Abstract
The role of catecholamines in ischemic preconditioning is unclear. Accordingly, the effects of tyramine-induced norepinephrine release and α1-receptor blockade were examined. Ischemic preconditioning with a 5-minute coronary occlusion 10 minutes before a 30-minute ischemic interval resulted in only 7.7±3.1% infarction of the risk area, significantly less than that in control rabbits with isolated 30-minute coronary occlusions (34.4±3.2%, P̃.01). Intravenous infusion of tyramine 10 minutes before 30 minutes of ischemia also protected the heart from infarction to an extent similar to that seen with ischemic preconditioning (6.9±2.4% infarction). This protection observed with tyramine infusion was eliminated by α1-receptor blockade with BE 2254 (36.8±2.6% infarction) but was unaffected by β-blockade with propranolol (10.5±2.4% infarction). Furthermore, the protection was unaffected when the tyramine-induced hypertension was attenuated by allowing blood to flow into a volume reservoir (3.9±0.8% infarction, P
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Thornton, J. D., Daly, J. F., Cohen, M. V., Yang, X. M., & Downey, J. M. (1993). Catecholamines can induce adenosine receptor-mediated protection of the myocardium but do not participate in ischemic preconditioning in the rabbit. Circulation Research, 73(4), 649–655. https://doi.org/10.1161/01.res.73.4.649
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