Pretanned leather shavings in a supplement mixture for steers: I. In situ and in vitro disappearance, ruminal fermentation, and organic matter, nitrogen, and fiber digestion.

Two digestion studies were conducted to evaluate the use of pretanned leather shavings as a component of a protein supplement. In Exp. 1, the in situ and in vitro disappearance of pretanned leather shavings and soybean meal was evaluated. Results revealed that less than 18.4% of the pretanned leather shavings was solubilized and disappeared when exposed to McDougall's buffer for 48 h, but there was 90.0% disappearance with 48-h exposure to a .1 N HCl/pepsin treatment and 97.0% disappearance with exposure to a two-stage digestion. In situ disappearance following 72 h in the rumen allowed 6.8% disappearance. Thus, leather shavings seem to be relatively indigestible in the rumen, but postruminal digestion may be possible. In Exp. 2, six Angus x Holstein steers, fitted with ruminal and duodenal cannulas, were used in a replicated 3 x 3 Latin square to evaluate ruminal and digestion effects of the following supplements combined with fescue hay at 1.7% of BW (DM basis): no supplementation (control); supplementation intraruminally with soybean meal at .07% of BW (as-fed basis); and supplementation intraruminally with a combination of soybean meal and pretanned leather shavings (17:8 ratio) at .05% of BW (isonitrogenous to soybean meal; as-fed basis). Ruminal fluid passage rate was greater and fluid turnover time was shorter in steers fed leather shavings than in those fed soybean meal (P = .10). Ruminal pH was lower (P = .04) for supplemented steers than for control steers and ruminal NH3 N concentration was greater (P = .01) in steers fed soybean meal than in those fed leather shavings. Total VFA concentration was increased (P = .02) by supplementation. Supplementation with soybean meal increased (P < .05) ruminal molar proportions of butyrate, valerate, and isovalerate compared with leather shavings. Duodenal OM flow and OM disappearing in the intestines were increased by supplementation (P < .10), but not by the type of supplement fed (P > .10). Ruminal digestion of OM and total tract OM digestion were unaffected (P > .10) by supplementation and the type of supplement fed. Flow and digestion of NDF were unaffected (P > .10) by the treatments. Flow of N and the quantity of N disappearing in the intestines were increased (P < .05) by supplementation but did not differ (P > .10) between supplementation groups. Microbial N flow, N utilization for net microbial protein synthesis, and ruminal N disappearance were unaffected (P > .10) by supplementation and the type of supplement provided. Combining pretanned leather shavings with soybean meal seemed to have no deleterious effects on digestion or fermentation and to allow for escape of some N to the lower tract.

Pretanned leather shavings in a supplement mixture for steers: II. Digesta kinetics, ruminal fermentation, and grazing behavior in steers grazing dormant wheatgrass pasture.

Twelve ruminally cannulated steers (Angus x Holstein; average initial BW = 533 +/- 3.28 kg) were randomly allotted to one of three treatments (four steers/treatment) to evaluate the use of pretanned leather shavings as a component of a protein supplement for steers grazing dormant intermediate wheatgrass (Thinopyrum intermedium Host). Steers were allotted to one of three treatments: 1) no supplement (control); 2) supplementation intraruminally at 0700 with soybean meal at .2% of BW (as-fed basis); 3) supplementation intraruminally with soybean meal and pretanned leather shavings (17:8 ratio, respectively) at .16% of BW (as-fed basis). Supplements were formulated so that intakes were isonitrogenous and were placed intraruminally once daily (0700). Sampling periods were conducted February 3 to 16 and February 17 to March 5, 1995. In situ organic matter disappearance of the soybean meal supplement was greater (P > .05) than that of the leather shavings supplement at all incubation times (1, 3, 6, 9, 12, 24, and 48 h). Data suggested that pretanned leather shavings within the leather shavings supplement were only 25% degradable within the rumen. Forage OM intake (control = 12.7, soybean meal = 12.7, and leather shavings = 13.4 g/kg of BW), grazing time, and grazing efficiency were not altered (P > .10) by supplementation or type of supplement provided but did increase between the February and March samplings. Total intake was increased (P = .09) with supplementation and reflected the addition of the protein supplements. Particulate and fluid passage estimates were unaffected (P > .10) by the supplements; however, gastrointestinal fill increased (P = .01) between the February and March samplings. Ruminal pH was lower (P = .04) and ruminal NH3 N concentration was greater (P = .02) for supplemented steers than for control steers, and supplementation treatments did not differ (P > .10). Total VFA concentrations were increased (P = .01) by supplementation but were not affected by type of supplement provided (P > .10). Ruminal molar proportions of acetate and propionate and the ratio of these two VFA did not differ (P > .10) between supplementation types. Nonetheless, supplementation increased molar proportions of butyrate (P = .04), valerate (P = .02), and isovalerate (P = .05), and leather shavings supplementation increased (P = .10) isobutyrate proportions over those in steers supplemented with soybean meal. Combining pretanned leather shavings with soybean meal seemed to have no deleterious effects on forage intake, digesta passage, grazing behavior, or ruminal fermentation and seemed to provide effects similar to those of soybean meal alone.

Ardacin for steers grazing endophyte-free fescue pasture: effects on live weight gain, forage intake, nitrogen and fiber digestion, ruminal fluid kinetics, ruminal fermentation, and serum hormones and metabolites.

Growth and digestion studies were conducted to evaluate the use of ardacin as a feedgrade antibiotic for enhancing digestive function and growth in grazing steers. In Exp. 1, 90 yearling steers (average initial BW of 248 kg) used in a randomized complete block design (block = weight group) grazed fescue pasture without supplementation (CON) or with daily supplements (DM basis) of .4% of BW supplemental ground corn (CRN) or .4% of BW supplemental corn supplying 120 mg of ardacin (ARD). In Exp. 2, 12 ruminally and duodenally cannulated steers and three ruminally cannulated steers (Hereford x Angus; average BW of 347 kg) were used to evaluate the effects of the same supplements used in Exp. 1 on ruminal fermentation and digestion. In Exp. 1, ARD-supplemented steers weighed more (P < .01) at the conclusion of the study than CRN steers, which together weighed more (P < .01) than CON steers. Average daily gain was greater (P < .10) in supplemented than in CON steers; ARD steers had greater (P < .01) ADG than CRN steers. In Exp. 2, forage intake and harvesting efficiency did not vary (P > .10) with supplementation or type of supplement, but total intake reflected (P = .03) the addition of corn to the forage diet. Addition of ardacin increased (P = .02) ruminal pH compared with CRN steers. Ardacin decreased ruminal molar proportions of acetate and increased (P = .01) propionate proportions when compared with CRN steers. Total tract N digestibility was affected (P < .10) by supplementation and by addition of ardacin to the diet. Addition of ardacin to the ground corn supplement increased ADG, in part by enhancing acetate:propionate ratios and increasing N digestion.

Determination of activable proacrosin/acrosin in bovine sperm using an irreversible isocoumarin serine protease inhibitor.

The activable proacrosin/acrosin levels in bovine sperm were examined using fluorescent staining and flow cytometry. The proportion of sperm with active acrosin were determined using the biotinylated isocoumarin serine protease inhibitor, Bi-Aca-Aca-OMe-IC (BIC). The presence of bound inhibitor on sperm was then determined by secondary labeling with avidin fluorescein conjugate. The proportion of sperm with activable proacrosin/acrosin was assessed by using detergent treatment to expose the active acrosin in intact sperm. The difference between untreated and detergent-treated aliquots was used to estimate the proportion of sperm with activable proacrosin/acrosin. In the 24-h stored samples from six bulls, the mean proportion of sperm with activable proacrosin/acrosin was 78.8 +/- 2.8%, whereas the mean proportion with exposed acrosin after cryopreservation of these samples was 55.8 +/- 4.1%. Significant differences (p < 0.05) were found among bulls in the proportion of sperm with activable proacrosin/acrosin both before and after cryopreservation. Activable proacrosin/acrosin levels in samples of cryopreserved sperm from five bulls were not correlated with fertility. These results do indicate, however, that the irreversible isocoumarin serine protease inhibitor BIC can be used to determine the proportion of sperm cells that retain activable proacrosin/acrosin after cryopreservation and thawing.

Supplemental cracked corn or wheat bran for steers grazing endophyte-free fescue pasture: effects on live weight gain, nutrient quality, forage intake, particulate and fluid kinetics, ruminal fermentation, and digestion.

Two experiments were conducted with beef steers (Exp. 1, average BW of 580 kg; Exp. 2, average BW of 247 kg) to evaluate the use of no supplements (CON) or daily supplementation with (OM basis) .34% of BW of cracked corn (CORN), .34% of BW of wheat bran (WBBW), or .48% of BW of wheat bran (WBISO; calculated to be isocaloric to CORN) on digestive responses (Exp. 1) and live weight gain (Exp. 2). In Exp. 1, type of supplement did not affect (P > .10) the dietary fiber or N constituents, but in vitro OM disappearance of the forage differed (P < .10) with supplementation and type of supplement fed. Supplemented steers consumed less (P < .05) forage and total OM. Particulate passage, fluid passage, and ruminal pH were not affected (P > .10) by supplementation. Ruminal NH3 N concentration showed (P < .05) a treatment x sampling time interaction and, in general, WBBW and WBISO steers had greater ruminal NH3 N than CORN and CON steers. Total VFA concentrations and molar proportions of propionate were lower (P < .10) in CON steers than in supplemented steers; no differences were noted (P > .10) among supplemented steers. Molar proportions of acetate were lower (P = .01) in supplemented steers than in CON steers and were greater (P = .03) in WBBW steers than in WBISO steers. Butyrate molar proportions were lower (P < .05) in CON steers than in supplemented steers and differed (P < .10) with type and quantity of supplement supplied. In situ forage NDF disappearance at 6, 9, and 24 h after feeding and rate of disappearance were greater (P < .05) in CON steers than in supplemented steers. In Exp. 2, CON steers weighed less (P = .01) than supplemented steers, CORN steers weighed more (P = .08) than wheat bran-supplemented steers, and WBISO steers weighed more (P = .02) than WBBW steers; ADG for 90 d followed a similar response. Results suggest that supplementation of wheat bran rather than corn did not seem to stop the reduction in forage intake or OM digestion associated with corn supplementation.

Cattle grazing a riparian mountain meadow: effects of low and moderate stocking density on nutrition, behavior, diet selection, and plant growth response.

Twelve ruminally cannulated and six intact crossbred beef steers were used in a randomized complete block design to evaluate the effects of stocking density of a riparian pasture in the Sierra Nevada mountains on grazing behavior, dietary selection, forage intake, digesta kinetics, and growth rates of Carex nebraskensis and Juncus balticus. Nine .5-ha pastures were assigned to one of three treatments: ungrazed (CON) or grazed to leave either 1,500 kg/ha (LOW) or 1,000 kg/ha (MOD). Two collections were conducted during the summer of 1992 (following winter drought) and 1993 (following above-average winter precipitation). Standing crop biomass was greater (P < .05) in grazed pastures than in CON pastures at initiation of grazing in 1992 but not in 1993. After grazing in both 1992 and 1993, a treatment x intrapasture location interaction was noted (P < .05). Tiller growth rates in both 1992 and 1993 were affected (P < .05) by a treatment x growth period interaction. Stocking density did not alter (P > .10) botanical or chemical composition of the diet in 1992, and only minor differences were noted (P < .05) in 1993. Forage intake, passage rate measures, and total time spent loafing did not differ (P > .10) between LOW and MOD steers. Within the mid-meadow area in 1992, loafing time was greater (P< .05) for MOD steers than for LOW steers. In 1993, a treatment x trial interaction was noted for loafing time in all three areas. Total time spent grazing was greater (P < .05) for MOD steers than for LOW steers in 1992 and was affected (P < .05) by a treatment x trial interaction in 1993. In 1992 grazing time along the streamside was greater (P < .05) for LOW steers than for MOD steers, and significant treatment x trial interactions were noted for grazing time spent along the forest edge and mid-meadow areas. In 1993, only streamside grazing time was influenced by treatment being greater (P < .05) for MOD steers than for LOW steers. In general, our data suggest that management decisions to reduce stocking densities may force cattle to congregate along streambanks and to concentrate grazing and loafing activities in those areas.

Steers grazing intermediate wheatgrass at various stages of maturity: effects on nutrient quality, forage intake, digesta kinetics, ruminal fermentation, and serum hormones and metabolites.

Six ruminally cannulated Holstein steers (average BW of 495 +/- 5 kg) grazed a 32-ha, nonirrigated, intermediate wheatgrass (Thinopyrum intermedium Host) pasture from April 10 through December 7. Sample collections were conducted in May, June, September, and November 1989. Total masticate N decreased (P < .05) and bound N increased (P < .05) with advancing forage maturity. Masticate in vitro OM disappearance was lower (P < .05) in November (40.5%) than in May (62.0%). Organic matter intake (grams/kilogram of BW) decreased (P < .05) at each sampling date (May = 35.7, June = 26.8, September = 20.0, November = 14.9). Correspondingly, particulate passage rate decreased and gastrointestinal mean retention time increased (P < .05) with advancing forage maturity. Extent and rate of NDF digestion were greater (P < .05) during May and June than during September and November. Ruminal NH3 N and total VFA concentrations were greater (P < .05) during May and June than during September and November. Advancing forage maturity did not alter (P > .10) serum growth hormone concentrations; however, nonesterified fatty acid concentrations were greater (P < .05) during September and November than during May and June. Serum insulin-like growth factor I decreased (P < .05) with advancing forage maturity. Seasonal changes in forage intake and ruminal fermentation suggest that animal performance might be increased if supplemental energy is provided early in the growing season of intermediate wheatgrass; however, supplemental protein would likely be needed as wheatgrass matures.

Effects of pregnancy on digesta kinetics and ruminal fermentation in beef cows.

Four pregnant and four nonpregnant, ruminally cannulated beef cows were used to evaluate the effects of the last trimester of pregnancy on digesta kinetics and ruminal fermentation. Before breeding, cows were allotted randomly either to pregnant (PR) or to nonpregnant (NP) groups; PR cows were bred at the first estrus after synchronization. All cows were fed long-stem fescue hay at 15 g of DM/kg of BW based on BW 120 d before parturition of pregnant cows (average BW of 642 kg). Collection periods, each lasting 9 d, began at 96, 68, 41, and 10 +/- 1.3 d before parturition. Particulate passage rate was greater (P < .05) and retention times and gastrointestinal fill were less (P < .05) for PR than for NP cows. Apparent total tract DM digestion, rate and extent (96-h in situ incubation) of NDF disappearance, and ruminal fluid kinetics were not affected (P > .10) by pregnancy. A physiological state x sampling day interaction was noted (P < .05) for ruminal NH3 N, total VFA concentrations, and molar proportions of butyrate. Ruminal pH and individual VFA proportions, however, did not differ (P > .10) between PR and NP cows, except for valerate, which was less (P < .05) for PR than NP cows. Results suggest that in late pregnancy with restricted feeding, passage rate of particulates increases without substantial changes in fermentation or extent of digestion.

Supplemental methionine and time of supplementation effects on ruminal fermentation, digesta kinetics, and in situ dry matter and neutral detergent fiber disappearance in cattle.

Two experiments were conducted to study the effects of methionine supplementation on ruminal fermentation and digesta kinetics. In Exp. 1, nine ruminally cannulated beef heifers (average initial BW = 527 kg) in a crossover design were fed low-quality grass hay and cottonseed meal with or without 11.4 g of supplemental methionine (polysaccharide-coated). Particulate and fluid kinetics, rate of DM and NDF disappearance, ruminal VFA and NH3 N concentrations, and pH were not altered (P > .10) by supplemental methionine; however, ruminal purine concentration was greater (P < .05) in methionine-supplemented heifers than in unsupplemented heifers. In Exp. 2, 12 ruminally cannulated Holstein steers (average initial BW = 622 kg) grazing a fescue pasture were allotted to one of three groups: no supplemental methionine (CON) or 11.4 g of supplemental methionine fed at 0700 (AM) or at 1200 (PM). Forage intake, particulate kinetics, ruminal fluid kinetics, pH, VFA, and NH3 N concentrations were not altered (P > .10) by supplemental methionine or supplementation time. In situ rate of DM and NDF disappearance was greater (P < .05) in supplemented steers than in CON steers; AM steers exhibited faster (P < .05) rates than PM steers. Overall, methionine supplementation of low-quality forage increased ruminal purine concentration but did not alter in situ fermentation or digesta passage, whereas supplementation at 0700, but not at 1200, of steers grazing fescue forage increased rate of NDF fermentation.

Steers grazing endophyte-free tall fescue: seasonal changes in nutrient quality, forage intake, digesta kinetics, ruminal fermentation, and serum hormones and metabolites.

Six ruminally cannulated Holstein steers (average BW 514 kg) grazed a 33-ha, unirrigated, endophyte-free, tall fescue (Festuca arundinacea Schreb.) pasture from April 10 through December 7, 1989. Samples were collected in May, June, September, and November 1989. Total masticate N was relatively constant (P > .10) throughout the year. Masticate in vitro OM disappearance was less (P < .05) in September (48.4%) and November (50%) than in May (60.6%) and June (56%). Ruminal NH3N concentrations (milligrams/deciliter) were greater (P < .05) during May (20.5) and June (17.8) than during September (9.4) and November (5.9). Organic matter intake (grams/kilogram of BW) and particulate passage rate (percentage/hour) were least (P < .05) in November (15.3; 2.6) and not different (P > .10) during May (23.7; 3.1), June (20.7; 3.1), and September (21.0; 3.0). Extent and rate of NDF digestion and ruminal total VFA did not differ (P > .10) across sampling dates. Serum glucose concentrations were not affected (P > .10) by sampling date, but serum urea N was greater (P < .05) during May and November than during June and September. Nonesterified fatty acid concentrations increased (P < .05) with advancing plant maturity. Serum insulin concentrations were greater (P < .05) during May than during other sampling periods; however, growth hormone concentrations were not altered (P > .10) by advancing plant maturity. Unirrigated fescue pasture maintained a high nutrient level throughout the grazing season, and masticate samples did not display the decrease in nutrient content often noted with other types of pasture forage.

Growth performance, serum hormones, and metabolite responses before and after weaning in lambs weaned at 42 days of age: effect of preweaning milk and postweaning alfalfa or grass hay diets.

Fourteen fall-born lambs were used to determine the effects of diet before and after weaning on intake, growth, serum hormones, and metabolite profiles. Before weaning, lambs were intensively sampled for 6 h at 35 and 42 d of age. Before sample collection, lambs were allowed to suckle, and milk intake was recorded. At 42 d of age, lambs were weaned and randomly allotted to ad libitum access to either alfalfa or grass hay. Blood samples were collected at 49 and 56 d of age for 6 h. Milk intake did not differ (P greater than .10) between groups. After weaning, lambs fed alfalfa hay consumed more (P less than .05) hay and had greater (P less than .05) ADG than lambs fed grass hay. Postweaning diet had no effect (P greater than .10) on serum insulin, growth hormone (GH), insulin:GH ratio, prolactin, cortisol, glucose, or nonesterified fatty acids (NE-FA) concentrations. Lambs consuming alfalfa had higher (P less than .05) serum urea nitrogen (SUN) at 49 and 56 d of age than lambs consuming grass. At 35 and 42 d of age, (P less than .05) serum insulin and insulin:GH ratio were higher (P less than .05) after milk intake than at 49 and 56 d of age after hay intake. Serum GH was higher (P less than .05) in lambs at 35 and 42 d of age for 2 h postfeeding, but by h 3 through 5, lambs consuming milk had lower (P less than .05) values than lambs consuming hay.(ABSTRACT TRUNCATED AT 250 WORDS)

Time of daily supplementation for steers grazing dormant intermediate wheatgrass pasture.

To compare the effects of time of daily protein supplementation on grazing behavior, forage intake, digesta kinetics, ruminal fermentation, and serum hormones and metabolites, 12 ruminally cannulated Holstein steers (449 and 378 kg average initial and final BW, respectively) were allotted to three groups. Treatments consisted of CON = no supplement, AM = cottonseed meal (.25% of BW) at 0600, and PM = cottonseed meal (.25% of BW) at 1200. Steers grazed a dormant (1.1% N) intermediate wheatgrass (Thinopyrum intermedium Host) pasture. Sampling trials occurred in December, January, and February. Supplementation altered (P = .01) time spent grazing; CON steers grazed approximately 1.5 h longer than supplemented steers. Supplemented steers lost less (P = .02) BW (-40 kg) than CON steers (-75 kg) did. Supplementation did not alter (P greater than .15) forage OM intake; however, total OM intake was greater (P = .01) for supplemented steers (22.3 g/kg of BW) than for CON (18.4 g/kg of BW) steers. Supplementation did not affect (P greater than .15) digesta kinetics. Extent of in situ NDF (96 h) and rate (%/h) of disappearance for supplemented steers was greater (P = .01) than for CON steers. Across all periods, ruminal NH3 N and total VFA concentrations were lower (P = .01) for CON steers than for supplemented steers. Serum insulin (ng/mL) concentration was lower (P = .03) and concentration of serum growth hormone (ng/mL) was higher (P = .02) for CON steers than for supplemented steers. Cottonseed meal supplementation enhanced utilization of intermediate wheatgrass; however, supplementation time had minimal effects on the variables measured.

Effects of cottonseed meal supplementation time on ruminal fermentation and forage intake by Holstein steers fed fescue hay.

Four ruminally cannulated Holstein steers (average BW 303 kg) were used in a 4 x 4 Latin square design digestion trial to study the influence of daily cottonseed meal (CSM; 1.6 g of CP/kg of BW) supplementation time on forage intake and ruminal fluid kinetics and fermentation. Steers were housed individually in tie stalls and were fed chopped fescue hay on an ad libitum basis at 0600 and 1400. Treatments were 1) control, grass hay only (CON) and grass hay and CSM fed once daily at 2) 0600 (EAM) 3) 1000 (MAM), or 4) 1400 (PM). Ruminal NH3 N concentrations reflected a time of supplementation x sampling time interaction (P less than .05); CON steers had the lowest (P less than .05) ruminal NH3 N concentrations at all times other than at 0600, 1000, 1200, and 2400, when they did not differ (P greater than .05) from at least one of the supplemented groups. Forage intake, ratio of bacterial purine:N, rate of DM and NDF disappearance, and ruminal fluid kinetics were not influenced (P greater than .05) by supplementation time. Total ruminal VFA differed (P less than .05) between CON and supplemented steers, as well as among supplemented steers (linear and quadratic effects P less than .05). Acetate, propionate, and valerate proportions were influenced (P less than .05) by a sampling time X supplementation time interaction. Under the conditions of this study, greater peak ammonia concentrations with morning supplementation than with afternoon supplementation did not stimulate ruminal fermentation or rate of NDF disappearance.

Digesta kinetics, ruminal fermentation characteristics and serum metabolites of pregnant and lactating ewes fed chopped alfalfa hay.

Eight ruminally cannulated ewes (four control and four bred; average BW = 85.7 kg), limit-fed alfalfa hay (1.86% BW), were used in two experiments to determine the effects of pregnancy and lactation on digestive function and serum metabolites. Seven-day sampling periods were used starting on d 102, 118 and 132 of gestation (Exp. 1) and d 14 and 32 of lactation (Exp. 2). Particulate (6.8 vs 4.9%/h; PPR) and fluid passage rates (13.9 vs 10.9%/h) were greater (P less than .05) and gastrointestinal mean retention time (28.9 vs 35.7 h) and fluid turnover time (FTT, 7.5 vs 9.5 h) were lesser (P less than .05) in pregnant than in nonpregnant ewes, respectively. Isobutyrate concentration was lower (P less than .05) in pregnant (1.7 mol/100 mol) than in nonpregnant (1.9 mol/100 mol) ewes. No differences (P greater than .10) were noted for any other ruminal fermentation measures between pregnant and nonpregnant ewes. In Exp. 2, no differences (P greater than .10) were noted in digesta kinetics or ruminal fermentation measures except for isobutyrate and isovalerate molar proportions and serum urea N (SUN) concentration. Isobutyrate, isovalerate and SUN concentrations (21.8 vs 26.1 mg/dl) were lower (P less than .05) in lactating ewes than in nonlactating ewes. Gastrointestinal fill (5.7 vs 7.7 g/kg BW) and FTT (9.3 vs 12.7 h) were lesser and DM digestion (66.7 vs 57.4%) was greater (P less than .05) in lactating than in nonlactating ewes. Data suggest that, during pregnancy, passage rate increases occur without affecting DM digestion and that, during lactation, PPR is not affected when ewes are limit-fed.

Effects of exogenous ovine growth hormone on reproduction, serum hormone profiles and milk characteristics in early-postpartum fine-wool ewes nursing single or twin offspring.

After parturition (Day 0), 31 mature spring-lambing, fine-wool ewes were randomly allotted to one of six groups. Treatments were lambs suckled (one or two) and ovine growth hormone (oGH; 0, 5 or 10 mg). Growth hormone was administered subcutaneously daily from Days 6 to 25. Milk characteristics were determined on Day 26. Ewes were observed for estrus beginning on Day 27. Serum insulin did not differ (P > 0.10) between suckling intensity before or after oGH treatment on Days 6, 15 or 25. Likewise, no difference (P > 0.10) in serum insulin was detected among ewes receiving 0, 5 or 10 mg oGH. Ewes suckling twins had higher (P < 0.05) serum growth hormone on Day 6 (before beginning oGH treatment) than ewes suckling single lambs. In ewes receiving 0, 5 and 10 mg oGH, serum growth hormone differed (P < 0.01) in a linear fashion 1 h after treatment was initiated on Day 6 and continued through Hour 6. Serum growth hormone on Days 15 and 25 differed among groups both before and after oGH was administered (P < 0.01). Suckling intensity did not affect (P > 0.10) milk or milk protein and fat yields; however, oGH increased (linear, P < 0.05) fat but did not affect milk or protein yields. Interval from parturition to estrus did not differ (P > 0.20) in ewes suckling single or twin offspring. Likewise, no differences (P > 0.20) in interval length were noted in ewes receiving 0, 5 or 10 mg oGH. Suckling intensity and oGH administration for 20 d had little effect on postpartum interval or milk characteristics during the first 30 d after lambing in fine-wool ewes.

Elimination of [14C]heptachlor from body stores of lactating ewes treated with ovine growth hormone.

Elimination of [14C]heptachlor from body burdens of sheep was measured using mature ewes nursing single offspring, and the influence of exogenous ovine growth hormone (oGH) on elimination was studied. Six ewes (62 +/- 2.5 kg BW) were dosed (i.p.) once with [14C]heptachlor (2.04 mg/kg Bw; .88 microCi/mg heptachlor) and three were treated additionally with oGH (oGH; 5 mg/d) for 21 d. Three additional ewes served as controls. Excreta were collected each day for 21 d. Milk and blood were collected every 3rd d until ewes were euthanized at d 21. 14C activity was measured in excreta, milk, blood and tissues. Total cumulative activity of [14C]heptachlor and(or) metabolites in excreta (21 d) did not differ (P greater than .20) in ewes given oGH (25 +/- 2%) vs none (23 +/- 2%). Milk yield and protein content were unaffected (P greater than .10) by oGH. Ewes given oGH eliminated 2.2 +/- 2% of total 14C dosage into milk during 21 d, whereas ewes untreated with oGH eliminated 1.3 +/- .2% (P less than .10); total 14C activity eliminated into milk plus excreta was similar for ewes given oGH or none (P greater than .10). For all six ewes, half-times (T1/2) for distribution and elimination of 14C activity (heptachlor and metabolites) were 1.5 d and 11.7 d, respectively. Blood concentrations of 14C activity during 21 d yielded elimination half-time as 23 d. Unlike bovines, which eliminate heptachlor slowly (T1/2 approximately 70 to 80 d) and mainly into milk fat, lactating ovines eliminated heptachlor and(or) metabolites mainly into excreta and about sixfold faster than bovines.

Reproductive, hormonal and milk characteristics in ewe lambs treated with ovine growth hormone before breeding.

One month before a fall breeding season, 30 6-mo-old fine-wool ewe lambs were allotted to one of three treatment groups consisting of either 0, 2.5 or 5 mg ovine growth hormone (oGH) daily for 10 d and then, on alternate days, for an additional 20 d. Five ewes from each treatment group were bled at hourly intervals for 8 h on Days 0 (first day of treatment), 9, 19 and 29. Milk yield and composition were examined on Day 21 post partum. Neither feed intake nor ewe weights differed (P > 0.20) among treatments. Serum insulin did not differ (P > 0.20) among treatments before or during the 5 h following treatment on Day 0 or 29; however, 6, 7 and 8 h after oGH administration, a linear, dose-dependent increase (P < 0.10) in serum insulin was noted. On Day 9, serum insulin differed linearly (P < 0.10) before and after treatment. On Day 19, serum insulin differed (P < 0.10) among the groups 2, 3, 6, 7 and 8 h following oGH treatment. One hour after treatment on Day 0, serum GH increased linearly (P < 0.01) among groups. Serum GH continued to rise 3 h after treatment and remained elevated through Hour 8 in ewes receiving oGH. Serum GH was increased (P < 0.01) before and after oGH administration on Days 9, 19 and 29 in GH-treated ewes. Percentage of ewes that cycled during treatment or breeding as determined by serum progesterone was similar (P > 0.20) among groups. Pregnancy rates did not differ (P > 0.20) in ewe lambs receiving 0 (70%), 2.5 (80%) and 5 (60%) mg oGH. No differences were detected (P > 0.40) in milk yield or composition among treatments. In fine-wool ewe lambs treated with 2.5 or 5 mg of exogenous oGH for 30 d before breeding, neither reproductive performance nor subsequent milk production were enhanced; however, these treatments increased serum GH and insulin.

Reproductive responses, progesterone profiles and ovarian characteristics of cycling, fine-wool ewes treated with an inhibitor of progesterone synthesis (epostane).

In Exp. 1, 45 fine-wool ewes received (sc) either 0, 50 or 100 mg epostane (3-beta-hydroxysteroid dehydrogenase inhibitor) to examine effects on return to estrus and conception rates. Treatments were imposed on d 10 of an estrous cycle (estrus = d 0) and jugular blood samples were collected once daily on d 8 and 9, twice daily on d 10 through 13 and once daily from d 14 until first post-treatment estrus or d 20 (15 ewes/treatment). Intensive samples were obtained hourly for 6 h after treatment (d 10; five ewes/treatment). Serum progesterone (P4) before treatment was similar among groups; but by 2 h after treatment, epostane-treated ewes had lower (P less than .10) values than controls. By 6 h post-treatment, serum P4 in ewes receiving 50 (1.0 ng/ml) and 100 (.9 ng/ml) mg epostane was well below control values (3.2 ng/ml). By 7 d after treatment, 93.3% of ewes treated with 50 mg epostane had recycled compared with 66.7 and 33.3% of those receiving 100 and 0 mg, respectively (P less than .10). Similarly, 93.3, 53.3 and 26.7% of ewes receiving 50, 100 or 0 mg epostane, respectively, lambed to breeding within 7 d of treatment (P less than .05). Overall conception rates during a 34-d breeding season were similar among groups. Preweaning performance of offspring did not differ among maternal treatments.(ABSTRACT TRUNCATED AT 250 WORDS)