Author:
Marks Gerald S.,McLaughlin Brian E.,Brown Leslie B.,Beaton Danielle E.,Booth Brian P.,Nakatsu Kanji,Brien James F.
Abstract
The current proposed mechanism of action of nitrovasodilator drugs involves biotransformation to nitric oxide, which is postulated to be the active vasodilator substance. Our objective was to determine whether nitric oxide was formed from two prototype nitrovasodilator drugs, glyceryl trinitrate (GTN) and sodium nitroprusside (SNP), after incubation with bovine pulmonary vein (BPV) preparations. GTN or SNP was incubated in an argon atmosphere with phosphate buffer, BPV homogenate, or the 10 000 × g supernatant fraction of the homogenate. Nitric oxide formation, as determined by a chemiluminescence – headspace gas method, was measurable following the incubation of SNP with BPV homogenate and 10 000 × g supernatant. There was no detectable formation of nitric oxide from the incubation of GTN with the two BPV preparations, although GTN was biotransformed to glyceryl dinitrate, as determined by gas–liquid chromatography. There was decreased recovery of nitric oxide during the incubation of authentic nitric oxide with the two BPV preparations as compared with buffer. In conclusion, formation of nitric oxide was measured for the interaction of SNP, but not GTN, with BPV preparations. However, the data do not exclude the possible formation of nitric oxide from GTN, as nitric oxide was shown to be sequestered or transformed by the BPV preparations.Key words: glyceryl trinitrate, sodium nitroprusside, nitric oxide formation, bovine pulmonary vein.
Publisher
Canadian Science Publishing
Subject
Physiology (medical),Pharmacology,General Medicine,Physiology
Cited by
39 articles.
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