Key result
L-648,051 increased the digoxin concentration required for ventricular premature beats and cardiac arrest and decreased ventricular tachycardia duration in isolated guinea-pig hearts.
Why the study?
Does the leukotriene D4 receptor antagonist L-648,051 reduce digoxin-induced arrhythmias in isolated guinea-pig hearts?
Does the leukotriene D4 receptor antagonist L-648,051 reduce digoxin-induced arrhythmias in isolated guinea-pig hearts?
The leukotriene D4 receptor antagonist L-648,051 may have beneficial effects in mitigating digoxin-induced arrhythmias in a preclinical model.
May support LTD4 antagonism for digoxin cardiotoxicity; leaves open translation from isolated guinea-pig hearts.
The effect of a leukotriene D4 (LTD4) receptor antagonist, L-648,051, was investigated in digoxin-induced cardiac toxicity in isolated guinea-pig hearts (Langendorff preparation). Digoxin infusion (25 microg.ml-1, 0.5 ml.min-1) increased perfusion pressure and contractile force initially, but decreased them later. The onset of first ventricular premature beats (VPBs) matched the increase phase, but the decrease phase was accompanied by ventricular tachycardia (VT) and fibrillation (VF). In the presence of L-648,051 (5 micromol. l-1), the initial phase was similar to that observed with digoxin alone, but the marked reduction was inhibited. This drug increased the concentration of digoxin required for VBSs and cardiac arrest, but it could not prevent the formation of VT and VF. The duration of VT was significantly decreased by L-648,051. It is concluded that the leukotriene receptor antagonist might have beneficial effects on digoxin-induced arrhythmias. Whether this effect depends on direct or indirect actions is uncertain.
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Gök et al. (1998) studied Digoxin-induced cardiac toxicity. L-648,051 vs. Digoxin alone was evaluated on Digoxin-induced arrhythmias and cardiac toxicity. L-648,051 increased the digoxin concentration required for ventricular premature beats and cardiac arrest and decreased ventricular tachycardia duration in isolated guinea-pig hearts.
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