The dose precision of PMSG in young and old sows in the process of biotechnical ovulation synchronization. 1. Comparison of diagnostic laparotomy

Treatment was applied, on two farms, to 272 gilts and 169 adult sows, 24 hours after discontinuation of Suisynchron application to the gilts or weaning of piglets of adult sows. Included were 600, 800 or 1,000 IU of PMSG for the gilts and 750, 1,000 oder 1,250 IU of the same batch (Pregmagon-Dessau) for the adult sows for ovarian stimulation. This was followed by application of 500 IU of HCG to the gilts or 300 micrograms Gn-RH vet. "Berlin-Chemie" + 300 IU HCG to the adult sows for synchronised ovulation. Laparotomy was performed on the gilts on the fifth day from PMSG application and on the adult sows on the fourth day. Average ovariotropic stimulation was "mild" in response to lower doses (14.8 follicles in gilts and 20.4 follicles in adult sows) but was "pronounced" in response to medium doses (19.4 or 22.7 follicles, respectively). The pharmacological concept of "mild" exogenic ovarian stimulation by low dosage at the threshold of effectiveness should deserve more attention, last but not least, for breeding aspects. The two groups of animals on both farms differed considerably from one another with regard to reactivity, which cannot be etiologically interpreted for the time being.     

The dose precision of PMSG for gilts and old sows in procedures for ovulation synchronization. 2. Organometric and histometric findings after diagnostic slaughtering

An account is given in this paper of organometric and histometric findings obtained, on three farms, N, B, and D, from ovaries, uteri, and oviducts of biotechnologically treated gilts and adult sows, using differentiated PMSG doses (600, 800, and 1,000 IU on gilts and adult sows of N and B; 500, 1,000, and 1,500 IU on gilts of D). Ovulation potentials were within the biological normal in response to low dosage (with an average of 12 to 15 follicles in gilts and 17 in adult sows). The 800 IU dose caused significant stimulation, which had to be interpreted as overstimulation for PMSG-sensitive probands of N. Ovarian reaction and induced cycle should by duly considered for interpretation of histometric findings.     

Experimental studies on the stimulation of prenatal development in swine by PMSG treatment in early pregnancy. 1. Clinical results of embryonic development in young slaughtered sows and litter results in young and old sows after PMSG treatment on the 11th day of pregnancy

Thirty-eight gilts were slaughtered on the 25th and 39th days of pregnancy, after they had received 400 I.U. PMSG treatment on the eleventh day of pregnancy. Treated and untreated animals in a group of 140 gilts and 195 adult sows were compared with each other for post-farrowing fertility performance. Weight development of embryos obtained from the slaughtered sows depended on the number of embryos alive. The survival rate of embryos from treated sows was about 5% higher than that recorded from untreated animals. Clearly increased litter sizes which, however, were associated with lower piglet birth weights were recorded from farrowing gilts and adult sows, following PMSG treatment. The conclusion is drawn that PMSG treatment, via luteotrophic action of luteinising hormone, is capable of stabilising pregnancy-related corpora lutei, resulting in higher litter sizes. Further studies will be necessary, and emphasis will have to be laid on the problem of weight development of newborn piglets, following litter-size boosting treatment.     

不同质量标准血促性素对杜长大后备母猪排卵数和繁殖性能的影响

血促性素（PMSG）是母猪繁殖调控的重要激素,文章采用效价为220单位/mg和2 580单位/mg PMSG,对后备母猪排卵数和繁殖性能影响进行了研究。高效价试验组与低效价对照组对杜长大后备母猪排卵数影响的试验中,静立发情率和排卵率虽有增高趋势,但差异不显著;平均每头母猪排卵数增加1.47枚,差异显著。高效价试验组与低效价对照组的定时输精试验中,待配分娩率提高11.27个百分点,差异显著;试验组的窝产总仔数和活仔数比对照组分别提高了0.39头和0.69头,差异均显著;试验组的窝产死胎数比对照组虽减少了0.30头,但差异不显著。     

Clinical study results of the embryonic development in gilts and brooding performance of gilts and sows after HCG treatment on the 11th day of pregnancy

Forty-four pregnant gilts were slaughtered on the 32nd and 33rd days of pregnancy, after 30 of them had received 100 or 400 IU of HCG on the eleventh day of pregnancy. Both doses had resulted in higher number of living embryos. Embryo survival rates of treated sows were up to 14.9 percent higher than those of untreated animals. Higher numbers of embryos had no adverse effect on their mass development. Fertility was measured of 77 HCG-treated and untreated gilts as well as of 54 adult sows. The number of non-pregnant sows which returned to oestrus was higher in the group of gilts and adult sows which had received treatment. The number of pregnant animals in the treated adult sow group was seven percent higher than that in the control group. Increased litter sizes were additionally recordable from those gilts and adult sows that had received HCG injections. Yet, those higher litter sizes were associated with lower weight of live-born piglets. In further studies more attention should be given to possible stimulation of LH secretion in early gravidity.     

Studies on the modification of sexual and breeding maturity in swine using gonadotrophic hormone preparations

Injection of low doses of PMSG-HCG gonadotrophin mixes to intensively raised prepuberal gilts, aged six months, stimulated sexual juvenile development prior to breeding use, the average being 255 days. First insemination of the test animals, following synchronisation of oestrus or ovulation, increased live births by 0.5 piglets per litter over the untreated controls. More controlled production experiments to test the new bioengineering approach are in preparation.     

The effect of various doses HCG on ovulation stimulation in gilts following previous biotechnical puberty induction

The effects of various doses of human chorionic gonadetropine (HCG) to stimulate ovulation in 86 gilts in which puberty had been induced by administration of 500 IU of pregnant mare serum (PMS) and 250 IU of HCG were established by slaughter. Only 26.9 per cent of the group without HCG had completed ovulation 120 hours from puberty induction, but 93.5 per cent had done so in the group which had received additional 500 IU or HCG 78 hours after the PMS/HCG injection. Ovulation was completed by 71.4 per cent of those sows which had been stimulated, using 250 IU of HCG. More accurate timing of ovulation in animals of one and the same group can be helpful in better insemination timing.     

Estrus and ovulation synchronization in Merino meat sheep. 2. Fertility outcome after estrus and ovulation synchronization with Cloprostenol "Jenapharm" and Gonovet "Berlin-Chemie" and term-oriented artificial insemination]

49 of 102 sheep of one production herd, which had returned to oestrus once or twice within the 1985 breeding season, were treated twice in a nine-day interval with the PGF2 alpha analogue Cloprostenol "Jenapharm". 53 animals received an additional dose of 10 micrograms of Gonavet "Berlin-Chemie". A lambing rate of merely 15% was achieved by subsequent term-oriented artificial insemination. 31 sheep still in oestrus one day after term-oriented artificial insemination were served, bringing the lambing rate from synchronisation of oestrus and ovulation to 26% and the lambing result to 154%. Serving of the remaining sheep in 2 subsequent oestric cycles, on balance, yielded lambing rates and results of the remaining sheep in 2 subsequent oestric cycles, on balance, yielded lambing rates and results which were higher with significance than those recorded from untreated sheep in the same herd.     

Conclusions on the use of Suisychron in the USSR

Suisynchron was applied to 2,258 gilts, including 850 from breeding farms. Forty-four pigs were checked to elucidate the influence of sexual maturity on the success of oestrus synchronisation. Suisynchron-Pr?mix was fed to the animals over 20 days, the daily dose for each pig having been 5 g. Twenty-four hours were allowed to elapse from the last administration before 1,500 I.U. PMSG were injected. Synchronised oestrus occurred in 81.2 per cent of all pigs between four and six days from serum injection.Fertilisation in response to first insemination was recorded from 72.9 percent of the pigs, their fertility rate being 9.7 piglets from each farrowing sow. The results of oestrus synchronisation obtained from fattening pigs were somewhat inferior to those recorded from pigs of breeding units. Suisynchron and serum of pregnant mares can synchronise oestrus in 91 per cent of all mateable sows with no previous cycle. The fertility rates recorded from such pigs did not exceed 59 per cent or were between 28.9 and 31.9 per cent lower than those recordable from pigs with a cycle history prior to the use of Suisynchron.     

The Duration of Ovulation in GnRH-Treated Gilts Following Seminal Plasma Infusion

Contents: The relationship between seminal plasma infusion and ovulation time in GnRH-treated gilts was investigated. Following oestrus synchronisation with Regumate (Roussel Uclaf) and PMSG (Pregmagon Dessau) 14 gilts were injected with 75 μg GnRH (Gonavet "Berlin-Chemie") 80 h after PMSG. Seven gilts received an additional intracervical infusion of 80 ml seminal plasma 16 h after GnRH. The laparoscopic observation of follicular development and ovulation started 24 h after GnRH injection in 6 to 1.5 h intervals up to the completion of ovulation. The mean interval between GnRH and completion of ovulation was 40.1 1.6 h in gilts treated with seminal plasma and 40.8 0.7 h in control gilts. There was no additional seminal plasma related effect on the advancement of ovulation compared to GnRH only.     

Effect of Insemination–Ovulation Interval and Addition of Seminal Plasma on Sow Fertility to Insemination of Cryopreserved Sperm

In swine, the use of frozen-thawed (FT) sperm for artificial insemination (AI) is limited because of poor sow fertility, possibly associated with a post-thaw capacitation-like status resulting in fewer fully viable sperm. Sow fertility to AI with FT sperm may improve with deeper deposition of sperm within the female tract, insemination very close to ovulation, or reversal of cryocapacitation by seminal plasma (SP). We performed two experiments to examine these suggestions. In experiment 1, 122 multiparous Yorkshire sows received 600 IU equine chorionic gonadotrophin at weaning and 5 mg pLH 80 h later to control time of ovulation. The predicted time of ovulation (PTO) was 38 h after pLH injection. Thereafter, sows were assigned on the basis of parity to a single AI of FT sperm at 2 h before PTO, or at 12 h before PTO, or FT sperm supplemented with 10% SP at 12 h before PTO. Control sows received fresh semen at 12 h before PTO. All semen doses were adjusted to 3 x 10(9) live cells and deposited into the cervix. Experiment 2 employed 99 multiparous crossbred sows and repeated the treatments of experiment 1 except that all FT inseminations were intrauterine. In both experiments, farrowing rates were lower (p < 0.01) following FT inseminations with no effect of time of insemination or of supplemental SP. In experiment 1, litter size was smaller following FT insemination (p < 0.05), but no effect on litter size was evident in experiment 2. Supplemental SP had no effect on litter size in either experiment. The lack of effect of either SP or timing of FT insemination on sow fertility suggests that the non-lethal sperm cryoinjury affecting fertility involves more than just cryocapacitation.     

Improving ovulation in gilts using anti-inhibin serum treatment combined with fixed-time artificial insemination

For successful batch farrowing, porcine oestrus and ovulation must be synchronized using fixed-time artificial insemination (FTAI). However, exogenous gonadotropins, which are currently used in FTAI, negatively affect gilt ovulation. Here, we aimed to improve sexually mature gilt superovulation efficiency using passive immunization against inhibin during FTAI. Altrenogest-treated gilts were challenged with 10 ml anti-inhibin serum (AIS group, n = 6), 1,000 IU pregnant mare serum gonadotropin (PMSG group, n = 6), or 10 ml goat serum (control group, n = 6). Gilts in the AIS and PMSG groups were inseminated according to the FTAI protocol, and gilts in the control group were inseminated during natural oestrus. When PMSG was replaced by AIS during FTAI of gilts, ovulation rate and embryos recovered were significantly greater in the AIS group as compared to the other two groups (p < .05). Especially the average number of 6–8-cell embryos in the AIS group was significantly higher than that in the PMSG group (p < .01). Moreover, the blastocyst number in the AIS group was significantly higher than that in the PMSG group and the control group (p < .05). But there was no significant difference in the blastocyst number between the PMSG group and the control group (p > .05). Besides, plasma levels of estradiol-β (E2) and progesterone (P4) were significantly greater in the AIS group as compared to the other two groups on Day 23 and D 27, respectively (p < .01). In summary, we devised an improved high-yield FTAI protocol for sexually mature gilts using AIS; this protocol had a greater superovulation efficiency than the FTAI using PMSG.     

Litter Size and Vagina–cervix Catheter Penetration Length in Gilts

As in other species, the reproductive tract in pigs increases in size with age and body weight, and the development of the reproductive tract depends on a balance between development of the pituitary–ovarian axis and the influence of metabolic hormones. Two experiments were conducted in prepubertal Duroc gilts, 150–180 days of age, to determine whether litter size is related to vaginal–cervix catheter penetration length during insemination. In experiment 1, oestrus was induced in 452 gilts with a combined dose of 400 IU Pregnant Mare Serum Gonadotrophine (PMSG) + 200 IU human chorionic gonadotropin (hCG). The gilts were classified into three catheter penetration length groups: Ih, ≤ 21 cm; IIh, > 21 and < 28 cm; IIIh, > 28 cm. The litter size was lowest in group Ih (7.35 ± 0.15) compared with groups IIh (7.81 ± 0.12; p < 0.05) and IIIh (10.0 ± 0.36; p < 0.001). In experiment 2, first oestrus was induced in 162 gilts by boar exposure. The gilts were classified into three catheter penetration length groups at insemination during their second oestrus: In, ≤ 24 cm; IIn, > 24 and < 26 cm; IIIn, > 26 cm. As in experiment 1, the litter size was lowest in the group with the shortest catheter penetration length (8.32 ± 0.19). The litter size was not different among gilts of groups IIn and IIIn (8.84 ± 0.35 and 9.56 ± 0.46, respectively), but litter size was lower (p < 0.05) in group In than in group IIn. Based on the combined data from both experiments, the correlation between the catheter penetration length and total number of piglets born was expressed as: y=5.346 ± 0.104x; r=0.361 (p < 0.05). Fertility rate was not different among the groups of gilts induced into oestrus by hormone treatment or inseminated in the second oestrus; however, the total fertility rate of boar‐exposed gilts was higher (p < 0.0001) than PMSG/hCG treated animals. Thus, it is possible to conclude that litter size at first farrowing is associated with vaginal–cervix catheter penetration length during insemination of the gilt.     

Reproductive failure associated with porcine parvovirus in an enzootically infected pig herd.

Two outbreaks of porcine parvovirus occurred in a unit of 380 sows, with a subsequent decrease in the size of gilts' litters. Of the 203 gilts and 64 primiparous sows which were seronegative at the time of insemination, 134 gilts and 55 primiparous sows seroconverted during pregnancy. Of the second parity sows nine of 271 were still seronegative at the time of insemination but all nine seroconverted during their third gestation. The gilts that seroconverted during their first pregnancy produced on average 0.9 fewer live piglets than the gilts that did not seroconvert. Second litter sows which seroconverted produced 0.3 fewer piglets than those which did not seroconvert. There were no significant differences between sows which seroconverted or did not seroconvert in the numbers of returns to service, or in the percentages of piglets which were born dead or died before weaning.     

Effect of human chorionic gonadotropin on preovulatory luteinizing hormone surge and ovarian hormone secretion in gilts

The influence of varying doses of human chorionic gonadotropin (hCG) on the preovulatory luteinizing hormone (LH) surge, estradiol-17 beta (E2) and progesterone (P4) was studied in synchronized gilts. Altrenogest (AT) was fed (15 mg X head-1 X d-1) to 24 cyclic gilts for 14 d. Pregnant mares serum gonadotropin (PMSG; 750 IU) was given im on the last day of AT feeding. The gilts were then assigned to one of four groups (n = 6): saline (I), 500 IU hCG (II), 1,000 IU hCG (III) and 1,500 IU hCG (IV). Human chorionic gonadotropin or saline was injected im 72 h after PMSG. No differences in ovulation rate or time from last feeding of AT to occurrence of estrus were observed. All gilts in Groups I and II expressed a preovulatory LH surge compared with only four of six and three of six in Groups III and IV, respectively. All groups treated with hCG showed a rapid drop (P less than .01) in plasma levels of E2 11, 17, 23 h after hCG injection when compared with the control group (35 h). The hCG-treated gilts exhibited elevated P4 concentrations 12 h earlier than the control group (3.1 +/- .5, 3.4 +/- .72, 3.1 +/- .10 ng/ml in groups II, III and IV at 60 h post-hCG vs .9 +/- .08 ng/ml in group I; P less than .05). These studies demonstrate that injections of ovulatory doses of hCG (500 to 1,500 IU) had three distinct effects on events concomitant with occurrence of estrus in gilts: decreased secretion of E2 immediately after hCG administration, failure to observe a preovulatory LH surge in some treated animals and earlier production of P4 by newly developed corpora lutea.     

Influence of PMSG and time of artificial insemination on fertility of progestogen-treated sheep in confinement

The need for pregnant mates' serum gonadotropin (PMSG) in breeding confined sheep by artificial insemination (AI) at progestogen-synchronized estrus was assessed in 152 adult crossbred ewes brought into season by a controlled light regimen. One-half of the ewes received 500 IU PMSG after intravaginal progestogen treatment; all ewes were inseminated either 54, 57 or 60 h after sponge removal or at 54 and again at 60 h. Based on progesterone determinations 18 d after AI, conception rates with single insemination 54, 57, or 60 h and double insemination at 54 and 60 h were 76, 72, 47 and 72%, respectively, among ewes receiving PMSG, compared to 17, 22, 47 and 43%, respectively, among ewes not give PMSG (P less than .01) Lambing rates were higher (P less than .01) with PMSG (67, 67, 37 and 61%) than without PMSG (11, 11, 26 and 33%). While there was only a small increase (.06 less than P less than .05) in litter size with PMSG, fecundity decreased (P less than .01) from 1.4 to .3 when PMSG was not used. These data indicate that, even with controlled lighting to induce estrous activity, additional stimulation of ovulation by PMSG at progestogen-synchronized estrus is necessary for normal fertility when confined sheep are bred by AI.     

Endocrine pathogenesis of postweaning anestrus in swine: response of the persistently anestrous sow to hormonal stimuli

The endocrine function of the individual components of the hypothalamo-hypophyseal-ovarian axis of the postweaning anestrous sow was evaluated by monitoring the sow's response to exogenous estradiol, gonadotropin releasing hormone (GnRH), and gonadotropins. Sows (4 to 6/group) not returning to estrus by 42.8 +/- 3.1 days after weaning were assigned to 1 of the following treatments: 10 micrograms of estradiol benzoate (EB)/kg of body weight; 200 micrograms of GnRH, 1,000 IU of pregnant mare's serum gonadotropin (PMSG); 1,000 IU of human chorionic gonadotropin (HCG); or 4 ml of saline solution plus 2 ml of corn oil. A preovulatory-like surge of luteinizing hormone [(LH) greater than 12 hours in duration] was observed in all weaned sows treated with EB. All EB-treated sows exhibited estrus and ovulated but none conceived. Sows given GnRH had transiently increased (less than 3 hours) LH concentrations that were not associated with estrus or ovulation. Treatment with PMSG caused an increase in peripheral concentrations of 17 beta-estradiol that was followed by an LH surge, estrus, ovulation, and conception. Treatment with HCG caused an increase in circulating concentrations of 17 beta-estradiol that was accompanied by a surge of LH in some sows and ovulation in all sows. Not all sows treated with HCG exhibited estrous behavior, but conception occurred in 2 of 3 sows that were mated at estrus. None of the sows treated with saline plus corn oil had consistent changes in circulatory concentrations of 17 beta-estradiol or LH and none exhibited estrus or ovulated.(ABSTRACT TRUNCATED AT 250 WORDS)     

定时输精对经产母猪繁殖性能及生殖激素的影响

试验旨在建立高效的经产母猪定时输精（timed artificial insemination,TAI）技术,研究了定时输精对经产母猪繁殖性能、断奶-分娩间隔、不同胎次母猪产仔性能及断奶后7 d内血清生殖激素水平的影响。选取309头2~8胎次二元（长×大）经产母猪,随机分为对照组和试验组,对照组母猪进行常规人工授精（artificial insemination,AI）,试验组母猪进行断奶后24 h注射PMSG 1 000 IU,间隔72 h注射GnRH 100 μg,在注射GnRH后24和40 h各输精1次的定时输精技术。通过统计两组母猪的断奶1周内发情率、受胎率、分娩率、窝均产仔数等,判断定时输精对经产母猪繁殖性能的影响;通过对断奶时间和分娩时间的统计,检测定时输精对经产母猪断奶-分娩间隔的影响;用放射免疫（RIA）方法检测2~4胎次母猪断奶1周内血清E₂、LH、FSH和P₄的含量,研究定时输精对母猪生殖激素的影响。结果显示,试验组母猪发情率显著高于对照组（P<0.05）,但两组间受胎率、分娩率差异不显著（P>0.05）,窝均产仔数、窝均合格仔数和繁殖效率有增加的趋势,但差异不显著（P>0.05）;定时输精显著缩短了母猪的断奶-分娩间隔（P<0.05）。在胎次方面,3~4胎母猪使用定时输精的效果较好,其发情率、受胎率和分娩率均显著高于对照组（P<0.05）。在生殖激素方面,试验组E₂水平在注射PMSG后迅速上升,且在定时输精处理后66~96 h内持续高于对照组（P<0.05）,试验组P₄水平在断奶后至配种前显著低于对照组（P<0.05）,但配种后快速升高,并高于对照组;LH和FSH的含量在两组间无显著差异。综上,定时输精可有效提高经产母猪的断奶发情率,并减少其非生产天数,可显著提高3~4胎母猪的繁殖性能。     

The effect of Oestrophan Spofa (synthetic analog of prostaglandin F2 alpha) added to the insemination dose on pregnancy and fertility in sows

Laboratory trials were conducted to study the effect of various concentrations of cloprostenol on the motility and morphological changes of the acrosomes of boar spermatozoa. As found, a cloprostenol concentration of 250 ng per ml of semen to 2500 ng per ml of diluted semen has no adverse effect on the motility of spermatozoa and on the morphological changes of their acrosomes. The concentration of 5000 ng of cloprostenol (in the Oestrophan Spofa product) per 1 ml of diluted semen negatively influences the motility of spermatozoa. An insemination dose of 100 ml of diluted sperm treated with 500 ng of cloprostenol was used for the artificial insemination of 152 sows; 166 sows of the same farm inseminated with untreated semen were used as controls. No gilts were included in the trial. Out of the 152 test sows, 113 conceived after the first insemination, i.e. 74.35%, and the average litter size was 10.04 piglets. In the control group, 125 sows delivered their litters, i.e. 75.30% of the total number, the average litter size being 9.96 piglets. Comparing the reproduction parameters of the experimental and control groups it can be said that the treatment of an insemination dose with 500 ng of cloprostenol immediately before insemination had no influence on the pregnancy rate and on the size of litters.     

Orientation studies of ovulation release in mice to test gonadotropic preparations. 2. FSH, PMSG and Gn-RH activity

The doses of FSH (follicle-stimulating hormone), PMSG (pregnant mare serum gonadotrophin), and gn-RH (gonadotrophin-releasing hormone) effective in terms of triggering ovulation were determined in a mouse ovulation test. Varying doses of the above preparations were subcutaneously injected, 48 hours after overstimulation by injection of 0.5 or 1.0 IU of PMSG. The animals were sacrificed for examination, after another 18-20 hours had passed. Roughly 50 per cent of all animals treated (threshold) in one and the same dosage group (n = 5) had ovulated in response to 0.02-0.1 IU of FSH per animal. The following FSH and PMSG dosages are recommended: 0.02, 0.04, 0.06, 0.08, and 0.1 IU of FSH, 0.6, 1.0, 1.4, 1.8, 2.2, 2.6, 3.0 IU of PMSG. When mouse ovulation tests were used in orientation studies, ovulation was regularly induced by Gn-RH doses per animal between 0.01 and 1.0 micrograms. Dosage spacings or increments should be specified with higher accuracy by further studies.