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Radiocontrast agents induce endothelin release in vivo and in vitro.
Author(s) -
Samuel N. Heyman,
Barbara A. Clark,
Ν. Kaiser,
Katherine Spokes,
Seymour Rosen,
Mayer Brezis,
F H Epstein
Publication year - 1992
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.v3158
Subject(s) - endothelin receptor , endothelin 1 , endocrinology , medicine , iohexol , atrial natriuretic peptide , nephropathy , endothelins , in vivo , chemistry , endothelium , pharmacology , renal function , biology , receptor , microbiology and biotechnology , diabetes mellitus
The intravascular administration of the ionic radiocontrast agent sodium iothalamate (2.9 g of iodine/kg body wt) to rats induced an increase in plasma concentration of immunoreactive endothelin from 21.3 +/- 1.2 to 36 +/- 3 fmol/mL, preceded by a transient rise in the plasma level of atrial natriuretic peptide and associated with a fall in RBF. Equi-iodine amounts of the nonionic agents ioxaglate and iohexol elicited similar or more marked changes in plasma endothelin, but hypertonic solutions of NaCl, mannitol, or glucose did not. Comparable levels of endothelin produced by infusions of endothelin-1 induced a reduction of up to 29% in RBF. Iothalamate and iohexol stimulated endothelin release from cultured bovine endothelial cells, suggesting a direct effect of ionic and nonionic agents on vascular endothelium. The data invite speculation that under some circumstances endothelin release might play a role in the circulatory changes caused by these compounds and in the pathogenesis of radiocontrast nephropathy.

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