Ovulation In Sows Research Articles

The influence of pre- and post-ovulatory insemination on sperm distribution in the oviduct, accessory sperm to the zona pellucida, fertilisation rate and embryo development in sows

The aim of present study was to investigate the influence of pre-compared with post-ovulatory insemination, on the distribution of spermatozoa in the oviduct, the accessory sperm counts on the zona pellucida and early embryonic development. Thirty-six crossbred multiparous sows (Swedish Landrace×Swedish Yorkshire) were artificially inseminated once either at 20–15 h before (group AIB) or at 15–20 h after (group AIA) ovulation by using a pooled semen of two boars. Thereafter, they were randomly allocated to one of five groups: slaughter at 5–6 h after AI (group I-AIB), at 20–25 h after ovulation (groups II-AIB and II-AIA), at 70 h after ovulation (groups III-AIB and III-AIA), on day 11 (groups IV-AIB and IV-AIA, first day of standing oestrus=day 1) and on day 19 (groups V-AIB and V-AIA). The plasma levels of oestradiol-17β and progesterone differed significantly ( P≤0.05 and P≤0.001, respectively) between AI before (group AIB) and after (group AIA) ovulation. All sows inseminated before ovulation (group I-AIB) had spermatozoa in the UTJ but this was found only in one of the late inseminated sows (group II-AIA). The number of oocytes with spermatozoa in the ZP differed significantly ( P≤0.001) between ‘group II-AIB’ and ‘group II-AIA’. Comparing fertilisation rate, the fertilisation rate in ‘group III-AIB’ was significantly ( P≤0.001) higher than in ‘group III-AIA’. A larger number of recovered embryos (on days 11 and 19) per sow in groups IV-AIB and V-AIB compared with IV-AIA and V-AIA were found. The embryos in group IV-AIB were also larger than embryos in group IV-AIA. In group V-AIA, no embryos were found. In conclusion, the results of this study showed that if insemination was performed at 15–20 after ovulation in sows that still were in standing oestrus, the transport of spermatozoa to the UTJ and oviduct was impaired and a lower proportion of oocytes with accessory spermatozoa to the zona pellucida was found compared with insemination before ovulation. In the late inseminated sows, fertilised oocytes and developed embryos were observed up to day 11 but no embryos were found at day 19.

Sincronização da ovulação em fêmeas suínas submetidas ao desmame precoce

Verificou-se a eficiência de protocolos para sincronizar a ovulação em porcas desmamadas precocemente. Trinta porcas com média de 4,4± 2,0 partos e estádio de lactação de 14,8± 0,7 dias foram distribuídas em três grupos de 10 animais: 1- nenhum tratamento hormonal; 2- 1000 UI de PMSG, via intramuscular (IM), 48h pós-desmame e 0,25mg de GnRH, IM, 72h após a aplicação do PMSG; 3- 1000 UI de PMSG, IM, 48h pós-desmame e 500 UI de hCG, IM, 72h após o PMSG. O momento da ovulação foi detectado por ultra-sonografia transretal. A taxa de sincronização (ovulação até 48h após aplicação de hCG ou GnRH) dos grupos 2 e 3 (94,7%) foi maior (P<0,01) que no grupo controle (40%). Com o uso dos protocolos de sincronização de ovulação, as fêmeas tratadas apresentaram, em relação ao grupo controle, tendência de maior taxa de prenhez (95% vs. 70%; P<0,10) e similares intervalo do desmame ao estro (96,5± 3,0 vs. 130,2± 31,4h) e número de leitões nascidos vivos por fêmea gestante no primeiro cio pós-desmame (10,9± 0,8 vs. 12,0± 0,9). Dessa maneira, os protocolos de sincronização usados neste estudo foram eficientes em sincronizar a ovulação, e podem viabilizar o uso da inseminação artificial em horários predeterminados.

Factors influencing estrus and ovulation in weaned sows as determined by transrectal ultrasound.

Characterization of factors influencing estrus and ovulation in sows may facilitate development of procedures for improving reproductive performance. The experiment was conducted in confinement during 1997 to 1999 using 174 Large White x Landrace sows. After weaning, sows were checked for estrus twice daily. In the 1st yr, transrectal ultrasound was performed once daily and in the 2nd yr twice daily at estrus and on every day until ovulation. The effects of lactation length (< or = 16 d, 17 to 24 d, 25 to 31 d or > or = 32 d), parity (1, 2, or > or = 3), season (winter, spring, summer, or fall) and weaning-to-estrus interval (3, 4, 5, or 6 to 8 d) and their interactions on estrual and ovulatory responses were studied. There was no effect of frequency of ultrasound on any response variable, so data across years were pooled. Percentage of sows expressing estrus within 8 d of weaning was influenced by lactation length (P < 0.001), with sows lactating < or = 16 d (35.2%) less likely to express estrus than sows lactating > or = 17 d (94%). A parity x season interaction was observed (P < 0.001) for estrus, with the lowest expression in parity 1 (73.0%) and parity 2 sows in fall (67.2%), compared with > or = parity 3 sows (98.1%). No explanatory variable had a significant effect on weaning-to-estrus interval (4.4 d) or on follicle size at estrus (8.1 mm). Ovulation hour after onset of estrus was affected by weaning-to-estrus interval (P < 0.01), with sows returning in 3 d ovulating at 46.2 h and between 6 and 8 d at 30.2 h. For sows that expressed estrus within 8 d of weaning, the percentage of sows ovulating was influenced by lactation length (P < 0.001) and weaning-to-estrus interval (P < 0.001). Sows that lactated < or = 16 d were less likely to ovulate (78.0%) than those lactating > or = 17 d (> 92%). Sows that returned to estrus in 3 d were also less likely to ovulate (79.5%) than sows returning > or = 4 d after weaning (> 92%). A parity x season interaction was also observed on ovulation (P < 0.001), with parity 1 and 2 sows less likely to ovulate after expressing estrus in fall and spring compared with parity 3 and greater sows. The data suggest lactation length, early return to estrus, and parity by season effects are associated with risk of failure to express estrus and ovulate.

Ovulation and Embryonic Developmental Rate Following hCG-stimulation in Sows

The hCG induced ovulation in sows was studied by use of ultrasonography, and an investigation of the development and diversity of the zygotes/embryos was performed at 24 h after ovulation. Crossbred sows (N = 48) were weaned (day 0) and checked for heat twice daily from day 3 onwards. From day 4, the ovaries were transrectally scanned twice daily. On day 4, the sows were given an injection of 750 iu hCG i.m. and inseminated 27 +/- 2 h (X +/- SD) and 38 +/- 1 h later. From 38 to 48 h after the hCG injection, the ovaries were scanned at 60 to 90 min intervals. At 24 h after ovulation the oviducts were surgically flushed in 18 sows. Out of the 48 sows, 34 showed heat at 12-36 h after the hCG-treatment and 14 showed heat before the hCG treatment. In the former group of sows, 20 (59%) ovulated within the interval of 38 to 48 h after the hCG treatment, and the follicular size immediately before ovulation was 7.8 +/- 0.6 mm. Among the sows which showed heat before hCG treatment only 7 (50%) ovulated within the above interval and the preovulatory follicle size was larger (8.3 +/- 0.5, p < 0.05) than in the former group of sows, which showed heat after the hCG treatment. The flushing of 18 sows yielded a total of 243 ova, 70 (29%) 1-cell stages, 160 (66%) 2-cell stages and 13 (5%) 4-cell stages. A pronounced difference in the degree of variation in embryonic development was seen between sows: 4 animals yielded 1- to 4-cell stages, one exclusively 2-cell stage. In conclusion, the control of ovulation in sows by hCG treatment will affect the follicular growth and the exact timing of ovulation can not always be relied on. It is strongly recommended to use ultrasonography to monitor the time of ovulation if this parameter is important. Ova recovered at 24 +/- 1 h after the median time of ovulation revealed a pronounced diversity (1- to 4-cell stage) within sows. No obvious relation with this embryonic diversity and the follicular size at ovulation was seen in these data.

Duration of estrus in relation to reproduction results in pigs on commercial farms.

This research was conducted to determine factors that influence duration of estrus, AI strategy, and reproduction results between and within commercial swine farms that use AI. Data from 15,186 sows and gilts on 55 farms for a period of 6.1+/-4.2 mo per farm were used in this study. The average duration of estrus was 48.4+/-1.0 h, ranging from 31 to 64 h, and was consistent from month to month within a farm (repeatability of 86%). Differences in duration of estrus between farms accounted for 23% of the total variation in duration of estrus. On most farms (n = 45), gilts showed a shorter (P < .05) duration of estrus than sows (40.8+/-1.1 h vs 48.5+/-1.0 h). The duration of first estrus after weaning was longer (P < .0001) compared with that of repeat-breeder sows (50.2+/-1.0 h vs 46.8+/-1.0 h). Duration of estrus decreased (P < .05) when interval from weaning to estrus increased from 4 to 6 d (56.0 +/- 1.2 h vs 45.8 +/-1.2 h). The regression of interval from onset to estrus to first AI and interval from weaning to estrus varied between farms and ranged from -7.4 to +1.3 h/d; four farms had a positive relationship. Farrowing rate decreased (P < .05) from 89.7+/-2.7% to 78.2+/-5.74 when the interval from weaning to estrus increased from 4 to 10 d. The litter size decreased (P < .05) from 11.7 to 10.6 pigs when the interval from weaning to estrus increased from 4 to 7 d. Compared with a single AI, double AI in sows and gilts resulted in a 4.3 and 7.0% higher (P < .05) farrowing rate, respectively. When the first AI was performed after expected ovulation, reproduction results were lower than when AI was performed before or at expected ovulation in sows. Duration of estrus was not related to farrowing rate or litter size in individual pigs. Number of inseminations per estrus, time of AI, and duration of estrus were correlated, which made it difficult to assess which of these factors was primarily related to the farrowing rate or litter size. Knowledge of average duration of estrus on farms and of factors that influence the duration of estrus on commercial farms can help to improve the efficiency of the AI strategy specific for each farm.

Seminal plasma does not advance ovulation in hCG-treated sows.

In gilts, seminal plasma treatment before or during the LH-surge has been found to advance ovulation in all animals by as much as 8 to 14 h. Two experiments were performed to assess whether such an advancement occurs in multiparous sows in which ovulation is induced by 750 i.u. hCG at 68 h after weaning. In both experiments, seminal plasma was inseminated at 4, 5 and 6 h after hCG (7 and 6 sows, respectively) and control sows (6 and 6 sows, respectively) were not inseminated. In Experiment 1, using Meishan semen, all sows ovulated between 38 and 44 h after hCG; no advancement of ovulation was seen due to treatment. In Experiment 2, using GY seminal plasma, 3 and 4 sows, respectively had started ovulation at 44 h after hCG. Again, no advancement of ovulation was seen due to treatment. Therefore, in both experiments, seminal plasma treatment within 4-6 h after hCG failed to advance ovulation to a similar extent as found in spontaneously ovulating gilts. It is unclear what causes this lack of effect. Maybe seminal plasma treatment does not advance hCG-induced ovulation or batches of seminal plasma differ in their ovulation-advancing properties.

Follicle Size and the Process of Ovulation in Sows as Studied with Ultrasound

In several experiments, transrectal ultrasound was used to count the number of follicles on both ovaries every half hour for the last 5 to 20 hours before ovulation. In 13 spontaneously ovulating sows, the deviation between the maximum follicle count and the corpora lutea count at 100 hours after ovulation was zero in 54% of the ovaries (14 of 26), 1 in 27%, 2 in 15% and more than 2 in 4% of the 26 ovaries (Soede et al., 1992). This deviation was not related to the corpora lutea count. Therefore, transrectal ultrasound offers a reliable method to count the number of pre-ovulatory follicles and assess the duration of ovulation. Slaughter of sows before, during or after ovulation as monitored with ultrasound, confirmed the accuracy of the technique as a tool to follow the process of ovulation. Results of experiments that study the duration of ovulation can only be used when the procedures used do not interfere with the processes involved. Effects of transrectal ultrasound on the duration of ovulation can not be studied directly, since no other noninvasive method is available. Therefore, in an experiment in which follicle growth and ovulation time in sows were synchronized, Soede and Kemp (1993a) used non-scanned control sows to trace effects of scanning on indirect parameters such as fertilisation rate, embryonic development, embryo diversity and accessory sperm count at Day 5 after ovulation. No effects of repeated transrectal ultrasound were found on any of the parameters studied. It was concluded, that transrectal ultrasound offers a reliable method for assessment of the duration of ovulation in sows and does not seem to interfere with the processes studied. In Table 1, a summary is given of the experiments in which the duration of ovulation was assessed. The duration of ovulation varied between sows from 1 to at most 7 h, but normally did not last longer than 2 to 3 hours. In the experiments, it was found that neither artificial insemination at 22 and 30 h after hCG (Exp. 3), nor stress conditions as caused by 2months of tethering (Exp. 4), nor advanced ovulation by decreasing the interval between PMSG

LH profile and advancement of ovulation after transcervical infusion of seminal plasma at different stages of oestrus in gilts.

The influence of a transcervical infusion of seminal plasma on preovulatory LH profiles and the advancement of ovulation after seminal plasma infusion for different times during oestrus were investigated using the single uterine horn infusion technique (Mariensee model), in combination with transcutaneous sonographic monitoring of the ovaries. Preparative surgery in 23 German Landrace gilts comprised the detachment of the left uterine horn from the corpus, leaving the caudal end open to the peritoneal cavity but sealing the corpus wound. In six gilts fitted with a permanent jugular vein catheter the patent horns were administered a transcervical infusion of seminal plasma (n = 5 cycles) or PBS (n = 4 cycles) immediately after the detection of oestrus by a teaser boar. In addition, 17 non-catheterized gilts received infusions of seminal plasma either 0 h (n = 3 gilts), 16 h (n = 7 gilts) or 24 h (n = 7 gilts) after the detection of oestrus. Seminal plasma infusion at the onset of oestrus provoked ovulation in the ipsilateral ovary of the treated horn 8.5 +/- 0.9 h earlier than in the contralateral (control) ovary. Seminal plasma did not influence the LH profile compared with PBS (P > 0.05), but shortened the interval between the LH peak and ipsilateral ovulation to 23.4 +/- 4.0 h compared with 31.8 +/- 3.4 h in the contralateral ovulation (P < or = 0.01). Infusion 16 h after the onset of oestrus reduced the effect to 4.6 +/- 3.8 h with a wide range of 0-8 h (P < 0.01). The effect was more pronounced in gilts with long intervals between the onset of oestrus and contralateral ovulation compared with earlier ovulation on the control ovary. Seminal plasma infusion less than 16 h before contralateral ovulation and 24 h after the detection of oestrus had no effect. It is concluded that transcervical infusion of seminal plasma early in oestrus synchronizes the variable intervals between the onset of oestrus and ovulation in sows by a locally active mechanism.

The effect of oxytocin on the time of ovulation, conception, and embryonic survival in swine

Three experiments were undertaken to assess the effect of a subcutaneous injection of oxytocin (OT, 10 IU) on the time of ovulation in 25 sows, conception rate and embryo survival in these sows, and conception rate and embryo survival in 82 crossbred gilts. The OT was given after the sows were detected in estrus (exp. 1) and after the first artificial insemination (AI) in exps. 2 and 3. The effect of a single AI or a second AI 18 h later on embryo survival in the gilts also was assessed. The gilts were from either a control (C) line or a line selected (S) for minimum backfat at market weight. In sows, OT versus no injection (NI) had no effect on the time of ovulation, as determined by transrectal ultrasonography (TU) when the injection was given at the detection of estrus (OT, 43.4 ± 3.4 h; NI, 47.3 ± 4.1 h), or after the first AI (OT 43.6 ± 3.2 h; NI 40.5 ± 3.0 h). Oxytocin had no effect on embryo survival in sows (OT, 78.1 ± 4.0%; NI, 76.4 ± 4.0%) or gilts (OT, 79.4 ± 3.0%; NI, 83.2 ± 2.2%). The number of inseminations had no effect on embryo survival (single, 80.3 ± 2.6%; twice, 82.0 ± 2.7%). Embryo survival was lower in S gilts (77.1 ± 2.8% vs. C, 87.1 ± 1.5%, P = 0.0092). These results show that OT had no effect on the time of ovulation in sows or embryo survival in sows or gilts. In gilts embryo survival was not altered by a second AI. Embryo survival was reduced in gilts selected for minimum backfat. Key words: Oxytocin, artificial insemination, ovulation, embryo survival

OESTRUS (STANDING RESPONSE FOR BOAR and MAN) and OVULATION IN SOWS

Reproduction in Domestic AnimalsVolume 31, Issue 2 p. 293-294 OESTRUS (STANDING RESPONSE FOR BOAR and MAN) and OVULATION IN SOWS N.M. Soede, N.M. Soede Department of Animal Husbandry, Agricultural University, Wageningen, The NetherlandsSearch for more papers by this authorC.C.H. Wetzels, C.C.H. Wetzels Department of Animal Husbandry, Agricultural University, Wageningen, The NetherlandsSearch for more papers by this authorB. Kemp, B. Kemp Department of Animal Husbandry, Agricultural University, Wageningen, The NetherlandsSearch for more papers by this author N.M. Soede, N.M. Soede Department of Animal Husbandry, Agricultural University, Wageningen, The NetherlandsSearch for more papers by this authorC.C.H. Wetzels, C.C.H. Wetzels Department of Animal Husbandry, Agricultural University, Wageningen, The NetherlandsSearch for more papers by this authorB. Kemp, B. Kemp Department of Animal Husbandry, Agricultural University, Wageningen, The NetherlandsSearch for more papers by this author First published: September 1996 https://doi.org/10.1111/j.1439-0531.1996.tb00064.xCitations: 3AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume31, Issue2September 1996Pages 293-294 RelatedInformation

Advanced ovulation in gilts by the intrauterine application of a low molecular mass pronase-sensitive fraction of boar seminal plasma

The shortening of the time interval between the onset of oestrus and ovulation in sows by the transcervical administration of seminal plasma was investigated in 23 German Landrace gilts, using the technique of single horn infusions (Mariensee model) in combination with the transcutaneous sonographic monitoring of ovaries. Preparative surgery comprised the detachment of the left uterine horn from the corpus, leaving the caudal end open to the peritoneal cavity but sealing the corpus wound. The left ovary was loosely tied to the ventral abdominal wall for better sonographic distinction. The animals were used in two to four consecutive cycles. After detection of oestrus by the teaser boar, the patent (right) horns were filled by transcervical infusion of 100 ml of a variety of test solutions. Ovulation was probed by transcutaneous sonography at intervals of 4 h thereafter. Native seminal plasma provoked ovulation in the ipsilateral ovary of the treated horn 10.7 h earlier than in the contralateral ovary. This effect was reduced to 7.3 h after charcoal treatment of seminal plasma; addition of 10 micrograms oestradiol restored the effect in full, while 10 micrograms of oestradiol in PBS shortened the time interval to only 3.3 h versus the control ovary. Little effect was seen with oestrone sulfate, none with prostaglandins in PBS or with PBS alone. The preliminary characterization of the nonsteroidal component of seminal plasma advancing ipsilateral ovulation after transcervical infusion suggests a proteinaceous nature. The activity resides in the 1-10 kDa fraction separated by ultrafiltration and is lost after treatment with pronase.

TIMING OF AI and OVULATION IN SOWS

TIMING OF AI and OVULATION IN SOWS

Follicular Development and Ovulation in Sows: Effect of hCG and GnRH Treatment

Follicular growth, chronology of ovulation and embryo morphology were compared in sows ovulating spontaneously and sows, in which the ovulation was attempted induced by hCG or GnRH. Indwelling catheters were placed on day 1 (weaning = day 0) in the ear veins of 18 sows, which were then randomly divided into 3 groups: a control group (N = 6), a group (N = 6) given 750 iu hCG (Physex) im 76h after weaning (hCG group) and a group (N = 6) given 500 micrograms GnRH (Fertagyl) im 76h (N = 3) or 100h after weaning (N = 3) (GnRH group). Follicular diameter and time of ovulation were monitored by ultrasonography every 4h from day 3 until ovulation or development of cysts by means of a sector scanner fitted with a 5.0/7.5 MHz multiangle probe. Heat detection was performed every 8h from day 3 until ovulation. On day 13, the sows were slaughtered, the number of corpora luteae (CL) was counted, and embryos were flushed from the uteri. The control group showed clear heat symptoms, and on day 3, the follicles were typically 3-7 mm and grew up to 7-10 mm over 2 days, where they remained for approximately 24h until ovulation took place 41h +/- 9h after first sign of standing heat. The hCG group exhibited no signs of heat, and the follicles only reached 5-8 mm in diameter at time of ovulation, which occurred 40h +/- 1h after hCG-injection. The GnRH group exhibited inconsistent signs of heat, and the follicles reached a maximum size of 7-12 mm in diameter where they remained for more than 24h. Only 2 sows in this group ovulated within 84-92h after the GnRH injection, and development of bursa cysts and cystic follicles was a common finding. The average number of CL was 18.2 +/- 5.7 per sow (N = 16, range: 3-27) with no significant difference between the groups. Total embryo recovery was 79 +/- 13% with no significant difference between groups. The embryo diversity calculated as standard deviation of the maximum diameter was higher in the hCG group as compared with the control group.(ABSTRACT TRUNCATED AT 400 WORDS)

Influence of stage of lactation, exogenous luteinizing hormone-releasing hormone, and suckling on estrus, positive feedback of luteinizing hormone, and ovulation in sows treated with estrogen1

The overall objective of this study was to investigate the LH response and occurrence of estrus and ovulation in sows treated with estradiol benzoate (EB) at mid- (d 14) or late (d 28) lactation. Experiment 1 tested the hypothesis that hourly pulses of LHRH given to sows treated with EB would cause a greater proportion to exhibit LH surges. Sows (n = 32) at mid- or late lactation were given (i.m.) corn oil (CO) or EB (10 micrograms/kg BW) at 0 h and no pulses or hourly pulses (100 ng/pulse) of the LHRH agonist des-Gly10,[D-ALA6]-LHRH ethylamide (LHRH-A) from 54 to 96 h, the anticipated period of positive feedback of LH. Blood samples for determination of estradiol-17 beta (E2) and LH were collected every 6 h from -12 to 120 h from sows treated with EB. Estrus was checked daily with a mature boar, and ovulation was assessed by measuring progesterone in blood 1 wk after estrus induced by EB or 2 wk after weaning at 34 +/- 1.4 d postpartum. Lactational estrus occurred in 0 of 16 and 15 of 16 sows given CO and EB, respectively; however, no sow ovulated in response to EB. Concentrations of LH were lower (P < .01) during mid- than during late lactation, and LHRH-A pulses had no effect on secretion of LH and E2. The LH concentrations during the pretreatment (-12 to 0 h), negative feedback (6 to 54 h), and positive feedback (60 to 96 h) periods at mid-lactation (.32 +/- .03, .22 +/- .01, and .54 +/- .08 ng/mL, respectively) differed (P < .01) from values at late lactation (.80 +/- .06, .49 +/- .02, and 1.47 +/- .17, respectively). Preovulatory-like surges of LH occurred in one of eight (peak 2.1 ng/mL) and seven of eight (peak 2.9 +/- 1 ng/mL) sows given EB at mid- and late lactation, respectively. Experiment 2 tested the hypothesis that the hypothalamus and pituitary of sows weaned 96 h before they were given EB would show a greater responsiveness than those weaned and given EB simultaneously. Sows (n = 16) at mid- or late lactation were treated with EB (10 micrograms/kg BW; i.m.), and one-half of the sows were suckled until the moment of EB treatment, whereas the other half had their litters weaned 96 h before treatment with EB.(ABSTRACT TRUNCATED AT 400 WORDS)

Effect of boar presence before and after weaning on estrus and ovulation in sows.

Two hundred sixty-two sows were used to investigate the effects of boar exposure during the last week of nursing (BPRE) and after weaning (BPOST) on the return to estrus. Because approximately one-half of the sows were weaning their first litter, a third factor, primiparous vs multiparous (LITT), was considered in the statistical analysis. To evaluate the effect of treatment on ovarian activity, the sows were also blood-sampled twice weekly for 3 wk after weaning for the measurement of plasma progesterone concentrations as an index of ovulation. Boar exposure after weaning was the most important stimulus of early ovulation and estrus after weaning (P less than .001). A greater proportion of first-litter sows exhibited estrus later (P less than .02) and ovulated later (P less than .09) than did multiparous sows. First-litter sows were unaffected (P greater than .10) by boar exposure before weaning. Multiparous sows were sensitive to boar exposure during nursing. Maximal boar exposure for these sows (BPRE + BPOST) resulted in 95% of sows in estrus and ovulating within 20 d of weaning. No boar exposure resulted in 45% and 38% anestrus and anovulatory sows. Boar exposure, either before or after weaning, was effective in reducing the number of anestrus and anovulatory sows to between 15 to 30%. The effects of BPRE and BPOST on return to ovulation were additive and approximately equal.