Pharmacokinetics and pharmacodynamics of growth hormone-releasing peptide-2: a phase I study in children.
Pihoker. C C; Kearns. G L GL; French. D D; Bowers. C Y CY
Key Findings
- A 1 µg/kg IV dose of GHRP‑2 quickly raised plasma growth hormone (GH) by about 68 ng/mL on average.
- GHRP‑2 showed a two‑phase clearance with a half‑life of roughly 0.55 hours and a clearance of 0.66 L/h·kg.
- The EC50 for GHRP‑2‑induced GH release was about 1.1 ng/mL, providing a quantitative target for dosing.
Practical Outcomes
- For biohackers, the study confirms that GHRP‑2 can reliably stimulate GH, but the data come from IV dosing in children, not typical adult self‑administration. The PK numbers and EC50 give a starting point for modeling sub‑cutaneous or oral regimens, though safety and dosing need further adult studies.
Summary
A small study gave kids with short stature a single tiny IV dose of GHRP‑2 and measured how the drug and growth hormone behaved in their blood. The peptide reliably boosted growth hormone levels, and the researchers worked out how fast it clears, how much spreads in the body, and the dose needed to get half‑maximal effect (EC50). This data can help design future dosing schedules, especially for non‑IV routes.
Abstract
Administration of GH-releasing peptide-2 (GHRP-2) represents a potential mode of therapy for children of short stature with inadequate secretion of GH. Requisite information to determine the dosing route and frequency for GHRP-2 consists of the pharmacokinetics (PK) and pharmacodynamics (PD) for this compound, neither of which have been previously evaluated in children. The purpose of this study was to characterize the PK and PD of GHRP-2 in children with short stature. Ten prepubertal children (nine boys and one girl; 7.7 +/- 2.4 yr old) received a single 1 microg/kg i.v. dose of GHRP-2 over 1 min, followed by repeated (n = 9) blood sampling over 2 h. GHRP-2 and GH were quantitated by specific RIA methods. PK parameters were calculated from curve fitting of GHRP-2 and GH vs. time data. Posttreatment plasma GH concentrations (normalized for pretreatment values) were used as the effect measurement. PD parameters were generated using the sigmoid Emax model. Disposition of GHRP-2 best fit a biexponential function. GHRP-2 PK parameters (mean +/- SD) were: alpha = 13.4 +/- 9.7 h(-1), beta = 1.3 +/- 0.3 h(-1), t(1/2beta) = 0.55 +/- 0.14 h, AUC(0-infinity) = 2.02 +/- 1.37 ng/mL x h, Cmax = 7.4 +/- 3.8 ng/mL, plasma clearance = 0.66 +/- 0.32 L/h x kg, and apparent volume of distribution = 0.32 +/- 0.14 L/kg. PK parameters for GH were: appearance rate constant = 5.9 +/- 3.1 h(-1), elimination t(1/2) = 0.37 +/- 0.15 h, lag time = 0.05 +/- 0.01 h, Cmax = 50.7 +/- 17.2 ng/mL, Tmax = 0.42 +/- 0.16 h, and AUC(0-infinity) = 47.9 +/- 26.1 ng/mL x h. PD parameters for GHRP-2 were: Ke0 = 1.13 +/- 0.94 h(-1), gamma = 13.15 +/- 9.44, E0 = 6.63 +/- 4.86 ng/mL (GH), Emax = 67.5 +/- 23.5 ng/mL (GH), and EC50 = 1.09 +/- 0.59 ng/mL. We concluded that 1) GHRP-2 produced a predictable and significant (i.e. compared to pretreatment values) increase in plasma GH concentrations; 2) the PK-PD link model enabled quantitative assessment of GHRP-2 modulation of serum GH levels; and 3) definition of the EC50 for GHRP-2 will enable PD and PK evaluations of extravascular dosing regimens for children.
Study Information
pubmed
1998
10.1210/jcem.83.4.4744