Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 2
2010 pubmed 289 citations

The kisspeptin system of the human hypothalamus: sexual dimorphism and relationship with gonadotropin-releasing hormone and neurokinin B neurons.

Hrabovszky. E E; Ciofi. P P; Vida. B B; Horvath. M C MC; Keller. E E; Caraty. A A; Bloom. S R SR; Ghatei. M A MA; Dhillo. W S WS; Liposits. Z Z; Kallo. I I

Key Findings

  • Kisspeptin neurons are far more abundant in female hypothalami than in males.
  • Kisspeptin‑positive fibers make direct contacts with GnRH‑producing cells, indicating a direct regulatory pathway.
  • About three‑quarters of kisspeptin cells in the infundibular nucleus also produce neurokinin B, linking two fertility‑related peptides.

Practical Outcomes

  • The data suggest that boosting kisspeptin signaling could affect reproductive hormone balance, especially in women, but no specific protocols or safe dosage ranges are provided. Biohackers interested in fertility or hormone modulation should view this as mechanistic background and await clinical studies before trying any kisspeptin‑based interventions.

Summary

Researchers mapped kisspeptin-producing cells in human brains and found they are more numerous in women, connect directly to hormone‑controlling GnRH neurons, and often also make another peptide called neurokinin B. This helps explain how kisspeptin influences fertility, but the study doesn’t give any dosing or treatment advice.

Abstract

Kisspeptin signaling via the kisspeptin receptor G-protein-coupled receptor-54 plays a fundamental role in the onset of puberty and the regulation of mammalian reproduction. In this immunocytochemical study we addressed the (i) topography, (ii) sexual dimorphism, (iii) relationship to gonadotropin-releasing hormone (GnRH) neurons and (iv) neurokinin B content of kisspeptin-immunoreactive hypothalamic neurons in human autopsy samples. In females, kisspeptin-immunoreactive axons formed a dense periventricular plexus and profusely innervated capillary vessels in the infundibular stalk. Most immunolabeled somata occurred in the infundibular nucleus. Many cells were also embedded in the periventricular fiber plexus. Rostrally, they formed a prominent periventricular cell mass (magnocellular paraventricular nucleus). Robust sex differences were noticed in that fibers and somata were significantly less numerous in male individuals. In dual-immunolabeled specimens, fine kisspeptin-immunoreactive axon varicosities formed axo-somatic, axo-dendritic and axo-axonal contacts with GnRH neurons. Dual-immunofluorescent studies established that 77% of kisspeptin-immunoreactive cells in the infundibular nucleus synthesize the tachykinin peptide neurokinin B, which is known to play crucial role in human fertility; 56 and 17% of kisspeptin fibers in the infundibular and periventricular nuclei, respectively, contained neurokinin B immunoreactivity. Site-specific co-localization patterns implied that kisspeptin neurons in the infundibular nucleus and elsewhere contributed differentially to these plexuses. This study describes the distribution and robust sexual dimorphism of kisspeptin-immunoreactive elements in human hypothalami, reveals neuronal contacts between kisspeptin-immunoreactive fibers and GnRH cells, and demonstrates co-synthesis of kisspeptins and neurokinin B in the infundibular nucleus. The neuroanatomical information will contribute to our understanding of central mechanisms whereby kisspeptins regulate human fertility.

Study Information

Provider

pubmed

Year

2010

Date

2010-06-01T00:00:00.000Z

DOI

10.1111/j.1460-9568.2010.07239.x

Citations

289

References

56