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Protocols · Growth Hormone

GHRP-6 dosage protocol

Dosage and protocol information sourced exclusively from PeptideDosages.com.

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Dosage and protocol figures on this page are reproduced only from the matching PeptideDosages.com protocol. The 3 ml table is arithmetic based on those source amounts and the listed vial sizes. Educational research only — not instructions or medical advice.

Dosage chart

The dosage amounts and schedules below come only from PeptideDosages.com. Syringe-unit figures are mathematical conversions of those source amounts using exactly 3 ml of bacteriostatic water. Educational reference only — not instructions or medical advice.

GHRP-6 · 10 mg Vial

GHRP-6 is dosed at 100 mcg–300 mcg daily via subcutaneous injection in educational protocols.

Typical daily range
300–900 mcg total (split into 3 doses with gradual titration).

Standard / Gradual Approach

Week/PhaseDose per Injection (mcg)
Weeks 1–2100 mcg
Weeks 3–4200 mcg
Weeks 5–12300 mcg

3 ml conversion

5 mg + 3 ml = 1.67 mg/ml. Choose your vial strength to update the units below.

Source doseU-100 syringe
100 mcg6.0 units
200 mcg12 units
300 mcg18 units

Mixing note: growth-hormone secretagogues like GHRP-6 are commonly reconstituted with 0.5 ml of acetic acid solution topped up with 2.5 ml of bacteriostatic water (3 ml total). Educational reference only — not instructions.

Source chart on peptidedosages.com

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GHRP-6: research background

What GHRP-6 Is

Growth hormone-releasing peptide-6 (GHRP-6) is a peptidyl growth hormone secretagogue (GHS) (PMID 9879640, PMID 30282322). It is a hexapeptide (PMID 9879640). Analogs of GHRP-6 have been synthesized, including azapeptide derivatives (PMID 32721647) and N-aminoimidazolidin-2-one (Aid) peptidomimetics (PMID 24697286). These analogs can help control peptide conformation or act as ligands for specific receptors (PMID 24697286, PMID 32721647). GHRP-6 is also referred to as a ghrelin mimetic due to its activity on the ghrelin receptor (PMID 19289567, PMID 38958606).

How It Is Thought to Work

GHRP-6 can act directly at the somatotroph, which are cells in the pituitary gland that produce growth hormone (PMID 8887178). As a ghrelin mimetic, GHRP-6 acts as an agonist of the ghrelin receptor (PMID 19289567). The ghrelin receptor is a seven-transmembrane (7-TM) receptor found to have increased expression in human carcinoma and heart failure (PMID 30282322). Some azapeptide analogs of GHRP-6 have been developed as selective ligands for CD36, a scavenger receptor involved in lipid uptake and atherosclerosis progression (PMID 32721647). GHRP-6 has also been observed to enhance the survival of renal tubular epithelial cells by activating the mTOR-P70 pathway in a laboratory setting (PMID 41327290).

Laboratory and Animal Studies Report

In male rats, GHRP-6 was primarily excreted in the bile after intravenous injection, showing a systemic plasma clearance (PMID 9879640). After intranasal application in rats, GHRP-6 showed moderate absorption, suggesting this route could be promising for systemic delivery (PMID 9879640). A self-assembling GHRP-6 peptide hydrogel was studied in a mouse model of acute kidney injury (AKI). This hydrogel treatment reprogrammed the metabolism of renal tubular epithelial cells, enriching spermidine, L-glutamine, and acetyl-CoA, and enhanced cell survival (animal study, PMID 41327290). In apoe-/- mice fed a high-fat, high-cholesterol diet, azapeptide analogs of GHRP-6 decreased lesion progression in the aortic arch and reduced aortic sinus lesion areas, indicating an anti-atherosclerotic effect. These effects were linked to a reduced ratio of inflammatory macrophages and lower plasma inflammatory cytokine levels, and were dependent on CD36 (animal study, PMID 32721647). In a rodent model of postoperative ileus (POI), a single dose of GHRP-6 (20 microg/kg) decreased the time to the first bowel movement (animal study, PMID 19289567). GHRP-6 reversed specific phenotypic effects of calorie restriction in mice related to gastric endocrine cell differentiation (animal study, PMID 38958606).

Human Evidence So Far

In short-statured children and adults with diagnosed growth hormone deficiency (GHD), intravenous GHRP-6 was used to evaluate pituitary GH reserve. Although a lower GH response to GHRP-6 was observed in GHD patients compared to normal children, there was considerable overlap (human study, PMID 8887178). A nearly complete blockade of GH response to GHRP-6, or combined GHRH plus GHRP-6, was found in patients with pituitary stalk transection, suggesting its potential as a diagnostic test for this condition (human study, PMID 8887178). A similar finding with combined GHRH plus GHRP-6 was observed in patients with adult-onset GHD, indicating its possible value in diagnosing this entity (human study, PMID 8887178).

Key Terms Explained

Pituitary GH reserve: The capacity of the pituitary gland to release growth hormone. Somatotroph: A cell in the pituitary gland that produces growth hormone. GHRH: Growth hormone-releasing hormone. Ghrelin receptor: A protein that binds ghrelin, influencing appetite and growth hormone release. CD36: A scavenger receptor that takes up modified lipoproteins, contributing to atherosclerosis. mTOR-P70 pathway: A signaling pathway involved in cell growth and metabolism. Renal tubular epithelial cells (TECs): Cells lining the kidney tubules, important for kidney function.

Studies cited in this section

Summarised from the PubMed abstracts listed above. Educational reference only — not medical advice or instructions.

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