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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 2
2007 pubmed 203 citations

Direct pituitary effects of kisspeptin: activation of gonadotrophs and somatotrophs and stimulation of luteinising hormone and growth hormone secretion.

Gutiérrez-Pascual. E E; Martínez-Fuentes. A J AJ; Pinilla. L L; Tena-Sempere. M M; Malagón. M M MM; Castaño. J P JP

Key Findings

  • Both the kisspeptin gene (KiSS-1) and its receptor (GPR56) are present in the pituitary of young male and female rats.
  • Kisspeptin-10 raises intracellular calcium in about 10% of pituitary cells, affecting both gonadotrophs (LH‑producing) and somatotrophs (GH‑producing).
  • Increasing concentrations of kisspeptin‑10 cause modest, dose‑related increases in LH and GH release, with maximal effects at 10⁻⁸ M, but these are smaller than the responses to GnRH or GHRH.

Practical Outcomes

  • For biohackers, the data suggest kisspeptin could be a mild way to boost LH and GH, but the evidence is limited to rat cells in a dish and the effect is weaker than standard hormonal triggers. Until human studies confirm safety and efficacy, kisspeptin‑10 isn’t ready for reliable self‑administration as a longevity or performance aid.

Summary

The study shows that kisspeptin-10 can directly trigger the release of luteinising hormone (LH) and growth hormone (GH) from rat pituitary cells, acting not only on the usual brain‑hypothalamus pathway but also right at the gland itself. The effect is dose‑dependent but weaker than the natural hormones that normally stimulate LH and GH.

Abstract

Recent, compelling evidence indicates that kisspeptins, the products of KiSS-1 gene, and their receptor GPR54, represent key elements in the neuroendocrine control of reproduction, and that they act primarily by regulating gonadotrophin-releasing hormone (GnRH) secretion at the hypothalamus. Conversely, and despite earlier reports showing GPR54 expression in the pituitary, the potential physiological roles of kisspeptins at this gland have remained elusive. To clarify this issue, cultures of rat pituitary cells were used to evaluate expression of KiSS-1 and GPR54, and to monitor the ability of kisspeptin-10 to stimulate Ca(2+) responses in gonadotrophs and to elicit luteinising hormone (LH) secretion in vitro. The results obtained show that both GPR54 and KiSS-1 are expressed in the pituitary of peripubertal male and female rats. Moreover, kisspeptin-10 induced a rise in free cytosolic Ca(2+) concentration ([Ca(2+)](i)) in approximately 10% of male rat pituitary cells. Intriguingly, kisspeptin-responsive cells included not only gonadotrophs, in which a 62.8 +/- 16.0%[Ca(2+)](i) rise was observed, but also somatotrophs, wherein kisspeptin induced a 60.3 +/- 5.5%[Ca(2+)](i) increase. Accordingly, challenge of dispersed pituitary cells with increasing kisspeptin-10 concentrations induced dose-related LH and growth hormone (GH) secretory responses, which were nevertheless of lower magnitude than those evoked by the primary regulators GnRH and GH-releasing hormone, respectively. In particular, 10(-8) M kisspeptin caused maximal increases in LH release (218.7 +/- 23.6% and 180.4 +/- 7.2% in male and female rat pituitary cells, respectively), and also stimulated maximally GH secretion (181.9 +/- 14.9% and 260.2 +/- 15.9% in male and female rat pituitary cells, respectively). Additionally, moderate summation of kisspeptin- and GnRH-induced LH responses was observed after short-term incubation of male rat pituitary cells. In conclusion, our results provide unequivocal evidence that kisspeptins exert direct pituitary effects in peripubertal male and female rats and suggest a possible autocrine/paracrine mode of action. The precise relevance and underlying mechanisms of this potential new actions of kisspeptins (i.e. the direct modulation of gonadotrophic and somatotrophic axis at the pituitary) deserve further analysis.

Study Information

Provider

pubmed

Year

2007

Date

2007-07-01T00:00:00.000Z

DOI

10.1111/j.1365-2826.2007.01558.x

Citations

203

References

42