Kisspeptin-10

Reproductive / Hormonal Peptideresearch

Also known as: KP-10, Metastin 45-54, KISS1-derived peptide

A 10-amino acid fragment of kisspeptin that is the most potent endogenous stimulator of GnRH release, playing a critical role in reproductive hormone regulation and fertility.

Overview

Kisspeptin-10 is the shortest bioactive fragment of the kisspeptin family, derived from the KISS1 gene product. It is the most potent known endogenous activator of the hypothalamic-pituitary-gonadal (HPG) axis, acting through the kisspeptin receptor (KISS1R/GPR54) on GnRH neurons to stimulate gonadotropin-releasing hormone secretion. This cascade leads to LH and FSH release, which in turn stimulates testosterone production in males and estrogen/progesterone in females. Kisspeptin-10 has garnered significant research interest for its potential in treating hypogonadism, infertility, and as a diagnostic tool for reproductive disorders. Clinical trials have demonstrated its ability to robustly stimulate LH release in both men and women. In the biohacking community, it is explored as a natural alternative to exogenous testosterone or hCG for maintaining endogenous hormone production.

Mechanism of Action

Kisspeptin-10 acts through the HPG axis: (1) Binds to KISS1R (GPR54) receptors on GnRH neurons in the hypothalamus; (2) Activates Gq/11 signaling, increasing intracellular calcium and depolarizing GnRH neurons; (3) Stimulates pulsatile GnRH release into the hypophyseal portal system; (4) GnRH acts on anterior pituitary gonadotropes to release LH and FSH; (5) LH stimulates Leydig cells (males) to produce testosterone or theca cells (females) for steroidogenesis; (6) FSH supports spermatogenesis in males and follicular development in females; (7) Subject to negative feedback from sex steroids, maintaining physiological regulation.

Molecular Formula

C56H78N14O12

Molecular Weight

1131.31 g/mol

Sequence

Tyr-Asn-Trp-Asn-Ser-Phe-Gly-Leu-Arg-Phe-NH2

Dosage Protocols

Dose Range

100mcg500mcg

Frequency

Once to twice daily

Route

subcutaneous

Cycle Length

4-8 weeks

Pulsatile dosing may be more physiological. Higher continuous doses can paradoxically desensitize the receptor. Some protocols use every-other-day dosing. Very short half-life (~30 minutes).

Source: Community protocols and clinical research extrapolation

Side Effects

EffectSeverity
Injection site discomfortmild
Facial flushingmild
Headachemild
Receptor desensitizationmoderate
Hormonal fluctuationsmoderate

Pros & Cons

Stimulates the entire HPG axis naturally, preserving endogenous hormone production and feedback

Human clinical trial data supporting robust LH and testosterone stimulation

Does not bypass natural regulatory mechanisms — maintains physiological pulsatility

Potential fertility applications in both sexes without exogenous hormone administration

Very short half-life (~30 min) requiring frequent dosing or pulsatile administration

Continuous dosing leads to receptor desensitization and reduced efficacy (tachyphylaxis)

Not yet approved for clinical use — research compound only

Testosterone elevation is modest compared to exogenous TRT or hCG

Research Studies

Legal Status

Not FDA-approved. Available as a research chemical. Used in clinical research settings for diagnostic and therapeutic purposes. No specific regulatory restrictions in most jurisdictions.

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