Abstract
The effects of ischaemia and reoxygenation on cardiac contractile function can be abrogated by ischaemic preconditioning (IPC). We tested whether β-adrenoceptor agonists could mimic IPC and whether IPC was dependent on β-adrenoceptor activation in rat-isolated cardiac tissues. Paced left atria and right ventricular strips were set-up in Krebs solution and isometric developed tension recorded. Ischaemia was simulated by replacing with hypoxic glucose-free Krebs solution for 30 min. IPC and isoprenaline (10−7 M) preconditioning for 10 min were examined. Developed tension post-reoxygenation was expressed as a percentage of the pre-ischaemic baseline. Recovery at 15 min was significantly increased by IPC in atria (47 ± 4.0% vs. 29.3 ± 1.7%, p < 0.05) and ventricles (39.0 ± 5.2% vs. 22.4 ± 2.8%, p < 0.05). At 60 min, isoprenaline-treated atria recovery (75.8 ± 16.6%) was significantly (p < 0.05) greater than controls (47.9 ± 2.3%). Propranolol (10−6 M) abolished both effects. Therefore, both IPC and β-adrenoceptor agonist-induced improvement of contractile recovery was propranolol-sensitive and β-adrenoceptor-mediated.
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Abbreviations
- βP:
-
β-adrenoceptor-mediated preconditioning
- IPC:
-
ischaemic preconditioning
- Pro:
-
propranolol
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Acknowledgement
This work was funded by a British Heart Foundation Studentship (FS-05-075-19397) awarded to P.E.P. for which the authors are grateful.
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Penson, P.E., Ford, W.R., Kidd, E.J. et al. Activation of β-adrenoceptors mimics preconditioning of rat-isolated atria and ventricles against ischaemic contractile dysfunction. Naunyn-Schmied Arch Pharmacol 378, 589–597 (2008). https://doi.org/10.1007/s00210-008-0331-6
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DOI: https://doi.org/10.1007/s00210-008-0331-6