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Research compoundEndocrine Signaling ResearchKP-102

GHRP-2

Also known as: Pralmorelin

GHRP-2 (pralmorelin) is a synthetic hexapeptide growth hormone secretagogue that acts on the ghrelin receptor (GHS-R1a). Research consists mainly of older hormone-release, rodent, cell and livestock studies.

Evidence: limited · Mostly rodent, cell and livestock studies

At a glance

Class
Synthetic hexapeptide growth hormone secretagogue (ghrelin-receptor agonist)
Developer
No active pharmaceutical developer identified
FDA status
Not FDA-approved
Human data
Older hormone-response studies exist; not detailed on this page
Animal / lab data
Mouse GH-release studies; rat and C2C12 muscle-cell studies; hamster heart model; yak growth study

Where it’s been studied

123
  • 1PituitaryGH release in GHRH-receptor-mutant (lit/lit) mice (2012)
  • 2Skeletal muscleDexamethasone muscle model, rat, plus C2C12 myocytes (2008); yak muscle protein (2016)
  • 3Heartδ-sarcoglycan-deficient TO-2 hamster heart-muscle model (2010)

Mechanism studied

Established: GHRP-2 is an agonist of the growth hormone secretagogue receptor (GHS-R1a) and raises circulating GH; in mice with a non-functional GHRH receptor it still produced a small GH rise, indicating GH release only partly dependent on the GHRH pathway [1]. Proposed: in rat muscle and C2C12 myocytes, GHRP-2 lowered expression of the muscle ubiquitin ligases atrogin-1 and MuRF1 independent of IGF-I, an effect blocked by a GHS-R1a antagonist [2].

What the research shows

StudyModelReported resultSource
GH response in GHRH-receptor-mutant mice [1]Mouse
Little (lit/lit) mice, heterozygous (lit/+) and wild-type C57BL/6J mice; single GHRP-2 challenge
Serum GH reached 9.3 ng/mL in lit/lit mice (vs 1.04 control), 34.5 in lit/+ and 163 ng/mL in wild-type mice.Peer-reviewed
Clinics 2012
Muscle ubiquitin ligases in a dexamethasone model [2]Rat
Dexamethasone-exposed rats (soleus muscle) and differentiated C2C12 mouse myocytes
GHRP-2 reduced dexamethasone-induced atrogin-1 mRNA and lowered MuRF1 mRNA; plasma and muscle IGF-I were unchanged; a GHS-R1a blocker abolished the cell effects.Peer-reviewed
Life Sciences 2008
GHRP-2 in a hamster heart-muscle model [3]Other animal
δ-sarcoglycan-deficient TO-2 hamsters (inherited heart-muscle model) versus untreated animals
Researchers reported less left-ventricular remodeling, better systolic function and lower myocardial oxidative-stress markers.Peer-reviewed
Circulation Journal 2010
GHRP-2 and growth in slow-growing yaks [4]Other animal
Growth-retarded one-year-old Qinghai plateau yaks; GHRP-2 and cysteamine compared
Researchers measured body-weight gain, somatotropic-axis hormones (GHRH, GH, IGF-I) and muscle protein deposition.Peer-reviewed
PLOS ONE 2016

Human trials are listed for research context only; outcomes are reported in the linked publications. Animal and lab results do not establish effects in humans.

Not currently stocked

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More in Endocrine Signaling Research

Sources

  1. Peroni CN et al. (2012). doi:10.6061/clinics/2012(03)11 Source
  2. Yamamoto D et al. (2008) Source
  3. Kato Y et al. (2010). doi:10.1253/circj.cj-09-0378 Source
  4. Hu R et al. (2016). doi:10.1371/journal.pone.0149461 Source
For research use only. Not for human or veterinary use. Not a drug, food or cosmetic, and not intended to diagnose, treat, cure or prevent any disease. This library summarizes published research for educational purposes. PureLab Performance Inc.