Article date: October 1994
By: Takahiro Fukuroda, Satoshi Ozaki, Masaki Ihara, Kiyofumi Ishikawa, Mitsuo Yano, Masaru Nishikibe, in Volume 113, Issue 2, pages 336-338
In the rabbit isolated pulmonary artery, neither the ETA receptor antagonist, BQ‐123 (10 μm), nor the ETB receptor antagonist, BQ‐788 (10 μm), inhibited the contractions induced by 1 nm endothelin‐1 (ET‐1). However, the combination of BQ‐123 and BQ‐788 completely inhibited the ET‐1‐induced contraction. In contrast, the ETB‐selective agonist, sarafotoxin S6c (1 nm)‐induced contraction was completely inhibited by BQ‐788 but not by BQ‐123. In receptor binding assays, [125I]‐ET‐1 specific binding to pulmonary arterial membranes was inhibited by BQ‐123 (1 μm) by approximately 20% and additive treatment with BQ‐788 (1 μm) completely inhibited the BQ‐123‐resistant component of [125I]‐ET‐1 specific binding. The present study demonstrates synergistic inhibition by BQ‐123 and BQ‐788 of ET‐1‐induced contraction of the rabbit pulmonary artery and the coexistence of ETA and ETB receptors, suggesting that the activation of either only ETA or only ETB receptors may be sufficient to cause complete vasoconstriction. Therefore, blockade of both receptor subtypes would be necessary for the inhibition of some ETA/ETB composite types of responses.
DOI: 10.1111/j.1476-5381.1994.tb16901.x
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