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Endocrinology2009; 150(6); 2813-2821; doi: 10.1210/en.2008-1698

Biological and anatomical evidence for kisspeptin regulation of the hypothalamic-pituitary-gonadal axis of estrous horse mares.

Abstract: The purpose of the present study was to evaluate the effects of kisspeptin (KiSS) on LH and FSH secretion in the seasonally estrous mare and to examine the distribution and connectivity of GnRH and KiSS neurons in the equine preoptic area (POA) and hypothalamus. The diestrous mare has a threshold serum gonadotropin response to iv rodent KiSS decapeptide (rKP-10) administration between 1.0 and 500 microg. Administration of 500 microg and 1.0 mg rKP-10 elicited peak, mean, and area under the curve LH and FSH responses indistinguishable to that of 25 microg GnRH iv, although a single iv injection of 1.0 mg rKP-10 was insufficient to induce ovulation in the estrous mare. GnRH and KiSS-immunoreactive (ir) cells were identified in the POA and hypothalamus of the diestrous mare. In addition, KiSS-ir fibers were identified in close association with 33.7% of GnRH-ir soma, suggesting a direct action of KiSS on GnRH neurons in the mare. In conclusion, we are the first to reveal a physiological role for KiSS in the diestrous mare with direct anatomic evidence by demonstrating a threshold-like gonadotropin response to KiSS administration and characterizing KiSS and GnRH-ir in the POA and hypothalamus of the diestrous horse mare.
Publication Date: 2009-02-19 PubMed ID: 19228887DOI: 10.1210/en.2008-1698Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research focused on the role of a protein called kisspeptin (KiSS) in regulating reproductive hormones in female horses. The researchers discovered that this protein appears to directly influence the cells responsible for producing these hormones, and demonstrated a certain dose range at which its administration triggers a response.

Study Objectives and Methodology

  • The study aimed to understand how kisspeptin (KiSS) affects the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which are critical for reproduction in female horses that are in their diestrus phase (non-reproductive period).
  • It also sought to investigate the network and distribution of GnRH (gonadotropin-releasing hormone) and KiSS neurons in the preoptic area (POA) and hypothalamus (key brain regions in hormone regulation) of the mare.
  • To achieve these aims, the researchers administered intravenous injections of a version of the KiSS protein derived from rodents (rKP-10) at different doses, and monitored the resultant LH and FSH responses.
  • They also examined GnRH and KiSS activity in the POA and hypothalamus in the diestrous mare.

Key Findings

  • The study found that the administration of rKP-10 causes a response in the production of LH and FSH within a certain dose range.
  • A further increase in the dose of rKP-10 caused a peak in LH and FSH levels equivalent to that of an injection of GnRH. However, even the highest dosage of rKP-10 tested was not enough to trigger ovulation in the mare.
  • The research also discovered that KiSS and GnRH-reactive cells are present in the POA and hypothalamus during the diestrus phase.
  • Moreover, KiSS fibers were identified in close proximity with approximately a third of GnRH-producing cells, suggesting a possible direct interaction between KiSS and GnRH neurons.

Conclusions and Implications

  • The findings of this study suggest that KiSS plays an important role in the endocrine regulation of the reproductive cycle in female horses during their diestrus phase.
  • The research also provides the first anatomical evidence of a direct interaction between KiSS and GnRH neurons in the mare, affirming a potential direct role of KiSS in the reproductive hormone regulation.
  • These insights could have significant implications in the understanding and potential treatment of reproduction-related disorders in horses and possibly other mammals, given the common role of these hormones in sexual maturity and reproduction.

Cite This Article

APA
Magee C, Foradori CD, Bruemmer JE, Arreguin-Arevalo JA, McCue PM, Handa RJ, Squires EL, Clay CM. (2009). Biological and anatomical evidence for kisspeptin regulation of the hypothalamic-pituitary-gonadal axis of estrous horse mares. Endocrinology, 150(6), 2813-2821. https://doi.org/10.1210/en.2008-1698

Publication

ISSN: 1945-7170
NlmUniqueID: 0375040
Country: United States
Language: English
Volume: 150
Issue: 6
Pages: 2813-2821

Researcher Affiliations

Magee, Christianne
  • Department of Biomedical Sciences, Animal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins, Colorado 80523, USA.
Foradori, Chad D
    Bruemmer, Jason E
      Arreguin-Arevalo, Jesus A
        McCue, Patrick M
          Handa, Robert J
            Squires, Edward L
              Clay, Colin M

                MeSH Terms

                • Animals
                • Estrous Cycle / drug effects
                • Estrous Cycle / physiology
                • Female
                • Follicle Stimulating Hormone / blood
                • Gonadotropin-Releasing Hormone / metabolism
                • Horses / physiology
                • Hypothalamo-Hypophyseal System / drug effects
                • Hypothalamo-Hypophyseal System / physiology
                • Hypothalamus / cytology
                • Hypothalamus / metabolism
                • Injections, Intravenous
                • Kisspeptins
                • Luteinizing Hormone / blood
                • Models, Animal
                • Neurons / metabolism
                • Oligopeptides / administration & dosage
                • Oligopeptides / physiology
                • Ovary / drug effects
                • Ovary / physiology
                • Ovulation / drug effects
                • Preoptic Area / cytology
                • Preoptic Area / metabolism
                • Reproduction / physiology
                • Tumor Suppressor Proteins / metabolism

                Citations

                This article has been cited 11 times.
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                  doi: 10.3390/ani10122249pubmed: 33266083google scholar: lookup
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