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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 3
2013 pubmed 55 citations

Effects of environmental endocrine disruptors and phytoestrogens on the kisspeptin system.

Patisaul. Heather B HB

Key Findings

  • Exogenous estrogenic compounds (BPA, PCBs, genistein) can disrupt kisspeptin signaling in a region‑, sex‑, and compound‑specific manner.
  • Disruption of kisspeptin is linked to altered timing of puberty, irregular estrous/menstrual cycles, and changes in socio‑sexual behavior.
  • Impaired kisspeptin signaling may contribute to broader health issues such as precocious puberty, unexplained infertility, and metabolic syndrome.

Practical Outcomes

  • For biohackers, the takeaway is to minimize exposure to BPA (found in plastics), PCBs (legacy pollutants) and high‑dose phytoestrogens if you’re concerned about reproductive and metabolic health. Choose BPA‑free containers, filter water, and be selective with soy‑rich foods. Monitoring and reducing these environmental chemicals could help maintain a healthy kisspeptin system and support longevity goals.

Summary

The review shows that chemicals like BPA, PCBs and the plant estrogen genistein can mess up the kisspeptin system, which is a key hormone pathway for puberty, fertility and metabolism. These disruptions depend on the brain region, sex, and the specific chemical, and they can cause early puberty in girls, irregular cycles, and even affect mood and metabolism.

Abstract

Sex steroid hormones, most notably estradiol, play a pivotal role in the sex-specific organization and function of the kisspeptin system. Endocrine--disrupting compounds are anthropogenic or naturally occurring compounds that interact with steroid hormone signaling. Thus, these compounds have the potential to disrupt the sexually dimorphic ontogeny and function of kisspeptin signaling pathways, resulting in adverse effects on neuroendocrine physiology. This chapter reviews the small but growing body of evidence for endocrine disruption of the kisspeptin system by the exogenous estrogenic compounds bisphenol A, polychlorinated biphenyl mixtures, and the phytoestrogen genistein. Disruption is region, sex, and compound specific, and associated with shifts in the timing of pubertal onset, irregular estrous cycles, and altered sociosexual behavior. These effects highlight that disruption of kisspeptin signaling pathways could have wide ranging effects across multiple organ systems, and potentially underlies a suite of adverse human health trends including precocious female puberty, idiopathic infertility, and metabolic syndrome.

Study Information

Provider

pubmed

Year

2013

DOI

10.1007/978-1-4614-6199-9_21

Citations

55

References

133