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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
2008 pubmed 47 citations

Exogenous kisspeptin does not alter photoperiod-induced gonadal regression in Siberian hamsters (Phodopus sungorus).

Greives. Timothy J TJ; Kriegsfeld. Lance J LJ; Demas. Gregory E GE

Key Findings

  • Exogenous kisspeptin did not prevent gonadal regression in short‑day hamsters.
  • Kisspeptin did not accelerate gonadal regrowth in hamsters that had already regressed.
  • Seasonal reproductive changes involve mechanisms beyond just the kisspeptin system.

Practical Outcomes

  • For biohackers, this work suggests that kisspeptin is unlikely to be useful for manipulating seasonal reproductive or hormonal cycles in humans. The findings don’t provide a new protocol or dosage guidance for longevity or performance purposes.

Summary

The study tested whether giving the hormone‑like peptide kisspeptin could stop or reverse the shrinking of reproductive organs that happens in hamsters when days get short. Across three experiments, giving kisspeptin didn’t change the outcome – hamsters still showed the same gonadal regression as untreated animals.

Abstract

In order to reproduce successfully, animals must integrate multiple environmental cues to synchronize breeding with favorable conditions. In temperate, seasonally breeding rodents, photoperiod acts as the primary seasonal cue. Long days are associated with reproductive development and maturation of the gonads whereas short days induce gonadal regression. The neuropeptide kisspeptin has potent stimulatory effects on reproductive development. Kisspeptin potently stimulates GnRH release and kisspeptin expression co-varies with photoperiod in seasonally breeding animals. Here we tested the hypothesis that reproductive involution in response to inhibitory day lengths results from reduced kisspeptin stimulation of the reproductive axis in seasonally breeding Siberian hamsters (Phodopus sungorus). If true, gonadal regrowth should be hastened by kisspeptin treatment in regressed hamsters and prevented in hamsters by treatment prior to and during regression. In Experiments 1 and 2 we tested the ability of kisspeptin to reverse gonadal regression. In Experiment 1, reproductively regressed hamsters received chronic kisspeptin via osmotic mini-pumps for 4 weeks. In Experiment 2, daily injections of kisspeptin were administered to regressed hamsters for 6 weeks. In Experiment 3, the ability of kisspeptin to block gonadal regression was tested; hamsters transferred to short days received daily injections of kisspeptin for 6 weeks. In all three studies, short-day animals receiving exogenous kisspeptin did not differ from short-day controls. Collectively, these results provide evidence that mechanisms in addition to those that converge on the kisspeptin system are likely critical for seasonal changes in the reproductive axis.

Study Information

Provider

pubmed

Year

2008

Date

2008-03-05T00:00:00.000Z

DOI

10.1016/j.ygcen.2008.02.017

Citations

47

References

38