Key result
HMA has a depressant action on cardiac Na+ channels and prolongs action potentials at concentrations that presumably affect Na+-H+ exchange in cardiac muscle.
Why the study?
Does 5-(N,N-hexamethylene)amiloride affect action potentials, intracellular Na+, and pH in guinea pig ventricular muscle in vitro?
Does 5-(N,N-hexamethylene)amiloride affect action potentials, intracellular Na+, and pH in guinea pig ventricular muscle in vitro?
HMA exerts a depressant action on cardiac Na+ channels and prolongs action potentials at concentrations that affect Na+-H+ exchange in cardiac muscle.
May confound NHE inhibition studies in cardiac muscle; leaves open selectivity and in vivo relevance.
We examined the effects of 5-(N,N-hexamethylene)amiloride (one of the Na(+)-H+ exchange blockers, HMA) and amiloride (AM) on action potentials (APs), intracellular Na+ activity, and pH using conventional and double-barreled ion-selective microelectrodes in guinea pig papillary muscle in vitro. Papillary muscle preparations were superfused with HEPES-buffered solution, and intracellular Na+ (aiNa+) and H+ (intracellular pH, pHi) activities were measured in quiescent preparations without stimulation. HMA at a concentration of 1 microM began to induce prolongation of action potential duration (APD) and at concentrations > 10 microM induced a decrease in action potential amplitude (APA), depolarization of resting membrane potential (RMP), prolongation of APD and depression of the maximum upstroke velocity (Vmax). HMA exerted dose-, time-, and rate-dependent reduction in Vmax. AM began to prolong APD at a concentration of 10 microM and at 1 mM induced depolarization of RMP, decreased Vmax and induced significant prolongation of APD. HMA (100 microM) induced a decrease in aiNa+ by 2-3 mM, but exerted no effects on pHi in normal Tyrode's solution. Under conditions of intracellular acidosis induced by exposure to K(+)-free solution, HMA produced a further decrease in pHi. Our results provide direct evidence that HMA has a depressant action on cardiac Na+ channels and prolongs AP at concentrations that presumably affect Na(+)-H+ exchange in cardiac muscle.
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Lai et al. (1994) studied this question. 5-(N,N-hexamethylene)amiloride (HMA) and amiloride (AM) was evaluated on Action potentials, intracellular Na+ activity, and pH. HMA has a depressant action on cardiac Na+ channels and prolongs action potentials at concentrations that presumably affect Na+-H+ exchange in cardiac muscle.
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