1 To date, only two mammalian endothelin (ET) receptors, termed ET A and ET B , have been cloned, sequenced and characterized. However, several functional studies of isolated blood vessels suggest that ET-1-induced contractions may be mediated by multiple ET A receptors. In this study, the ET A receptors in renal arteries isolated from Wistar rats were characterized by isometric tension recording and radioligand binding techniques. 2 ET-1, sarafotoxin S6b (StxS6b) and ET-3 produced concentration-dependent contraction with similar response maxima in endothelium-denuded arteries, whereas the ET B receptor-selective agonist StxS6c was inactive. ET-1 and StxS6b were equipotent and 30 times more potent than ET-3. This agonist pro®le, together with the ®ndings that the ET A receptor-selective antagonists, BQ-123 and FR-139317 caused concentration-dependent, rightward shifts of the concentration-e ect curves to each agonist indicated that ET-1-induced contractions in rat renal artery were mediated via ET A receptors. 5 Thus, di erences in BQ-123 potency against ET-1 and StxS6b-induced contractions in rat renal arteries might be due to di erences in the kinetics of agonist binding, rather than due to the existence of atypical ET A receptors.
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