Dose dependency of the pharmacokinetics and acute lipolytic actions of growth hormone

J Clin Endocrinol Metab. 2002 Oct;87(10):4691-8. doi: 10.1210/jc.2002-020563.

Abstract

The sensitivity to GH is subject to substantial interindividual variations, which has been attributed to differences in age, sex, and body composition. We investigated 18 healthy nonobese men (aged 24-56 yr) on four occasions. The pharmacokinetics and acute lipolytic effects of GH were evaluated using iv bolus injections of either placebo or GH (1, 3, and 6 micro g/kg(-1)). Body composition was determined by computed tomography and bioimpedance measurements, and the lipolytic response was assessed through measurements of circulating lipid intermediates and adipose tissue microdialysis. The metabolic clearance rate was dose dependently reduced with increasing GH doses (57.2 +/- 5.1, 45.2 +/- 3.8, and 39.2 +/- 2.4 ml/min(-1) per meter(-2) following injection of 1, 3, and 6 micro g/kg(-1) GH, respectively, P < 0.001), and half-time was increased (14.2 +/- 0.6, 16.2 +/- 0.4, and 18.0 +/- 0.5 min, respectively, P < 0.0001). The pharmacokinetic variables were not correlated to age or body composition at any GH dose, but GH-binding protein was the major predictor of metabolic clearance rate following the two highest GH doses as indicated by multivariate regression analysis (r(2) = 0.55, P < 0.001 and r(2) = 0.35, P = 0.012, respectively). There was a significant dose-response relationship between injected GH and the subsequent increments in lipid intermediates, but the integrated lipolytic response was not correlated to GH pharmacokinetics, age, or body composition at any GH dose. Taken together, our findings suggest that differences in GH-binding protein concentrations, which possibly reflect GHR expression, determine GH pharmacokinetics rather than age or body composition per se.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / metabolism
  • Adult
  • Body Composition
  • Carrier Proteins / blood
  • Electric Impedance
  • Human Growth Hormone / administration & dosage*
  • Human Growth Hormone / blood
  • Human Growth Hormone / pharmacokinetics*
  • Humans
  • Insulin-Like Growth Factor I / analysis
  • Lipids / blood
  • Lipolysis / drug effects*
  • Male
  • Metabolic Clearance Rate
  • Microdialysis
  • Middle Aged
  • Placebos
  • Regression Analysis
  • Tomography, X-Ray Computed

Substances

  • Carrier Proteins
  • Lipids
  • Placebos
  • Human Growth Hormone
  • Insulin-Like Growth Factor I
  • somatotropin-binding protein