Multiple subtypes of endothelin receptors in human and porcine tissues: Characterization by ligand binding, affinity labeling, and regional distribution

R. Takayanagi, K. Ohnaka, C. Takasaki, M. Ohashi, H. Nawata

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13 Citations (Scopus)

Abstract

To characterize the properties and the distribution of endothelin (ET) receptor subtypes, we have examined the ligand selectivity and the molecular weight (Mr) of [125I]ET-1 and [125I]ET-3 binding sites in various tissues of human and pigs. ET-1 and ET-2 showed almost identical potencies in displacing the bound [125I]ET-1 in all of the tissues examined. ET-3, sarafotoxin S6b (SRTX-b), and sarafotoxin S6C (SRTX-c) displaced the [125I]ET-1 with nearly the same sensitivity as ET-1 (IC50= 0.07-3.0 nM) in brain, kidney, liver, and adrenal, whereas the three peptides showed very weak competition (IC50= 40-500 nM) against [125I]ET-1 binding in atria, aorta, lung, stomach, and uterus. The Bmaxvalue for [125I]ET-3 was 83% of that for [125I]ET-1 in human liver membranes, whereas the Bmaxfor [125I]ET-3 was only 12% of that for [125I]ET-1 in human atrial membranes. [125I]ET-3 bound to liver and atrial membranes was displaced by ET/SRTX isopeptides almost equipotently. Two proteins with Mrof 110 and 50 kDa were specifically affinity-labeled with [125I]ET-1 in porcine lung membranes. The above findings indicated that two distinct subclasses of ET receptors, namely ET-1/ET-2-speeific and ET/SRT family common receptors, were distributed in various proportions in mammalian tissues.

Original languageEnglish
Pages (from-to)S127-S130
JournalJournal of Cardiovascular Pharmacology
Volume17
DOIs
Publication statusPublished - 1991

All Science Journal Classification (ASJC) codes

  • Pharmacology
  • Cardiology and Cardiovascular Medicine

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