Key takeaways
- ✓GHRH analogues act on the GHRH receptor; ghrelin mimetics act on the GHS receptor.
- ✓The two pathways are distinct and can be studied separately or together.
- ✓Short half-life and receptor desensitisation shape how each is used in experiments.
The GHRH receptor family
Growth-hormone-releasing hormone (GHRH) is a 44-residue hypothalamic peptide. Sermorelin is its 1-29 fragment, the shortest piece that keeps full activity. CJC-1295 and tesamorelin are modified analogues designed to last longer; tesamorelin is a full-length 44-residue analogue that is an approved medicine for a specific indication.
The ghrelin receptor family
Ghrelin is a gut hormone that activates the GHS receptor (GHS-R1a). GHRP-6, hexarelin and ipamorelin are synthetic ligands for it, developed before ghrelin itself was discovered. They differ in potency and selectivity: ipamorelin is reported as more selective for GH release, while GHRP-6 and hexarelin show broader hormonal effects in the published work.
Pulsatility and desensitisation
GH is naturally released in pulses. Cell and animal studies show that continuous receptor stimulation can blunt the response, and hexarelin is a well-documented example. This is why exposure pattern is a core design variable in secretagogue research.
Reading the downstream markers
Most studies track GH itself and IGF-1, the liver-derived mediator of GH signalling. Because IGF-1 integrates over hours, it behaves very differently from the minute-scale GH pulses.
Compounds mentioned
CJC-1295
GHRH analogue
Ipamorelin
Selective ghrelin-receptor agonist
Tesamorelin
Stabilised full-length GHRH analogue
GHRP-6
First-generation ghrelin-receptor agonist
Sermorelin
Shortest fully active fragment of GHRH
Hexarelin
Potent synthetic ghrelin-receptor agonist
More guides
Cite this page
peptide.wiki. (2026). Growth hormone secretagogues explained: GHRH analogues versus ghrelin mimetics. peptide.wiki. https://www.peptide.wiki/guides/growth-hormone-secretagogues-explained