Lactogenesis signals the shift from uterine nutrient transfer to the fetus to neonatal nourishment at the mammary gland. Metabolic adaptations involved in this process are under endocrine regulation. Key events include an increase in blood flow to mammary tissue, a decrease in nutrient utilization by peripheral tissues and an increase in nutrient utilization by mammary tissue for milk synthesis. Deficits of certain substrates during early lactation require mobilization of those substrates from depot stores. Changes in metabolism of various tissues are related to changes in hormone receptor populations of those tissues and hormone concentrations in blood. Hormone receptors are therefore the primary mechanism by which information from the endocrine systems is linked to cellular metabolism. Endocrine changes at parturition result in dramatic changes in receptor populations of key tissues such as adipose and mammary tissues. Knowledge in this area, however, is incomplete. Relationship between hormone receptors and specific cellular metabolic pathways remains unresolved. (

Third-crop mixed grass-legume forage and corn were ensiled in 70-tonne bunker silos to evaluate the effects of a commercial carbohydrase enzyme-inoculant mixture (220 ml/tonne) and an experimental enzyme-inoculant mixture (264 ml/tonne) on silage fermentation and composition, ruminal degradation, and milk production. Twelve Jersey and 24 Holstein early lactation cows were fed one of four TMR at 32.5:32.5:35.0 haycrop silage:corn silage:concentrate (DM basis) containing a combination of treated and untreated silages from d 2 to 100 of lactation. Bunker silages were incubated twice in situ in fistulated cows in each dietary treatment to determine rates of DM and NDF degradation. Treatment of haycrop silage significantly reduced silage pH and acetic acid concentration and increased titratable acidity, lactic acid concentration, lactate: acetate ratio, and DM and NDF disappearances after 24 h of ruminal incubation. Treated haycrop silage increased DMI:BW ratio and daily production of milk, milk protein, and SNF of early lactation cows. Application of the experimental mixture to corn silage did not change silage fermentation or composition, except that the concentration of NH3 was reduced. Enxyme-treated corn silage did not improve DMI and slightly reduced daily milk production in early lactation cows.

With Three Text-figures)The experiments to be described were undertaken for two main reasons, primarily to compare the oourso and the control of mammary development in the males and females of two related species; and secondarily, to see how far the sheep might be used as a small, convenient substitute for the cow in studies of udder growth. To anticipate with regard to the second point, it became very clear that argument from one species to the other would be quite unjustified. MATERIAL AXD METHODS Sheep.To obtain a normal series, a flock of mixed-age Romney ewes was run with marked Romnoy rams, and animals were killed at monthly stages of pregnancy dated from the last recorded hoat. Enough were slaughtered to yield two male and two female foetuses at each stage from 2 months onward, and at each month at least two of the ewes killed were 2-tooths pregnant for the first time and the udders of these were retained to illustrate development during pregnancy. Table 1 gives Table 1. Details of sheep foetuses and pregnant ewes

Mature, pregnant Hereford cows (n = 17) were used to determine the effect of nutrition and body energy reserves on fetal development, concentrations of nutrients and estrogens in placental fluids, and on progesterone, estrogens and placental lactogen in maternal plasma. On d 145 of gestation, cows were assigned by breeding date to two groups and fed to achieve either a thin (TH; n = 8) or a moderate (M; n = 9) body condition score (BCS) by d 195 of gestation. Body weights, BCS, estrogens, placental lactogen and progesterone in plasma were determined weekly between d 200 and 256 of gestation. Cows were slaughtered on d 259 +/- 1 of gestation, and amnionic and allantoic fluids were sampled and analyzed for concentrations of protein, fructose and estrogens. Body weights and BCS were less (P less than .01) for TH (419 kg; 3.7) than for M (511 kg; 5.7) cows at slaughter. Uterine weights were less (P less than .07), but chorioallantoic weights were greater (P less than .07) in TH than in M cows. Cotyledonary weights were greater (P less than .05) for TH than for M cows, and total fructose in amnionic fluid was reduced (P less than .01) in TH compared with M cows. Concentrations of estradiol, estrone and placental lactogen were greater between d 240 and 256 of gestation for TH than for M cows. We conclude that nutrient intake and(or) BCS of beef cows during late gestation influence placental weight, fructose in amnionic fluid, and placental lactogen, estrone and estradiol in plasma.

The influence of supplemental protein during gestation on maternal hormones and fetal growth was determined in composite beef heifers. At AI, 118 heifers were stratified by BW within each composite genotype (BeefX = 1/2 Senepol, 1/4 Brahman, 1/8 Charolais, 1/8 Red Angus and CBX = 1/2 Senepol, 1/4 Brahman, 1/4 Charolais) into 4 treatment groups: high high (HH = 1.4 kg CP/d for first and second trimesters of gestation), high low (HL = 1.4 kg of CP/d for first trimester and 0.4 kg of CP/d for second trimester), low high (lowH = 0.4 kg CP/d for first trimester and 1.4 kg of CP/d and for second trimester), or low low (LL = 0.4 kg CP/d for first and second trimesters). Maternal plasma IGF-I and -II, total IGFBP, and leptin concentrations were determined at 14 d before AI and at d 28, 82, 179, and 271 post-AI (mean gestation length 286 d), and leptin concentrations were also determined at calving. Increased dietary protein increased maternal plasma IGF-I (P < 0.001 on d 28, 82, and 179), IGF-II (P = 0.01 on d 82; P = 0.04 on d 271), and total IGFBP (P = 0.002 on d 82; P = 0.005 on d 179; P = 0.03 on d 271). Maternal plasma IGF-I at d 271 was negatively associated with calf crown-rump length at birth (P = 0.003). BeefX had greater birth weight calves (P = 0.01), greater IGF-II (P < 0.001), increased ratios of IGF-I:total IGFBP (P = 0.008) and IGF-II:total IGFBP (P < 0.001), and reduced total IGFBP compared with CBX (P = 0.02). Increased dietary protein during second trimester increased maternal plasma leptin at calving (P = 0.005). Maternal plasma leptin near term was positively associated with heifer BCS (P = 0.02) and with calf birth weight (P = 0.04), and at calving was positively associated with heifer age at AI (P = 0.02). These findings suggest that maternal dietary protein, age, and genotype influence plasma concentrations of metabolic hormones and fetal growth in Bos indicus-influenced heifers.