Kisspeptins: a multifunctional peptide system with a role in reproduction, cancer and the cardiovascular system.
Mead. E J EJ; Maguire. J J JJ; Kuc. R E RE; Davenport. A P AP
Key Findings
- Kisspeptin triggers the GnRH hormone cascade, making it essential for puberty and reproductive hormone regulation.
- Kisspeptin can suppress tumor metastasis by altering cell movement and stickiness.
- Kisspeptin receptors are found in blood vessels linked to atherosclerosis and cause strong vasoconstriction; they are also highly expressed in the placenta, suggesting a role in pregnancy.
Practical Outcomes
- For biohackers, kisspeptin might be a future target for influencing fertility or hormonal balance, but there is no safe, tested dosage or protocol yet. Its vascular effects mean any self‑experimentation could affect blood pressure. At present, the information is mainly scientific background rather than actionable guidance.
Summary
Kisspeptin is a small protein that helps start puberty by turning on the hormone cascade that controls reproduction. It also appears to slow down cancer spread, is involved in pregnancy, and can tighten blood vessels, especially in areas prone to artery disease. However, the paper is a broad review and does not give any dosing or practical protocols for using kisspeptin.
Abstract
Orphan G-protein-coupled receptors that have recently been paired with their cognate ligand are an often untapped resource for novel drug development. The KISS1 receptor (previously designated GPR54) has been paired with biologically active cleavage peptides of the KiSS-1 gene product, the kisspeptins (KP). The focus of this review is the emerging pharmacology and physiology of the KP. Genetic linkage analysis in humans revealed that mutations in KISS1 (GPR54, AXOR12 or hOT7T175) result in idiopathic hypogonadotrophic hypogonadism and knockout mouse studies confirmed this finding. Identification of KISS1 (GPR54) as a molecular switch for puberty subsequently led to the discovery that KP activate the GnRH cascade. Prior to the role of KISS1 (GPR54) in puberty being described, KP had been shown to be inhibitors of tumour metastasis across a range of cancers. Subsequently the mechanism of this inhibition has been suggested to be via altered cell motility and adhesiveness. PCR detected highest expression of KP and KISS1 (GPR54) in placenta, and changes in KP levels throughout pregnancy and expression in trophoblasts suggests a role in placentation. Placentation and metastasis are invasive processes that require angiogenesis. Investigation of KISS1 (GPR54) and KP in vasculature revealed discrete localisation of KISS1 (GPR54) to blood vessels prone to atherosclerosis and a potent vasoconstrictor action. A role for KP has also been shown in whole body homeostasis. KP are multifunctional peptides and further investigation is required to fully elucidate the complex pathways regulated by these peptides and how these pathways integrate in the whole body system.
Study Information
pubmed
2007
2007-05-21T00:00:00.000Z
10.1038/sj.bjp.0707295
63
79