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2. Evidence for a specific receptor site for lidocaine, quinidine, and bupivacaine associated with cardiac sodium channels in guinea pig ventricular myocardium. Clarkson CW, Hondeghem LM. Circ Res; 1985 Apr; 56(4):496-506. PubMed ID: 2579747 [Abstract] [Full Text] [Related]
3. Mechanism for bupivacaine depression of cardiac conduction: fast block of sodium channels during the action potential with slow recovery from block during diastole. Clarkson CW, Hondeghem LM. Anesthesiology; 1985 Apr; 62(4):396-405. PubMed ID: 2580463 [Abstract] [Full Text] [Related]
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10. Stereoselective effects of the enantiomers of bupivacaine on the electrophysiological properties of the guinea-pig papillary muscle. Vanhoutte F, Vereecke J, Verbeke N, Carmeliet E. Br J Pharmacol; 1991 May; 103(1):1275-81. PubMed ID: 1878762 [Abstract] [Full Text] [Related]
13. Depression of myocardial contractility in vitro by bupivacaine, etidocaine, and lidocaine. Lynch C. Anesth Analg; 1986 Jun; 65(6):551-9. PubMed ID: 2422988 [Abstract] [Full Text] [Related]
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15. Effects of lidocaine alone and in combination with tetraethylammonium on the maximum upstroke velocity in guinea-pig papillary muscles. Ban T, Kojima M, Ichiyama M, Sada H, Hamamoto T. Arzneimittelforschung; 1989 Jul 21; 39(7):770-4. PubMed ID: 2551305 [Abstract] [Full Text] [Related]
17. Electrophysiological effects of EGIS-7229, a new antiarrhythmic agent, in isolated mammalian and human cardiac tissues. Pankucsi C, Bányász T, Magyar J, Gyönös I, Kovács A, Varró A, Szénási G, Nánási PP. Naunyn Schmiedebergs Arch Pharmacol; 1997 Mar 21; 355(3):398-405. PubMed ID: 9089672 [Abstract] [Full Text] [Related]
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