number, and milk yield on inorganic phosphorus of plasma and milk were measured with 40 Holstein cows. Dietary treatments were 1.0% calcium, .31% phosphorus; 1.0% and .54%; 1.8% and .30%; 1.7% and .54%. Blood and milk samples were taken at wk 6 postpartum and every 5th wk thereafter. Inorganic phosphorus in plasma and milk was higher for cows in first lactation than multiparous cows. Cows which calved in November to December had the highest inorganic phosphorus in plasma but the lowest in milk. Month of year affected inorganic phosphorus in milk but not in plasma. Inorganic phosphorus in plasma increased as milk yields decreased and as inorganic phosphorus in milk decreased. Dietary phosphorus affected inorganic phosphorus in plasma but not in milk. The correlation between inorganic phosphorus in milk and plasma was -.15. These data indicate the limitations of using inorganic phosphorus in plasma or milk as sole or primary means of determining nutritional phosphorus status of lactating cows.

Animals↗