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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 2
2006 pubmed 137 citations

KiSS-1 and reproduction: focus on its role in the metabolic regulation of fertility.

Tena-Sempere. Manuel M

Key Findings

  • Kisspeptin neurons are central controllers of the gonadotropic axis and puberty onset.
  • Low energy states suppress hypothalamic KiSS‑1 expression, leading to reduced fertility.
  • Administering kisspeptin or normalizing leptin levels can restore reproductive hormone function in undernourished or diabetic animal models.

Practical Outcomes

  • For biohackers focused on fertility, the data imply that severe calorie restriction may impair reproductive hormones via kisspeptin loss. Supporting energy balance or exploring kisspeptin‑based supplements could help maintain fertility, but human dosing and safety are not yet defined.

Summary

Kisspeptin, a brain chemical made by the KiSS-1 gene, is a key switch for starting puberty and keeping the reproductive hormone system running. When the body is low on energy (like during dieting or illness), kisspeptin levels fall, which can shut down fertility. Giving extra kisspeptin or boosting leptin (the fat‑cell hormone) can reverse this shutdown in animal studies, suggesting a link between energy balance and reproductive health.

Abstract

Unraveling of the master role of kisspeptins, the products of the KiSS-1 gene, and their receptor, GPR54, in the control of reproduction has been a major breakthrough in contemporary neuroendocrinology. Indeed, since the disclosure of their reproductive dimension in late 2003, an ever-growing number of genetic, molecular, physiologic and pharmacological studies have defined the crucial role of KiSS-1 neurons as central processors for the dynamic regulation of the gonadotropic axis and its full activation at puberty. Yet, the potential role of the hypothalamic KiSS-1 system as an intermediary factor for the well-known interplay between energy status and reproduction initially received little attention. Recent data, however, strongly suggest a prominent role of KiSS-1 in the metabolic control of fertility, as expression of KiSS-1 gene at the hypothalamus is down-regulated in conditions of negative energy balance and kisspeptin administration is capable of overcoming the hypogonadotropic state observed in undernutrition and disturbed metabolic conditions. Leptin, the adipocyte hormone signaling the size of body energy stores, is likely to play a pivotal role in the metabolic control of the KiSS-1 system, since kisspeptin neurons express leptin receptors and leptin is able to normalize defective KiSS-1 gene expression in models of impaired gonadotropin secretion linked to hypoleptinemia, such as the ob/ob mouse and streptozotocin-induced diabetic rat. In sum, these data provide strong evidence for a central role of kisspeptins and GPR54 as molecular conduits for the metabolic regulation of reproductive function - a phenomenon with potential physiopathologic and therapeutic implications.

Study Information

Provider

pubmed

Year

2006

Date

2006-08-29T00:00:00.000Z

DOI

10.1159/000095549

Citations

137

References

39