Attenuated vasoconstrictor responses to endothelin in afferent arterioles during a high-salt diet

Am J Physiol Renal Physiol. 2007 Apr;292(4):F1208-14. doi: 10.1152/ajprenal.00280.2006. Epub 2007 Jan 9.

Abstract

Endothelin-1 (ET-1) is increased in rats on a high-salt (HS) diet and participates in salt-dependent hypertension. Afferent arterioles (AA) are important for long-term blood pressure control, and therefore we hypothesized that a HS diet would alter their responsiveness to ET-1. Sprague-Dawley rats were fed either a normal-salt (NS; 0.66% NaCl) or HS (8%) diet for 1 wk. Diameters of AA were determined in response to increasing concentrations of big ET-1, ET-1, sarafotoxin 6c (S6c), or norepinephrine (NE), using the blood-perfused juxtamedullary nephron technique. ET-1 responses were also determined during blockade of endothelin type A (ET(A)) or type B (ET(B)) receptors with 10 nM ABT-627 or 30 nM A-192621, respectively. Expression of ET(A) and ET(B) receptors was determined in renal microvessels. Responses of AA to big ET-1, ET-1, and S6c were significantly attenuated during a HS diet (e.g., response to 10(-10) M ET-1 in NS vs. HS rats: -52.5 +/- 10.2 vs. +5.6 +/- 11.3% of control diameter; P < 0.05), with no change in the responses to NE. ET(B), but not ET(A) receptor blockade abolished the different response to ET-1 between the NS and HS groups. ET(B) receptor expression in renal microvessels was increased in response to HS (17.7 +/- 2.4 vs. 6.6 +/- 3.0% of beta-actin, P = 0.02), whereas ET(A) receptor expression was unchanged. These results suggest that the reduced vasoconstrictor response of AA to endothelin peptides during a HS diet is mediated by increased vasodilatory function of endothelial ET(B) receptors. By preserving renal blood flow, this may be an important mechanism to restore sodium balance during a HS diet.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arterioles / drug effects
  • Arterioles / physiology*
  • Blood Pressure / drug effects
  • Endothelin-1 / physiology*
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Endothelin A / biosynthesis
  • Receptor, Endothelin B / biosynthesis
  • Sodium, Dietary / administration & dosage*
  • Vasoconstriction / drug effects*

Substances

  • Endothelin-1
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Sodium, Dietary