Analyze Diet
Veterinary research communications2026; 50(6); 527; doi: 10.1007/s11259-026-11472-1

Endocrine and uterine hemodynamic differences between intra- and interspecific equine pregnancies during early gestation.

Abstract: Interspecific equine pregnancies (mare x donkey) are associated with altered endocrine patterns and increased pregnancy loss; however, the relationship between hormonal dynamics, luteal activity, and uterine hemodynamics in relation to conceptus origin remains incompletely understood. This study aimed to evaluate the influence of conceptus origin on endocrine profiles, supplementary corpora lutea (SCL) formation, and uterine hemodynamics, and to investigate the relationships among these variables. Twenty mares were initially included; however, six were excluded due to pregnancy loss or incomplete follow-up, resulting in a final sample of 14 mares (six stallion-derived and eight donkey-derived pregnancies). Serum progesterone (P4), equine chorionic gonadotropin (eCG), SCL number, and uterine artery Doppler indices, including pulsatility index (PI) and resistivity index (RI), were evaluated at Days 49, 63, 84, and 98 of gestation. Donkey-derived pregnancies showed significantly lower P4 and eCG concentrations, reduced SCL formation, and lower uterine PI and RI compared to stallion-derived pregnancies (p < 0.05). While stallion-derived pregnancies remained relatively stable over time, donkey-derived pregnancies showed progressive declines in P4 and eCG concentrations, accompanied by reductions in uterine PI and RI. Positive correlations were observed between P4 and PI (r = 0.846; p < 0.001) and between eCG and PI (r = 0.733; p = 0.015). All pregnancies were maintained to term. These findings indicate that conceptus origin is associated with distinct endocrine and uterine hemodynamic patterns, supporting integrated hormonal-vascular adaptations in equine pregnancy.
Publication Date: 2026-08-25 PubMed ID: 42640365PubMed Central: 12322513DOI: 10.1007/s11259-026-11472-1Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

Plain Language Overview

  • This study investigated how pregnancies from different species of equines (horse mares bred with either horse stallions or donkeys) differ in their hormone levels, formation of hormone-producing structures, and blood flow in the uterus during early pregnancy.
  • It found that interspecies pregnancies (mare x donkey) showed distinct hormonal and uterine blood flow patterns compared to same-species pregnancies (mare x stallion), which helps explain differences in pregnancy maintenance and loss.

Detailed Explanation

Background and Objectives

  • Interspecific equine pregnancies occur when a mare is bred with a donkey, producing a mule or hinnies.
  • These pregnancies are known for differing endocrine (hormonal) patterns and have higher risks of pregnancy loss compared to standard horse-to-horse pregnancies.
  • The specific interactions among hormones, the formation and activity of supplementary corpora lutea (SCL, structures on the ovary that produce progesterone), and blood flow parameters in the uterus related to the origin of the conceptus (offspring) are not fully understood.
  • The study aimed to:
    • Evaluate how conceptus origin (stallion-derived vs. donkey-derived) influences hormonal profiles, SCL formation, and uterine blood flow.
    • Analyze how these variables relate to each other during early pregnancy (Days 49 to 98).

Methodology

  • Twenty mares were initially included; however, data from 14 mares were analyzed due to losses or incomplete monitoring.
  • Pregnancy groups:
    • 6 mares with stallion-derived pregnancies (horse x horse)
    • 8 mares with donkey-derived pregnancies (horse x donkey)
  • Measurements taken at gestational Days 49, 63, 84, and 98 included:
    • Serum progesterone (P4) concentrations
    • Equine chorionic gonadotropin (eCG) concentrations, a hormone related to supporting pregnancy
    • Counting the number of supplementary corpora lutea (SCL), indicative of luteal activity
    • Uterine artery Doppler indices: pulsatility index (PI) and resistivity index (RI), which measure blood flow resistance and pulsatility in uterine arteries

Key Findings

  • Donkey-derived pregnancies showed significantly:
    • Lower progesterone (P4) and equine chorionic gonadotropin (eCG) levels compared to stallion-derived pregnancies
    • Reduced formation of supplementary corpora lutea (SCL)
    • Lower uterine artery pulsatility index (PI) and resistivity index (RI), indicating different uterine blood flow patterns
  • Stallion-derived pregnancies remained relatively stable for hormone concentrations and uterine blood flow indices throughout the study period.
  • Donkey-derived pregnancies showed a progressive decline in both P4 and eCG, alongside decreases in uterine PI and RI over time.
  • Statistically significant positive correlations were observed:
    • Between progesterone (P4) levels and pulsatility index (PI) (correlation coefficient r = 0.846, p < 0.001)
    • Between equine chorionic gonadotropin (eCG) and pulsatility index (PI) (r = 0.733, p = 0.015)
  • All pregnancies, despite these differences, were maintained to term.

Interpretation and Significance

  • The data support the conclusion that the origin of the conceptus (horse vs donkey sperm) influences endocrine activity, luteal function, and uterine blood flow during early pregnancy in mares.
  • Lower progesterone and eCG along with fewer supplementary corpora lutea in donkey-derived pregnancies suggest altered luteal support, which may explain some increased pregnancy risks observed previously in interspecific pregnancies.
  • Lower PI and RI values indicate reduced resistance in uterine arterial blood flow, which may be an adaptive or compensatory vascular response to lower hormone concentrations.
  • The strong correlations between hormone levels and blood flow indices highlight an integrated relationship between endocrine support and uterine vascular adaptations during pregnancy.
  • Understanding these differences is important for managing interspecific equine pregnancies and improving pregnancy outcomes.

Cite This Article

APA
Campos DG, Campos IS, Silva PHH, Bringel B, Douglas RH, Pinna AE, Jacob JCF, Portela VM, Amaral CDS, Antoniazzi AQ. (2026). Endocrine and uterine hemodynamic differences between intra- and interspecific equine pregnancies during early gestation. Vet Res Commun, 50(6), 527. https://doi.org/10.1007/s11259-026-11472-1

Publication

ISSN: 1573-7446
NlmUniqueID: 8100520
Country: Switzerland
Language: English
Volume: 50
Issue: 6
PII: 527

Researcher Affiliations

Campos, Diego Guedes
  • Laboratory of Reproductive Biotechnology (BIOREP), Federal University of Santa Maria (UFSM), Santa Maria, RS, Brazil. diegoguedescampos@hotmail.com.
Campos, Isabela Syllos
  • Department of Veterinary Pathology and Diagnostic Imaging, Fluminense Federal University (UFF), Niterói, RJ, Brazil.
Silva, Paulo Henrique Hümmelgen
  • Laboratory of Reproductive Biotechnology (BIOREP), Federal University of Santa Maria (UFSM), Santa Maria, RS, Brazil.
Bringel, Beatriz
  • BET Reproductive Laboratory, Lexington, KY, USA.
Douglas, Robert H
  • BET Reproductive Laboratory, Lexington, KY, USA.
Pinna, Aline Emerim
  • Department of Veterinary Pathology and Diagnostic Imaging, Fluminense Federal University (UFF), Niterói, RJ, Brazil.
Jacob, Julio Cesar Ferraz
  • Department of Animal Reproduction and Evaluation, Institute of Animal Science (IZ), Federal Rural University of Rio de Janeiro (UFRRJ), Seropédica, RJ, Brazil.
Portela, Valério Marques
  • Laboratory of Reproductive Biotechnology (BIOREP), Federal University of Santa Maria (UFSM), Santa Maria, RS, Brazil.
Amaral, Carolina Dos Santos
  • Laboratory of Reproductive Biotechnology (BIOREP), Federal University of Santa Maria (UFSM), Santa Maria, RS, Brazil. carolina.amaral@ufsm.br.
Antoniazzi, Alfredo Quites
  • Laboratory of Reproductive Biotechnology (BIOREP), Federal University of Santa Maria (UFSM), Santa Maria, RS, Brazil.

MeSH Terms

  • Animals
  • Female
  • Pregnancy
  • Horses / physiology
  • Uterus / blood supply
  • Uterus / physiology
  • Progesterone / blood
  • Pregnancy, Animal / physiology
  • Hemodynamics
  • Equidae / physiology
  • Chorionic Gonadotropin / blood
  • Corpus Luteum / physiology

Conflict of Interest Statement

Declarations. Ethics approval and animal welfare: All procedures involving animals were approved by the Animal Ethics Committee of the Universidade Federal Fluminense (CEUA/UFF; protocol no. 001/19) and were conducted in accordance with institutional and national guidelines for animal care and use. Consent to participate: Not applicable. Consent to publish: Not applicable. Competing interests: The authors declare no competing interests.

References

This article includes 36 references
  1. Allen WR, Moor RM. The origin of the equine endometrial cups. I. Production of PMSG by fetal trophoblast cells.. J Reprod Fertil 29(2):313–316.
    doi: 10.1530/jrf.0.0290313google scholar: lookup
  2. Allen WR, Short RV. Interspecific and extraspecific pregnancies in equids: anything goes.. J Hered 88(5):384–392.
  3. Allen WR, Stewart F. Equine placentation.. Reprod Fertil Dev 13(7–8):623–634.
    doi: 10.1071/rd01063pubmed: 11999314google scholar: lookup
  4. Allen WR, Kydd J, Boyle MS, Antczak DF. Between-species transfer of horse and donkey embryos: a valuable research tool.. Equine Vet J 17(S3):53–62.
  5. Allen WR, Skidmore JA, Stewart F, Antczak DF. Effects of fetal genotype and uterine environment on placental development in equids.. J Reprod Fertil 98(1):55–60.
    doi: 10.1530/jrf.0.0980055pubmed: 8345479google scholar: lookup
  6. Balaro MFA, Santos AS, Moura LFGM, Fonseca JF, Brandão FZ. Luteal dynamic and functionality assessment in dairy goats by luteal blood flow, luteal biometry, and hormonal assay.. Theriogenology 95:118–126.
  7. Barbosa LA, Maran AP, Almeida MER, Guimarães EC, Bringel B, Douglas RH, Lima TFG, Silva ESM. Plasma estradiol and endometrial edema profile in acyclic mares after single administration of 17-β estradiol, estradiol benzoate and estradiol cypionate.. Reprod Domest Anim 60:e70108.
    doi: 10.1111/rda.70108pubmed: 40760876pmc: 12322513google scholar: lookup
  8. Boeta M, Zarco L. Progesterone and equine chorionic gonadotropin concentrations around the time of pregnancy loss in mares impregnated by donkeys or stallions.. J Equine Vet Sci 25(12):531–538.
  9. Boeta M, Zarco L. Luteogenic and luteotropic effects of eCG during pregnancy in the mare.. Anim Reprod Sci 130(1–2):57–62.
  10. Bollwein H, Weber F, Woschée I, Stolla R. Transrectal Doppler sonography of uterine and umbilical blood flow during pregnancy in mares.. Theriogenology 61(2–3):499–509.
    doi: 10.1016/s0093-691x(03)00225-5pubmed: 14662147google scholar: lookup
  11. Bollwein H, Heppelmann M, Lüttgenau J. Ultrasonographic Doppler use for female reproduction management.. Vet Clin North Am Food Anim Pract 32(1):149–164.
    doi: 10.1016/j.cvfa.2015.09.005pubmed: 26922117google scholar: lookup
  12. Brinsko SP, Blanchard TL, Varner DD, Schumacher J, Love CC, Hinrichs K. Pregnancy: physiology and diagnosis.. Manual of Equine Reproduction, 3th edn. Elsevier, Missouri, pp 85–93.
  13. Campos DG, Ferreira CSC, Oliveira LFPS, Jacob JCF, Pinna AE. US Doppler in the monitoring of hemodynamic alterations of the supplementary corpus luteum in cyclic mares.. J Equine Vet Sci 125:104695.
  14. Canisso IF, Panzani D, Miró J, Ellerbrock RE. Key aspects of donkey and mule reproduction.. Vet Clin North Am Equine Pract 35(3):607–642.
    doi: 10.1016/j.cveq.2019.08.014pubmed: 31672204google scholar: lookup
  15. Carluccio A, Bucci R, Fusi J, Robbe D, Veronesi MC. Effect of age and reproductive status on reproductive indices in horse mares carrying mule pregnancies.. Heliyon 6(10):e05175.
    doi: 10.1016/j.heliyon.2020.e05175pubmed: 33083622pmc: 7551364google scholar: lookup
  16. Conley AJ. Review of the reproductive endocrinology of the pregnant and parturient mare. Theriogenology 86(1):355–365.
  17. Cuervo-Arango J, Domingo-Ortiz R. Systemic treatment with high dose of flunixin-meglumine is able to block ovulation in mares by inducing hemorrhage and luteinisation of follicles. Theriogenology 75:707–714.
  18. Enders AC, Meadows S, Stewart F, Allen WR. Failure of endometrial cup development in the donkey-in-horse model of equine abortion. J Anat 188(Pt 3):575–589.
    pubmed: 8763475pmc: 1167486
  19. Fanelli D, Moroni R, Bocci C, Camillo F, Rota A, Panzani D. Interspecific and intraspecific artificial insemination in domestic equids. Animals 13(4):582.
    doi: 10.3390/ani13040582pubmed: 36830369pmc: 9951644google scholar: lookup
  20. Ferreira JC, Meira CD. Aplicação da ultrassonografia colorida Doppler em programas de transferência de embriões equinos. Cienc Rural 41(6):1063–1069.
  21. Ferreira CSC, Morais RDCL, Andrade ABP, Balaro MFA, Ribas JAS, Gomes GM. Spectral Doppler ultrasound in selecting an equine embryo receiver. Reprod Dom Anim 55:747–752.
    doi: 10.1111/rda.13676google scholar: lookup
  22. Figueira LM, Fonseca JF, Arashiro E, Souza-Fabjan J, Ribeiro A, Oba E. Colour Doppler ultrasonography as a tool to assess luteal function in Santa Inês ewes. Reprod Domest Anim 50(4):643–650.
    doi: 10.1111/rda.12543pubmed: 25970377google scholar: lookup
  23. Ginther OJ. Ultrasonic imaging and animal reproduction: color-Doppler ultrasonography. .
  24. Ginther OJ. How ultrasound technologies have expanded and revolutionized research in reproduction in large animals. Theriogenology 81(1):112–125.
  25. Ginther OJ, Utt MD. Doppler ultrasound in equine reproduction: principles, techniques, and potential. J Equine Vet Sci 24(12):516–526.
  26. Henneke DR, Potter GD, Kreider JL, Yeates BF. Relationship between condition score, physical measurements and body fat percentage in mares. Equine Vet J 15(4):371–372.
  27. Lemos SG, Campos DG, Ferreira CS, Balaro MF, Cunha LE, Pinna AE. Uterine vascularization in mares bred to donkeys or stallions. Pesq Vet Bras 37(8):877–882.
  28. Meira CD, Ferreira JC, Silva ESM, Ignácio FS. Developmental aspects of early pregnancy in mares. Anim Reprod 9(3):166–172.
  29. Murphy BD. Equine chorionic gonadotropin: an enigmatic but essential tool. Anim Reprod 9(3):223–230.
  30. Oliveira M, Campos IS, Campos DG, Ferreira CSC, Souza GN, Pinna AE. Uterine artery doppler indices in mares carrying horse and donkey pregnancies. Cienc Rural 56(5):e20250177.
  31. Ousey JC, Kölling M, Newton R, Wright M, Allen WR. Uterine haemodynamics in young and aged pregnant mares measured using Doppler ultrasonography. Equine Vet J Suppl 41:15.
  32. Pugliesi G, Rezende RG, Silva JCB, Lopes E, Nishimura TK, Baruselli OS. Uso da ultrassonografia Doppler em programas de IATF e TETF em bovinos. Rev Bras Reprod Anim 41(1):140–150.
  33. Silva LA, Gastal EL, Gastal MO, Beg MA, Ginther OJ. Relationship between vascularity of the preovulatory follicle and establishment of pregnancy in mares. Anim Reprod 3(3):339–346.
  34. Teixeira ACB, Valle GR, Riveros JAN, Diniz JHW, Wenceslau RR, Monteiro GA. Effects of equine chorionic gonadotropin on ovulatory and luteal characteristics of mares submitted to a P4-based protocol of ovulation induction with hCG. J Equine Vet Sci 94:103233.
    doi: 10.1016/j.jevs.2020.103233pubmed: 33077076google scholar: lookup
  35. Urias-Castro C, Zarco L, Boeta AM. The role of equine chorionic gonadotropin in the stimulation of luteal steroidogenesis in mares carrying horse or mule pregnancies. J Equine Vet Sci 50:1–7.
  36. Vilanova XM, De Briyne N, Beaver B, Turner PV. Horse welfare during equine chorionic gonadotropin (eCG) production. Animals 9(12):1053.
    doi: 10.3390/ani9121053google scholar: lookup

Citations

This article has been cited 0 times.