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The Journal of endocrinology1977; 73(3); 419-425; doi: 10.1677/joe.0.0730419

Influence of foetal genotype on the follicle-stimulating hormone:luteinizing hormone ratio of pregnant mare serum gonadotrophin.

Abstract: Rat testicular radioreceptor assays specific for FSH and LH were used to determine the FSH:LH ratio of PMSG produced by horse, donkey, mule and hinny conceptuses. Measurements of FSH and LH activities in PMSG produced both in vivo and in vitro by the four types of conceptuses showed that the genotype of the foetus markedly influences the FSH:LH ratio of PMSG. The FSH:LH ratio of PMSG produced by the horse conceptus was around unity whereas the ratio of PMSG produced by the donkey conceptus was as low as 0-2. Furthermore, the hybrid mule and hinny conceptuses both produced PMSG with an FSH:LH ratio which was approximately midway between those of the horse and donkey.
Publication Date: 1977-06-01 PubMed ID: 874396DOI: 10.1677/joe.0.0730419Google Scholar: Lookup
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  • Journal Article

Summary

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The research investigates how the genetic makeup of a foetus influences the ratio of follicle-stimulating hormone (FSH) to luteinizing hormone (LH) in the serum of pregnant mares. It found that the ratio varies significantly between different species; the ratio in horses was approximately 1:1, while in donkeys it was considerably lower.

Methodology

  • To carry out this research, the scientists utilized Rat testicular radioreceptor assays – analytical procedures that specifically detect and measure the levels of FSH and LH hormones.
  • The scientists examined pregnant mare serum gonadotrophin (PMSG) produced from the pregnant females of horses, donkeys, mules and hinnies.
  • This investigation included assessing the hormone ratio in PMSG both from in vivo (inside the body) and in vitro (outside the body in a controlled environment) production by the conceptuses (early stages of foetal development).

Findings

  • The results show that the genotype – the set of genes characteristic of the foetus – significantly influences the FSH:LH ratio in PMSG.
  • Specifically, the hormone ratio in horses was around 1:1, suggesting an equal presence of FSH and LH hormones. However, the ratio in donkeys was significantly lower (0.2), indicating a dominance of LH over FSH.
  • Interestingly, the hybrid species – mules and hinnies – presented a PMSG hormone ratio approximately halfway between those of horses and donkeys.

Implications

  • The variability of the FSH:LH ratio based on the foetus’ genotype implies that species-specific signalling mechanisms might be at work in hormone production, potentially impacting reproductive strategies employed by different species.
  • The research may have significant implications in terms of understanding species-specific reproductive physiology and potentially influence breeding and conservation strategies for these animal species.

Cite This Article

APA
Stewart F, Allen WR, Moor RM. (1977). Influence of foetal genotype on the follicle-stimulating hormone:luteinizing hormone ratio of pregnant mare serum gonadotrophin. J Endocrinol, 73(3), 419-425. https://doi.org/10.1677/joe.0.0730419

Publication

ISSN: 0022-0795
NlmUniqueID: 0375363
Country: England
Language: English
Volume: 73
Issue: 3
Pages: 419-425

Researcher Affiliations

Stewart, F
    Allen, W R
      Moor, R M

        MeSH Terms

        • Animals
        • Female
        • Fetus / physiology
        • Follicle Stimulating Hormone / analysis
        • Genotype
        • Gonadotropins, Equine / analysis
        • Horses / metabolism
        • Luteinizing Hormone / analysis
        • Perissodactyla / metabolism
        • Pregnancy
        • Rats

        Citations

        This article has been cited 2 times.
        1. 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.
        2. Enders AC, Meadows S, Stewart F, Allen WR. Failure of endometrial cup development in the donkey-in-horse model of equine abortion.. J Anat 1996 Jun;188 ( Pt 3)(Pt 3):575-89.
          pubmed: 8763475