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Waberski D, Weitze KF, Lietmann C, et al. The initial fertilizing capacity of longerm-stored liquid boar semen following pre- and postovulatory insemination. Theriogenology. 1994;41(7):1367-77doi: 10.1016/0093-691x(94)90188-o.
Waberski, D., Weitze, K. F., Lietmann, C., Lübbert Zur Lage, W., Bortolozzo, F. P., Willmen, T., & Petzoldt, R. (1994). The initial fertilizing capacity of longerm-stored liquid boar semen following pre- and postovulatory insemination. Theriogenology, 41(7), 1367-77. https://doi.org/10.1016/0093-691x(94)90188-o
Waberski, D, et al. "The initial fertilizing capacity of longerm-stored liquid boar semen following pre- and postovulatory insemination." Theriogenology vol. 41,7 (1994): 1367-77. doi: https://doi.org/10.1016/0093-691x(94)90188-o
Waberski D, Weitze KF, Lietmann C, Lübbert Zur Lage W, Bortolozzo FP, Willmen T, Petzoldt R. The initial fertilizing capacity of longerm-stored liquid boar semen following pre- and postovulatory insemination. Theriogenology. 1994;41(7):1367-77. doi: 10.1016/0093-691x(94)90188-o. PMID: 16727491.
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Theriogenology. 1994;41(7):1367-77. doi: 10.1016/0093-691x(94)90188-o.

The initial fertilizing capacity of longerm-stored liquid boar semen following pre- and postovulatory insemination.

Theriogenology

D Waberski, K F Weitze, C Lietmann, W Lübbert Zur Lage, F P Bortolozzo, T Willmen, R Petzoldt

Affiliations

  1. Institute for Reproductive Medicine, Veterinary School of Hannover Bünteweg 15, D-30559 Hannover, Germany.

PMID: 16727491 DOI: 10.1016/0093-691x(94)90188-o

Abstract

In pigs, high variation is seen in the duration of estrus and in the time of ovulation. This is one of a wide range of factors not related to semen quality, which possibly influences the results of field insemination trials. Experiment 1 (n=81 gilts) was performed to determine the influence of the time of ovulation on the fertilizing capacity of liquid boar semen stored up to 118 h. The objective of Experiment 2 (n=102 gilts) was to study the fertilizing potential of semen stored up to 120 h in 2 different extenders, Androhep and Beltsville Thawing Solution (BTS), by means of postovulatory AI. Inseminations were performed 0 to 4 h after ovulation in order to standardize the trial conditions. Fertilization rates based on Day-2 to Day-4 embryos, and the number of accessory spermatozoa per zona pellucida did not differ between semen stored for 0 to 48 and 48 to 87 h in gilts ovulating within 12 after insemination (Experiment 1). Gilts with an interval of 12 to 24 h between AI and ovulation had lower fertility results using semen stored for more than 48 h. A further decrease was observed when semen storage exceeded 87 h in those gilts ovulating later than 24 h after insemination. The time of ovulation has to be considered as being a major factor of variation in the fertility results of AI trials. In Experiment 2, fertilization rates and numbers of accessory spermatozoa decreased between semen stored for 0 to 24 and 24 to 48 h in BTS, and between semen stored for 0 to 24 and 48 to 72 h in Androhep. Significant differences in fertility between diluents were seen only when using semen stored for more than 96 h, with semen extended with Androhep giving the higher results. The results indicate that the decrease in fertilizing capacity due to in vitro aging of spermatozoa cannot be prevented even during the first days of storage.

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