Mature Gilts Research Articles

Influence of the number of microinjected embryos transfer-red, oestrus—Behaviour and body weight of the recipient on the success rate of a gene transfer programme in pig

The objective of this study was to assess the effect of various aspects of pronuclear DNA microinjection on the early development of porcine ova in utero. Estrus was synchronized and superovulation was achieved in sexually mature gilts by the administration of allyl trenbolone, PMSG and hCG. Donor gilts were bred at 12 and 24 h after the onset of estrus. Ova were recovered between 60 and 62 h after the administration of hCG. One-cell ova that exhibited pronuclei after centrifugation were randomly allocated in equal numbers from each donor across one of two pairs of treatments: micro-DNA (ova were injected with two gene constructs that code for the human complement regulatory proteins decay accelerating factor and membrane cofactor protein) and control (ova were centrifuged only) or micro-buffer (ova were injected with buffer only) and pierced (a pipette was inserted into one pronucleus). Ova were transferred by treatment pairs to recipients. Treatments were segregated by oviduct. Ova were recovered after 120 h in utero, fixed and stained with 1% orcein. The proportion of ova that possessed ≥80 nuclei, the mean number of nuclei present and proportion of ova that formed blastocysts were all significantly (P<0.05) greater for control and pierced ova than for micro-DNA and micro-buffer ova. No difference in these parameters was observed between micro-DNA and micro-buffer ova. These results demonstrate that pronuclear microinjection of a buffer alone can adversely affect the early development of porcine ova in utero.

Pulsatile administration of gonadotropin-releasing hormone agonist to gilts actively immunized against gonadotropin-releasing hormone.

Sexually mature gilts (n = 20) were actively immunized against GnRH. Primary and booster immunizations of GnRH conjugated to bovine serum albumin induced production of antibodies in all gilts. Nineteen of the gilts became acyclic with suppressed concentrations of gonadotropins and estradiol. Intravenous challenges with 100 micrograms GnRH and 5 micrograms D-(Ala6, des-Gly-NH2(10)) ethylamide GnRH (a GnRH agonist that did not cross-react with antibodies produced by the gilts) caused release of LH and FSH, indicating maintenance of secretory capacity of pituitary gonadotropes in the immunized animals. Gilts were given 100 ng GnRH agonist at 2-h intervals for 72 h (n = 4) or 144 h (n = 10) or did not receive agonist (n = 5). Blood samples were taken every 6 h, and detectable concentrations of LH were observed in 42% and 52% of samples taken from gilts treated with or without agonist. In contrast, serum concentrations of FSH and estradiol were undetectable. Reproductive tracts and anterior pituitaries were taken from gilts at the conclusion of pulsatile administration of GnRH agonist or at 144 h for controls. Pituitary concentration of LH and FSH, uterine wet and dry weight, and size of the uterus were similar among groups. Paired ovarian weights for treated gilts pulsed with GnRH agonist for 72 h were heavier (P less than .05); however, ovaries from all immunized gilts were atrophied without follicular structures.(ABSTRACT TRUNCATED AT 250 WORDS)

The effects of zearalenone on reproduction in swine. I. The relationship between ingested zearalenone dose and anestrus in non-pregnant, sexually mature gilts

Ninety-nine sexually mature, non-pregnant gilts were checked for estrus daily with a mature boar and then allocated at estrus (D O) to receive 2 kg/d of a diet containing 0, 1, 5 or 10 ppm purified zearalenone between D 5 and 20 of the estrous cycle during two seasons of the year (winter and summer). None of the gilts exhibited any visual signs of “hyperestrogenism” and there was no effect of season on interestrous interval (P > 0.05). A significant effect of zearalenone dose on inter-estrous interval was detected (P < 0.001). Gilts receiving 0 or 1 ppm had similar inter-estrous intervals (21.0 ± 0.3 and 21.5 ± 0.8 d, respectively) whereas gilts receiving 5 and 10 ppm had extended cycles (29.2 ± 2.9 and 32.7 ± 3.3 d, respectively). Plasma progesterone concentrations at D 19 to 21 were higher in gilts with extended cycles (P < 0.001) and corpora lutea (CL) were present at laparotomy. Some 86% of these retained CL underwent spontaneous regression resulting in the onset of estrus within the next 30 d. Fecal zearalenone concentrations rose during ingestion of contaminated diets and declined to pretreatment values within 2 d (1 ppm) to 8 d (10 ppm) of the cessation of treatment. These data show that feeding zearalenone at concentrations of 5 to 10 ppm from D 5 to 20 of the estrous cycle causes luteal maintenance and extended inter-estrous intervals. Spontaneous regression of these CL usually occurs within 30 d after zearalenone is removed from the diet. Fecal zearalenone analysis does not appear to be an effective method for determining prior exposure to zearalenone when carried out more than a few days following the last ingestion of zearalenone.

Low concentrations of zearalenone in diets of mature gilts.

Four groups of sixteen gilts were each individually fed diets containing 0, 3, 6 or 9 ppm pure zearalenone starting the day after they exhibited puberal estrus. They were artificially inseminated twice at subsequent heat periods. Fifteen of the 30 gilts not exhibiting estrus within 80 d of the start of the experiment were slaughtered and their reproductive tracts examined. The remaining 15 gilts that did not return to estrus were fed the control diet after 80 d to determine the effect on return to estrus. Eighty-eight percent of the gilts fed 6 or 9 ppm zearalenone became pseudopregnant as confirmed by plasma progesterone levels and(or) examination of their reproductive tracts. However, three animals fed the two higher levels of zearalenone conceived and farrowed. No conclusions can be made regarding the effect of zearalenone on litter size due to the relatively few numbers of gilts fed the higher levels of zearalenone that farrowed. Gilts fed diets containing 6 or 9 ppm zearalenone returned to estrus spontaneously (n = 7) or following injection of cloprostenol (n = 8) approximately 45 d after the removal of zearalenone from their diet.

Utero-ovarian venous concentrations of prostaglandin E 2 (PGE 2 and prostaglandin F2α ( PGF2α) following PGE 2 intrauterine infusions

The uterine horns and utero-ovarian veins of nine crossbred mature gilts were bilaterally cannulated on day 9 of the estrous cycle (day 0 - first day of estrus). Each uterine horn in treated gilts (N=5) was infused with 150 μg PGE 2 in 3 ml of saline at 0900 h on day 12, 15 and 18 of the estrous cycle. Control gilts ( N=4) received 3 ml saline intrauterine infusions on the corresponding day. Blood samples were collected from the utero-ovarian veins 15 min before each infusion and for the following 6 h with 15, 30 and 60 min intervals through the first, second and third two-hour periods, respectively. Venous concentrations of PGE 2 and PGF 2 α were determined by radioimmunoassay procedures. Infusion of PGE 2 resulted in an immediate elevation in PGE 2 concentration in utero-ovarian venous drainage. Coincident elevations of PGF 2 α utero-ovarian venous concentrations were observed after PGE 2 infusion. Plasma PGF 2α concentrations in the utero-ovarian veins were elevated (P<.01) in PGE 2 treated gilts for one hour post-treatment. The duration of PGE 2 and PGE 2 α elevations as well as the peak values were influenced by day of the cycle.

Active immunization of gilts against gonadotropin-releasing hormone: effects on secretion of gonadotropins, reproductive function, and responses to agonists of gonadotropin-releasing hormone.

Sexually mature gilts were actively immunized against gonadotropin-releasing hormone (GnRH) by conjugating GnRH to bovine serum albumin, emulsifying the conjugate in Freund's adjuvant, and giving the emulsion as a primary immunization at Week 0 and as booster immunizations at Weeks 10 and 14. Antibody titers were evident by 2 wk after primary immunization and increased markedly in response to booster immunizations. Active immunization against GnRH caused gonadotropins to decline to nondetectable levels, gonadal steroids to decline to basal levels, and the gilts to become acyclic. Prolactin concentrations in peripheral circulation were unaffected by immunization against GnRH. The endocrine status of the hypothalamic-pituitary-ovarian axis was examined by giving GnRH and two agonists to GnRH and by ovariectomy. An i.v. injection of 100 micrograms GnRH caused release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) in control animals, but not in gilts immunized against GnRH. In contrast, administration of 5 micrograms D-(Ala6, des-Gly-NH2(10] ethylamide or 5 micrograms D-(Ser-t-But6, des-Gly-NH2(10] ethylamide resulted in immediate release of LH and FSH in both control and GnRH-immunized gilts. Circulating concentrations of LH and FSH increased after ovariectomy in the controls, but remained at nondetectable levels in gilts immunized against GnRH. Prolactin concentrations did not change in response to ovariectomy. We conclude that cyclic gilts can be actively immunized against GnRH and that this causes cessation of estrous cycles and inhibits secretion of LH, FSH, and gonadal steroids.(ABSTRACT TRUNCATED AT 250 WORDS)

Regression of induced corpora lutea by human chorionic gonadotropin in prepuberal gilts.

The effect of daily injections of human chorionic gonadotropin (HCG) on luteal maintenance in hysterectomized prepuberal gilts induced to ovulate and in hysterectomized mature gilts was studied. Twenty-four pre-puberal gilts, 120 to 130 d of age, were induced to ovulate with 1,000 IU pregnant mare serum gonadotropin followed 72 h later with 500 IU HCG. Nine of the 24 prepuberal gilts (bred controls) were artificially inseminated on d 0 (d 0 = d after HCG). Mature gilts that had displayed one or more estrous cycles of 17 to 22 d were used (d 0 = onset of estrus). All gilts, except the bred controls, were totally hysterectomized on d 6 to 9 and their corpora lutea (CL) marked with charcoal. From d 10 through 29, eight prepuberal and 10 mature hysterectomized gilts received daily injections of 500 IU HCG in saline while seven prepuberal and eight mature hysterectomized gilts received daily injections of saline vehicle. Jugular blood samples were quantitated by radioimmunoassay for estrogen and 13,14-dihydro-15-keto prostaglandin F2 alpha (PGFM), a metabolite of prostaglandin F2 alpha. One bred control gilt was pregnant on d 30, indicating that the prepuberal gilts used in the experiment were prepuberal. All mature gilts and six of seven prepuberal gilts that received saline had maintained CL to d 30. Eight of 10 mature gilts that received HCG had maintained CL to d 30, while only two of eight (P less than .05) prepuberal gilts that received HCG maintained CL to d 30. All gilts receiving HCG had numerous follicles and accessory luteal structures.(ABSTRACT TRUNCATED AT 250 WORDS)

Inhibition of pregnancy with indomethacin in mature gilts and prepuberal gilts induced to ovulate.

Twenty prepuberal (P) gilts, 56.5 +/- 1.1 kg body weight, were induced to ovulate with 1000 IU of pregnant mare's serum gonadotropin followed 72 h later by 500 IU of human chorionic gonadotropin (hCG), and bred by artificial insemination (AI) with 50 ml fresh pooled boar semen the day after hCG treatment (Day 0). Eighteen mature (M) gilts, 120.6 +/- 1.7 kg body weight, were bred by AI each day of estrus using pooled semen from the same boars (onset of estrus = Day 0). One-half of each group was fed the prostaglandin (PG) synthesis inhibitor indomethacin (IND), at 10 mg/kg body weight, or control (C) feed twice daily on Days 10 to 25. Blood samples taken by venipuncture on Days 10, 15, 20 and 25 were quantitated for progesterone (P4) and 13,14-dihydro-15-keto-PGF2 alpha (PGFM) by radioimmunoassay. Ovaries were examined on Day 26. All M-C gilts were pregnant, whereas 3 of 9 M-IND gilts (P less than 0.05) and none of the P gilts (P less than 0.01) were pregnant. Three of the 6 nonpregnant M-IND gilts displayed estrus on Day 21. The 3 remaining M-IND gilts had maintained corpora lutea (CL) on Day 26. Only corpora albicantia were present in P gilts on Day 26. Serum P4 concentrations for M-C gilts, nonpregnant M-IND gilts with maintained CL, and pregnant M-IND gilts were not different. Serum P4 for all nonpregnant gilts in which CL had regressed by Day 25 decreased to less than 5 ng/ml on Day 20.(ABSTRACT TRUNCATED AT 250 WORDS)

An evaluation of the erythrocyte glutamate-oxaloacetate Transaminase activity coefficient as a biochemical indicator Of vitamin B-6 status in mature gilts

An experiment was conducted to evaluate the erythrocyte glutamate-oxaloacetate transaminase activity coefficient (EGOT-Ac) as a biochemical indicator of vitamin B-6 status and to document clinical effects of a B-6 deficiency in mature swine. A 12% crude protein diet, formulated with cornstarch and an isolated soy protein, was analyzed to contain .24 ppm B-6. Sixty-one gilts, initially averaging 111 kg, were individually fed 1.9 kg daily of a diet providing .45, 1.8, or 90 mg B-6/d (treatments (Trt) 1, 2 and 3, respectively). In addition, another group of gilts was fed 90 mg B-6 for the initial 57 d then switched to the diet providing .45 mg B-6 for the remainder of the experiment (Trt 4). On d 0, 57 and 121 animals from each Trt were killed and samples of the semitendinosus (ST) and semimembranosus (SM) were collected. Following a 24-h chill, the entire SM and ST were dissected from the carcass and weighed Blood was sampled on d 0 and monthly thereafter. The EGOTAc was determined by measuring the glutamate-oxaloacetate transaminase (GOT) activity in isolated, hemolized erythrocytes with and without pyridoxal phosphate added to the reaction mixture.

Reproductive development in young boars exposed to sexually mature, nonpregnant sows and gilts

Thirty Yorkshire boars were allotted by litter to one of two treatment groups. Fifteen boars were reared, from 14 to 22 wk of age, in fenceline contact with mature sows and gilts that were randomly exhibiting estrus. Fifteen littermates of these boars, reared without exposure to females, served as controls. Boar-to-boar sexual behaviors were observed 1 hour daily from 16 to 22 wk of age. At ages 14 to 30 wk, boars were weighed at 4-wk intervals. Five boars per treatment were slaughtered when 22 wk old and twelve others (six per treatment) when 30 wk old. Vesicular gland, bulb of the prostate gland, bulbourethral gland, and each testis, cauda epididymis, and combined caput and corpus epididymis were closely trimmed and weighed. Left cauda epididymal sperm and left testis elongated spermatids were determined by homogenization and hemacytometer counting. At 26, 30, and 38 wk of age, boars were tested for mating efficiency by exposure to an estrous gilt. Boars exposed to females tended to be lighter at 22 wk and were lighter at 30 wk (P<.05). Total male-to-male sexual acts from 16 to 22 wk were correlated with mating-efficiency score at 26 and 30 wk (r = .69 and .68, respectively; (P<.05)). Correlation between testicle size and total testicle elongated spermatids was high at 30 wk of age (r = .92; P<.001). Results indicated that exposing young boars to mature females had limited effects on the boars' reproductive development; however, there were strong indications of a relationship between boar behavior during rearing and postpuberal mating performance.

Absorption of [formula omitted][formula omitted] endotoxin from the small intestines of mature non-pregnant gilts

The small intestines of 31 mature crossbred gilts were infused with Escherichia coli endotoxin through permanent jejunostomies. A total of 86 infusions were done. The endotoxin was absorbed after 4 infusions. Evidence of absorption included variations in body temperatures, decline in white blood cell counts, detection of the endotoxin in circulating blood plasma samples by a limulus amebocyte lysate gelation test, and abnormal clinical signs. E. coli endotoxin placed in the small intestines of normal, healthy, mature gilts does not readily cause illness.

Estrus and ovulation in gilts fed a synthetic progestogen

A synthetic progestogen, allyl trenbolone (AT), was fed to sexually mature gilts to determine the effective doses for the control of estrus and ovulation. Gilts were assigned to a control group and 5 treatment groups receiving 10.0, 12.5, 15.0, 17.5 or 20.0 mg of AT mixed in .45 kg of feed/head/day for 18 consecutive days. Ovarian morphology was determined by laparotomy following estrus or at 10 days post-treatment. AT suppressed estrus in all gilts during treatment. Estrus was effectively synchronized in treated gilts. The average interval from withdrawal of progestogen treatment to estrus was 4.5 days for 48 of 50 treated gilts that were in estrus within 10 days after treatment. The average ovulation rate in treated gilts was similar to control gilts. No detrimental side effects, due to treatment, were observed with the possible exception of a slight increase in the incidence of cystic follicles.

Lipid metabolism and [formula omitted] production of progesterone and prostaglandin F during induced regression of porcine corpora lutea

The effects of Cloprostenol administration on porcine luteal lipid and arachidonic acid accumulation were examined in relation to luteal in vitro progesterone and prostaglandin F synthesis in 18 mature gilts at day 12 of the estrous cycle. Basal and net in vitro release of progesterone from luteal tissue was depressed at 8 hr after treatment whereas net in vitro release of prostaglandin F was elevated at 8 hr. Inclusion of copper dithiothreitol or reduced glutathione in the incubation media resulted in minor alterations of in vitro release of progesterone and prostaglandin F and no changes in composition of luteal lipids or fatty acids. Luteal contents of triglyceride had increased by 8 hr after treatment whereas contents of free and esterified cholesterols had increased by 32 hr after Cloprostenol administration. Luteal contents of phospholipid and free fatty acids were not affected by Cloprostenol administration. At 32 hr after treatment, percentages and content of arachidonic acid had increased in luteal cholesterol esters and triglycerides. Although arachidonic acid percentages increased in luteal free fatty acids and phospholipids, calculated arachidonic acid contents did not change following Cloprostenol administration. Induced luteal regression was associated with decreased in vitro progesterone release, increased in vitro prostaglandin F release, and accelerated lipid and arachidonic acid accumulation within the corpus luteum. The effects of altered lipid metabolism on release of prostaglandin F could not be defined. However, availability of arachidonic acid did not appear to be rate-limiting in relation to luteal in vitro prostaglandin F synthesis.

Prostaglandin F concentrations in utero-ovarian vein plasma of prepuberal and mature gilts

Prostaglandin F (PGF) and progestins in utero-ovarian vein (UOV) plasma during the late luteal phase of the estrous cycle in unbred mature gilts and following induced ovulation in unbred prepuberal gilts were determined. Prepuberal gilts (120 to 130 days of age) were induced to ovulate with Pregnant Mare Serum Gonadotropin and Human Chorionic Gonadotropin (HCG). The day following HCG was designated as Day 0. Mature gilts which had displayed two or more estrous cycles of 18 to 22 days (onset of estrus = Day 0) were used. Polyvinyl catheters were inserted into the UOV of all gilts and blood was collected at 15 min intervals from 0800 to 1045 hr on Days 10 through 20 or Days 12 through 18. Plasma PGF concentrations in the mature gilts were elevated on Days 13, 14, 15, 16 and 17, whereas, plasma PGF concentrations in the prepuberal gilts were elevated only on Days 15, 16 and 17 resulting in a reproductive age (mature vs prepuberal) by day interaction ( P<.01). In addition, the PGF concentrations on Days 13 through 17 were consistently greater in the mature gilts than in the prepuberal gilts as was the overall mean PGF concentration (1.95 vs .83 ng/ml). The average peak PGF concentration throughout the sampling period (4.6 vs 2.5 ng/ml; P<.01) and the average peak PGF concentration prior to luteal regression (3.8 vs 1.1 ng/ml; P<.05) were also greater in the mature than in the prepuberal gilts. Based on these results, we suggest that luteal regression in the bred prepuberal gilt following induced ovulation may not be due to an excessive production of the uterine luteolysin, but rather that the induced corpora lutea (CL) of the prepuberal gilt may be more sensitive to the uterine luteolysin than the spontaneously formed CL of the mature gilt.

Corpus luteum susceptibility to prostaglandin F 2α (PGF 2α) luteolysis in hysterectomized prepuberal and mature gilts

The susceptibility of induced corpora lutea (CL) of prepuberal gilts and spontaneously formed CL of mature gilts to prostaglandin F 2α (PGF 2α) luteolysis was studied. Prepuberal gilts (120 to 130 days of age) were induced to ovulate with Pregnant Mare Serum Gonadotropin and Human Chorionic Gonadotropin (HCG). The day following HCG was designated as Day 0. Mature gilts which had displayed two or more estrous cycles of 18 to 22 days were used (onset of estrus = Day 0). Gilts were laparotomized on Day 6 to 9, their CL marked with sterile charcoal and totally hysterectomized. On Day 20, gilts were injected IM with either distilled water (DW), 2.5 mg PGF 2α or 5.0 mg PGF 2α. An additional group of prepuberal gilts was injected with 1.25 mg PGF 2α, a dose of PGF 2α equivalent, on a per kilogram body weight basis, to the 2.5 mg PGF 2α dose given to the mature gilts. The percentages of luteal regression on Day 27 to 30 for mature and prepuberal gilts given DW, 2.5 mg PGF 2α and 5.0 mg PGF 2α were 0.0 vs 4.4, 43.5 vs 96.8 and 47.7 vs 91.6, respectively; the percentage of luteal regression for the prepuberal gilts given 1.25 mg PGF 2α was 75.1. These results indicate that induced CL of the prepuberal gilt were more susceptible to PGF 2α luteolysis than spontaneously formed CL of the mature gilt and that pregnancy failure in the prepuberal gilt could be due to increased susceptibility of induced CL to the natural luteolysin.

Intraperitoneal insemination, sperm transport and capacitation in the pig

Intraperitoneal insemination was studied in a total of 58 pigs, both to ascertain the success of this route of sperm deposition with the eventual use of frozen-thawed boar semen in mind and to estimate the timing of capacitation in the absence of uterine exposure of spermatozoa. Ovulation was controlled in mature gilts, and 5–20 ml freshly collected semen containing approximately 10 8 spermatozoa per ml introduced through the peritoneum either by means of mid-ventral laparotomy or using a 3.5-in (ca. 9 cm) × 18-gauge hypodermic needle. Embryo development to the morula and blastocyst stage appeared chronologically and cytologically normal after intraperitoneal insemination, but the timing of semen deposition was critical: optimal levels of fertilization (60%) arose from insemination in the 12 h preceding ovulation. Fertility was never comparable to that found after natural mating due to the inefficiency of sperm transport into the oviducts and the absence of significant sperm reservoirs. The timing of sperm capacitation after intraperitoneal insemination was not reduced when compared with that found after insemination directly into the oviducts, indicating a negligible contribution of peritoneal exposure to this process. Spermatozoa were not phagocytosed in the oviducts, but rather descended to the uterus at the same time as the developing embryos or degenerating eggs, the sperm flagellum usually being separated from the head by this stage.

Corpus Luteum Function following Subtotal Hysterectomy in the Prepuberal Gilt

SUMMARY The effect of subtotal hysterectomy- on maintenance of induced corpora lutea (CL) in prepuberal gilts, 120 to 130 days of age, was studied. Ovulation was induced with 1,000 IU Pregnant Mare Serum Gonadotropin (PMSG) followed 72 hr later with 500 IU Human Chorionic Gonadotropin (HCG). Thirteen gilts (bred controls) were inseminated on Day 0 (Day following HCG=Day 0). Fifty gilts were laparotomized on Days 6 through 9, their CL marked with charcoal and the gilts subtotally hysterectomized so that the amount of cervix and uterus left intact was: group 1 (n=13), posterior half of cervix; group 2 (n=12), cervix and posterior half of the uterine body; group 3 (n=12), cervix and uterine body; group 4 (n=13), posterior half of cervix and anterior 15% of one uterine horn. At necropsy (Day 30), three bred control gilts were pregnant while the ovaries of the remaining controls had only corpora albicantia (CA) present. The percentage of CL maintained to Day 30 for groups 1 through 4 were, respectively; 85.7, 65.9, 37.1 and 31.2. Based on these results, we suggest that, unlike mature gilts in which at least 25% of one uterine horn must be present to cause luteal regression and in which the presence of only the uterine body fails to cause luteal regression, as little as 15% of one uterine horn or the uterine body left intact will cause regression in the prepuberal gilt.

Development of capacity to secrete progesterone-induced protein by the porcine uterus.

Prepubertal gilts at various ages were treated for 15 days with gonadal steroids (estradiol and progesterone). On Day 15 the uteri were flushed with buffered saline to recover the secreted protein. The protein recovered was quantitated and analyzed by polyacrylamide gel electrophoresis. In a series of experiments it was found that gilts do not possess the ability to respond to exogenous gonadal steroids by secreting a complete adult pattern of uterine specific proteins until about 140 days of age. A partial pattern of uterine specific proteins was observed from about 112 days of age. This indicates that the ability to secrete all uterine specific proteins is not developed at the same time, but rather occurs during the period from 4 to 5 months of age. Even when gilts were able to secrete the entire pattern, the quantity of induced protein was normally much less than that in mature gilts.

Plasma hormone levels and fertility in pigs induced to superovulate with PMSG.

Summary. Seventy-one mature gilts were allocated to a 3×2×2 factorial experiment consisting of three doses of PMSG (0, 600 or 1200 i.u.), two levels of food intake on the 1st day of oestrus (none or double the normal daily amount of food), and two times of autopsy after mating (Day 6 or Day 24). The PMSG was administered by a single subcutaneous injection on Day 15 of the oestrous cycle and animals were mated on the first 2 days of the subsequent oestrus. Blood samples were collected in order to assess the effects of PMSG and superovulation on the secretion of oestrogen, LH, and progesterone. Ovulation rate was significantly increased by PMSG treatment (P≤0·001) but was not affected by food intake at oestrus. The number of normal embryos at slaughter on Day 6 or Day 24 after mating was significantly increased by PMSG treatment compared to that in the control animals, but embryonic losses by Day 24 were greatly increased in the gilts treated with PMSG. The plasma oestrogen concentration before oestrus was increased by PMSG treatment. The magnitude of the LH surge on the 1st day of oestrus was not affected by PMSG, but oestrus and the preovulatory LH surge were advanced by about 1 day. Mean plasma progesterone concentrations after mating were increased by PMSG treatment.

Developmental Abnormalities of Female Sexual Organs in Swine

One thousand reproductive organs from gilts were collected during the period March-August at a slaughterhouse in central Sweden. The organs were inspected in respect of congenital defects and certain reproductive physiological data. The results are recorded in Tables 1–6. Figs. 1–7 show some types of malformations. The total frequency of malformations was 22.1 %, of which 14 % cysts in mesosalpinx and 4.1 % partial duplication of the vagina. The remainder consisted of general developmental defects and of local defects in the tubular genital tract. Malformations with presumed effect on fertility were found in 4.5 % of all organs examined, of which 0.8 % presumably caused permanent sterility and 3.7 % lowered fertility (small litters). Hydrometra was found in 33 cases, 2 of which in sexually mature gilts. The left ovary contained more corpora lutea than the right, and the mean weight of the left ovary was greater than that of the right, both in sexually mature and prepuberal gilts. Of 202 sexually mature gilts examined 16.9 % had cystic corpora lutea in their ovaries as a rule 2–4 in each ovary.