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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 1
2012 pubmed

Altered placental expression of kisspeptin and its receptor in pre-eclampsia.

Cartwright. Judith E JE; Williams. Paula Juliet PJ

Key Findings

  • KISS1 (kisspeptin) expression is reduced in placentas from pre‑eclampsia cases
  • KISS1R (kisspeptin receptor) expression is increased in pre‑eclampsia placentas
  • Protein and mRNA levels of both kisspeptin and its receptor match each other

Practical Outcomes

  • This research is mainly relevant to pregnancy health and does not provide actionable advice for general longevity or performance optimization. It suggests kisspeptin pathways are involved in pre‑eclampsia, but there are no dosing or protocol recommendations for non‑pregnant individuals.

Summary

The study looked at a protein called kisspeptin and its receptor in the placenta and found that in women with pre‑eclampsia, kisspeptin levels are lower while its receptor levels are higher, which may affect how the placenta develops.

Abstract

Kisspeptin, originally identified as metastatin, important in preventing cancer metastasis, has more recently been shown to be important in pregnancy. Roles indicated for kisspeptin in pregnancy include regulating trophoblast invasion and migration during placentation. The pregnancy-specific disorder pre-eclampsia (PE) is now accepted to begin with inadequate trophoblast invasion and the current study therefore sets out to characterise placental expression of both kisspeptin (KISS1) and its receptor (KISS1R) throughout pregnancy and in PE. Placental tissue was obtained from women undergoing elective surgical termination of early pregnancy (n=10) and from women following Caesarean section at term in normal pregnancy (n=10) and with PE (n=10). Immunohistochemistry of paraffin embedded sections and western immunoblotting were performed to assess protein localisation and expression. Quantitative real-time PCR was carried out to evaluate mRNA expression of both KISS1 and KISS1R. Protein and mRNA expression was found to mirror each other with KISS1 expression found to be reduced in PE compared with that in normal term pregnancy. Interestingly, KISS1R expression at both the mRNA and protein levels was found to be increased in PE compared with that in normal term pregnancy. The current findings of increased KISS1R expression may represent a mechanism by which functional activity of KISS1 is higher in PE than in normal pregnancy. Higher levels of activity of KISS1R may be involved in inhibition of trophoblast invasion and angiogenesis, which are associated with PE.

Study Information

Provider

pubmed

Year

2012

Date

2012-04-23T00:00:00.000Z

DOI

10.1530/joe-12-0091