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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 2
2021 pubmed 5 citations

Mutual Interactions Between GnRH and Kisspeptin in GnRH- and Kiss-1-Expressing Immortalized Hypothalamic Cell Models.

Kanasaki. Haruhiko H; Tumurbaatar. Tuvshintugs T; Tumurgan. Zolzaya Z; Oride. Aki A; Okada. Hiroe H; Kyo. Satoru S

Key Findings

  • Kisspeptin‑10 raises Kiss‑1 (kisspeptin) mRNA and protein levels in both AVPV‑derived (mHypoA‑50) and ARC‑derived (mHypoA‑55) hypothalamic cell lines.
  • In ARC‑derived cells (mHypoA‑55), kisspeptin‑10 also increases GnRH expression, whereas in AVPV‑derived cells (mHypoA‑50) GnRH levels stay unchanged.
  • Both kisspeptin‑10 and GnRH stimulate the activity marker c‑Fos in these hypothalamic cells, indicating neuronal activation.

Practical Outcomes

  • For self‑experimenters, this research mainly adds basic knowledge about how kisspeptin interacts with reproductive hormone pathways; it does not provide dosing guidelines, safety data, or direct performance benefits. Until human studies are done, kisspeptin‑10 remains a research tool rather than a practical supplement for longevity or metabolic health.

Summary

The study shows that the short peptide kisspeptin‑10 can boost its own production and, in some hypothalamic cells, also increase the production of GnRH, another hormone that controls reproduction. This effect was seen in mouse brain cell lines and in rat fetal brain cells, suggesting a feedback loop between kisspeptin and GnRH in the brain.

Abstract

Kisspeptin and gonadotropin-releasing hormone (GnRH) are central regulators of the hypothalamic-pituitary-gonadal axis and control female reproductive functions. Recently established mHypoA-50 and mHypoA-55 cells are immortalized hypothalamic neuronal cell models that originated from the anteroventral periventricular nucleus (AVPV) and arcuate nucleus (ARC) regions of the mouse hypothalamus, respectively. mHypoA-50 or mHypoA-55 cells were stimulated with kisspeptin-10 (KP10) and GnRH, after which the expression of kisspeptin and GnRH was determined. Primary cultures of fetal rat brain cells were also examined. mHypoA-50 and mHypoA-55 cells expressed mRNA for Kiss-1 (which encodes kisspeptin) and GnRH as well as receptors for kisspeptin and GnRH. We found that Kiss-1 mRNA expression was significantly increased in mHypoA-50 AVPV cells by KP10 and GnRH stimulation. Kisspeptin protein expression was also increased by KP10 and GnRH stimulation in these cells. In contrast, GnRH expression was unchanged in mHypoA-50 AVPV cells by KP10 and GnRH stimulation. In mHypoA-55 ARC cells, kisspeptin expression was also significantly increased at the mRNA and protein levels by KP10 and GnRH stimulation; however, GnRH expression was also upregulated by KP10 and GnRH stimulation in these cells. KP10 and estradiol (E2) both increased Kiss-1 gene expression in mHypoA-50 AVPV cells, but combined stimulation with KP10 and E2 did not potentiate their individual effects on Kiss-1 gene expression. On the other hand, E2 did not increase Kiss-1 gene expression in mHypoA-55 ARC cells, and the KP10-induced increase of Kiss-1 gene expression was inhibited in the presence of E2 in these cells. KP10 and GnRH significantly increased c-Fos protein expression in the mHypoA-50 AVPV and mHypoA-55 ARC cell lines. In primary cultures of fetal rat neuronal cells, KP10 significantly increased Kiss-1 gene expression, whereas GnRH significantly increased GnRH gene expression. We found that kisspeptin and GnRH affected Kiss-1- and GnRH-expressing hypothalamic cells and modulated Kiss-1 and/or GnRH gene expression with a concomitant increase in c-Fos protein expression. A mutual- or self-regulatory system might be present in Kiss-1 and/or GnRH neurons in the hypothalamus.

Study Information

Provider

pubmed

Year

2021

Date

2021-07-15T00:00:00.000Z

DOI

10.1007/s43032-021-00695-z

Citations

5

References

47