Abstract
Background: Propofol may decrease myocardial contractility via actions on the β-adrenoceptor-mediated signal transduction. The aim of this study was to evaluate the effect of propofol via β-adrenoceptor-mediated signal transduction by measuring the tissue levels of cAMP (cyclic adenosine monophosphate). Methods: The effects of propofol on β-adrenoceptor mediated cascades were measured with cAMP concentrations, which were stimulated by agonists (l-isoproterenol, GTPγS, and forskolin) of each step of β-adrenoceptor-mediated cascades. Results: While the production of cAMP stimulated by isoproterenol, GTPγS, or forskolin are increased (P < 0.05), application of each concentration of propofol (0.1, 1, 10, 100 μM) did not alter the levels of cAMP. Conclusions: Considering that propofol did not alter the tissue cAMP levels when stimulated by isoproterenol, GTPγS, and forskolin, propofol appears to have no effect on the β-adrenoceptor signaling pathway in guinea pig ventricular myocardium. Copyright © Korean Society of Anesthesiologists, 2010.
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Chang, C. H., Roh, G. U., & Park, W. K. (2010). Effects of propofol on β-adrenoceptor-mediated signal transduction in cardiac muscle; role of cAMP. Korean Journal of Anesthesiology, 58(4), 374–377. https://doi.org/10.4097/kjae.2010.58.4.374
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