Lack of inhibition of glyceryl trinitrate by diphenyleneiodonium in bovine coronary artery

Recent studies indicate that diphenyleneiodonium is a potent inhibitor of glyceryl trinitrate-induced relaxation in rat aorta precontracted with phenylephrine. We have explored the generality of this action in bovine coronary artery precontracted with the thromboxane A 2 mimetic, 9,11-dideoxy-11α,9α...

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Veröffentlicht in:European journal of pharmacology 1996-10, Vol.314 (3), p.347-350
Hauptverfasser: De la Lande, Ivan S., Philp, Theron, Stafford, Irene, Horowitz, John D.
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Sprache:eng
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Zusammenfassung:Recent studies indicate that diphenyleneiodonium is a potent inhibitor of glyceryl trinitrate-induced relaxation in rat aorta precontracted with phenylephrine. We have explored the generality of this action in bovine coronary artery precontracted with the thromboxane A 2 mimetic, 9,11-dideoxy-11α,9α-epoxy-methano-prostaglandin F 2α (U46619). Diphenyleneiodonium 0.3 μM was without effect (endothelium absent) or caused mild potentiation (0.3 μM or 10 μM; endothelium present) of the relaxant response to glyceryl trinitrate. Lack of inhibition was not due to U46619, since inhibition was still prominent in rat aorta precontracted with this agent. It is concluded that diphenyleneiodonium distinguishes between cellular mechanisms mediating vasodilator responses to glyceryl trinitrate in rat aorta and bovine coronary artery.
ISSN:0014-2999
1879-0712
DOI:10.1016/S0014-2999(96)00729-7