Neurokinin B stimulates GnRH release in the male monkey (Macaca mulatta) and is colocalized with kisspeptin in the arcuate nucleus.
Ramaswamy. Suresh S; Seminara. Stephanie B SB; Ali. Barkat B; Ciofi. Philippe P; Amin. Nisar A NA; Plant. Tony M TM
Key Findings
- A single injection of NKB or its agonist senktide triggers a strong LH surge via GnRH release.
- Repeated or pulsed activation of the NKB receptor does not maintain pulsatile GnRH/LH secretion, unlike kisspeptin.
- NKB and kisspeptin are found together in the same brain cells of the arcuate nucleus, suggesting they work together but have different effects on hormone pulse generation.
Practical Outcomes
- For biohackers, this means NKB‑based compounds might be useful for a brief LH boost but aren’t suitable for long‑term hormonal modulation. Kisspeptin remains the more promising target for sustaining GnRH/LH pulses if you’re looking to influence reproductive hormones over time.
Summary
The study shows that activating the neurokinin B (NKB) pathway in male monkeys can cause a quick jump in the hormone LH, which signals the brain to release GnRH, but doing this repeatedly doesn’t keep the hormone pulses going like kisspeptin does. In other words, NKB can give a short‑term boost but isn’t good for sustained hormone rhythm control.
Abstract
Human genetics indicate that kisspeptin and neurokinin B (NKB) signaling are necessary for generating pulsatile LH release and therefore for initiation of puberty and maintaining gonadal function. In the present study, male monkeys were employed to examine 1) whether activation of the NKB receptor (NK3R) is associated with GnRH release, and 2) hypothalamic localization of these peptides using immunofluorescence histochemistry. Agonadal juveniles, in which pituitary responsiveness to GnRH was heightened by GnRH priming, were employed to indirectly examine GnRH-releasing actions of NK3R and kisspeptin receptor agonists by tracking LH after their i.v. injection. Castrated adults were used for immunohistochemistry. Single i.v. injections of NKB or senktide (an NK3R agonist) elicited robust LH discharges that were abolished by GnRH receptor antagonism (acyline) confirming the ligands' hypothalamic action. Intermittent infusion of senktide (1-min pulse every hour for 4 h), in contrast to that of kisspeptin, failed to sustain pulsatile GnRH release. Repetitive senktide injections did not compromise the GnRH-releasing action of kisspeptin. NKB and kisspeptin were colocalized in perikarya of the arcuate nucleus and in axonal projections to the median eminence, confirming earlier findings in sheep. These results are consistent with the human genetics, and indicate that although brief activation of NK3R stimulates GnRH release, repetitive stimulation of this pathway, in contrast to that of kisspeptin receptor, fails to sustain pulsatile GnRH release. In addition, the data provide a platform for future elucidation of the interactions between NKB and kisspeptin that are required for generating pulsatile GnRH release in primates.
Study Information
pubmed
2010
2010-06-23T00:00:00.000Z
10.1210/en.2010-0223
248
32