The objective of this study was to characterize the uterine leukocyte influx after artificial insemination (AI).

Yorkshire x Landrace gilts were used to determine the effect of spermatozoa and seminal plasma on postbreeding uterine leukocyte influx. Estrus detection was performed with a boar at 12-h intervals following synchronization with 400 IU eCG and 200 IU of hCG. All gilts were AI once, 24 h after the detection of estrus following random assignment to a 2x2x3 factorial arrangement of treatments (sperm or sperm-free AI doses), AI dose medium (seminal plasma or PBS), and lavage time following AI. Gilts were treated with sperm (5x10(9) spermatozoa; SPZ; n = 30) or sperm-free (SF; n = 30) doses containing either 100 mL of seminal plasma (SP; n = 15/treatment) or PBS (n = 15/treatment). Uterine lavage was performed once on each gilt (n = 20/time) at one of three times after AI (6, 12, or 36 h) to determine the total number of uterine leukocytes. The leukocytes consisted predominately (92 to 99%) of polymorphonuclear neutrophilic granulocytes (PMN). There was an AI x medium interaction on uterine PMN numbers. The number of uterine PMN recovered from gilts inseminated with sperm suspended in PBS was greater than the number of PMN recovered from the uterine lumen of gilts inseminated with sperm in SP, SP alone, or PBS alone (P<.05). Furthermore, SP accelerated the rate of uterine clearance when suspended with sperm cells during the first 36 h following AI (P<.05). These results indicate that seminal plasma suppresses PMN migration into the uterus following breeding and enhances the rate of disappearance of uterine inflammation.

The objective of this experiment was to determine the reproductive performance and factors that affect on-farm application of low-dose intrauterine insemination (IUI) in sows. Four hundred twenty-two sows were used in a simple arrangement of four treatments to determine the effect of spermatozoa per dose (0.5 x 10(9), 1 x 10(9), or 4 x 10(9) IUI, and 4 x 10(9) with a conventional catheter) on the main effects of conception, litter size, and farrowing rate. Following weaning at approximately 18 d after parturition, estrus detection was performed daily in the presence of a mature boar. At the time of estrus detection, sows were blocked for parity (1, 2, or 3+), weaning-to-estrus interval (WEI; 3, 4, or 5 d), and assigned randomly to be serviced twice with semen from the same boar(s). Treatment services were equally divided among three technicians. Delivery of acceptable numbers of spermatozoa per dose with either device (IUI or conventional) produced similar reproductive performances; however, farrowing rate, total pigs born, and total born alive decreased (P < 0.05) when suboptimal numbers (< or = 1 x 10(9)) of spermatozoa were used with IUI. Treatment interactions with parity were not detected and were removed from the final model. Treatment interactions with WEI on farrowing rate were detected (P < 0.05), and sows with WEI of 3 d had a markedly lower (P < 0.05) farrowing rate than all other treatment groups. The results from this experiment suggest that placement of semen at the beginning of the uterine horn with conventional volumes and spermatozoa numbers produces results similar to placement of semen in the cervical cavity with a conventional AI catheter. Although there is little published evidence of reproductive performances in a commercial setting with suboptimal numbers of spermatozoa, these results suggest that insemination beyond the cervix does not offset effects of suboptimal numbers of spermatozoa.

Yorkshire x Landrace sows and gilts were used in a 3x2 factorial arrangement of treatments to determine the effect of uterine inflammation induced by either killed spermatozoa (KS) or bacterial lipopolysaccharide (LPS) on the fertility of a subsequent, optimally timed AI. Estrus was detected with a mature boar twice daily. Twelve hours after the first detection of estrus, females received intrauterine infusions of an inflammatory stimulus consisting of a 100-mL dose of extender containing 3x10(9) KS (n = 40), 20 microg of LPS (n = 40; positive control) or extender alone (n = 40; negative control). An insemination was performed 12 to 18 h later with 3x10(9) motile spermatozoa (i.e., fertile AI) suspended in either 100 mL of seminal plasma (SP; n = 60) or extender replenished with of estrogens (5 microg of estradiol-17beta, 4.5 microg of estrone sulfate, and 2 microg of estrone; n= 60). Transcutaneous ultrasound was performed at the time of fertile AI and again 24 h later to detect the presence or absence of preovulatory follicles. A fertile AI performed within 24 h before ovulation was considered optimal. Conception (CR) and farrowing rates (FR) were greater in females that received a fertile AI diluted with SP compared with extender (P<.01), and there was a significant (P<.05) treatment x fertile AI dilution medium interaction for both CR and FR. Females that received a fertile AI 12 h after infusion of extender had similar CR and FR regardless of fertile AI dilution medium. After inducing an inflammatory response with either KS or LPS, CR and FR were higher in females that received a fertile AI diluted with SP compared with fertile AI dilution with extender (P<.05). The effects of treatment and AI dilution media and their interactions were not significant for litter size in females that farrowed. These results show that the fertility of a subsequent AI can be impaired when semen is deposited into an inflamed environment created by an earlier AI, and this impairment was offset by inclusion of SP in the subsequent insemination.

A study was conducted with 360 gilts and sows from four herds to determine whether fertility was affected when the final of multiple inseminations was performed in late estrus or metestrus (late insemination). Sows and gilts were inseminated at 24-h intervals immediately after the detection of estrus. After receiving a first insemination, females were paired according to parity and estrus status on d 2 of estrus. Each pair set was inseminated with extended semen from the same semen collection(s). Control females were inseminated once on d 1 if they were not in estrus on d 2 (n = 31) or on both days if they were in estrus on d 2 (n = 149). Late inseminated females in each pair were managed and inseminated in the same manner as control females and then inseminated again 24 h later regardless of estrus status. Overall reproductive performance was similar among the four herds. Late insemination caused a drop in farrowing rate in parity 1 and 2 females (23 and 22%; P < .05 and P < .01, respectively) and average litter size decreased by 1.1 pigs per litter (P < .05) regardless of parity. There were no differences in either litter size or farrowing rate between late inseminated females in estrus and those that were in metestrus at the time of their last insemination.