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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 2
2005 pubmed

Repetitive activation of hypothalamic G protein-coupled receptor 54 with intravenous pulses of kisspeptin in the juvenile monkey (Macaca mulatta) elicits a sustained train of gonadotropin-releasing hormone discharges.

Plant. Tony M TM; Ramaswamy. Suresh S; Dipietro. Meloni J MJ

Key Findings

  • A single 1‑minute IV infusion of kisspeptin‑10 triggers an immediate LH surge in juvenile monkeys.
  • Hourly repeat doses sustain a pulsatile LH (and FSH) release pattern for at least 48 hours.
  • Blocking GnRH receptors with acyline eliminates the kisspeptin‑induced LH response, confirming the effect works through GnRH.

Practical Outcomes

  • The study shows kisspeptin can reliably activate the reproductive hormone cascade in primates, suggesting it could be a tool for influencing LH/FSH levels. However, the experiments used high‑dose IV administration in juvenile monkeys, a method not feasible or safe for self‑experimentation. Biohackers should view this as mechanistic proof rather than a ready‑to‑use protocol, and await research on safer delivery routes and dosing for humans.

Summary

In young male rhesus monkeys, giving a short IV dose of the peptide kisspeptin-10 every hour for two days caused the brain to release a steady stream of hormone signals (GnRH) that led to repeated spikes in LH and FSH, the hormones that start puberty. The effect stopped when a drug that blocks GnRH receptors was used, showing the response depends on the normal GnRH pathway.

Abstract

The purpose of the present study was to further examine the hypothesis that activation of G protein-coupled receptor 54 (GPR54) signaling at the end of the juvenile phase of primate development is responsible for initiation of gonadarche and the onset of puberty. Accordingly, we determined whether repetitive iv administration of the GPR54 receptor agonist kisspeptin-10 (2 microg as a brief 1-min infusion once every hour for 48 h) to the juvenile male rhesus monkey would prematurely elicit sustained, pulsatile release of hypothalamic GnRH, the neuroendocrine trigger for gonadarche. GnRH release was monitored indirectly by measuring LH secretion from the in situ pituitary, the GnRH responsiveness of which had been heightened before the experiment with an intermittent iv infusion of synthetic GnRH. Agonadal animals (n = 4) were employed to eliminate any confounding and secondary effects of changing feedback signals from the testis. The first brief infusion of kisspeptin-10 evoked an LH discharge that mimicked those produced by GnRH priming, and this was followed by a train of similar LH discharges in response to hourly activation of GPR54 by repetitive kisspeptin-10 administration. Concomitant treatment with a GnRH receptor antagonist, acyline, abolished kisspeptin-10-induced LH release. Repetitive kisspeptin-10 administration also provided a GnRH-dependent signal to FSH secretion. These findings are consistent with the notion that, in primates, the transition from the juvenile (attenuated GnRH release) to pubertal (robust GnRH release) state is controlled by activation of GPR54 resulting from increased expression of hypothalamic KiSS-1 and release of kisspeptin in this region of the brain.

Study Information

Provider

pubmed

Year

2005

Date

2005-11-10T00:00:00.000Z

DOI

10.1210/en.2005-1261