Evaluation of progesterone deficiency as a cause of fetal death in mares with experimentally induced endotoxemia

Peter F. Daels From the Department of Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616 (Daels, Stabenfeldt, Hughes), and the Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Swedish University of Agricultural Sciences, S-75007 Uppsala, Sweden (Odensvik, Kindahl).

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George H. Stabenfeldt From the Department of Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616 (Daels, Stabenfeldt, Hughes), and the Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Swedish University of Agricultural Sciences, S-75007 Uppsala, Sweden (Odensvik, Kindahl).

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John P. Hughes From the Department of Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616 (Daels, Stabenfeldt, Hughes), and the Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Swedish University of Agricultural Sciences, S-75007 Uppsala, Sweden (Odensvik, Kindahl).

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Kristina Odensvik From the Department of Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616 (Daels, Stabenfeldt, Hughes), and the Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Swedish University of Agricultural Sciences, S-75007 Uppsala, Sweden (Odensvik, Kindahl).

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Hans Kindahl From the Department of Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616 (Daels, Stabenfeldt, Hughes), and the Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, Swedish University of Agricultural Sciences, S-75007 Uppsala, Sweden (Odensvik, Kindahl).

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SUMMARY

The role of decreased luteal activity in embryonic loss after induced endotoxemia was studied in mares 21 to 35 days pregnant. Fourteen pregnant mares were treated daily with 44 mg of altrenogest to compensate for the loss of endogenous progesterone secretion caused by prostaglandin F (pgf) synthesis and release following intravenous administration of Salmonella typhimurium endotoxin. Altrenogest was administered daily from the day of endotoxin injection until day 40 of gestation (group 1; n = 7), until day 70 (group 2; n = 5), or until day 50 (group 3; n = 2).

In all mares, secretion of pgf, as determined by the plasma 15-keto-13,14-dihydro-pgf concentrations, followed a biphasic pattern, with an initial peak at 30 minutes followed by a second, larger peak at 105 minutes after endotoxin injection. Plasma progesterone concentrations decreased in all mares to values < 1 ng/ml within 24 hours after endotoxin injection.

In group 1, progesterone concentrations for all mares were < 1 ng/ml until the final day of altrenogest treatment. In 6 of 7 mares in group 1, the fetuses died within 4 days after the end of treatment, with progesterone concentrations < than 1 ng/ml at that time. In the mare that remained pregnant after the end of treatment, plasma progesterone concentration was 1.6 ng/ml on day 41 and increased to 4.4 ng/ml on day 44.

In group 2, all mares remained pregnant, even though plasma progesterone concentrations were < 1 ng/ml in 4 of 5 mares from the day after endotoxin injection until after the end of altrenogest treatment. One group-2 mare appeared to develop a secondary corpus luteum before day 70, with progesterone concentrations greater than 1 ng/ml from day 36 through day 70.

Daily altrenogest administration consistently prevented pregnancy loss, which usually follows induced endotoxemia. Altrenogest administration offers a reliable and practical treatment for the prevention of fetal loss following endotoxemia in mares < 2 months pregnant.

One group-3 mare remained pregnant, and in the other mare, fetal death was diagnosed 8 days after endotoxin administration, although this mare was still being treated with altrenogest. In that case fetal death was believed to be unrelated to the treatment.

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