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Journal of animal science1980; 50(3); 490-495; doi: 10.2527/jas1980.503490x

Induction of abortion in mares with equimate: effect on secretion of progesterone, PMSG and reproductive performance.

Abstract: Thirty-two light-horse mares were confirmed to be pregnant and assigned to one of four treatments: (1) injected with 250 micrograms of Equimate on day 70 and again on day 77 if abortion had not occurred; (2) injected with 250 micrograms of Equimate on day 70 and every 24 hr until abortion occurred (maximum four injections); (3) injected with 250 micrograms of Equimate on day 70 and every 12 hr until abortion (maximum eight injections); and (4) injected with 250 micrograms of Equimate once only on day 35 of gestation. Mares were observed four times daily for incidence of abortion or side effects. Estrual behavior was monitored daily and follicular activity either daily or every third or fourth day until estrus and ovulation. Samples of jugular blood were obtained at 0600 hr day -1 and every 6 hr until the first day of estrus after abortion, or for 2 weeks after abortion if estrus had not occurred, or for 1 week after treatment for mares that had not aborted. A single injection of Equimate terminated pregnancy in all but one mare injected on day 35, but none of the mares given an injection on day 70 and 77 aborted. Multiple injections of Equimate beginning on day 70 of gestation terminated pregnancy in all mares. Fewer (P less than .05) injections were required for abortion of mares injected daily. During the immediate week post-treatment, concentrations of progesterone decreased (P less than .05) in all mares injected with Equimate, but overall concentrations were greater (P less than .05) for mares injected once on day 70 than for those in the other three groups. Equimate did not affect secretion of PMSG in the day 70 group of mares. Estrus and ovulation after abortion were delayed (P less than 0.05) for mares injected daily or twice daily beginning on day 70 compared to those injected once on day 35. Thus, rebreeding of these mares during the same breeding season in which they were aborted would be difficult.
Publication Date: 1980-03-01 PubMed ID: 7364685DOI: 10.2527/jas1980.503490xGoogle Scholar: Lookup
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  • Journal Article

Summary

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The research paper discusses a study conducted on thirty-two light-horse mares to ascertain the impact of Equimate, a drug used to induce abortion, as well as the drug’s effects on progesterone secretion, PMSG secretion, and overall reproductive performance. The results indicate that multiple administrations of Equimate could successfully terminate a pregnancy, with progesterone levels dropping following treatment. However, the findings also highlight the possibility of delay in estrus and ovulation following abortion, especially in mares administered the drug more frequently.

Experimental Design and Process

  • The experiment involved thirty-two light-horse mares that were confirmed to be pregnant. They were randomly divided into four groups, each subjected to a different treatment protocol involving Equimate administration.
  • The first group received 250 micrograms of Equimate on the 70th day of pregnancy, and again on the 77th day if abortion didn’t occur. The second group received the same dose every 24 hours starting from the 70th day until abortion occurred, with a maximum limit of four injections. The third group received the same dose every 12 hours from the 70th day until abortion occurred, capped to a maximum of eight injections. The last group received a one-time dose of 250 micrograms on the 35th day of gestation.
  • All mares were monitored four times daily for signs of abortion or side effects. Additionally, their estrual behavior and follicular activity were tracked daily, or every third or fourth day until estrus and ovulation.
  • Blood samples were drawn at 0600 hr day -1 and every six hours until the first day of estrus after abortion, or for two weeks after abortion if estrus did not occur. For mares who didn’t abort, samples were obtained one week after treatment.

Key Findings

  • Except for one mare in group 4, a single dose of Equimate successfully terminated the pregnancy in all mares in this group. However, none of the mares in the first group (who received injections on the 70th and 77th day) aborted. Multiple Equimate injections starting from the 70th day led to successful abortion in all mares.
  • Progesterone levels decreased in all mares post-Equimate treatment. However, overall progesterone concentrations were significantly higher in mares who received only one injection on the 70th day compared to the other groups.
  • Equimate did not impact PMSG secretion in the group of mares that were injected on the 70th day.
  • The occurrence of estrus and ovulation was delayed in mares injected daily or twice daily starting on the 70th day, compared to those injected once on the 35th day. The study concludes that this delay could complicate rebreeding of these mares in the same breeding season.

Cite This Article

APA
Squires EL, Hillman RB, Pickett BW, Nett TM. (1980). Induction of abortion in mares with equimate: effect on secretion of progesterone, PMSG and reproductive performance. J Anim Sci, 50(3), 490-495. https://doi.org/10.2527/jas1980.503490x

Publication

ISSN: 0021-8812
NlmUniqueID: 8003002
Country: United States
Language: English
Volume: 50
Issue: 3
Pages: 490-495

Researcher Affiliations

Squires, E L
    Hillman, R B
      Pickett, B W
        Nett, T M

          MeSH Terms

          • Abortifacient Agents / administration & dosage
          • Abortifacient Agents / pharmacology
          • Abortion, Induced / veterinary
          • Animals
          • Female
          • Gestational Age
          • Gonadotropins, Equine / metabolism
          • Horses / metabolism
          • Horses / physiology
          • Progesterone / metabolism
          • Reproduction / drug effects

          Citations

          This article has been cited 1 times.
          1. Bosu WT, McKinnon AO. Induction of abortion during midgestation in mares.. Can Vet J 1982 Dec;23(12):358-60.
            pubmed: 17422207