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Vertebrate reproductive science and technology
RESEARCH ARTICLE

Caudal vena cava progesterone and LH release patterns on Day 14 of gestation in primiparous sows

L. L. Hoving A C , S. M. Haen B D , B. F. A. Laurenssen A , O. A. T. Peltoniemi B , B. Kemp A and N. M. Soede A
+ Author Affiliations
- Author Affiliations

A Adaptation Physiology Group, Wageningen University, PO Box 338, 6700 AH Wageningen, The Netherlands.

B Department of Production Animal Medicine, Faculty of Veterinary Medicine, University of Helsinki, Paroninkuja 20, 04920 Saarentaus, Finland.

C Present address: Cargill Premix and Nutrition, Veerlaan 17-23, 3072 AN Rotterdam, The Netherlands.

D Corresponding author. Email: silke.haen@helsinki.fi

Reproduction, Fertility and Development 29(3) 476-481 https://doi.org/10.1071/RD15016
Submitted: 14 January 2015  Accepted: 5 August 2015   Published: 9 October 2015

Abstract

The aim of the present study was to explore the relationship between systemic and local progesterone secretion and LH pulsatility during implantation in the pig. Differences in progesterone concentrations measured locally in the caudal vena cava and systemically in the jugular vein were studied in eight primiparous sows on Day 14 of pregnancy. LH pulsatility was analysed for its effects on the local progesterone-releasing pattern. Mean (± s.d.) progesterone concentrations in the vena cava (65.5 ± 19.8 ng mL–1) were approximately double basal concentrations (33.6 ± 13.1 ng mL–1). Basal concentrations of progesterone and LH were calculated as the average of the lowest six values. Basal caudal vena cava and mean jugular (27.6 ± 1.5 ng mL–1) progesterone concentrations did not differ significantly. Pre- and postprandial jugular progesterone concentrations were significantly different in the morning and afternoon (P = 0.025 and 0.023). Mean LH ranged from 0.24 to 0.43 ng mL–1 and was approximately double as high as basal LH in individual sows. In 60.8% of cases, LH pulses were followed by a progesterone pulse within 1 h. In conclusion, the present study showed that corpus luteum function appears to respond to LH pulsatility on Day 14 of pregnancy. However, the response varies at the level of individual sows. In addition, systemic postprandial decreases in progesterone were confirmed on Day 14 of pregnancy.

Additional keywords: corpus luteum, early pregnancy, progesterone metabolisation, second parity.


References

Anderson, L. L., Dyck, G., Mori, H., Henricks, D., and Melampy, R. (1967). Ovarian function in pigs following hypophysial stalk transection or hypophysectomy Am. J. Physiol. 212, 1188–1194.
| 1:CAS:528:DyaF2sXktlSns7c%3D&md5=94766edbfe012b6dabf0e14bb5668d8bCAS | 6023876PubMed |

Athorn, R. Z., Stott, P., Bouwman, E. G., Ashman, R., O’Leary, S., Nottle, M., and Langendijk, P. (2011). Direct ovarian–uterine transfer of progesterone increases embryo survival in gilts Reprod. Fertil. Dev. 23, 921–928.
Direct ovarian–uterine transfer of progesterone increases embryo survival in giltsCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhtVOrtb7P&md5=3355996306897ec37ce6f5d4a074de0dCAS | 21871211PubMed |

Athorn, R. Z., Stott, P., Bouwman, E. G., Chen, T. Y., Kennaway, D. J., and Langendijk, P. (2013). Effect of feeding level on luteal function and progesterone concentration in the vena cava during early pregnancy in gilts Reprod. Fertil. Dev. 25, 531–538.
Effect of feeding level on luteal function and progesterone concentration in the vena cava during early pregnancy in giltsCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXjslejtrg%3D&md5=a0b2d025c4c5a62e74e8ec58cd310067CAS | 23464500PubMed |

Baird, D. T., Horton, R., Longcope, C., and Tait, J. F. (1969). Steroid dynamics under steady-state conditions Recent Prog. Horm. Res. 25, 611–664.
| 1:CAS:528:DyaE3cXkvFKhs7Y%3D&md5=023cbaacbfdb7c4618b7c7092d7821f2CAS | 4900738PubMed |

Bedford, C. A., Harrison, F. A., and Heap, R. B. (1974). Splanchnic, uterine, ovarian and adrenal uptake of progesterone and 20 alpha-dihydroprogesterone in the pregnant and non-pregnant sheep J. Endocrinol. 62, 277–290.
Splanchnic, uterine, ovarian and adrenal uptake of progesterone and 20 alpha-dihydroprogesterone in the pregnant and non-pregnant sheepCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE2MXhsFaktrs%3D&md5=22e9ec37505d1d448301cf94fd48deb5CAS | 4415865PubMed |

Benoit, A. M., and Dailey, R. A. (1991). Catheterization of the caudal vena cava via the lateral saphenous vein in the ewe, cow, and gilt: an alternative to utero-ovarian and medial coccygeal vein catheters J. Anim. Sci. 69, 2971–2979.
| 1:STN:280:DyaK3MzlvVWntA%3D%3D&md5=09d1ec7de14ee571dcc7eaaf0546918eCAS | 1885407PubMed |

Brüssow, K.-P., Schneider, F., Tuchscherer, A., Egerszegi, I., and Rátky, J. (2008). Comparison of luteinizing hormone, leptin and progesterone levels in the systemic circulation (vena jugularis) and near the ovarian circulation (vena cava caudalis) during the oestrous cycle in Mangalica and Landrace gilts J. Reprod. Dev. 54, 431–438.
Comparison of luteinizing hormone, leptin and progesterone levels in the systemic circulation (vena jugularis) and near the ovarian circulation (vena cava caudalis) during the oestrous cycle in Mangalica and Landrace giltsCrossref | GoogleScholarGoogle Scholar | 18787307PubMed |

Brüssow, K.-P., Schneider, F., Wollenhaupt, K., and Tuchscherer, A. (2011). Endocrine effects of GnRH agonist application to early pregnant gilts J. Reprod. Dev. 57, 242–248.
Endocrine effects of GnRH agonist application to early pregnant giltsCrossref | GoogleScholarGoogle Scholar | 21157124PubMed |

Cosgrove, J. R., Booth, P. J., and Foxcroft, G. R. (1991). Opioidergic control of gonadotrophin secretion in the prepubertal gilt during restricted feeding and realimentation J. Reprod. Fertil. 91, 277–284.
Opioidergic control of gonadotrophin secretion in the prepubertal gilt during restricted feeding and realimentationCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXksVahur0%3D&md5=bc64974661c69b32fbc04bc3ca6d6515CAS | 1899888PubMed |

Ellicott, A. R., and Dziuk, P. J. (1973). Minimum daily dose of progesterone and plasma concentration for maintenance of pregnancy in ovariectomized gilts Biol. Reprod. 9, 300–304.
| 1:CAS:528:DyaE2cXms1ymsw%3D%3D&md5=0474d1285b38804c5865adbfdc0cdf8dCAS | 4747560PubMed |

Geisert, R. D., Renegar, R. H., Thatcher, W. W., Roberts, R. M., and Bazer, F. W. (1982). Establishment of pregnancy in the pig: I. Interrelationships between preimplantation development of the pig blastocyst and uterine endometrial secretions Biol. Reprod. 27, 925–939.
Establishment of pregnancy in the pig: I. Interrelationships between preimplantation development of the pig blastocyst and uterine endometrial secretionsCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3sXjt1Wrtw%3D%3D&md5=426c91695655e752024b730e4c8cd66bCAS | 6959653PubMed |

Hoving, L. L., Soede, N., Feitsma, H., and Kemp, B. (2012a). Lactation weight loss in primiparous sows: consequences for embryo survival and progesterone and relations with metabolic profiles Reprod. Domest. Anim. 47, 1009–1016.
Lactation weight loss in primiparous sows: consequences for embryo survival and progesterone and relations with metabolic profilesCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhvFKgtb0%3D&md5=a4c60a5eb3d05298031a6cd2d084c773CAS | 22420822PubMed |

Hoving, L. L., Soede, N. M., Feitsma, H., and Kemp, B. (2012b). Embryo survival, progesterone profiles and metabolic responses to an increased feeding level during second gestation in sows Theriogenology 77, 1557–1569.
Embryo survival, progesterone profiles and metabolic responses to an increased feeding level during second gestation in sowsCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XltVKkt7g%3D&md5=2af813dc484370d7a30206b674b5faafCAS | 22342593PubMed |

Magness, R. R., Reynolds, L. P., and Ford, S. P. (1986). Evidence for uterine metabolism of progesterone during early pregnancy in the pig Theriogenology 25, 551–558.
Evidence for uterine metabolism of progesterone during early pregnancy in the pigCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL28XksFCktLo%3D&md5=3f02c05907a7acf0efc1e06177ad75ffCAS | 16726145PubMed |

Miller, H. M., Foxcroft, G. R., Squires, J., and Aherne, F. X. (1999). The effects of feed intake and body fatness on progesterone metabolism in ovariectomized gilts J. Anim. Sci. 77, 3253–3261.
| 1:CAS:528:DC%2BD3cXktFehtA%3D%3D&md5=88ff97a5502afae3ada87f6acc588165CAS | 10641872PubMed |

Nase, B. R., Hagen, D. R., Kavanaugh, J. F., and Griel, L. C. (1985). Effect of partial stepwise luteectomy in pregnant gilts on maternal and fetal concentrations of progesterone Biol. Reprod. 33, 88–92.
Effect of partial stepwise luteectomy in pregnant gilts on maternal and fetal concentrations of progesteroneCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2MXkvFyqtL0%3D&md5=8f85e60901fd5b1e53bc628bf5fd51dbCAS | 4063446PubMed |

Parvizi, N., Elsaesser, F., Smidt, D., and Ellendorff, F. (1976). Plasma luteinizing hormone and progesterone in the adult female pig during the oestrous cycles, late pregnancy and lactation, and after ovariectomy and pentobarbitone treatment J. Endocrinol. 69, 193–203.
Plasma luteinizing hormone and progesterone in the adult female pig during the oestrous cycles, late pregnancy and lactation, and after ovariectomy and pentobarbitone treatmentCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE28XktFOkt7o%3D&md5=8bb720a8d8ad429d29583ffe8fbd22cdCAS | 1270963PubMed |

Peltoniemi, O. A. T., Easton, B. G., Love, R. J., Klupiec, C., and Evans, G. (1995). Effect of chronic treatment with a GnRH agonist (Goserelin) on LH secretion and early pregnancy in gilts Anim. Reprod. Sci. 40, 121–133.
Effect of chronic treatment with a GnRH agonist (Goserelin) on LH secretion and early pregnancy in giltsCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28Xjt1Gnsw%3D%3D&md5=4953134fae4e5ab33d62787faa5876c1CAS |

Pope, W. F. (1988). Uterine asynchrony: a cause of embryonic loss Biol. Reprod. 39, 999–1003.
Uterine asynchrony: a cause of embryonic lossCrossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaL1M7hvVCjtQ%3D%3D&md5=d862ea0496f44e27475b6bb66014b80aCAS | 3064819PubMed |

Prime, G. R., and Symonds, H. W. (1993). Influence of plane of nutrition on portal blood flow and the metabolic clearance rate of progesterone in ovariectomized gilts J. Agric. Sci. 121, 389–397.
Influence of plane of nutrition on portal blood flow and the metabolic clearance rate of progesterone in ovariectomized giltsCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2cXht1Ghurw%3D&md5=3f719d727a0754181085fd634d24e06fCAS |

Soede, N. M., Helmond, F. A., Schouten, W. G., and Kemp, B. (1997). Oestrus, ovulation and peri-ovulatory hormone profiles in tethered and loose-housed sows Anim. Reprod. Sci. 46, 133–148.
Oestrus, ovulation and peri-ovulatory hormone profiles in tethered and loose-housed sowsCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2sXjsVeisbk%3D&md5=f9f61046e6026564dccafb401a371ebfCAS | 9231254PubMed |

Tast, A., Love, R. J., Clarke, I. J., and Evans, G. (2000). Effects of active and passive gonadotrophin-releasing hormone immunization on recognition and establishment of pregnancy in pigs Reprod. Fertil. Dev. 12, 277–282.
Effects of active and passive gonadotrophin-releasing hormone immunization on recognition and establishment of pregnancy in pigsCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXks1amtbw%3D&md5=fc24635f5e752e2bc616a66d88ab6199CAS | 11451018PubMed |

Virolainen, J. V., Love, R. J., Tast, A., and Peltoniemi, O. A. T. (2005). Plasma progesterone concentration depends on sampling site in pigs Anim. Reprod. Sci. 86, 305–316.
Plasma progesterone concentration depends on sampling site in pigsCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXit1Cjtbg%3D&md5=cc50c26a8aee8ecb41b2007e291bd282CAS | 15766808PubMed |