1. Academic Validation
  2. Stimulation of growth hormone by kisspeptin antagonists in ewes

Stimulation of growth hormone by kisspeptin antagonists in ewes

  • J Endocrinol. 2018 May;237(2):165-173. doi: 10.1530/JOE-18-0074.
J T Smith 1 A Roseweir 2 3 M Millar 4 I J Clarke 5 R P Millar 6 7
Affiliations

Affiliations

  • 1 School of Human SciencesThe University of Western Australia, Perth, Western Australia, Australia.
  • 2 Academic Unit of SurgerySchool of Medicine, University of Glasgow, Royal Infirmary, Glasgow, UK.
  • 3 Unit of Experimental TherapeuticsInstitute of Cancer Sciences, University of Glasgow Glasgow, UK.
  • 4 Queen's Medical Research InstituteUniversity of Edinburgh, Edinburgh, UK.
  • 5 Department of PhysiologyMonash University, Clayton, Victoria, Australia.
  • 6 Centre for NeuroendocrinologyDepartment of Immunology and Physiology, University of Pretoria, Pretoria, South Africa robertpetermillar@gmail.com.
  • 7 Institute for Infectious Diseases and Molecular MedicineUniversity of Cape Town, Cape Town, South Africa.
Abstract

Kisspeptin signalling is indispensable for fertility, stimulating gonadotropin-releasing hormone (GnRH) secretion and mediating gonadal steroid feedback on GnRH neurons. Moreover, kisspeptin neurons have been implicated in Other non-reproductive neuroendocrine roles. Kisspeptin appears to also regulate growth hormone secretion but much of the data appear contradictory. We sought to clarify a potential role of kisspeptin in growth hormone (GH) regulation by examining the effect of kisspeptin antagonists on GH secretion in ewes under various physiological conditions. Our data show clear and robust increases in GH secretion following lateral ventricle or third ventricle infusion of kisspeptin antagonists p-234 and p-271 in either ovariectomized or anestrous ewes. Central infusion of kisspeptin-10 had no effect on GH secretion. To determine the level at which kisspeptin may influence GH secretion, we examined expression of the cognate Kisspeptin Receptor, GPR54, in pituitary cells and showed by immunocytochemistry that the majority of somatotropes express GPR54 while expression was largely negative in Other pituitary cells. Overall, we have demonstrated that blocking kisspeptin signalling by antagonists stimulates GH secretion in ewes and that this is likely mediated by inhibiting endogenous kisspeptin activation of GPR54 expressed on somatotropes. The findings suggest that endogenous kisspeptin inhibits GH secretion through GPR54 expressed on somatotropes.

Keywords

hypothalamus; neuroendocrinology; neuropeptide; reproduction.

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