Interaction between hypothalamic peptides in a superfused pituitary cell system.
Vigh. S S; Schally. A V AV
Key Findings
- CRF causes dose‑related ACTH release in pituitary cells
- Synthetic GH‑RF (including sermorelin) causes dose‑related GH release
- GH‑RF and CRF interact with other peptides (vasopressin, substance P, PHI‑27) to modulate hormone output
Practical Outcomes
- For biohackers, the data suggest that using GH‑releasing peptides alone may not give predictable results because other neuropeptides can boost or blunt the effect. Combining sermorelin with agents that affect vasopressin or substance P could change GH levels, but no specific dosing guidance is provided, so any such experiments should be approached cautiously and monitored closely.
Summary
The study shows that synthetic growth‑hormone‑releasing peptides (like sermorelin) trigger a dose‑dependent release of growth hormone from pituitary cells, and that this effect can be altered by other brain chemicals such as vasopressin and substance P, meaning hormone release is a complex, interacting system.
Abstract
Recently two hypothalamic releasing factors have been isolated, sequenced and synthesized: corticotropin-releasing factor (CRF) from sheep and rat hypothalami; and growth hormone-releasing factor (GH-RF) from tumors in human pancreas (hpGH-RF) and from rat hypothalami (rhGH-RF). Their biological potencies were tested by various laboratories in vivo and in vitro using rat pituitary cell cultures and the pituitary quarters method. In the present study, we investigated the dynamics of the release of pituitary hormones and the interaction between CRF and hGH-RF and several brain peptides in a pituitary cell-superfusion system. A dose-related ACTH release was found when the cells were superfused with different doses of synthetic CRF. Synthetic hGH-RF44, hGH-RF40, hGH-RF1-29 and purified porcine hypothalamic GH-RF caused similar dose-related releases of GH. In this system, we demonstrated interactions between CRF and vasopressin, CRF and SP, hGH-RF and vasopressin and hGH-RF and PHI-27. We conclude that the control of pituitary hormone secretion is a complex process; several factors may interact with each releasing or inhibiting factor to modulate their effects.
Study Information
pubmed
1984
1984-12-31T00:00:00.000Z
10.1016/0196-9781(84)90282-1
45
37