Adrenal endothelin-1 levels are not associated with aldosterone secretion in primary aldosteronism

Eur J Endocrinol. 2009 Mar;160(3):453-8. doi: 10.1530/EJE-08-0828. Epub 2008 Dec 10.

Abstract

Background: Endothelin-1 (ET-1) may function as an aldosterone secretagogue and, in turn, aldosterone can upregulate ET-1 expression. Hence, the existence of a feedforward loop involving ETs and aldosterone has been speculated in primary aldosteronism (PA). In the present study, we sought to examine ET-1 secretion from the adrenal glands in patients with PA.

Design: We determined ET-1 levels in blood samples obtained during adrenal venous sampling of patients affected by PA (n=17). Furthermore, we examined the mRNA expression of the ET system in tissue samples from aldosterone-producing adenomas (APAs, n=9) and control normal adrenals (n=3).

Methods: Blood ET-1 levels were determined by RIA. Tissue mRNA expression of the ET system was assayed with Affymetrix microarrays.

Results: ET-1 levels did not differ between inferior vena cava and adrenal vein blood in both bilateral adrenal hyperplasia and APA patients. Moreover, cortisol-normalized ET-1 levels did not show lateralized adrenal ET-1 secretion in APAs. Through gene expression profiling with microarray performed in a distinct set of APA individuals (n=9), we confirmed the adrenal expression of a complete ET system, but we did not detect a significant upregulation of ET components within the APA tissue compared with normal adrenals.

Conclusions: The present data argue against the hypothesis of increased ET-1 secretion from APAs and do not support a general role for adrenal ET-1 in the vascular pathophysiology of PA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoma / metabolism
  • Adenoma / physiopathology
  • Adrenal Gland Neoplasms / metabolism
  • Adrenal Gland Neoplasms / physiopathology
  • Adrenal Glands / metabolism*
  • Aged
  • Aldosterone / blood
  • Aldosterone / metabolism*
  • Aspartic Acid Endopeptidases / genetics
  • Endothelin-1 / blood*
  • Endothelin-1 / genetics
  • Endothelin-Converting Enzymes
  • Female
  • Humans
  • Hyperaldosteronism / metabolism*
  • Hyperaldosteronism / physiopathology
  • Male
  • Metalloendopeptidases / genetics
  • Middle Aged
  • RNA, Messenger / metabolism
  • Receptor, Endothelin A / genetics
  • Receptor, Endothelin B / genetics

Substances

  • Endothelin-1
  • RNA, Messenger
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Aldosterone
  • Aspartic Acid Endopeptidases
  • Metalloendopeptidases
  • Endothelin-Converting Enzymes