Serum half-life of pituitary gonadotropins is decreased by sulfonation and increased by sialylation in women

J Clin Endocrinol Metab. 2009 Mar;94(3):958-64. doi: 10.1210/jc.2008-2070. Epub 2008 Dec 30.

Abstract

Context: The gonadotropins are secreted from the human pituitary as spectra of isoforms with different degrees of sulfonation and sialylation of the oligosaccharides, modifications suspected to determine their half-lives in the circulation.

Objectives: Our objectives were to determine the isoform composition of the serum gonadotropins during GnRH receptor blockade, and to estimate the half-lives in circulation of isoforms with 0-1-2-3 sulfonated N-acetylgalactosamine (SO(3)-GalNAc) residues.

Design/participants: Serum samples were collected in seven healthy women before and up to 20 h after administration of the NAL-GLU GnRH antagonist.

Main outcome measures: The number of sialic acid and SO(3)-GalNAc residues per LH and FSH molecule and the distribution of molecules with 0-1-2-3 sulfonated residues were measured. The half-lives were estimated by monoexponential decay.

Results: More sialylated and less sulfonated gonadotropin isoforms remain longer in circulation during GnRH receptor blockade. LH isoforms with two and three sulfonated residues per molecule had shorter half-lives compared with those with zero and one (109 and 80 vs. 196 and 188 min; P < 0.01). FSH isoforms with one and two sulfonated residues had shorter half-lives than those with zero (485 and 358 vs. 988 min; P < 0.01).

Conclusions: The decline in LH and FSH during GnRH receptor blockade is associated with a decrease in sulfonated and increase in sialylated residues. The rapid disappearance of LH isoforms with two and three SO(3)-GalNAc residues suggests their removal by hepatic SO(3)-GalNAc-receptors similar to those in rodents. Episodical secretion of spectra of isoforms with different half-lives is expected to lead to continuous changes in gonadotropin isoform compositions in blood.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetylgalactosamine / metabolism
  • Electrophoretic Mobility Shift Assay
  • Female
  • Follicle Stimulating Hormone / blood*
  • Gonadotropin-Releasing Hormone / antagonists & inhibitors
  • Half-Life
  • Humans
  • Luteinizing Hormone / blood*
  • N-Acetylneuraminic Acid / metabolism*
  • Protein Isoforms
  • Sulfonic Acids / metabolism*

Substances

  • Protein Isoforms
  • Sulfonic Acids
  • Gonadotropin-Releasing Hormone
  • Luteinizing Hormone
  • Follicle Stimulating Hormone
  • N-Acetylneuraminic Acid
  • Acetylgalactosamine