Influence of sexual maturity of donor on in vivo survival of transferred porcine embryos.

A study was conducted to determine whether embryos recovered from first-estrous (pubertal) and second-estrous gilts differed in survival when transferred to first- or third-estrous recipients. Embryos were recovered surgically from first- and second-estrous donors 48-72 h postmating and 6-10 normal embryos/zygotes (1-4 cells) were transferred to oviducts (3-5 embryos/ampulla) of nonmated synchronous first- (n = 40) or third- (n = 15) estrous recipients. Blood samples were collected from the jugular vein of recipient gilts on Days 3, 12, and 30 of gestation and the sera were analyzed for progesterone and free (unconjugated) estrogens by use of radioimmunoassays. Recipient gilts were subsequently slaughtered between Days 30 and 40 to assess embryonic losses. Mean number of ovulations was lower among first-estrous vs. third-estrous recipients (8.9 +/- 0.7 vs. 11.4 +/- 0.7; p < 0.05). Percentage of recipients that maintained pregnancy was similar between first- and third-estrous gilts (67.5 vs. 60.0%) and recovery of total conceptuses (normal and degenerating) resulting from transfer of one-cell- and cleavage-stage embryos did not differ among first- vs. third-estrous gilts (76.1 vs. 78.2%). Similarly, percentage of viable fetuses in first-estrous gilts that were pregnant from transfer of one-cell- and cleavage-stage embryos was not different from that of third-estrous gilts (69.3 vs. 75.6%). Percentages of total conceptuses and viable fetuses in first- and third-estrous gilts that were recipients of cleavage-stage embryos only also did not differ (p > 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

Effect of insulin and adrenergic agonists on glucose transport of porcine adipocytes.

1. Insulin increased basal 2-deoxyglucose uptake in isolated swine adipocytes by 75%. In the absence of insulin, isoproterenol did not inhibit basal 2-deoxyglucose transport. 2. Adenosine deaminase plus isoproterenol or theophylline alone reduced insulin effect by 10 and 40%, respectively. Isoproterenol alone or with 2-chloroadenosine did not inhibit insulin effect on glucose transport activity. 3. Insulin effect was inhibited by isoproterenol in the presence of theophylline but not in the presence of adenosine deaminase. 4. These results suggest that catecholamines do not counter-regulate basal and insulin-stimulated glucose transport in swine adipocytes.

Heteroaromatic analogues of the alpha 2-adrenoreceptor partial agonist clonidine.

A 1,4-dioxane analogue (1) of the alpha 2-adrenoreceptor partial agonist clonidine (2) has previously been shown to possess an interesting but complex pharmacological profile. In this study, from a series of other heterocyclic analogues of clonidine, the 1,4-oxazines 6 and 12 were found to resemble 1 in that they are partial alpha 2-agonists in the periphery and are excluded from the central nervous system. However, when given directly into the brain, they behave as pure alpha 2-antagonists.

Comparison of in vitro development of embryos collected from the same gilts at first and third estrus.

In vitro development of embryos collected from the same gilts mated at first and third estrus was compared. Embryos from one to eight cells were collected from gilts 36 to 48 h after detection of estrus. Embryos were cultured for 8 d in Whitten's medium in a humidified atmosphere of 5% CO2 in air at 37 degrees C and were observed daily. No differences were detected among percentages of one- to eight-cell embryos developing into morulae from gilts in first or third estrus (P greater than .05). Similar percentages of one- to two-cell embryos from gilts mated at first and third estrus developed into blastocysts (45.8 and 55.2%, respectively), expanded blastocysts (10.4 and 24.1%, respectively) and hatching blastocysts (4.2 and 3.4%, respectively; P greater than .05). Fewer three- to eight-cell embryos from gilts in first estrus than from gilts in third estrus developed into blastocysts (63.4 and 91.1%) and expanded blastocysts (14.6 and 55.6%; P less than .01). Similar percentages of embryos with abnormal morphology were observed among morulae developing from one- to eight-cell embryos collected from gilts mated at first and third estrus (14.9 and 9.9%, respectively; P greater than .05). In contrast, more morphologically abnormal embryos were observed among blastocysts developing from gilts mated at first estrus than at third estrus (31.2% and 14.0%, respectively; P less than .05). The results suggest that the reduced in vitro development of embryos collected from gilts mated at first estrus may be due to an aberration in blastocoel formation and expansion.

Suppressed development of cultured mouse and swine embryos by diethylstilbestrol.

Effects of prolonged exposure to the synthetic estrogen diethylstilbestrol (DES) on in vitro development of early mouse and swine embryos were investigated. Two-cell mouse embryos cultured in Whitten's medium (WM) for 192 h were exposed to 10(-4), 10(-7) or 10(-10) M DES dissolved in 1, 10(-3) or 10(-6)% ethanol, respectively. One-cell to eight-cell swine embryos were cultured in WM for 192 h containing 10(-4) or 10(-7) M DES dissolved in 1 and 10(-3)% ethanol, respectively. Embryos cultured in WM containing 1 (0 DES1), 10(-3) (0 DES2) or 10(-6)% ethanol (0 DES3) served as controls. Hatching was inhibited (P less than .05) in mouse embryos cultured in 10(-4) M DES (3.0 +/- 2.1% vs 0 DES1, 25.1 +/- 3.7%). Similar (P greater than .10) percentages of mouse embryos hatched in 10(-7) M DES (36.4 +/- 5.4% vs 0 DES2, 29.1 +/- 5.7%) and 10(-10) M DES (44.4 +/- 4.4% vs 0 DES3, 38.9 +/- 5.3%). Diethylstilbestrol at a concentration of 10(-4) M failed to affect the development of one- to eight-cell swine embryos into blastocysts. However, compared with 0 DES2, 10(-7) M DES reduced (P less than .05) the number of swine blastocysts developing from one- to two-cell (36 vs 78%) and three- to four-cell embryos (50 vs 84%). No significant effects of 10(-7) M DES were detected on the ability of six- to eight-cell swine embryos to develop into blastocysts.(ABSTRACT TRUNCATED AT 250 WORDS)

Ovulation and embryonic survival in pubertal gilts treated with gonadotropin releasing hormone.

An experiment was conducted to evaluate the effect of exogenous gonadotropin releasing hormone (GnRH) on ovulation and embryonic survival in pubertal gilts. Gilts were assigned in replicates to a control (n = 10) and treatment (n = 10) group. Treatment consisted of an iv injection of 200 micrograms of GnRH immediately after initial mating on the first day of detected estrus. Control gilts were similarly injected with physiological saline. Blood samples were collected from the anterior vena cava immediately prior to injection, thereafter at 15-min intervals for 90 min, and subsequently, before slaughter on d 30 of gestation. Serum samples were analyzed for luteinizing hormone (LH) and progesterone by radioimmunoassay. Treatment with GnRH increased the quantity of LH released (P less than .05), with highest serum concentrations (ng/ml, means +/- SE) of gonadotropin in treated gilts (17.3 +/- 3.5) occurring at 75 min post-injection. In control gilts, serum concentrations of LH were not affected by injection of saline. Mean number of ovulations in treated gilts was also greater (P less than .05) than that of control animals (14.5 +/- .7 vs 12.1 +/- .6). However, treatment with GnRH did not enhance the number of attached conceptuses (normal and degenerating) present (treated, 10.9 +/- .9 vs control, 10.5 +/- .7) nor the percentage of viable fetuses (treated, 74.7 +/- 6.9 vs control, 83.5 +/- 5.0%) on d 30 of gestation. Although GnRH increased ovulation rate, mean weight of corpora lutea of treated and control gilts did not differ (402.8 +/- 16.3 vs 389.5 +/- 11.3 mg, respectively).(ABSTRACT TRUNCATED AT 250 WORDS)

Factors contributing to early embryonic mortality in gilts bred at first estrus.

Gilts bred at first (n = 18) and third (n = 18) estrus were assigned in replicates of equal numbers to be slaughtered on d 3, 15 and 30 post-mating to assess fertilization rate, embryonic losses and serum concentrations of estrogen (estradiol-17 beta + estrone) and progesterone. Mean number of ovulations was lower among gilts bred at first vs third estrus (12.2 vs 14.5; P less than .05), with no difference in fertilization rate (100 vs 98%). Embryonic survival was lower (P less than .05) among gilts bred at first vs third estrus on d 15 (78.1 vs 95.4%) and 30 (66.7 vs 89.4%) of gestation. Serum estrogen (pg/ml) and progesterone (ng/ml) levels, although lower in gilts bred at first vs third estrus, were not significantly different at the three stages of gestation studied. The ratio of progesterone to estrogen in gilts bred at first estrus was higher than in those bred at third estrus on d 15 (439 +/- 71 vs 210 +/- 17) and 30 (597 +/- 106 vs 179 +/- 50), but was lower on d 3 (187 +/- 37 vs 444 +/- 123; stage of gestation X estrous period interaction, P less than .05). These data suggest that changes in the ratio of systemic levels of estrogen and progesterone may be related to early embryonic mortality in gilts bred at pubertal estrus.

Improving sow efficiency by management to enhance opportunity for nutritional intake by neonatal piglets.

Starvation, primarily during the first week postpartum, is the direct or indirect cause of at least one-half of preweaning mortalities in healthy herds. Causes of starvation originate from characteristics of the dam, of the litter and of individual piglets. A major cause of starvation is congenital weakness associated with birth weights less than 1000 g. Increasing energy during late gestation shows inconsistent effects on birth weight; some dietary component energy sources appear to improve stamina of newborn and(or) energy content of sow's milk with favorable effects on survival. Total or partial supplemental nutrient intake supplied by caretakers, automated feeding devices or transfer of piglets to foster dams are the primary means of providing enhanced nutrient intake opportunity. Nutrient intake from non-dam sources ranges from temporary tube-feeding, administered by caretakers to excessively small or weak pigs, to self-feeding by pigs from simple or sophisticated dispensers of sow milk substitutes. Transfer of piglets to foster dams as a nutrient intake source is most successful when characteristics such as size of dam, size of teats, stage of lactation and temperament are in harmony with characteristics affecting pigs' needs. If other dams are not available, sows 2 to 3 wk into lactation can serve as foster dams for large and strong newborn piglets after resident litters are removed. Planning for availability of appropriate foster dams, based on prior or projected prolificacy and other sow and litter traits, should be done at time of assembling each mating group. Research results show that, on a weight-to-weight basis, pigs requiring artificial or foster dam rearing perform similarly to other pigs and thus justify management to secure their survival.

Estrus, ovulation, conception and embryo survival in confinement-managed gilts of three weight groups.

Puberty, cycling, ovulation, conception and embryo survival were determined for gilts managed by a specific regimen in confinement. At weights of 70 to 80, 91 to 100 and 109 to 116 kg (groups A, B, C, respectively) gilts were (1) moved from rearing pens to pens in a separate broodstock building, (2) housed in groups of eight to 10 with unfamiliar penmates and (3) exposed to boar presence in an adjoining pen. Groups A and B were mated at third estrus; group C was mated at first estrus. For the three groups 76, 79 and 79%, respectively, of allotted gilts mated; of these 21, 13 and 11%, respectively, showed estrus again and were remated. Ten, 10 and 11%, respectively, were not pregnant when slaughtered at 25 to 28 d of postmating. Average days on experiment to first estrus were 14, 15 and 16 for groups A, B and C; mean interval between estrous periods was 21 d. Ovulations (13.3, 12.9 and 12.6) and live embryos (11.6, 11.1 and 10.7, respectively) did not differ significantly among groups. None of the reproduction traits were significantly associated with differences in mean age or weight among the three groups at breeding.(ABSTRACT TRUNCATED AT 250 WORDS)

Effect of Feeding Lactobacilli on the Coliform and Lactobacillus Flora of Intestinal Tissue and Feces from Piglets 1.

Development of fecal Lactobacillus and coliform in healthy newborn pigs during the first 48 h after birth was studied. Lactobacilli were detected (104 per g) in the feces of newborn pigs as early as 4 h after birth and colifroms by 8 h (105 per g). By 24 h the two types were present in near equal numbers (104 to 105/g). A frozen concentrate of a human isolate of Lactobacillus lactis was fed to piglet litters (8 to 10 animals per litter) from the time of their birth. Bottle feeding resulted in reduced fecal coliforms in nursing pigs but lactobacilli were not increased in number. After 54 days of treatment, the Lactobacillus to coliform ratio (L/C) was 1280:1; in control pigs not fed lactobacilli, the ratio was 2: 1. A continued suppression of coliforms was observed for 30 days after treatment was discontinued. The influence of Lactobacillus on the bacterial flora of the gastrointestinal tract was studied. With scouring pigs, enteropathogenic Escherichia coli (EEC) were present in larger numbers in tissue homogenates of the tract than in the lumen. The virulence of the EEC found prosent was confirmed by experimental infection in pigs. In control, nonscouring pigs only non-EEC were isolated from tissue sections. In Lactobacillus -fed pigs, E. coli was reduced to low numbers; also, the few E. coli observed were non-enteropathogenic. There were higher numbers of lactobacilli in tissue sections of Lactobacillus -fed pigs than in control and scouring pigs. The lactobacilli isolated from tissue homogenates of the treated animals resembled biochemically and serologically (fluorescent antibody staining) the Lactobacillus which was fed. Histological studies were done to observe the bacteria in frozen sections of washed intestine obtained from Lactobacillus -fed pigs; staining revealed large numbers of gram-positive bacilli. On the other hand, control pigs which died of scouring revealed many coliform types present. Pigs in groups receiving colostrum and lactobacilli did well; no evidence of diarrhea was seen and many lactobacilli were observed in tissue throughout the small intestine. Even after the challenge with EEC serotype 09:K:NM, these two groups of pigs did not show any signs of disease and few coliform types (cocco-bacillary forms) were observed. Pigs not receiving colostrum but only lactobacilli did not scour before challenge and many lactobacilli were present in tissue from the small intestine. However, 72 h after challenge these latter animals revealed symptons of diarrhea and coliforms were seen in the small intestine tissue in addition to lactobacilli.