Key result
Dihydropyridines reduce reperfusion enzyme release and contracture in rat hearts but higher doses increase cardiodepression.
Why the study?
Do dihydropyridine calcium antagonists reduce ischemia-reperfusion injury in isolated rat hearts?
Do dihydropyridine calcium antagonists reduce ischemia-reperfusion injury in isolated rat hearts?
Dihydropyridine calcium antagonists provide anti-ischemic protection in isolated rat hearts, but their varying washout rates and cardiodepressant effects influence the recovery of reperfusion function.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for dihydropyridine calcium antagonists in ischemia-reperfusion; leaves open clinical translation given dose-dependent cardiodepression in this model.
A comparison was made of the anti-ischemic effects of dihydropyridine calcium antagonists in isolated globally ischemic rat hearts. Pretreatment with amlodipine, nifedipine, nitredipine, or nisoldipine reduced reperfusion enzyme (lactate dehydrogenase) release and contracture after 25 min of global ischemia and 30 min of reperfusion. Increasing concentrations of all compounds resulted in proportionally smaller reductions in the severity of ischemia, with larger decreases in nonischemic tissue contractility occurring. Reperfusion function was significantly improved at 30 min with nifedipine only; however, at 60 min reperfusion function was significantly improved for all except nisoldipine. Washout data from nonischemic hearts (rate of disappearance of cardiodepressant effects) showed that the dihydropyridines washed out in the following order (fastest to slowest): nifedipine greater than nitrendipine greater than nisoldipine greater than amlodipine. Thus, these dihydropyridines are anti-ischemic, though at higher concentrations cardiodepressant effects increase disproportionately. Differences in washout also effect the ability of these compounds to improve reperfusion function.
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Grover et al. (2008) studied Global ischemia. Dihydropyridine calcium antagonists (amlodipine, nifedipine, nitrendipine, nisoldipine) was evaluated on Reperfusion enzyme (lactate dehydrogenase) release, contracture, and reperfusion function. Pretreatment with dihydropyridine calcium antagonists reduced reperfusion enzyme release and contracture in isolated ischemic rat hearts, though higher concentrations increased cardiodepression.
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