The pharmacokinetics of acyl, des-acyl, and total ghrelin in healthy human subjects.

Journal Article (Journal Article)

BACKGROUND: Ghrelin stimulates GH secretion and regulates energy and glucose metabolism. The two circulating isoforms, acyl (AG) and des-acyl (DAG) ghrelin, have distinct metabolic effects and are under active investigation for their therapeutic potentials. However, there is only limited data on the pharmacokinetics of AG and DAG. OBJECTIVES: To evaluate key pharmacokinetic parameters of AG, DAG, and total ghrelin in healthy men and women. METHODS: In study 1, AG (1, 3, and 5 μg/kg per h) was infused over 65 min in 12 healthy (8 F/4 M) subjects in randomized order. In study 2, AG (1 μg/kg per h), DAG (4 μg/kg per h), or both were infused over 210 min in ten healthy individuals (5 F/5 M). Plasma AG and DAG were measured using specific two-site ELISAs (study 1 and 2), and total ghrelin with a commercial RIA (study 1). Pharmacokinetic parameters were estimated by non-compartmental analysis. RESULTS: After the 1, 3, and 5 μg/kg per h doses of AG, there was a dose-dependent increase in the maximum concentration (C(max)) and area under the curve (AUC(0-last)) of AG and total ghrelin. Among the different AG doses, there was no difference in the elimination half-life, systemic clearance (CL), and volume of distribution. DAG had decreased CL relative to AG. The plasma DAG:AG ratio was ~2:1 during steady-state infusion of AG. Infusion of AG caused an increase in DAG, but DAG administration did not change plasma AG. Ghrelin administration did not affect plasma acylase activity. CONCLUSIONS: The pharmacokinetics of AG and total ghrelin appears to be linear and proportional in the dose range tested. AG and DAG have very distinct metabolic fates in the circulation. There is deacylation of AG in the plasma but no evidence of acylation.

Full Text

Duke Authors

Cited Authors

  • Tong, J; Dave, N; Mugundu, GM; Davis, HW; Gaylinn, BD; Thorner, MO; Tschöp, MH; D'Alessio, D; Desai, PB

Published Date

  • June 2013

Published In

Volume / Issue

  • 168 / 6

Start / End Page

  • 821 - 828

PubMed ID

  • 23482590

Pubmed Central ID

  • PMC3740531

Electronic International Standard Serial Number (EISSN)

  • 1479-683X

Digital Object Identifier (DOI)

  • 10.1530/EJE-13-0072


  • eng

Conference Location

  • England