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Kisspeptin-10

KP-10, Metastin (45-54), Kisspeptin-10 (human), KiSS-1

Quick Stats
Studies 877
Trials 47
Score 1
2018 pubmed

Stimulation of growth hormone by kisspeptin antagonists in ewes.

Smith. J T JT; Roseweir. A A; Millar. M M; Clarke. I J IJ; Millar. R P RP

Key Findings

  • Kisspeptin antagonists (p‑234, p‑271) infused into the brain sharply increased GH secretion in ewes
  • Direct infusion of kisspeptin‑10 had no effect on GH levels
  • Most somatotropes in the pituitary express the kisspeptin receptor GPR54

Practical Outcomes

  • The study shows that blocking kisspeptin can boost growth hormone in sheep, but the technique (central brain infusion) isn’t practical for humans. There’s no ready‑to‑use dosage or supplement recommendation, so biohackers can’t directly apply this finding yet.

Summary

In sheep, stopping the normal kisspeptin signal with special blockers caused a clear rise in growth hormone, while giving kisspeptin itself didn’t change hormone levels. The hormone‑producing cells in the pituitary have the kisspeptin receptor, indicating that the body’s own kisspeptin normally keeps growth hormone in check.

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.

Study Information

Provider

pubmed

Year

2018

Date

2018-03-16T00:00:00.000Z

DOI

10.1530/joe-18-0074