Why the study?
Does induction of glyceryl trinitrate tolerance affect large coronary artery responsiveness to non-catecholamine constrictor agents in a bovine isolated coronary artery model?
Does induction of glyceryl trinitrate tolerance affect large coronary artery responsiveness to non-catecholamine constrictor agents in a bovine isolated coronary artery model?
In a bovine coronary artery model, GTN tolerance induction does not cause rebound vasoconstriction to non-catecholamine constrictors upon GTN withdrawal.
GTN tolerance spares non-catecholamine constrictor responses in bovine coronaries; leaves open rebound mechanisms and human translation.
Recent clinical studies have raised the possibility that intermittent nitrate dose regimens, while limiting the extent of nitrate tolerance development, may trigger rebound aggravation of ischaemia after abrupt withdrawal of nitrate. To date, only limited studies have been performed to examine the mechanism of this phenomenon. 2. In a bovine isolated coronary artery model, we tested the hypothesis that induction of glyceryl trinitrate (GTN) tolerance might affect large coronary artery responsiveness to a variety of non-catecholamine constrictor agents. Glyceryl trinitrate tolerance was induced by pre-exposure to GTN (10 mumol/L) for 60 min followed by 15 min washout. In some experiments, the effect of prior endothelial removal on putative interactions was also examined. 3. Our results showed that GTN tolerance did not affect responses to KCl, the thromboxane A2 mimetic U46619, endothelin-1 and 5-HT, irrespective of presence or absence of endothelium. None of the constrictor agents tested induced endothelium-dependent constriction. 4. We conclude that in this model of GTN tolerance induction, there is no evidence of 'rebound' vasoconstriction to this group of non-catecholamine vasoconstrictors with GTN withdrawal.
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Zhang et al. (1995) studied this question.
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