Electrophysiological interactions between quinidine-lidocaine and quinidine-phenytoin in guinea-pig papillary muscle-Reference-Cited by-同舟云学术

Electrophysiological interactions between quinidine-lidocaine and quinidine-phenytoin in guinea-pig papillary muscle

Published:1985 Issue:4 Volume:331 Page:369-375
ISSN:0028-1298
Container-title:Naunyn-Schmiedeberg's Archives of Pharmacology
language:en
Short-container-title:Naunyn-Schmiedeberg's Arch. Pharmacol.

Author:

S�nchez-Chapula Jos�

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF00500822.pdf

Reference30 articles.

1. Bean BP, Cohen CJ, Tsien RW (1983) Lidocaine block of cardiac sodium channels. J Gen Physiol 81:613?642

2. Campbell TJ (1983) Improtance of physico-chemical properties in determining the kinetics of the effects of class I antiarrhythmic drugs on maximum rate of depolarization in guinea-pig ventricle. Br J Pharmacol 80:33?40

3. Chen CM, Gettes LS (1976) Combined effects of rate, membrane potential, and drugs on maximum rate of rise ( $$\dot V_{\max }$$ ) of action potential upstroke of guinea-pig papillary muscle. Circ Res 38:464?469

4. Clarkson CW, Hondeghem LM (1984) Electrophysiological evidence that local anaesthetics and antiarrhythmic drugs bind to a specific receptor site in cardiac sodium channels: displacement of bupivacaine by lidocaine. Proc West Pharmacol Soc 27:23?25

5. Cohen CJ, Bean P, Tsien RW (1984) Maximal upstroke velocity as an index of available sodium conductance. Circ Res 54:636?651

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