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Theriogenology1992; 38(4); 695-710; doi: 10.1016/0093-691x(92)90032-m

Initiation of superovulation in mares 5 or 12 days after ovulation using equine pituitary extract with or without GnRH analogue.

Abstract: Cyclic mares were assigned to 1 of 3 treatments (n=15 per group): Group 1 received equine pituitary extract (EPE; 25 mg, i.m.) on Day 5 after ovulation; Group 2 received EPE on Day 12 after ovulation; while Group 3 received 3.3 mg of GnRH analogue (buserelin implant) on the day of ovulation and 25 mg, i.m. EPE on Day 12. Mares in each group were given 10 mg PGF2alpha on the first and second day of EPE treatment. The EPE treatment was continued daily until the first spontaneous ovulation, at which time 3,300 IU of human chorionic gonadotropin (hCG) were given to induce further ovulations. Mares in estrus with a >or=35 mm follicle were inseminated every other day with pooled semen from 2 stallions. Embryo recovery was attempted 7 days after the last ovulation. Follicular changes and embryo recovery during 15 estrous cycles prior to treatment were used as control data. During treatment, the number of follicles>or=25 mm was higher (P0.05) to that of mares treated with buserelin implants (Group 3). Initiation of EPE treatment on Day 5 resulted in a greater (P0.05). The conclusions were 1) EPE initiated in early diestrus increased follicular development and ovulation and 2) treatment with GnRH analogue marginally improved response to EPE treatment.
Publication Date: 1992-10-01 PubMed ID: 16727172DOI: 10.1016/0093-691x(92)90032-mGoogle Scholar: Lookup
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Summary

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The research focused on the impact of beginning superovulation treatment in mares either 5 or 12 days after ovulation, using equine pituitary extract (EPE) either alone or in combination with a GnRH analogue. It found that starting the treatment at day 5 resulted in more ovulation, and using the GnRH analogue showed slight enhancement in response to the EPE treatment.

Experimental Groups and Treatments

  • The study involved three groups each with 15 cyclic mares. Each group was subjected to slightly different treatment methods.
  • Group 1 received equine pituitary extract (EPE) on Day 5 after ovulation, Group 2 got the EPE on Day 12, while Group 3 had a combination of a 3.3 mg GnRH analogue (buserelin implant) on the day of ovulation, and EPE on Day 12.
  • All groups were administered with 10 mg PGF2alpha on the first and second day of EPE treatment, intended to contract the uterus and regress the corpus luteum.

Procedure and Results

  • The EPE treatment was continued daily till the first spontaneous ovulation. When that happened, each mare was given a dose of 3,300 IU of human chorionic gonadotropin (hCG) to induce further ovulations.
  • Any mare in estrus with a follicle of 35 mm or larger was inseminated every two days with pooled semen from two stallions. The researchers then attempted to recover embryos seven days after their last ovulation.
  • The researchers used follicular changes and embryo recovery during 15 estrous cycles prior to treatment as control data.
  • It was observed that there was a significantly higher number of follicles of size 25 mm or larger in mares treated with EPE on day 5 compared to those treated on day 12 or control mares. However, this number was similar to mares that got the buserelin implants (Group 3).

Findings and Conclusion

  • Initiation of the EPE treatment on Day 5 resulted in a more significant number of ovulations (2.9) than on Day 12 (1.1) or in the control mares (1.3).
  • However, the number of embryos recovered was similar across all groups – Day 5 (1.2), Day 12 (1.0), buserelin (0.9) and control (0.9) groups.
  • Two conclusions were drawn: Firstly, superovulation initiated early in diestrus using EPE leads to increased follicular development and ovulation. Secondly, the use of a GnRH analogue moderately enhances the response to EPE treatment.

Cite This Article

APA
Dippert KD, Hofferer S, Palmer E, Jasko DJ, Squires EL. (1992). Initiation of superovulation in mares 5 or 12 days after ovulation using equine pituitary extract with or without GnRH analogue. Theriogenology, 38(4), 695-710. https://doi.org/10.1016/0093-691x(92)90032-m

Publication

ISSN: 0093-691X
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 38
Issue: 4
Pages: 695-710

Researcher Affiliations

Dippert, K D
  • Animal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins, CO 80523, USA.
Hofferer, S
    Palmer, E
      Jasko, D J
        Squires, E L

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