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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 2
2013 pubmed 71 citations

Interactions between kisspeptins and neurokinin B.

Navarro. Víctor M VM

Key Findings

  • Kisspeptin and neurokinin B are crucial gatekeepers of puberty and fertility.
  • Loss‑of‑function mutations in their genes or receptors lead to delayed sexual maturation and infertility.
  • Neurokinin B stimulates LH release by acting on kisspeptin‑dependent pathways within KNDy neurons.

Practical Outcomes

  • Understanding this hormone interplay suggests that future biohacks could target kisspeptin or neurokinin B pathways to modulate reproductive hormones, but the current research offers no direct dosing or protocol guidance.

Summary

The study explains how two brain chemicals, kisspeptin and neurokinin B, work together to control the release of hormones that start puberty and keep the reproductive system running. It shows that problems with these chemicals can cause delayed puberty or infertility, and that neurokinin B helps trigger hormone bursts by acting on kisspeptin‑producing neurons.

Abstract

Reproductive function is tightly regulated by an intricate network of central and peripheral factors; however, the precise mechanism triggering critical reproductive events, such as puberty onset, remains largely unknown. Recently, the neuropeptides kisspeptin (encoded by Kiss1) and neurokinin B (NKB, encoded by TAC3 in humans and Tac2 in rodents) have been placed as essential gatekeepers of puberty. Studies in humans and rodents have revealed that loss-of-function mutations in the genes encoding either kisspeptin and NKB or their receptors, Kiss1r and neurokinin 3 receptor (NK3R), lead to impaired sexual maturation and infertility. Kisspeptin, NKB, and dynorphin A are co-expressed in neurons of the arcuate nucleus (ARC), so-called Kisspeptin/NKB/Dyn (KNDy) neurons. Importantly, these neurons also co-express NK3R. Compelling evidence suggests a stimulatory role of NKB (or the NK3R agonist, senktide) on LH release in a number of species. This effect is likely mediated by autosynaptic inputs of NKB on KNDy neurons to induce the secretion of gonadotropin-releasing hormone (GnRH) in a kisspeptin--dependent manner, with the coordinated actions of other neuroendocrine factors, such as dynorphin, glutamate, or GABA. Thus, we have proposed a model in which NKB feeds back to the KNDy neuron to shape the pulsatile release of kisspeptin, and hence GnRH, in a mechanism also dependent on the sex steroid level. Additionally, NKB may contribute to the regulation of the reproductive function by metabolic cues. Investigating how NKB and kisspeptin interact to regulate the gonadotropic axis will offer new insights into the control of GnRH release during puberty onset and the maintenance of the reproductive function in adulthood, offering a platform for the understanding and treatment of a number of reproductive disorders.

Study Information

Provider

pubmed

Year

2013

DOI

10.1007/978-1-4614-6199-9_15

Citations

71

References

122