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Endothelin‐A receptor antagonist inhibits angiotensin II and noradrenaline in man
Author(s) -
Wenzel R. R.,
Rüthemann J.,
Bruck H.,
Schäfers R. F.,
Michel M. C.,
Philipp Th.
Publication year - 2001
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1046/j.0306-5251.2001.01422.x
Subject(s) - vasoconstriction , vasodilation , angiotensin ii , medicine , endocrinology , antagonist , endothelin 1 , endothelin receptor , chemistry , agonist , renin–angiotensin system , pharmacology , receptor , blood pressure
Aims Endothelin‐1 (ET‐1) is a potent vasoconstrictor produced by the vascular endothelium. The interactions of ET with the mediators of the sympathetic nervous system and the renin‐angiotensin‐system in humans are unclear. Methods We studied the effects of the ET A ‐selective antagonist BQ‐123 and the ET B ‐selective antagonist BQ‐788 (both 10 −10 −10 −8 m ) on ET‐1 (10 −16 −10 −10 m ), angiotensin II (AT, 10 −16 −10 −10 m ) and noradrenaline (NA, 10 −16 −10 −10 m ) induced vasoconstriction in the human skin microcirculation in vivo in 25 healthy male volunteers using laser Doppler flowmetry and double injection technique. Results BQ‐123 caused a dose‐dependent vasodilatation (maximum effect: + 949 ± 84 AUC‐PU, P < 0.001), whereas BQ‐788 induced mild vasoconstriction (maximum effect: −388 ± 96 AUC‐PU, P < 0.01). In the presence of BQ‐123, but not BQ‐788, ET‐1, AT and NA caused markedly less vasoconstriction at any tested agonist dose; the effect was most pronounced on ET‐1 (maximum effect at 10 −14 m : + 814 ± 93 AUC‐PU vs ET alone, P < 0.001), followed by noradrenaline (maximim effect at 10 −16 m : + 580 ± 107 AUC‐PU vs NA alone, P < 0.01) and angiotensin II (maximim effect at 10 −14 m : + 493 ± 111 AUC‐PU vs AT alone, P < 0.001). Conclusions ET A ‐selective antagonism inhibits vasoconstriction to AT and NA in vivo in healthy subjects. This beneficial effect may be useful for the treatment of patients with cardiovascular disease including hypertension especially in combination therapy with sympatholytic agents and inhibitors of the renin‐angiotensin system.