Analyze Diet

Transport of spermatozoa in the reproductive tracts of mares.

Abstract: A scintigraphic method was developed to study sperm migration in the reproductive tracts of mares. Mares (n=5) and stallions (n=2) were used to test various steps of the procedure and three other mares and a stallion were used to study sperm transportation. A radiolabelling solution was prepared from 99mTc (Technetium-99m) and hexamethyl propylene amine oxime. The highest labelling of spermatozoa (57-72%) was obtained by incubation of the spermatozoa with the radiolabelling solution for 20 min at 20 degrees C. Radioactivity outside the spermatozoa was removed by centrifugation and by two subsequent washings with skimmed milk extender. The labelled spermatozoa were inseminated into the uterine bodies of detomidine-sedated mares undergoing oestrus and scintigraphic images were obtained for 4.5 h after insemination. Both dynamic (two pictures s(-1), 2 min multiple scans, 64 x 64 matrix) and static scans (20 s, 64 x 64 matrix) were used to image the mares. The attenuation of gamma radiation in the vagina and uterus was determined for each mare. Radioactive spermatozoa were found in the tips of the uterine horns for the first time at about 8-20 min after insemination. The frequency of uterine contractions varied considerably among mares and ranged from five to 65 contractions during the first 30 min after insemination. Within 1 h after insemination most of the sperm activity was in the uterus. At 2.5 h after insemination, most of the spermatozoa had left the uterus and were either in the vagina or had escaped into the vulva and been discharged. At 4.5 h after insemination there was hardly any sperm activity in the uterus and a small amount of activity only in the vagina; most spermatozoa had been eliminated from the mares.
Publication Date: 2000-01-01 PubMed ID: 20681171
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.

The research study outlines the development of a scintigraphic method to monitor sperm movement in mares’ reproductive tracts, utilizing a radiolabelling solution prepared from Technetium-99m and hexamethyl propylene amine oxime.

Research Methodology

  • The researchers developed a scintigraphic method specifically for studying sperm migration in the reproductive tracts of mares.
  • The study involved five mares and two stallions for preliminary tests, and an additional three mares and one stallion for the main experiment.
  • An isotopic radiolabelling solution was created using Technetium-99m and hexamethyl propylene amine oxime, which was then used to label the spermatozoa.
  • To ensure optimized labelling, spermatozoa were incubated with the radiolabelling solution for 20 minutes at 20 degrees Celsius, which resulted in a labelling rate of 57-72%.

Procedure and Findings

  • Any radioactivity outside the spermatozoa was eliminated by centrifugation and washing with skimmed milk extender.
  • The radiolabelled sperm was then introduced into the uterine bodies of detomidine-sedated mares in oestrus and scintigraphic images were obtained over a period of 4.5 hours post-insemination.
  • The movements of the sperm were tracked using both dynamic and static scans.
  • Results indicated that the radiolabelled sperms reached the uterine horns approximately 8-20 minutes after insemination. The number of uterine contractions in the 30 minutes following insemination ranged from 5 to 65 across the different mares.
  • After one hour post-insemination, the majority of the sperm activity was found in the uterus. At the 2.5-hour mark, most sperm had exited the uterus and were either in the vagina or discharged.
  • By the 4.5-hour mark, few traces of sperm activity were detected in the uterus, with minimal activity in the vagina as most spermatozoa had been eliminated from the mares.

Implications of the Study

  • This study delivers a novel method to explore and monitor sperm movement in the equine reproductive tract, enhancing understanding of equine fertility and potentially informing the development of fertility treatments for horses.
  • The findings also provide new insights, quantitatively and qualitatively, into the kinetics of sperm migration within the mare’s reproductive tract.

Cite This Article

APA
Katila T, Sankari S, Mäkelä O. (2000). Transport of spermatozoa in the reproductive tracts of mares. J Reprod Fertil Suppl(56), 571-578.

Publication

ISSN: 0449-3087
NlmUniqueID: 0225652
Country: England
Language: English
Issue: 56
Pages: 571-578

Researcher Affiliations

Katila, T
  • Department of Clinical Veterinary Sciences, Faculty of Veterinary Medicine, University of Helsinki, Finland.
Sankari, S
    Mäkelä, O

      MeSH Terms

      • Animals
      • Female
      • Genitalia, Female / physiology
      • Horses / physiology
      • Insemination, Artificial / veterinary
      • Male
      • Radionuclide Imaging / veterinary
      • Spermatozoa / physiology

      Citations

      This article has been cited 4 times.
      1. Marey MA, Ma D, Yoshino H, Elesh IF, Zinnah MA, Fiorenza MF, Moriyasu S, Miyamoto A. Sperm induce proinflammatory responses in the uterus and peripheral blood immune cells of artificially inseminated cows. J Reprod Dev 2023 Apr 3;69(2):95-102.
        doi: 10.1262/jrd.2022-124pubmed: 36775285google scholar: lookup
      2. Marey MA, Aboul Ezz M, Akthar I, Yousef MS, Imakawa K, Shimada M, Miyamoto A. Sensing sperm via maternal immune system: a potential mechanism for controlling microenvironment for fertility in the cow. J Anim Sci 2020 Aug 18;98(Suppl 1):S88-S95.
        doi: 10.1093/jas/skaa147pubmed: 32810249google scholar: lookup
      3. Catalán J, Padilla L, Maside C, Martínez-Hernández J, Yánez-Ortiz I, Tvarijonaviciute A, Barranco I, Bonet S, Miró J, Yeste M. Redox profiling of preovulatory follicular fluid in the donkey is species-specific, and contributes to modulate sperm function. Sci Rep 2025 Feb 23;15(1):6522.
        doi: 10.1038/s41598-025-91422-0pubmed: 39988588google scholar: lookup
      4. Akthar I, Kim Y, Umehara T, Kanno C, Sasaki M, Marey MA, Yousef MS, Haneda S, Shimada M, Miyamoto A. Activation of sperm Toll-like receptor 2 induces hyperactivation to enhance the penetration to mucus and uterine glands: a trigger for the uterine inflammatory cascade in cattle. Front Immunol 2023;14:1319572.
        doi: 10.3389/fimmu.2023.1319572pubmed: 38179051google scholar: lookup