Mechanisms responsible for the heterogeneous coronary microvascular response to nitroglycerin.
- 1 March 1991
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation Research
- Vol. 68 (3) , 847-855
- https://doi.org/10.1161/01.res.68.3.847
Abstract
Nitroglycerin dilates large (greater than or equal to 100 microns) but not small coronary arterial microvessels, and a putative metabolite of nitroglycerin, S-nitroso-L-cysteine, has been shown in vitro to dilate both large and small coronary microvessels. Based on this evidence, we tested the hypothesis that the lack of response of small coronary microvessels was due to an inability of small coronary microvessels to convert nitroglycerin into its vasoactive metabolite and examined possible explanations for this phenomenon. We studied left ventricular epicardial microvessels in vivo using video microscopy and stroboscopic epi-illumination in anesthetized, open-chest dogs. Diameters were determined while the epicardium was suffused with nitroglycerin, S-nitroso-L-cysteine, or S-nitroso-D-cysteine (all 10 microM) and nitroglycerin in the presence of L- or D-cysteine (100 microM). None of the agents affected systemic hemodynamics. Nitroglycerin dilated large arterioles (20 +/- 2%) but not small arterioles (1 +/- 1%). Both S-nitroso-L-cysteine and S-nitroso-D-cysteine were potent dilators of all size classes of microvessels. Concomitant application of L-cysteine and nitroglycerin evoked dilation in small microvessels (22 +/- 4%, p less than 0.5 versus nitroglycerin alone) and larger microvessels (27 +/- 6%, p = NS versus nitroglycerin alone). D-Cysteine did not alter the microvascular response to nitroglycerin in either small (7 +/- 4%, p = NS versus nitroglycerin alone) or large (18 +/- 3%, p = NS versus nitroglycerin alone) microvessels. Neither L-cysteine nor D-cysteine had a direct effect on microvascular diameter. These findings suggest that 1) sulfhydryl groups are required for the conversion of nitroglycerin to its vasoactive metabolite; 2) the interaction between nitroglycerin and sulfhydryl residues is a stereospecific process, indicating either an intracellular mechanism or a membrane-associated enzymatic reaction; and 3) a lack of available sulfhydryl groups may be responsible for the lack of response of small coronary arterioles to nitroglycerin.Keywords
This publication has 18 references indexed in Scilit:
- Nitric oxide formation during microsomal hepatic denitration of glyceryl trinitrate: Involvement of cytochrome P-450Published by Elsevier ,2004
- Tolerance to nitroglycerin is caused by reduced guanylate cyclase activationJournal of Molecular and Cellular Cardiology, 1989
- Guanylate cyclase activation by organic nitrates in not mediated via nitriteJournal of Molecular and Cellular Cardiology, 1988
- Effects of ethacrynic acid and cystamine on sodium nitroprusside-induced relaxation, cyclic GMP levels and guanylate cyclase activity in rat aortaGeneral Pharmacology: The Vascular System, 1987
- In Vivo Induction and Reversal of Nitroglycerin Tolerance in Human Coronary ArteriesNew England Journal of Medicine, 1987
- Prevention and Reversal of Nitrate Tolerance in Patients with Congestive Heart FailureNew England Journal of Medicine, 1987
- Effects of Glyceryl Trinitrate on Endothelium-Dependent and -Independent Relaxation and Cyclic GMP Levels in Rat Aorta and Human Coronary ArteryJournal of Cardiovascular Pharmacology, 1987
- Evidence for a correlation between nitric oxide formation by cleavage of organic nitrates and activation of guanylate cyclaseJournal of Molecular and Cellular Cardiology, 1985
- Investigations into the role of sulfhydryl groups in the mechanism of action of the nitratesCanadian Journal of Physiology and Pharmacology, 1982
- Requirement of thiols for activation of coronary arterial guanylate cyclase by glyceryl trinitrate and sodium nitrite possible involvement of S-nitrosothiolsBiochimica et Biophysica Acta (BBA) - General Subjects, 1980