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Acta Veterinaria Scandinavica logoLink to Acta Veterinaria Scandinavica
. 1995 Dec 1;36(4):489–498. doi: 10.1186/BF03547663

Endocrine Changes after Mating in Pregnant and Non-Pregnant Llamas and Alpacas

Hormonelle förändringar efter befadening hos dräktiga och icke drägliga lamor och alpakor

MA Aba 110,, M Forsberg 110, Η Kindahl 210, J Sumar 310, L-E Edqvist 110
PMCID: PMC8095409  PMID: 8669376

Abstract

Plasma concentrations of oestradiol-17ß, progesterone, 15-keto–dihydro–PGF and luteinizing hormone (LH) were monitored in llamas and alpacas after mating with an intact male. Concentrations of LH and PGF metabolite were high immediately after copulation. Ovulation occurred in 92% of the animals. The first significant increases in progesterone were recorded on day 4 after mating. In non-pregnant animals the lifespan of the corpus luteum was estimated to be 8–9 days. Luteolysis occurred in association with the release of PGF. In pregnant animals, a transient decrease in progesterone concentrations was observed between days 8 and 18 in both species. No significant changes in PGF secretion were registered during this period. Oes– tradiol–17ß concentrations were high on the day of mating, declined to low values on day 4, and started to increase again on day 8. Peak values after luteolysis in non-pregnant animals were significantly higher than those registered in pregnant ones. Furthermore, concentrations of oestradiol-17ß were elevated for a longer period in non–pregnant than in pregnant animals. The results suggest that progesterone from the corpus luteum exerts a negative influence on follicular activity in pregnant animals by reducing oes– tradiol-17ß secretion.

Keywords: oestradiol-17ß, Prostaglandin F, early pregnancy

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Acknowledgments

We thank Dr. J. Roser and Dr. H. Papkoff for supplying the LH antiserum and the equine LH standard. The Swedish Agency for Research in Developing Countries (SAREC), Swedish International Development Agency (SIDA) and Department of Physiopa–thology, Faculty of Veterinary Sciences, UNCPBA, Tandil, Argentina, are acknowledged for financial support.

References

  1. Adams GP, Sumar J, Ginther OJ. Effects of lac–tational and reproductive status on ovarian follic–ular waves in llamas (Lama glama) J. Reprod. Fert. 1990;90:535–545. doi: 10.1530/jrf.0.0900535. [DOI] [PubMed] [Google Scholar]
  2. Adams GP, Sumar J, Ginther OJ. Form and function of the corpus luteum in llamas. Anim. Re–prod. Sci. 1991;24:128–138. [Google Scholar]
  3. Bravo PW, Fowler ME, Stabenfeldt GH, Lasley BL. Ovarian follicular dynamics in the llama. Biol. Reprod. 1990;43:579–585. doi: 10.1095/biolreprod43.4.579. [DOI] [PubMed] [Google Scholar]
  4. Bravo PW, Fowler ME, Stabenfeldt GH, Lasley BL. Endocrine responses in the llama to copulation. Theriogenology. 1990;33:891–899. doi: 10.1016/0093-691X(90)90824-D. [DOI] [PubMed] [Google Scholar]
  5. Bravo PW, Stabenfeldt GH, Fowler ME, Lasley BL. Urinary steroids in the periparturient and Postpartum periods through pregnancy in llamas. Theriogenology. 1991;36:267–278. doi: 10.1016/0093-691X(91)90385-Q. [DOI] [PubMed] [Google Scholar]
  6. Bravo PW, Stabenfeldt GH, Fowler ME, Lasley BL. Pituitary response to repeated copulation and/or gonadotropin–releasing hormone administration in llamas and alpacas. Biol. Reprod. 1992;47:884–888. doi: 10.1095/biolreprod47.5.884. [DOI] [PubMed] [Google Scholar]

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