Arrhythmogenic effects induced by coronary conversion of pulmonary big endothelin to endothelin : Aggravation of this phenomenon in heritable hyperlipidemi

Objectives. We investigated whether endogenous pulmonary big endothelin has arrhythmogenic properties under normal conditions and in heritable hyperlipidemia. Background. Endothelin (ET), one of the most potent vasoconstrictors, is known to induce ventricular arrhythmias. It is unclear, however, whether its precursor, big endothelin, released from the lung, contributes to arrhythmogenesis. Methods. In lung-heart model in which Langendorff heart is serially perfused with the effluent from the isolated lung of the same animal, we evaluated arrhythmias in control and in Watanabe heritable hyperlipidemic (WHHL) rabbits. Results. In both controls (n = 12) and WHHL (n = 8), serial perfusion evoked decrease in coronary flow (controls, −11 ± 3%; WHHL, −25 ± 6%) and fourfold increase of ventricular extrasystoles (VES) (controls, 40.7 ± 8; WHHL, 40.2 ± 5 VES/40 min, p < 0.05). However, WHHL developed more and longer nonsustained ventricular tachycardias (VT) compared with controls (incidence, 1.38 ± 1.1 vs. 0.33 ± 0.5 VT/40 min, p < 0.05; length, 14.36 ± 3.1 vs. 7.25 ± 1.5 beats/VT, p < 0.05). Arrhythmias were not ischemia-induced because corresponding mechanical flow reduction had no arrhythmogenic effect (n = 6 in controls and WHHL). Although vasoconstriction disappeared entirely, arrhythmias were only partly suppressed by ET antagonists (BQ-123, 2 μmol/liter; A-127722, 20 μmol/liter). The ET-converting enzyme inhibitor phosphoramidon (50 μmol/liter) completely suppressed arrhythmias and vasoconstriction. The ETB antagonists (IRL-1038, 4 μmol/liter; IRL-1025, 5 μmol/liter) had no effect (n = 6). Conclusions. Endogenous pulmonary big ET produces arrhythmogenic effects that are aggravated in heritable hyperlipidemia. These effects, requiring coronary conversion of big ET into ET, are partly ETA-mediated and ETB-independent