GHRP-2
Also known as: Pralmorelin, GPA-748, KP-102 D, KP-102 LN, KP-102D, KP-102LN, Growth hormone-releasing peptide 2, D-Ala-D-(β-naphthyl)-Ala-Ala-Trp-D-Phe-Lys-NH2
Growth Hormone Secretagogue (GHS) / Synthetic Growth Hormone-Releasing Peptide (GHRP) / Ghrelin Receptor Agonist
What it is
GHRP-2 is a synthetic hexapeptide (D-Ala-D-β-naphthylAla-Ala-Trp-D-Phe-Lys-NH2) that acts as a potent agonist at the growth hormone secretagogue receptor (GHS-R1a / ghrelin receptor), a G-protein-coupled receptor distinct from the GHRH receptor (PMID 9798733, PMID 51). It stimulates GH secretion from pituitary somatotrophs through a mechanism involving protein kinase C (PKC) and intracellular calcium signalling, distinct from the cAMP/PKA pathway used by GHRH. GHRP-2 acts at both pituitary and hypothalamic levels, and its GH-releasing effect is synergistic with that of GHRH (PMID 9186261, PMID 9465289). Beyond GH release, GHRP-2 also stimulates ACTH/cortisol and prolactin secretion (PMID 9285939, PMID 45), and does not stimulate arginine vasopressin (AVP) secretion in healthy men. It acts as a synthetic mimic of ghrelin, the endogenous GHS-R1a ligand. GHRP-2 has also been shown to bind CD36, a scavenger receptor for oxidized LDL, and to exert antioxidant effects in vascular tissue independent of GH. In granulosa cells, GHRP-2 attenuates PKC-mediated inflammation via inhibition of p38, JNK, and NF-κB pathways.
Class: Growth Hormone Secretagogue (GHS) / Synthetic Growth Hormone-Releasing Peptide (GHRP) / Ghrelin Receptor Agonist
What it's studied for
- Diagnostic test for adult growth hormone deficiency (AGHD) Human observational
- 100 µg GHRP-2 IV in 77 healthy subjects and 58 GHD patients; peak GH cut-off of 15 µg/L (9 µg/L with WHO 98/574 standard) distinguished GHD from controls with high reliability. Test showed favourable reproducibility and mild influence of age and adiposity. PMID 17609397 Chihara K et al. European Journal of Endocrinology (2007)
- GHRP-2 test compared to ITT and arginine test in 71 Japanese adults with pituitary tumours. GHRP-2 sensitivity 81.3% and specificity 94.5% for severe AGHD vs ITT. Median peak GH 28.88 µg/L with GHRP-2 vs 9.38 µg/L with ITT. PMID 23079545 Kinoshita Y et al. Endocrine Journal (2013)
- Review: GHRP-2 test recommended in Japan as convenient and safe GH stimulating test; cut-off for severe AGHD is peak GH ≤9 ng/mL (9 µg/L). PMID 25070016 Fukuda I et al. Neurologia medico-chirurgica (2014)
- Preoperative GHRP-2 test peak GH values in NFPA patients reflected severity of hypopituitarism and predicted postoperative recovery of GH secretion. Cut-off for severe AGHD is ≤9 ng/mL. PMID 31776295 Soga A et al. Endocrine Journal (2020)
- In 65 elderly patients (≥65 yr) with non-functioning pituitary NETs, GH response to GHRP-2 test correlated significantly with adrenocortical function; optimal cut-off for peak GH 8.08 ng/mL (sensitivity 85.2%, specificity 86.8%) for predicting adrenocortical insufficiency. PMID 37295337 Teramoto S et al. Growth Hormone & IGF Research (2023)
- Diagnostic test for GH deficiency in children Human observational
- 2 µg/kg GHRP-2 IV in 56 children with growth disorders; peak GH significantly lower in GHD (median 3.39 µg/L) vs non-GHD (25.10 µg/L). Cross-specificity point at 15 µg/L. Test was safe and required ≤1 hour. PMID 20662346 Asakura Y et al. Journal of Pediatric Endocrinology & Metabolism (2010)
- In 23 adolescents, GH response to GHRP-2T was robustly high in idiopathic GHD and short stature groups (medians 88.9 and 90.1 ng/mL respectively) but low in organic/genetic GHD (median 3.4 ng/mL). Authors suggest current cut-off may miss some GHD patients in adolescents. PMID 38958228 Onuki T et al. Journal of Pediatric Endocrinology & Metabolism (2024)
- Diagnosis of secondary adrenal failure / HPA axis assessment Human observational
- GHRP-2 test in 47 patients: cut-off of 11.6 µg/dL for peak cortisol predicted secondary hypoadrenalism with 88.9% specificity and 89.7% sensitivity. ACTH/cortisol responses to GHRP-2 did not correlate with CRH test, suggesting direct pituitary ACTH stimulation. PMID 27020037 Arimura H et al. Endocrine Journal (2016)
- In 6 patients with hypothalamo-pituitary disorders who failed ITT, significant ACTH release was observed during GHRP-2 test, suggesting GHRP-2 may directly stimulate ACTH secretion. PMID 20431231 Kimura T et al. Endocrine Journal (2010)
- Diagnosis of GH secretory status in pituitary tumor patients / overweight subjects Human observational
- In 104 patients with NFPA or Rathke's cyst, 43% had severe GHD by GHRP-2 test. BMI, free thyroxine, and tumor height significantly predicted peak GH response. Overweight (OR 3.86) was significantly associated with severe GHD. PMID 35452483 Seki Y & Ichihara A. PLoS One (2022)
- GH secretion (GHRP-2 load test) negatively correlated with BMI (r=-0.59), visceral adipose tissue, and subcutaneous adipose tissue in 28 obese subjects. Response markedly improved after laparoscopic sleeve gastrectomy. PMID 28623445 Ohara E et al. Obesity Surgery (2017)
- Treatment of prolonged critical illness / hyposomatotropism in ICU patients Human RCT
- Continuous GHRP-2 infusion (1 µg/kg/h) in 26 critically ill adults caused 4–6-fold increase in mean GH concentration and 61% rise in serum IGF-I within 24 h. GHRH + GHRP-2 combination caused further 2-fold increase in GH over GHRP-2 alone. PMID 9024260 Van den Berghe G et al. Journal of Clinical Endocrinology & Metabolism (1997)
- RCT in 33 critically ill men: GHRP-2 alone (1 µg/kg/h continuous) reactivated GH secretion and normalized IGF-I. Combined GHRP-2+TRH+GnRH reactivated GH, TSH, and LH axes with beneficial metabolic effects; ureagenesis reduced only with TRH co-treatment. PMID 12030918 Van den Berghe G et al. Clinical Endocrinology (2002)
- Continuous GHRP-2 infusion (1 µg/kg/h) in critically ill patients synchronized serum profiles of GH, TSH and PRL; GHRH or TRH alone did not produce this synchronization. PMID 10037246 Van den Berghe G et al. European Journal of Endocrinology (1999)
- Stimulation of food intake / appetite (orexigenic effect) Human RCT
- Subcutaneous infusion of GHRP-2 (1 µg/kg/h for 270 min) in 7 lean healthy males increased ad libitum food intake by 35.9 ± 10.9% vs saline. All subjects increased intake. GH AUC significantly elevated during GHRP-2 infusion. PMID 15699539 Laferrère B et al. Journal of Clinical Endocrinology & Metabolism (2005)
- Treatment of short stature / GH deficiency in children (intranasal or oral administration) Human observational
- 15 children with short stature received intranasal GHRP-2 (5–15 µg/kg, 2–3x/day) for up to 24 months; height velocity increased from 3.7 to 6.1 cm/year at 6 months. GH-binding protein concentrations rose significantly. Well tolerated. PMID 9390009 Pihoker C et al. The Journal of Endocrinology (1997)
- Oral GHRP-2 (900 µg/kg b.i.d.) for 12 months in 10 prepubertal GHD children: 7/10 reported increased appetite in first 6 months; BMI SDS trended upward but did not reach statistical significance. PMID 14513874 Mericq V et al. Journal of Pediatric Endocrinology & Metabolism (2003)
- Modulation of GH secretory dynamics in healthy adults (mechanistic/pharmacodynamic studies) Human RCT
- Prospective RCT in 26 older men: continuous GHRP-2 infusion combined with GHRH pulses; pulsatile GH correlated positively with testosterone and negatively with BMI. Mean GH under GHRP-2 predicted jointly by estradiol (positively) and BMI (negatively). PMID 23101768 Norman C et al. American Journal of Physiology (2013)
- In 10 healthy men, SSTR-2/-5 agonist octreotide (1 µg/kg SC) suppressed GHRP-2 (1 µg/kg IV)-stimulated GH secretory burst mass, frequency, and irregularity, demonstrating interactive control of GH secretion. PMID 15356066 Iranmanesh A et al. Journal of Clinical Endocrinology & Metabolism (2004)
- Vascular antioxidant effects (animal/in vitro) Animal studies only
- GHRP-2 (20 µg twice daily SC) in ApoE-/- mice for 12 weeks: increased circulating IGF-I, decreased interferon-gamma by 66%, decreased aortic superoxide and 12/15-lipoxygenase expression; did not reduce atherosclerotic plaque area. PMID 19819949 Titterington JS et al. Endocrinology (2009)
- Anti-inflammatory effects in ovarian granulosa cells (in vitro) In vitro only
- GHRP-2 attenuated PKC activator (PDD)-induced COX-2 and IL-8 expression in KGN human granulosa cells, reduced PGE2 and IL-8 secretion, and inhibited p38, JNK, and NF-κB signalling pathways. PMID 27548147 Chao YN et al. International Journal of Molecular Sciences (2016)
- Growth performance and muscle protein deposition in animals with growth retardation Animal studies only
- GHRP-2 injection in growth-retarded yaks significantly enhanced average daily gain, myofiber diameter and area, serum GH and IGF-1 levels, and upregulated GHR, IGF-1R, and protein synthesis pathway (PI3K/AKT/mTOR) mRNA in liver and skeletal muscle. PMID 26894743 Hu R et al. PLoS One (2016)
- Cachexia / wasting syndrome treatment (proposed) Mixed
- Narrative review identifies GHRP-2 as a potential pharmacological option in cachexia treatment; notes that evidence-based recommendations for its use are not yet available. PMID 35758863 Celichowska M et al. Journal of Pain & Palliative Care Pharmacotherapy (2022)
- Diagnostic tool for TSH-producing pituitary adenomas Human observational
- In 5 patients with TSH-producing adenomas, 2 (40%) showed >50% increase in TSH after GHRP-2 test. GHRP-2 fails to induce TSH in normal subjects; proposed as potential additional diagnostic tool alongside TRH test. PMID 29973439 Kageyama K et al. Endocrine Journal (2018)
Community-reported dosing
| Route | Dose | Frequency / Duration | Population / context | Source tier |
|---|---|---|---|---|
| Intravenous (IV) bolus | 100 µg (single dose) | Single administration; blood sampled over 2 h | human | Research PMID 17609397 |
| Intravenous (IV) | 2 µg/kg | Single administration; blood sampled over 1 h | human | Research PMID 20662346 |
| Subcutaneous infusion | 1 µg/kg/h | 270-minute infusion | human | Research PMID 15699539 |
| Intravenous (IV) continuous infusion | 1 µg/kg/h (continuous infusion) | 5 days | human | Research PMID 12030918 |
| Intravenous (IV) continuous infusion | 1 µg/kg/h (preceded by 1 µg/kg bolus) | 21-hour infusion over 2 consecutive nights | human | Research PMID 9024260 |
| Intravenous (IV) continuous infusion | 1 µg/kg/h | 21-hour continuous infusion | human | Research PMID 10037246 |
| Intranasal (therapeutic); Intravenous (bolus for acute testing) | 5–15 µg/kg per dose (acute IV bolus 1 µg/kg; intranasal 5–20 µg/kg for GH response testing; therapeutic intranasal 5–15 µg/kg) | 6–24 months (therapeutic intranasal phase); initial 3 months twice daily then 3 times daily | human | Research PMID 9390009 |
| Oral | 900 µg/kg b.i.d. (orally) | 12 months | human | Research PMID 14513874 |
| Intravenous (IV) over 1 min | 1 µg/kg | Single dose; blood sampled over 2 h | human | Research PMID 9543135 |
| Intravenous (IV) continuous infusion | 1 µg/kg/h | 24-hour continuous infusion | human | Research PMID 10946861 |
| Intravenous (IV) bolus | 1 µg/kg | Single bolus; sessions repeated on separate days | human | Research PMID 15356066 |
| Intravenous (IV) bolus | 100 µg | Single intravenous bolus; measurements over 60 min | human | Research PMID 19907099 |
| Intravenous (IV) bolus | 1 µg/kg and 2 µg/kg | Single bolus | human | Research PMID 9285939 |
| Intravenous (IV) bolus | 2.0 µg/kg | Single bolus | human | Research PMID 10195374 |
| Intravenous (IV) bolus | 1 µg/kg bolus | Single bolus per session | human | Research PMID 11004017 |
| Intravenous (IV) | 100 µg (single dose) | Single administration; detected in DBS up to 4 h post-injection | human | Research PMID 33197153 |
| Intravenous (IV) | 100 µg | Single intravenous administration | human | Research PMID 25249726 |
| Not specified for GH replacement context | Initial low dose 3 µg/kg body weight/day (GH replacement therapy reference, not GHRP-2 treatment dose) | Ongoing with dose titration | human | Research PMID 25070016 |
| Subcutaneous (SC) | 20 µg twice daily | 12 weeks | animal | Research PMID 19819949 |
| Injection (route not further specified in abstract) | Not explicitly stated (GHRP-2 injection group vs control in yaks) | Study period not specified in abstract | animal | Research PMID 26894743 |
| Intravenous and subcutaneous | Not explicitly stated per kg; chronic administration studied | 7–30 days | human | Research PMID 8887169 |
| subcutaneous injection | 100 mcg | 3x daily (upon waking, post-workout, before bed) | male bodybuilders and performance-focused biohackers seeking GH pulse amplification | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 200 mcg | 3x daily (upon waking, post-workout, before bed) | experienced male bodybuilders and biohackers tolerant to GHRP side effects | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 300 mcg | 3x daily (upon waking, post-workout, before bed) | advanced bodybuilders pushing for maximum GH output per pulse | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 100 mcg | 2x daily (upon waking, before bed) | biohackers and anti-aging focused adults seeking moderate GH support with minimal side effects | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 100 mcg | once daily, 30 minutes before bed | general biohackers and older adults prioritizing sleep-related GH pulse and recovery | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 100 mcg | 3x daily, co-injected with Mod GRF 1-29 (CJC-1295 no-DAC) 100 mcg | intermediate-to-advanced biohackers and bodybuilders using GHRP+GHRH stacks | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 200 mcg | 3x daily, co-injected with Mod GRF 1-29 (CJC-1295 no-DAC) 100 mcg | experienced bodybuilders running aggressive GHRP+GHRH stacks for maximum GH output | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 100 mcg | once daily, 30 minutes pre-workout or post-workout (fasted state) | performance-oriented athletes and bodybuilders using GHRP-2 for intra-cycle recovery support | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 50 mcg | 2x daily (upon waking, before bed) | beginners, females, or older adults starting GHRP-2 for the first time to assess tolerance | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 100 mcg | 3x daily, co-injected with CJC-1295 with DAC 2 mg (dosed 1-2x per week separately) | biohackers and bodybuilders using a long-acting GHRH alongside GHRP-2 for convenience | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
| subcutaneous injection | 100 mcg | 3x daily, co-injected with Ipamorelin 100 mcg as a replacement or transition protocol | biohackers comparing or cycling between GHRPs, or layering for additive pulse effect | [S] Claude Sonnet 4.6 — synthesized from aggregate training data |
Tier key: Research = PMID-cited study · [C] = scraped community source · [S] = model-synthesized from aggregate community reports (softer evidence). How we source.
References
- [1] PMID 17609397 — 100 µg GHRP-2 IV in 77 healthy subjects and 58 GHD patients; peak GH cut-off of 15 µg/L (9 µg/L with WHO 98/574 standard) distinguished GHD from controls with h
- [2] PMID 23079545 — GHRP-2 test compared to ITT and arginine test in 71 Japanese adults with pituitary tumours. GHRP-2 sensitivity 81.3% and specificity 94.5% for severe AGHD vs IT
- [3] PMID 25070016 — Review: GHRP-2 test recommended in Japan as convenient and safe GH stimulating test; cut-off for severe AGHD is peak GH ≤9 ng/mL (9 µg/L).
- [4] PMID 31776295 — Preoperative GHRP-2 test peak GH values in NFPA patients reflected severity of hypopituitarism and predicted postoperative recovery of GH secretion. Cut-off for
- [5] PMID 37295337 — In 65 elderly patients (≥65 yr) with non-functioning pituitary NETs, GH response to GHRP-2 test correlated significantly with adrenocortical function; optimal c
- [6] PMID 20662346 — 2 µg/kg GHRP-2 IV in 56 children with growth disorders; peak GH significantly lower in GHD (median 3.39 µg/L) vs non-GHD (25.10 µg/L). Cross-specificity point a
- [7] PMID 38958228 — In 23 adolescents, GH response to GHRP-2T was robustly high in idiopathic GHD and short stature groups (medians 88.9 and 90.1 ng/mL respectively) but low in org
- [8] PMID 27020037 — GHRP-2 test in 47 patients: cut-off of 11.6 µg/dL for peak cortisol predicted secondary hypoadrenalism with 88.9% specificity and 89.7% sensitivity. ACTH/cortis
- [9] PMID 20431231 — In 6 patients with hypothalamo-pituitary disorders who failed ITT, significant ACTH release was observed during GHRP-2 test, suggesting GHRP-2 may directly stim
- [10] PMID 35452483 — In 104 patients with NFPA or Rathke's cyst, 43% had severe GHD by GHRP-2 test. BMI, free thyroxine, and tumor height significantly predicted peak GH response. O
- [11] PMID 28623445 — GH secretion (GHRP-2 load test) negatively correlated with BMI (r=-0.59), visceral adipose tissue, and subcutaneous adipose tissue in 28 obese subjects. Respons
- [12] PMID 9024260 — Continuous GHRP-2 infusion (1 µg/kg/h) in 26 critically ill adults caused 4–6-fold increase in mean GH concentration and 61% rise in serum IGF-I within 24 h. GH
- [13] PMID 12030918 — RCT in 33 critically ill men: GHRP-2 alone (1 µg/kg/h continuous) reactivated GH secretion and normalized IGF-I. Combined GHRP-2+TRH+GnRH reactivated GH, TSH, a
- [14] PMID 10037246 — Continuous GHRP-2 infusion (1 µg/kg/h) in critically ill patients synchronized serum profiles of GH, TSH and PRL; GHRH or TRH alone did not produce this synchro
- [15] PMID 15699539 — Subcutaneous infusion of GHRP-2 (1 µg/kg/h for 270 min) in 7 lean healthy males increased ad libitum food intake by 35.9 ± 10.9% vs saline. All subjects increas
- [16] PMID 9390009 — 15 children with short stature received intranasal GHRP-2 (5–15 µg/kg, 2–3x/day) for up to 24 months; height velocity increased from 3.7 to 6.1 cm/year at 6 mon
- [17] PMID 14513874 — Oral GHRP-2 (900 µg/kg b.i.d.) for 12 months in 10 prepubertal GHD children: 7/10 reported increased appetite in first 6 months; BMI SDS trended upward but did
- [18] PMID 23101768 — Prospective RCT in 26 older men: continuous GHRP-2 infusion combined with GHRH pulses; pulsatile GH correlated positively with testosterone and negatively with
- [19] PMID 15356066 — In 10 healthy men, SSTR-2/-5 agonist octreotide (1 µg/kg SC) suppressed GHRP-2 (1 µg/kg IV)-stimulated GH secretory burst mass, frequency, and irregularity, dem
- [20] PMID 19819949 — GHRP-2 (20 µg twice daily SC) in ApoE-/- mice for 12 weeks: increased circulating IGF-I, decreased interferon-gamma by 66%, decreased aortic superoxide and 12/1
- [21] PMID 27548147 — GHRP-2 attenuated PKC activator (PDD)-induced COX-2 and IL-8 expression in KGN human granulosa cells, reduced PGE2 and IL-8 secretion, and inhibited p38, JNK, a
- [22] PMID 26894743 — GHRP-2 injection in growth-retarded yaks significantly enhanced average daily gain, myofiber diameter and area, serum GH and IGF-1 levels, and upregulated GHR,
- [23] PMID 35758863 — Narrative review identifies GHRP-2 as a potential pharmacological option in cachexia treatment; notes that evidence-based recommendations for its use are not ye
- [24] PMID 29973439 — In 5 patients with TSH-producing adenomas, 2 (40%) showed >50% increase in TSH after GHRP-2 test. GHRP-2 fails to induce TSH in normal subjects; proposed as pot
- [25] PMID 9543135 — 1 µg/kg Intravenous (IV) over 1 min (human)
- [26] PMID 10946861 — 1 µg/kg/h Intravenous (IV) continuous infusion (human)
- [27] PMID 19907099 — 100 µg Intravenous (IV) bolus (human)
- [28] PMID 9285939 — 1 µg/kg and 2 µg/kg Intravenous (IV) bolus (human)
- [29] PMID 10195374 — 2.0 µg/kg Intravenous (IV) bolus (human)
- [30] PMID 11004017 — 1 µg/kg bolus Intravenous (IV) bolus (human)
- [31] PMID 33197153 — 100 µg (single dose) Intravenous (IV) (human)
- [32] PMID 25249726 — 100 µg Intravenous (IV) (human)
- [33] PMID 8887169 — Not explicitly stated per kg; chronic administration studied Intravenous and subcutaneous (human)
- [34] PMID 9798733 — in-prose reference
- [35] PMID 51 — in-prose reference
- [36] PMID 9688350 — in-prose reference
- [37] PMID 9186261 — in-prose reference
- [38] PMID 9465289 — in-prose reference
- [39] PMID 45 — in-prose reference
- [40] PMID 25869809 — in-prose reference
- [41] PMID 8950613 — in-prose reference
- [42] PMID 28400207 — in-prose reference
- [43] PMID 42395176 — in-prose reference
- [44] PMID 30051972 — in-prose reference
- [45] PMID 12938517 — in-prose reference
- [46] PMID 31758732 — in-prose reference
- [47] PMID 20552695 — in-prose reference