4.7 Article

Serum Half-Life of Pituitary Gonadotropins Is Decreased by Sulfonation and Increased by Sialylation in Women

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 94, Issue 3, Pages 958-964

Publisher

ENDOCRINE SOC
DOI: 10.1210/jc.2008-2070

Keywords

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Funding

  1. Academic Laboratory, University Hospital, Uppsala, Sweden
  2. National Institutes of Health [NIH R01 AG13241]

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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 (SO3-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 SO3-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 SO3-GalNAc residues suggests their removal by hepatic SO3-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. (J Clin Endocrinol Metab 94: 958-964, 2009)

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