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Journal of reproduction and fertility1981; 62(2); 527-536; doi: 10.1530/jrf.0.0620527

Biological functions and receptor binding activities of equine chorionic gonadotrophins.

Abstract: The role of equine chorionic gonadotrophin (CG, formerly termed Pregnant Mare serum Gonadotrophin, PMSG) in maintaining equine pregnancy was investigated by examining the effects of this hormone on the maternal ovaries during early gestation and relating these findings to the receptor binding activities of CG in vitro. Measurement of plasma progestagen profiles in mares and donkeys carrying horse, donkey, mule ( female horse X male donkey) and hinny (female donkey X male horse) conceptuses confirmed that CG induced several secondary ovulations and thus maintained maternal progestagen concentrations. However, in mares carrying horse and mule conceptuses and in donkeys carrying donkey conceptuses the growth of the follicles that gave rise to the secondary corpora lutea occurred before CG was secreted and the CG did not express any FSH-like activity. Nevertheless, in donkeys carrying hinny pregnancies the CG secreted by the hinny conceptus stimulated massive follicular growth in addition to luteinization, presumably because of an enhanced sensitivity of donkey ovaries to hinny CG which, as demonstrated in previous studies, is a mixture of horse and donkey CG and hence has considerably more FSH-like activity than normal donkey CG. In-vitro receptor binding experiments showed that both horse and donkey gonadal tissues possessed a low binding affinity for horse CG compared to that exhibited by equivalent gonadal tissues of other species. Furthermore, horse CG bound with low, but significant, affinity to horse and donkey LH receptors and donkey FSH receptors, but exhibited negligible binding to horse FSH receptors. We suggest that in equids the receptor-mediated refractoriness to the gonadotrophic activities of the intraspecific chorionic gonadotrophin protects the ovaries during pregnancy.
Publication Date: 1981-07-01 PubMed ID: 6265633DOI: 10.1530/jrf.0.0620527Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research article delves into the role of equine chorionic gonadotrophin (CG) in maintaining equine pregnancy. The researchers studied the effects of CG on maternal ovaries during early pregnancy, demonstrating that CG induces multiple secondary ovulations, ensuring necessary progestagen levels. They found that the growth of follicles resulting in secondary corpora lutea predates the secretion of CG. Additionally, certain pregnancy types stimulated mass follicular growth in addition to luteinization. The study further examined the binding activities of CG to its receptors, uncovering notably low binding affinity when horse CG binds to equivalent gonadal tissues of other species.

Role of Equine Chorionic Gonadotrophin

  • In the study, the research team investigated the role of equine chorionic gonadotrophin (CG) in maintaining equine pregnancies. They found that CG helped ensure stifling maternal progestagen concentrations, crucial for sustaining the pregnancy.
  • Interestingly, they observed that the growth of follies that lead to the creation of secondary corpora lutea often occurred before the secretion of CG itself, thus ruling the hormone out from being directly responsible for this particular process.

Impact of Different Pregnancies

  • The research also noted varied impacts on follicular growth depending on the type of pregnancy. In donkeys carrying hinny pregnancies (a result of breeding a female donkey with a male horse), the CG produced by the hinny conceptus fostered significant follicular growth in addition to luteinization. This unique growth pattern may be linked to the enhanced sensitivity of donkey ovaries to ‘hinny CG’ which produces more FSH-like activity than normal donkey CG.

Receptor Binding Activities of CG

  • Further in-vitro experiments were conducted to unearth the receptor binding activities of CG. Both horse and donkey gonadal tissues exhibited significantly low binding affinity to horse CG compared to the affinity exhibited by equivalent gonadal tissues in other species.
  • The same horse CG bound modestly to horse LH receptors and donkey FSH receptors. However, it exhibited marginal binding when applied to horse FSH receptors.
  • This pattern indicates a distinct receptor-mediated resistance to the gonadotrophic activities of the chorionic gonadotrophin in equids. The researchers suggest this might serve to protect the ovaries during pregnancy, preventing any potential hormonal overwhelm.

Cite This Article

APA
Stewart F, Allen WR. (1981). Biological functions and receptor binding activities of equine chorionic gonadotrophins. J Reprod Fertil, 62(2), 527-536. https://doi.org/10.1530/jrf.0.0620527

Publication

ISSN: 0022-4251
NlmUniqueID: 0376367
Country: England
Language: English
Volume: 62
Issue: 2
Pages: 527-536

Researcher Affiliations

Stewart, F
    Allen, W R

      MeSH Terms

      • Animals
      • Corpus Luteum / metabolism
      • Female
      • Gonadotropins, Equine / blood
      • Gonadotropins, Equine / metabolism
      • Horses / metabolism
      • Horses / physiology
      • Male
      • Ovarian Follicle / growth & development
      • Ovarian Follicle / metabolism
      • Perissodactyla / metabolism
      • Perissodactyla / physiology
      • Pregnancy
      • Pregnancy, Animal
      • Progestins / blood
      • Receptors, Cell Surface / metabolism
      • Receptors, FSH
      • Receptors, LH
      • Testis / metabolism

      Citations

      This article has been cited 9 times.
      1. Byambaragchaa M, Park A, Gil SJ, Lee HW, Ko YJ, Choi SH, Kang MH, Min KS. Luteinizing hormone-like and follicle-stimulating hormone-like activities of equine chorionic gonadotropin β-subunit mutants in cells expressing rat luteinizing hormone/chorionic gonadotropin receptor and rat follicle-stimulating hormone receptor. Anim Cells Syst (Seoul) 2021;25(3):171-181.
        doi: 10.1080/19768354.2021.1943708pubmed: 34262660google scholar: lookup
      2. Stella ED, Ramos AA, de Ruediger FR, Dantas A, Yamada PH, Codognoto VM, Salgado LC, Brochine S, Oba E. Evaluation of buffaloes' follicular dynamics and stress state under different ovulation synchronization protocols. Anim Reprod 2018 Aug 16;15(2):102-107.
      3. Reineri PS, Piccardi MB, Arroquy J JI, Fumagalli A, Coria MS, Hernández O, Bó G, Palma GA. Hormones and monensin use to improve pregnancy rates in grazing lactating beef cows in the semiarid region of Argentina. Anim Reprod 2018 Aug 16;15(1):56-63.
      4. Byambaragchaa M, Lee SY, Kim DJ, Kang MH, Min KS. Signal Transduction of Eel Luteinizing Hormone Receptor (eelLHR) and Follicle Stimulating Hormone Receptor (eelFSHR) by Recombinant Equine Chorionic Gonadotropin (rec-eCG) and Native eCG. Dev Reprod 2018 Mar;22(1):55-64.
        doi: 10.12717/DR.2018.22.1.055pubmed: 29707684google scholar: lookup
      5. Antczak DF, de Mestre AM, Wilsher S, Allen WR. The equine endometrial cup reaction: a fetomaternal signal of significance. Annu Rev Anim Biosci 2013 Jan;1:419-42.
      6. Casarini L, Lispi M, Longobardi S, Milosa F, La Marca A, Tagliasacchi D, Pignatti E, Simoni M. LH and hCG action on the same receptor results in quantitatively and qualitatively different intracellular signalling. PLoS One 2012;7(10):e46682.
        doi: 10.1371/journal.pone.0046682pubmed: 23071612google scholar: lookup
      7. Songsasen N, Woodruff TK, Wildt DE. In vitro growth and steroidogenesis of dog follicles are influenced by the physical and hormonal microenvironment. Reproduction 2011 Jul;142(1):113-22.
        doi: 10.1530/REP-10-0442pubmed: 21502334google scholar: lookup
      8. Wang Y, Gao Z, Zhang Q, Guo X, Xia W, Gu X, Zeng W. Unraveling the Transcriptomic Profiles of Large and Small Donkey Follicles. Genes (Basel) 2025 May 20;16(5).
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      9. Baruselli PS, de Abreu LÂ, Catussi BLC, Oliveira ACDS, Rebeis LM, Gricio EA, Albertini S, Sales JNS, Rodrigues CA. Use of new recombinant proteins for ovarian stimulation in ruminants. Anim Reprod 2023;20(2):e20230092.
        doi: 10.1590/1984-3143-AR2023-0092pubmed: 37720727google scholar: lookup