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Interactions between Verapamil and Digoxin in Langendorff‐Perfused Rat Hearts: The Role of Inhibition of P‐glycoprotein in the Heart
Author(s) -
Aylin Arici Mualla,
Kilinc Emrah,
Demir Omer,
Ates Mehmet,
Yesilyurt Alaattin,
Gelal Ayse
Publication year - 2010
Publication title -
basic and clinical pharmacology and toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.805
H-Index - 90
eISSN - 1742-7843
pISSN - 1742-7835
DOI - 10.1111/j.1742-7843.2010.00574.x
Subject(s) - verapamil , digoxin , inotrope , perfusion , medicine , diltiazem , in vivo , chemistry , pharmacology , endocrinology , heart failure , calcium , biology , microbiology and biotechnology
P‐glycoprotein (P‐gp) is expressed in tumour cells as well as normal tissues including heart. Modulation of P‐gp transport in vivo may lead to increased drug penetrance to tissues with resulting increases in toxicity. We aimed to investigate the effects of P‐gp on the isolated heart by digoxin infusion in the absence and presence of verapamil. The study was performed in Langendorff isolated perfused rat hearts. After a 20 min. stabilisation period with Tyrode Buffer, digoxin (125 μg/5 mL) was infused for 10 min. in the control group (n = 7). The same dose of digoxin was infused during perfusion with verapamil (1 n m ) containing Tyrode Buffer (n = 8) in the study group. Outflow concentration and cardiac parameters of digoxin were measured at frequent intervals for 40 min. AUEC (0–40 min) for left ventricular developed pressure was significantly increased in the presence of verapamil (4260 ± 39.37 mmHg min versus 4607 ± 98.09 mmHg min; 95% CI ‐587.7 to −105.8; p = 0.0083). The significant increases in left ventricular developed pressure were at 20, 25, 30, 35 and 40 min. AUC (0–40 min) value for outflow digoxin concentration‐time curve was significantly lower in the presence of verapamil. Verapamil increased the positive inotropic effect of digoxin, probably through the inhibition of P‐gp, which effluxes digoxin out of cardiac cells.