Open-access Additional effects using progestins in mares on levels of thyroid hormones and steroids in neonates

Abstract

The risk of pregnancy loss in mares leads to the use of exogenous hormones to help pregnancy maintenance. The objective was to evaluate the proportion of thyroid hormones and steroids in neonates, in the following postpartum period, born to mares fed with synthetic progesterone and to verify the existence of a correlation between the level of progesterone between mother and neonate. Twenty-seven mares and their foals were used. The animals were divided into 5 experimental groups: group 1 (control, without hormonal supplementation), group 2 (random samples fed to 120 days of pregnancy with long-term progesterone), group 3 (mares fed with short-term progesterone as of 280.º day of pregnancy), group 4 (mares fed with long-term progesterone as of 280.º day of pregnancy) and group 5 (mares fed with synthetic hormone [altrenogest] as of 280.º day of pregnancy). The animal’s blood collection took place immediately after parturition for the hormonal measurement. The hormones measured in neonates were total T3, free T4, TSH, progesterone and cortisone. In mares, only levels of progesterone. The groups of neonates showed no difference on levels of total T3, free T4, TSH and progesterone. There was no difference on levels of progesterone in mares among the groups. Neonates from groups 4 and 5 had higher and lower cortisone levels, respectively. No neonate showed clinical change. There was also no correlation between levels of progesterone in mares and foals. Thus, hormonal supplementation with long-term progesterone as of 280 days of pregnancy leds to an increase in the neonate's cortisone levels, in the meantime, supplementation with altrenogest as of 280 days of pregnancy caused a decrease on cortisone levels in foals, despite clinical signs have not been observed on these animals.

Keywords:  altrenogest; progesterone; cortisone; equine; pregnancy

Introduction

The high economic cost of a pregnancy by embryo transfer in mares and the great value of the live foal make professionals fear the failure of pregnancies and adhere to the use of exogenous/synthetic progesterone (Allen, 2001; DeLuca et al., 2011). There is no proven method to select which mares should be supplemented, causing the medication to be applied indiscriminately. Massive supplementation of the herd has not shown changes in rates of early pregnancy loss and percentage of alive foals for the last 12 years; besides, the period of greatest loss (15-42 days of pregnancy) remains similar in groups with and without exogenous progesterone (Rose et al., 2018).

In women, it has been described that exogenous progesterone supplementation can suppress the transcription of some genes, including some which are responsible for the production of cytokines and the proliferation of T cells after the introduction of antigens, which would impact the susceptibility to pathogens (Bamberger et al., 2000; Koubovec et al., 2004; Huijbregts et al., 2013). Although many studies have demonstrated the anti-inflammatory effect of progesterone in the context of reproduction, there is little understanding about its cellular and molecular actions that can generate immunomodulation (Goddard et al., 2013)

In fetus, in a period close to the birth, the adrenal gland becomes able to produce cortisone (Silver, 1990; Fowden and Silver, 1995; Fowden et al., 2012). Since adrenocortical activity increases prepartum, it is expected to find high levels of plasmatic cortisone in newborns in their first hours of life (Fowden et al., 2012; Silver et al., 1984; Lester, 2005). Foals that have undergone stress from disease, such as sepsis, have higher levels of total cortisone, and this value can be higher on those that did not survive (Panzani et al., 2009; Hart and Barton, 2011).

Another process that occurs close to the birth, is an increase in thyroid hormones, namely triiodothyronine (T3), thyroxine (T4) and even thyrotrophin (TSH) (Jeffcott et al., 1982; LeBlanc et al., 2004). Thyroid hormones have a direct action on fetal metabolism, especially on oxygen consumption, glucose and thermoregulation (Forhead and Fowden, 2014). Horses have one of the highest levels of flowing thyroid hormones, with the level at birth being 10-20 higher than adults (Knottenbelt et al., 2004). Along with cortisone, triiodothyronine (T3) seems to be critical for lung maturation (Forhead and Fowden, 2014; Barker et al., 1991; Ramminger et al., 2002). Thus, the effects of hypothyroidism in neonates are much more severe than in adults since the actions of thyroid hormones are crucial for the development of nervous and skeletal systems (Frank et al., 2002).

Knowledge about the consequences of the use of synthetic hormones in foals of mares with supplementation is almost non-existent, despite the evidence that altrenogest (derived from 19-norethisterone steroid), the most currently used, may be able to cross the placental boundaries, and its high levels described as causing problems in the newborn's life (Neuhauser et al., 2008, 2009; Palm et al., 2010). Thus, the objective of this study was to evaluate the hormonal levels of newborns in the immediate postpartum of mares submitted to different supplementation protocols with synthetic progesterone and to verify the correlation between the mother's progesterone levels with the newborn's hormonal levels of progesterone.

Methods

This project was approved and developed in accordance with the guidelines of the Ethics Committee on the Use of Animals of the Faculty of Veterinary Medicine and Zootechnics of the University of São Paulo, under protocol number 9874130317/2019.

Twenty-seven pregnant mares and their foals were selected through a suitable sample, all of them being of the Mangalarga Marchador breed, from a owner in São Roque, São Paulo, Brazil.

The animals were kept in coast-cross paddocks where they also received balanced feed twice a day and water uninterruptedly. All health protocols were carried out as recommended for horses and their respective stages of life. Mares were vaccinated for rhinopneumonia (Vencofarma, Brasil®) in fifth, seventh and ninth pregnancy months. Still, in the ninth month were applied tetanus, encephalomyelitis and influeza vaccines (Vencofarma, Brasil®). The animals were used exclusively for the experiment. All mares were inseminated with the same stallion during 2014-2015 breeding season and submitted to the same management. The pregnancy was monitored, every 30 days, with evaluation of fetal and placenta viability, and the births attended to ensure a promptly intervention in case of problems.

Soon after birth, all necessary parameters to evaluate the physical health and viability of the foal were measured and recorded, or possible complications arising from the intervention of the experiment.

Five experimental groups were defined, namely:

  • GROUP 1 (control): pregnant mares that were not submitted to supplementation with exogenous hormones (n=4);

  • GROUP 2 (treatment 1): Supplemented non-cycling receivers (induced to an artificial cycle). They received estradiol cypionate for three days after the embryo donor's ovulation. On the fourth day, 1500 mg of long-lasting natural progesterone (P4-LA) was administered. Once the embryo was retrieved on the eighth day after the donor's ovulation, another application of P4-LA in the receiver and the embryo transfer was performed. When pregnancy was confirmed, P4-LA was applied every 7 days until 120 days of pregnancy (n=4);

  • GROUP 3 (treatment 2): Hormonal supplementation (P4-CA). As of 280 days of pregnancy, the mares received 225 mg of short-term natural progesterone once a day until the foal's birth (n=5);

  • GROUP 4 (treatment 3): Hormonal supplementation (P4 - LA). As of 280 days of pregnancy, the mares received 1500 mg of long-term natural progesterone (P4-LA) once a week until the birth of the foal (n=5);

  • GROUP 5 (treatment 4): Hormonal supplementation with hormone derived from 19-norethisterone steroid (E-19N) (altrenogest). As of 280 days of pregnancy, the mares received 300mg of (E-19N) once a week until the foal's birth (n=4).

To perform serum hormone dosages in mares and foals, plasma was used and collection was carried out immediately after parturition, in 10 minutes maximum.

The dosage of progesterone in mares was performed using the radioimmunoassay (RIA) technique, following the protocol described by the manufacturer (Beckman Coulter, Immunotech/USA).

The levels of triiodothyronine (T3) and thyroxine (T4), progesterone and cortisone in foals were also determined using the Radioimmunoassay (RIA) technique and different commercial diagnostic kits were used (Coat-A-Count - Diagnostic Products Corporation/USA kit was used to T3 and T4; Beckman Coulter, Immunotech/USA kit was used to progesterone and cortisone). For the thyrotrophin test (TSH), the enzyme-linked immunosorbent assay (ELISA) was performed.

The data obtained were analyzed using Minitab®19 (Minitab, 2019).

The Shapiro-Wilk test was used to verify the normality of data distribution. For data that did not show normal distribution (free T4 and TSH) the Kruskal-Wallis test was used to compare the average. For variables with normal distribution (mother’s P4 and newborn’s P4, total T3 and cortisone), Analysis of Variance (ANOVA) was performed to detect the average difference of each hormone among groups, with a significance level of 5%. Thus, in cases where ANOVA detected significant interaction among groups (p<0,05), the Tukey's range test was applied. The Dunnett's test was also performed, adopting a 95% confidence interval, when applicable.

Pearson's correlation was used to calculate the relationship between progesterone from the mother and progesterone from the neonate.

Result

When comparing the plasmatic concentration average of TSH, T3, T4 and progesterone, in newborn foals from the groups of the experiment, no statistical difference was observed (p=0,46) (p=0,71), respectively. When comparing cortisone average among the groups, a difference was observed (p≤0,001), and after performing the Dunnett's test, it was found that cortisone average in groups 4 (11,10) and 5 (1, 16) was higher and lower when compared to the control group (5.88), respectively (Table 1).

Table 1
Means and standard error of hormonal dosages of TSH, T3, T4 and progesterone in newborn foals and adult mares in the five experimental groups.

In the analysis of the comparison of the dosage of progesterone in mares, it was observed that there is a significant difference among the groups (p≤0,001), however, after performing the Tukey's range test, it was not possible to identify among which groups there was this difference in the average.

Pearson's correlation, to verify if the level of natural progesterone in mares was correlated with the concentration in foals, showed that there was no relationship considering the two types of average (correlation coefficient: 0,208).

Discussion

Our study evaluated the level (in the immediate postpartum period) of some important hormones for the development of the neonate, since few studies have evaluated the effect of supplementation with synthetic progesterone in horses (Neuhauser et al., 2008, 2009; Palm et al., 2010; Jackson et al., 1986; Shoemaker et al., 1989; Ousey et al., 2002; Fedorka et al., 2019; Müller et al., 2019).

Changes in thyroid hormones levels in the intrauterine period can trigger permanent changes in the structure and function of tissues and organs (Forhead and Fowden, 2014). The investigation of thyroid dysfunction in horses has many difficulties due to multisystemic and non-specific effects (Messer et al., 1998). A study compared the levels of thyroid hormones in mares and neonates of different properties in relation to the reference values ​​and found a high percentage of animals with T3, T4 and TSH values ​​below the normal range, although none of them presented typical signs of apparent gland dysfunction (Messer et al., 1998). In our study, in addition to not having suggestive physical characteristics of thyroid disorders, neonates from different groups did not show any difference considering the levels of total T3, free T4 and TSH.

In relation to TSH, among the few studies that measure it in equine neonates, it has been observed that the hormone level is the same for foals and adult horses; on the other hand, there seems to be a difference considering those who were born premature and sick in comparison to healthy ones, with the first group presenting a lower level of TSH (Berg et al., 2007; Breuhaus, 2014). Since the level of thyroid hormones in foals is higher, it is likely that there is a different functioning between the hypothalamic pituitary adrenal (HPA) axis of adults and neonates (Breuhaus, 2014). We found no difference in TSH levels when comparing the groups and there are no previous references that discuss the possible influence of exogenous progesterone supplementation on the thyroid gland and this shows that our treatment groups do not interfered in measurement.

As for the level of progesterone in newborns, we also did not find a relationship between the use of hormones in the mother and changes in the levels found in foals. Literature reports that progesterone levels are high at birth but tend to decrease over the first day postpartum and become undetectable on the second day in healthy foals (Holtan et al., 1991; Chavatte et al., 1997). However, in sick foals, levels are high at birth and remain in the following days, with the highest levels found in animals with more severe impairments (Houghton et al., 1991; Rossdale et al., 1995). When there is a higher level of progesterone in foals born to supplemented mares, a slow or non-existent response to external stimulus is expected due to the possible sedative effects that progesterone derivatives have, as they cross the blood-brain barrier (BBB) and reach the central nervous system (Madigan et al., 2012). Thus, given the fact that we measured the progesterone level in a single moment and all animals were born healthy, the decay of the plasma level was expected. Another possibility would be the inability of the dosage test to detect exogenous progesterone. This hypothesis is in the literature, considering that the type of hormonal dosage test may interfere with the measurement, leading to false results, as it would only detect endogenous progesterone; in other words, it has been indicated that the synthetic hormone (altrenogest) does not have a cross-reactivity with the immunoassay antibodies (Wynn et al., 2018). Thus, we concluded that the use of synthetic hormone in mares did not interfere with the measured levels in neonates in our experiment, or the dosage test was not able to detect exogenous progesterone, indicating a limitation of this study.

As for the level of progesterone in the mares in the postpartum period, although we found a difference among the groups in the Analysis of variance (ANOVA), in the subsequent tests (Tukey and Dunnett), this difference was not found. We believe that the large variation in data, added to the low sample size, may have contributed to this inability to detect differences in means. Corroborating our finding, other studies found no difference in the level of endogenous progesterone after using altrenogest, depending on the dosage test used (Jackson et al., 1986; Willmann et al., 2011). Another study, however, managed to differentiate the level of endogenous and exogenous progesterone after application of altrenogest, but used other techniques for measurements, such as radioimmunoassay (RIA) and Gas chromatography (GC), respectively (Ousey et al., 2002). As well as the situation of foals, we believe that for this synthetic hormone, the type of hormonal test used, radioimmunoassay (RIA), may have been inefficient in differentiation. Knowing the altrenogest immunomodulatory effects in nonpregnant mares, and understanding the limitation of hormonal dosage tests, we consider that this topic requires more sample robust studies, so that this hypothesis can be discussed in pregnant mares and their respective neonates.

The cortisone level average in neonates was lower in group five (treatment with altrenogest) and higher in group four (treatment with long-term progesterone) when compared to the control group (group one). Contradicting our results, other studies found higher plasmatic cortisone levels in those groups supplemented with synthetic hormone (altrenogest), but this difference disappeared after 15 minutes of birth. These changes in cortisone level appeared to be associated with time of delivery, insofar as those animals treated with synthetic hormone had a longer time of delivery than the control group (Neuhauser et al., 2008, 2009; Palm et al., 2010). In our study, we did not have any prolonged action delivery that could justify the increase in cortisone in group four. Another distinction between our study and the literature is the method of administration; while we use the injectable form of the product, which has a lower absorption rate but a longer blood circulation time, other works show us a daily oral administration, therefore altering the plasmatic cortisone levels at the time of measurement (Machnik et al., 2007; McConaghy et al., 2016).

A limitation of our research was not evaluating the immune response despite the existing relationship between cortisone and the immune system. Existing studies try to understand the regulation of the immune system by glucocorticoids, such as cortisone, mainly because these hormones act in multiple ways (Cain and Cidlowski, 2017). However, the inhibition of cytokine production has been considered as the most relevant phenomenon of the immunosuppressive effects of glucocorticoids (Riccardi et al., 2002). Therefore, in our study, given the variation in cortisone levels which was found in the experimental groups, somehow, we believe that it may have modulated the newborns' immune system. Such parameters would need to be measured, and the foals would need to be monitored for a longer time than we proposed in this study.

Conclusion

There were no differences in the levels of total T3, free T4, TSH and progesterone in the neonates and in the levels of progesterone in the mares of the different groups, the small sample of animals evaluated may be the reason why no differences were observed. However, we found a higher level of cortisone in neonates in the group supplemented with long-lasting progesterone and a lower level of cortisone in the group supplemented with altrenogest. We believe that supplementation with altrenogest and natural progesterone is related to oscillations in cortisone found in neonates in the supplemented groups (groups 4 and 5). However, more studies need to be carried out to elucidate this influence.

Acknowledgements

We thank to the São Paulo Research Foundation (FAPESP) for financing the research project and paper publication (protocol number 2011/23120-6).

  • Financial support: This work has been supported by the São Paulo Research Foundation (FAPESP) under protocol number 2011/23120-6.
  • How to cite: Porto ACRC, Redoan MA, Massoco CO, Furtado PV, Oliveira CA. Additional effects using progestins in mares on levels of thyroid hormones and steroids in neonates. Anim Reprod. 2023;20(4):e20230029. https://doi.org/10.1590/1984-3143-AR2023-0029

References

  • Allen WR. Luteal deficiency and embryo mortality in the mare. Reprod Domest Anim. 2001;36(3-4):121-31. http://dx.doi.org/10.1046/j.1439-0531.2001.d01-43.x
    » http://dx.doi.org/10.1046/j.1439-0531.2001.d01-43.x
  • Bamberger AM, Jenatschke S, Schulte HM, Löning T, Bamberger MC. Leukemia inhibitory factor (LIF) stimulates the human HLA-G promoter in JEG3 choriocarcinoma cells. J Clin Endocrinol Metab. 2000;85(10):3932-6. http://dx.doi.org/10.1210/jcem.85.10.6849
    » http://dx.doi.org/10.1210/jcem.85.10.6849
  • Barker PM, Walters DV, Markiewicz M, Strang LB. Development of the lung liquid reabsorptive mechanism in fetal sheep: synergism of triiodothyronine and hydrocortisone. J Physiol. 1991;433(1):435-49. http://dx.doi.org/10.1113/jphysiol.1991.sp018436
    » http://dx.doi.org/10.1113/jphysiol.1991.sp018436
  • Berg EL, McNamara DL, Keisler DH. Endocrine profiles of periparturient mares and their foals. J Anim Sci. 2007;85(7):1660-8. http://dx.doi.org/10.2527/jas.2006-771
    » http://dx.doi.org/10.2527/jas.2006-771
  • Breuhaus BA. Thyroid function and dysfunction in term and premature equine neonates. J Vet Intern Med. 2014;28(4):1301-9. http://dx.doi.org/10.1111/jvim.12382
    » http://dx.doi.org/10.1111/jvim.12382
  • Cain DW, Cidlowski JA. Immune regulation by glucocorticoids. Nat Rev Immunol. 2017;17(4):233-47. http://dx.doi.org/10.1038/nri.2017.1
    » http://dx.doi.org/10.1038/nri.2017.1
  • Chavatte P, Holtan D, Ousey JC, Rossdale PD. Biosynthesis and possible biological roles of progestagens during equine pregnancy and in the newborn foal. Equine Vet J. 1997;29(24):89-95. http://dx.doi.org/10.1111/j.2042-3306.1997.tb05084.x
    » http://dx.doi.org/10.1111/j.2042-3306.1997.tb05084.x
  • DeLuca CA, McCue PM, Patten ML, Squires EL. Effect of a nonsurgical embryo transfer procedure and/or altrenogest therapy on endogenous progesterone concentration in mares. J Equine Vet Sci. 2011;31(2):57-62. http://dx.doi.org/10.1016/j.jevs.2010.12.002
    » http://dx.doi.org/10.1016/j.jevs.2010.12.002
  • Fedorka CE, Ball BA, Walker OF, Conley AJ, Corbin CJ, Lu KG, Hanneman JM, Troedsson MHT, Adams AA. Alteration of the mare’s immune system by the synthetic progestin, altrenogest. Am J Reprod Immunol. 2019;82(2):e13145. http://dx.doi.org/10.1111/aji.13145
    » http://dx.doi.org/10.1111/aji.13145
  • Forhead AJ, Fowden AL. Thyroid hormones in fetal growth and prepartum maturation. J Endocrinol. 2014;221(3):R87-103. http://dx.doi.org/10.1530/JOE-14-0025
    » http://dx.doi.org/10.1530/JOE-14-0025
  • Fowden AL, Forhead AJ, Ousey JC. Endocrine adaptations in the foal over the perinatal period. Equine Vet J. 2012;44(41):130-9. http://dx.doi.org/10.1111/j.2042-3306.2011.00505.x
    » http://dx.doi.org/10.1111/j.2042-3306.2011.00505.x
  • Fowden AL, Silver M. Comparative development of the pituitary-adrenal axis in the fetal foal and lamb. Reprod Domest Anim. 1995;30(4):170-7. http://dx.doi.org/10.1111/j.1439-0531.1995.tb00141.x
    » http://dx.doi.org/10.1111/j.1439-0531.1995.tb00141.x
  • Frank N, Sojka J, Messer NT 4th. Equine thyroid dysfunction. Vet Clin North Am Equine Pract. 2002;18(2):305-19. http://dx.doi.org/10.1016/S0749-0739(02)00007-X
    » http://dx.doi.org/10.1016/S0749-0739(02)00007-X
  • Goddard LM, Ton AN, Org T, Mikkola HKA, Iruela-Arispe ML. Selective suppression of endothelial cytokine production by progesterone receptor. Vascul Pharmacol. 2013;59(1-2):36-43. http://dx.doi.org/10.1016/j.vph.2013.06.001
    » http://dx.doi.org/10.1016/j.vph.2013.06.001
  • Hart KA, Barton MH. Adrenocortical insufficiency in horses and foals. Vet Clin North Am Equine Pract. 2011;27(1):19-34. http://dx.doi.org/10.1016/j.cveq.2010.12.005
    » http://dx.doi.org/10.1016/j.cveq.2010.12.005
  • Holtan DW, Houghton E, Silver M, Fowden AL, Ousey J, Rossdale PD. Plasma progestagens in the mare, fetus and newborn foal. J Reprod Fertil Suppl. 1991;44:517-28.
  • Houghton E, Holtan D, Grainger L, Voller BE, Rossdale PD, Ousey JC. Plasma progestagen concentrations in the normal and dysmature newborn foal. J Reprod Fertil Suppl. 1991;44:609-17.
  • Huijbregts RPH, Helton ES, Michel KG, Sabbaj S, Richter HE, Goepfert PA, Hel Z. Hormonal contraception and HIV-1 Infection: medroxyprogesterone acetate suppresses innate and adaptive immune mechanisms. Endocrinology. 2013;154(3):1282-95. http://dx.doi.org/10.1210/en.2012-1850
    » http://dx.doi.org/10.1210/en.2012-1850
  • Jackson SA, Squires EL, Nett TM. The effect of exogenous progestins on endogenous progesterone secretion in pregnant mares. Theriogenology. 1986;25(2):275-9. http://dx.doi.org/10.1016/0093-691X(86)90062-2
    » http://dx.doi.org/10.1016/0093-691X(86)90062-2
  • Jeffcott LB, Rossdale PD, Leadon DP. Haematological changes in the neonatal period of normal and induced premature foals. J Reprod Fertil Suppl. 1982;32:537-44.
  • Knottenbelt D, Holdstock N, Madigan J. Equine neonatal medicine and surgery. Philadelphia: Saunders; 2004. Perinatal review; p. 15-43.
  • Koubovec D, Berghe WV, Vermeulen L, Haegeman G, Hapgood JP. Medroxyprogesterone acetate downregulates cytokine gene expression in mouse fibroblast cells. Mol Cell Endocrinol. 2004;221(1-2):75-85. http://dx.doi.org/10.1016/j.mce.2004.03.006
    » http://dx.doi.org/10.1016/j.mce.2004.03.006
  • LeBlanc MM, MacPherson M, Sheerin P. Ascending placentitis: what we know about pathophysiology, diagnosis, and treatment. In: AAEP Annual Convention [Internet]; 2004; Denver. Lexington, KY: American Association of Equine Practitioners; 2004 [cited 2021 Jul 27]. Available from: https://www.ivis.org/library/aaep/aaep-annual-convention-denver-2004/ascending-placentitis-what-we-know-about-pathophysiology-diagnosis-and-treatment#read
    » https://www.ivis.org/library/aaep/aaep-annual-convention-denver-2004/ascending-placentitis-what-we-know-about-pathophysiology-diagnosis-and-treatment#read
  • Lester GD. Maturity of the neonatal foal. Vet Clin North Am Equine Pract. 2005;21(2):333-55. http://dx.doi.org/10.1016/j.cveq.2005.04.001
    » http://dx.doi.org/10.1016/j.cveq.2005.04.001
  • Machnik M, Hegger I, Kietzmann M, Thevis M, Guddat S, Schänzer W. Pharmacokinetics of altrenogest in horses. J Vet Pharmacol Ther. 2007;30(1):86-90. http://dx.doi.org/10.1111/j.1365-2885.2007.00820.x
    » http://dx.doi.org/10.1111/j.1365-2885.2007.00820.x
  • Madigan JE, Haggettt EF, Pickles KJ, Conley A, Stanley S, Moeller B, Toth B, Aleman M. Allopregnanolone infusion induced neurobehavioural alterations in a neonatal foal: is this a clue to the pathogenesis of neonatal maladjustment syndrome? Equine Vet J. 2012;109-12(41):109-12. http://dx.doi.org/10.1111/j.2042-3306.2011.00504.x
    » http://dx.doi.org/10.1111/j.2042-3306.2011.00504.x
  • McConaghy FF, Green LA, Colgan S, Morris LH. Studies of the pharmacokinetic profile, in vivo efficacy and safety of injectable altrenogest for the suppression of oestrus in mares. Aust Vet J. 2016;94(7):248-55. http://dx.doi.org/10.1111/avj.12459
    » http://dx.doi.org/10.1111/avj.12459
  • Messer NT 4th, Thomas Riddle W, Traub-Dargatz JL, Dargatz DA, Refsal KJ, Thompson DL. Thyroid hormone levels in thoroughbred mares and their foals at parturition. AAEP Proc. 1998;44:248-51.
  • Minitab. Minitab®19 [Internet]. 2019 [cited 2021 Jul 27]. Available from: https://www.minitab.com
    » https://www.minitab.com
  • Müller V, Curcio BR, Toribio RE, Feijó LS, Borba LA, Canisso IF, Nogueira CEW. Cortisol, progesterone, 17α-OH-progesterone, and pregnenolone in foals born from mare’s hormone-treated for experimentally induced ascending placentitis. Theriogenology. 2019;123:139-44. http://dx.doi.org/10.1016/j.theriogenology.2018.06.024
    » http://dx.doi.org/10.1016/j.theriogenology.2018.06.024
  • Neuhauser S, Palm F, Ambuehl F, Aurich C. Effects of altrenogest treatment of mares in late pregnancy on parturition and on neonatal viability of their foals. Exp Clin Endocrinol Diabetes. 2008;116(7):423-8. http://dx.doi.org/10.1055/s-2008-1065367
    » http://dx.doi.org/10.1055/s-2008-1065367
  • Neuhauser S, Palm F, Ambuehl F, Möstl E, Schwendenwein I, Aurich C. Effects of altrenogest treatment of mares in late pregnancy on parturition and on neonatal viability of their foals. Equine Vet J. 2009;41(6):572-7. http://dx.doi.org/10.2746/042516409X394481
    » http://dx.doi.org/10.2746/042516409X394481
  • Ousey J, Rossdale P, Palmer L, Houghton E, Grainger L, Fowden A. Effects of progesterone administration to mares during late gestation. Theriogenology. 2002;58(2-4):793-5. http://dx.doi.org/10.1016/S0093-691X(02)00743-4
    » http://dx.doi.org/10.1016/S0093-691X(02)00743-4
  • Palm FM, Schenk I, Neuhauser S, Schubert D, Machnik M, Schänzer W, Aurich C. Concentrations of altrenogest in plasma of mares and foals and in allantoic and amniotic fluid at parturition. Theriogenology. 2010;74(2):229-35. http://dx.doi.org/10.1016/j.theriogenology.2010.02.006
    » http://dx.doi.org/10.1016/j.theriogenology.2010.02.006
  • Panzani S, Villani M, McGladdery A, Magri M, Kindahl H, Galeati G, Martino PA, Veronesi MC. Concentrations of 15-ketodihydro-PGF2alpha, cortisol, and progesterone in the plasma of healthy and pathologic newborn foals. Theriogenology. 2009;72(8):1032-40. http://dx.doi.org/10.1016/j.theriogenology.2009.06.015
    » http://dx.doi.org/10.1016/j.theriogenology.2009.06.015
  • Ramminger SJ, Inglis SK, Olver RE, Wilson SM. Hormonal modulation of Na(+) transport in rat fetal distal lung epithelial cells. J Physiol. 2002;544(2):567-77. http://dx.doi.org/10.1113/jphysiol.2002.022459
    » http://dx.doi.org/10.1113/jphysiol.2002.022459
  • Riccardi C, Bruscoli S, Migliorati G. Molecular mechanisms of immunomodulatory activity of glucocorticoids. Pharmacol Res. 2002;45(5):361-8. http://dx.doi.org/10.1006/phrs.2002.0969
    » http://dx.doi.org/10.1006/phrs.2002.0969
  • Rose BV, Firth M, Morris B, Roach JM, Wathes DC, Verheyen KLP, de Mestre AM. Descriptive study of current therapeutic practices, clinical reproductive findings and incidence of pregnancy loss in intensively managed thoroughbred mares. Anim Reprod Sci. 2018;188:74-84. http://dx.doi.org/10.1016/j.anireprosci.2017.11.011
    » http://dx.doi.org/10.1016/j.anireprosci.2017.11.011
  • Rossdale PD, Ousey JC, McGladdery AJ, Prandi S, Holdstock N, Grainger L, Houghton E. A retrospective study of increased plasma progestagen concentrations in compromised neonatal foals. Reprod Fertil Dev. 1995;7(3):567-75. http://dx.doi.org/10.1071/RD9950567
    » http://dx.doi.org/10.1071/RD9950567
  • Shoemaker CF, Squires EL, Shideler RK. Safety of altrenogest in pregnant mares and on health and development of offspring. J Equine Vet Sci. 1989;9(2):69-72. http://dx.doi.org/10.1016/S0737-0806(89)80030-9
    » http://dx.doi.org/10.1016/S0737-0806(89)80030-9
  • Silver M, Ousey JC, Dudan FE, Fowden AL, Knox J, Cash RS, Rossdale PD. Studies on equine prematurity 2: post natal adrenocortical activity in relation to plasma adrenocorticotrophic hormone and catecholamine levels in term and premature foals. Equine Vet J. 1984;16(4):278-86. http://dx.doi.org/10.1111/j.2042-3306.1984.tb01927.x
    » http://dx.doi.org/10.1111/j.2042-3306.1984.tb01927.x
  • Silver M. Prenatal maturation, the timing of birth and how it may be regulated in domestic animals. Exp Physiol. 1990;75(3):285-307. http://dx.doi.org/10.1113/expphysiol.1990.sp003405
    » http://dx.doi.org/10.1113/expphysiol.1990.sp003405
  • Willmann C, Budik S, Walter I, Aurich C. Influences of treatment of early pregnant mares with the progestin altrenogest on embryonic development and gene expression in the endometrium and conceptus. Theriogenology. 2011;76(1):61-73. http://dx.doi.org/10.1016/j.theriogenology.2011.01.018
    » http://dx.doi.org/10.1016/j.theriogenology.2011.01.018
  • Wynn MAA, Esteller-Vico A, Legacki EL, Conley AJ, Loux SC, Stanley SD, Curry TE Jr, Squires EL, Troedsson MH, Ball BA. A comparison of progesterone assays for determination of peripheral pregnane concentrations in the late pregnant mare. Theriogenology. 2018;106:127-33. http://dx.doi.org/10.1016/j.theriogenology.2017.10.002
    » http://dx.doi.org/10.1016/j.theriogenology.2017.10.002

Publication Dates

  • Publication in this collection
    18 Dec 2023
  • Date of issue
    2023

History

  • Received
    09 Mar 2023
  • Accepted
    24 Oct 2023
location_on
Colégio Brasileiro de Reprodução Animal Coronel José dias Bicalho, 1224, CEP: , 31275-050, Belo Horizonte, MG - Brasil, Tel.: 55-31-3491 7122 - Belo Horizonte - MG - Brazil
E-mail: animreprod.journal@gmail.com
rss_feed Acompanhe os números deste periódico no seu leitor de RSS
Acessibilidade / Reportar erro