Distal-less 3 haploinsufficiency results in elevated placental oxidative stress and altered fetal growth kinetics in the mouse.

Distal-less 3 (Dlx3)(-/-) mice die at E9.5 presumably due to an abnormal placental phenotype including reduced placental vasculature and secretion of placental growth factor. To examine the role of Dlx3 specifically within the epiblast, Dlx3 conditional knockout mice were generated using an epiblast-specific Meox2(CreSor) allele. Dlx3(-/fl), Meox2(CreSor) animals were born at expected frequencies and survived to weaning providing indirect evidence that loss of Dlx3 within the trophoectoderm plays a critical role in fetal survival in the Dlx3(-/-) mouse. We next examined the hypothesis that loss of a single Dlx3 allele would have a negative impact on placental and fetal fitness. Dlx3(+/-) mice displayed reduced fetal growth beginning at E12.5 compared with Dlx3(+/+) controls. Altered fetal growth trajectory occurred coincident with elevated oxidative stress and apoptosis within Dlx3(+/-) placentas. Oral supplementation with the superoxide dismutase mimetic, Tempol, rescued the fetal growth and placental cell death phenotypes in Dlx3(+/-) mice. To determine the potential mechanisms associated with elevated oxidative stress on the Dlx3(+/-) placentas, we next examined vascular characteristics within the feto-placental unit. Studies revealed reduced maternal spiral artery luminal area in the Dlx3(+/-) mice receiving water; Dlx3(+/-) mice receiving Tempol displayed maternal spiral artery luminal area similar to control Dlx3(+/+) mice. We conclude that reduced Dlx3 gene dose results in diminished fetal fitness associated with elevated placental cell oxidative stress and apoptosis coincident with altered vascular remodeling. Administration of antioxidant therapy ameliorated this feto-placental phenotype, suggesting that Dlx3 may be required for adaptation to oxidative stresses within the intrauterine environment.

Dietary energy source and density: effects of roughage source, roughage equivalent, tallow level, and steer type on feedlot performance and carcass characteristics.

The effects of roughage level (10, 20, or 30% roughage equivalent [RE]), roughage source (alfalfa vs cottonseed hulls), roughage regimen (constant RE vs 2% RE during the mid-finishing period), tallow level (1.2 vs 4.6%), and steer type (British crossbred [BRITX] vs Bos indicus crosses [BRX]) were evaluated in three experiments with a common allotment and several overlapping treatments. Steers (n = 432; initial weight = 326 +/- 26 kg) were divided into three BW blocks and allotted randomly to 72 pens and 24 treatments. Steers were fed steam-flaked, sorghum grain-based finishing diets for 124 to 166 d. Diets with 20% RE decreased gain efficiency and 30% RE diets decreased both gain (linear, P < .07) and efficiency (linear, P < .001) compared with 10% RE diets. Reducing roughage level during the mid-finishing period improved overall gain efficiency 2, 7, and 24% (P > .2, < .05, and < .001, respectively) for the 10, 20, and 30% RE diets, respectively. Steers fed cottonseed hulls consumed more feed (9.6 vs 8.8 kg/d, P < .001) but tended to gain less (1.53 vs 1.58 kg/d, P = .11) than steers fed alfalfa, were leaner, and had fewer carcasses grading Choice (62 vs 77%, P < .05). Feeding 4.6% tallow decreased DMI (P < .05) and improved gain efficiency (P < .05) compared with 1.2% tallow. The BRITX steers consumed more feed (6%, P < .001) but were somewhat less efficient (3.5%, P < .05) than BRX steers. Carcasses from BRITX steers tended to be fatter than carcasses from BRX steers and more of them graded Choice (62 vs 37%, P < .01). Commercial BRX steers did not perform as well as BRITX steers on higher-energy-density diets (4.6% tallow or variable roughage regimen). Knowledge of the genetic background of feeder cattle can be important in the selection of dietary energy density and marketing expectations.

Corn supplementation of lambs grazing alfalfa.

We investigated the effects of supplementing Rambouillet x Suffolk wether lambs grazing irrigated 'Cimarron' alfalfa (Medicago sativa L.) with three levels (0 [C0], 123 [C123], and 247 [C247] g of DM.lamb-1.d-1) of cracked corn. Each treatment group also received 190 g of a supplement designed to prevent bloat. Replicated pastures (three per treatment) grown on a fine, mixed, thermic Torretic Paleustoll soil were grazed rotationally (forage plus supplement allowance of 6.5% of BW/d) by lambs for 85 d during spring 1992. Supplemental corn levels were analyzed as single degree of freedom contrasts for linear and quadratic effects. At the start of the experiment, lambs weighed 30.7 +/- .32 kg. Average daily gains for C0 C123, and C247 were 141, 154, and 169 g/d, respectively. Lamb production per hectare increased quadratically (P < .01) with increasing corn level (C0 [716 kg of lamb/ha], C123 [816 kg of lamb/ha], and C247 [964 kg of lamb/ha]). Supplementation with C247 vs C0 increased carcass weights (11%), dressing percentage (6%), and backfat thickness (30%). Plasma urea N (PUN) concentrations did not differ (P > .10) between C0 and C123 after 27 d of corn supplementation, but after 75 d PUN concentrations between C0 and C123 had decreased (P < .10) by 11%. For C247, PUN concentrations after 27 and 75 d of corn supplementation had decreased (P < .10) by 17 and 18%, respectively, compared with C0. Plasma urea N concentrations increased (P < .01) linearly (r2 = .93) with an increase in digestible CP:DE ratio (DP:DE).(ABSTRACT TRUNCATED AT 250 WORDS)

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)

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.

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.

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.