GHRP-6
Growth Hormone Releasing Peptide-6, Growth hormone-releasing hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2
Ghrelin and GHRP-6 enhance electrical and secretory activity in GC somatotropes.
Dominguez. Belisario B; Felix. Ricardo R; Monjaraz. Eduardo E
Key Findings
- Chronic (96âhour) exposure to ghrelin or GHRPâ6 raises the firing frequency of spontaneous action potentials in GHâproducing pituitary cells.
- Both peptides increase wholeâcell inward current density, indicating enhanced ion flow that drives cell excitability.
- Inhibiting Naâș or Lâtype CaÂČâș channels cuts down GHRPâ6âinduced GH release, showing these currents are crucial for hormone secretion.
Practical Outcomes
- For biohackers, the data supports the idea that GHRPâ6 can boost growth hormone by making pituitary cells more electrically active, but the work is done in a cell line, not humans. It suggests that dosing strategies aiming for sustained exposure might be more effective, yet realâworld protocols still need human studies to confirm safety and optimal dosing.
Summary
The study shows that giving ghrelin or the synthetic peptide GHRP-6 to pituitary cells in a dish makes those cells fire more often and release more growth hormone. This happens because the peptides increase the flow of positive ions into the cells, which boosts their electrical activity. Blocking those ion channels reduces the hormone release, confirming their role.
Abstract
It is well established that pituitary somatotropes fire spontaneous action potentials (SAP) which generate Ca(2+) signals of sufficient amplitude to trigger growth hormone (GH) release. It is also known that ghrelin and synthetic GH-releasing peptides (GHRPs) stimulate GH secretion, though the mechanisms involved remain unclear. In the current report, we show that the chronic (96h) treatment with ghrelin and GHRP-6 increases the firing frequency of SAP in the somatotrope GC cell line. This action is associated with a significant increase in whole-cell inward current density. In addition, long-term application of Na(+) or L-type Ca(2+) current antagonists decreases GHRP-6-induced release of GH, indicating that the ionic currents that give rise to SAP play important roles for hormone secretion in the GC cells. Together, our results suggest that ghrelin and GHPR-6 may increase whole-cell inward current density thereby enhancing SAP firing frequency and facilitating GH secretion from GC somatotropes.
Study Information
pubmed
2007
2007-04-20T00:00:00.000Z
10.1016/j.bbrc.2007.04.085