Evidence that both ETA and ETB receptor subtypes are involved in the in vivo aldosterone secretagogue effect of endothelin-1 in rats

Res Exp Med (Berl). 1996;196(3):145-52. doi: 10.1007/BF02576836.


Endothelins (ET) are a family of vasoconstrictor peptides, secreted by vascular endothelium, which act through two main subtypes of receptors: ETA and ETB. ET-1 is known to stimulate aldosterone (ALDO) secretion by adrenal zona glomerulosa (ZG), and in vitro its effect was recently found to be exclusively mediated by ETB receptors. In this study the involvement of ETA and ETB in the mediation of the in vivo acute ALDO secretagogue action of ET-1 was investigated by the use of their selective antagonists BQ-123 and BQ-788, respectively. The bolus intraperitoneal administration of ET-1 dose-dependently raised both basal and angiotensin II (ANG II)-enhanced plasma ALDO concentration (PAC) in rats. Both antagonists counteracted the stimulatory effect of ET-1 on basal PAC, and when administered together completely annulled it. Conversely, only BQ-788 reversed the effect of ET-1 on ANG II-enhanced PAC. ET-1 increased systolic blood pressure (BP) in normal rats, but not in animals simultaneously administered ANG II. The hypertensive effect of ET-1 was completely abolished by BQ-123, and not affected by BQ-788. In light of these findings the following conclusions can be drawn: (i) the in vivo ALDO secretagogue action of ET-1 is mediated by both ETA and ETB, this latter subtype of ET receptors playing a major role; and (ii) the mechanism whereby ETA participates in this in vivo effect of ET-1 is indirect, and probably connected with the ET-1-induced rise in BP and adrenal blood flow.

MeSH terms

  • Adrenal Cortex / chemistry
  • Adrenal Cortex / physiology
  • Aldosterone / metabolism*
  • Angiotensin II / blood
  • Angiotensin II / drug effects
  • Animals
  • Blood Pressure / drug effects
  • Dose-Response Relationship, Drug
  • Endothelin Receptor Antagonists
  • Endothelin-1 / pharmacology*
  • Male
  • Oligopeptides / pharmacology
  • Peptides, Cyclic / pharmacology
  • Piperidines / pharmacology
  • Rats
  • Rats, Wistar
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Receptors, Endothelin / agonists
  • Receptors, Endothelin / physiology*


  • Endothelin Receptor Antagonists
  • Endothelin-1
  • Oligopeptides
  • Peptides, Cyclic
  • Piperidines
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Receptors, Endothelin
  • Angiotensin II
  • BQ 788
  • Aldosterone
  • cyclo(Trp-Asp-Pro-Val-Leu)