Molecular Interaction of Droperidol with Human Ether-a-go-go-related Gene Channels: Prolongation of Action Potential Duration without Inducing Early Afterdepolarization
Schwoerer, Alexander P. M.D.*; Blütner, Carmen B.Sc.†; Brandt, Sven M.D.‡; Binder, Stephan M.Sc.§; Siebrands, Cornelia C. Ph.D.∥; Ehmke, Heimo M.D.#; Friederich, Patrick M.D.**
Background: The cardiac safety of droperidol given at antiemetic doses is a matter of debate. Although droperidol potently inhibits human ether-a-go-go-related gene (HERG) channels, the molecular mode of this interaction is unknown. The role of amino acid residues typically mediating high-affinity block of HERG channels is unclear. It is furthermore unresolved whether droperidol at antiemetic concentrations induces action potential prolongation and arrhythmogenic early afterdepolarizations in cardiac myocytes.
Methods: Molecular mechanisms of HERG current inhibition by droperidol were established using two-electrode voltage clamp recordings of Xenopus laevis oocytes expressing wild-type and mutant channels. The mutants T623A, S624A, V625A, Y652A, and F656A were generated by site-directed mutagenesis. The effect of droperidol on action potentials was investigated in cardiac myocytes isolated from guinea pig hearts using the patch clamp technique.
Results: Droperidol inhibited currents through HERG wild-type channels with a concentration of half-maximal inhibition of 0.6–0.9 μm. Droperidol shifted the channel activation and the steady state inactivation toward negative potentials while channel deactivation was not affected. Current inhibition increased with membrane potential and with increasing duration of current activation. Inhibition of HERG channels was similarly reduced by all mutations. Droperidol at concentrations between 5 and 100 nm prolonged whereas concentrations greater than 300 nm shortened action potentials. Early afterdepolarizations were not observed.
Conclusions: Droperidol is a high-affinity blocker of HERG channels. Amino acid residues typically involved in high-affinity block mediate droperidol effects. Patch clamp results and computational modeling allow the hypothesis that interaction with calcium currents may explain why droperidol at antiemetic concentrations prolongs the action potential without inducing early afterdepolarizations.
DROPERIDOL is a highly potent butyrophenone that has been commonly used for more than 30 yr in the therapy of postoperative nausea and vomiting.1,2
High doses of droperidol (0.25 mg/kg) given for the induction and maintenance of anesthesia have been reported to prolong the QT interval in perioperative patients.3
After several cases of excessive QT-prolongation leading to fatal arrhythmias associated with the use of droperidol at high doses, the US Food and Drug Administration released a “black box” warning in 2001.††
As a consequence, the clinical use of droperidol in postoperative nausea and vomiting therapy has decreased dramatically.2
However, not a single case of cardiac arrhythmia has been reported after application of droperidol at antiemetic doses (0.625–1.25 mg).2,4
Furthermore, droperidol given at antiemetic doses does not seem to be associated with a clinically significant prolongation of the QT interval.5
Also, the cardiotoxic potential of droperidol at antiemetic doses has not been addressed in controlled clinical trials.2,4,6,7
The cardiac safety of droperidol in postoperative nausea and vomiting therapy, therefore, remains a matter of debate.
Prolongation of the QT interval reflects an increase of action potential duration (APD) in ventricular cardiomyocytes. Contradicting results have been obtained in animal studies regarding the effects of droperidol on APD and its potential to induce early afterdepolarizations (EADs).8–12
Some authors demonstrated action potential (AP) shortening,8,9
whereas others reported AP prolongation11,12
or no effect on APD.10
Drug-induced prolongation of cellular APD and induction of torsades de pointes ventricular arrhythmia is often caused by high-affinity block of the delayed rectifying K+
The channel underlying IKr
is encoded by the human ether-a-go-go
-related gene (HERG).14,15
High-affinity block of HERG channels is transmitted by two aromatic amino acid residues in the S6 helix (Tyr652 and Phe656) and by several residues located at the base of the pore helix (Thr623, Ser624, Val625).16–20
Based on the concentration of half-maximal inhibition (IC50
) value for inhibition of HERG channels, droperidol may be regarded as a high-affinity blocker.12
Currently, however, it is unknown whether the amino acid residues typically mediating high-affinity block are involved in the interaction of droperidol with HERG channels. Furthermore, it is unknown whether droperidol interacts with these channels in a way mechanistically similar to high-affinity blockers such as dofetilide and E-4031.19,21
Therefore, despite the “black box” warning of the US Food and Drug Administration on the cardiac safety of droperidol, several issues of the cardiotoxic profile of droperidol remain unresolved. The molecular mode of interaction of the drug with HERG channels has not been defined. Furthermore, it is unclear whether droperidol at antiemetic concentrations induces AP prolongation and early afterdepolarizations in ventricular cardiomyocytes. The aim of our study, therefore, was to characterize the molecular mode of interaction of droperidol with HERG channels. In addition, it was intended to suggest a possible explanation why droperidol may not induce EADs despite its interaction with HERG channels.
Materials and Methods
All animal experiments were conducted in accordance with institutional guidelines and approved by local authorities (Ministry of Science and Health, Hamburg, Germany).
Solutions and Chemicals
Ringer's solution contained 75 mm NaCl, 2 mm KCl, 2 mm CaCl2
, 1 mm MgCl2
, 5 mm Na-pyruvate, and 5 mm HEPES, titrated to pH 7.5 with NaOH. Two-electrode voltage clamp experiments were performed using different extracellular solutions: HERG and HERG mutants were investigated using NaCl-79 solution, which contained 79.5 mm NaCl, 2 mm KCl, 2 mm CaCl2
, 1 mm MgCl2
, and 5 mm HEPES, pH adjusted to 7.5 with NaOH. NaCl-95 solution used for measurement of IKs
contained 95 mm NaCl, 2 mm KCl, 1 mm MgCl2
, 1 mm CaCl2
, and 10 mm HEPES, titrated to pH 7.40 with tris-(hydroxymethyl)-aminomethane. Cardioplegic solution contained 15 mm NaCl, 9 mm KCl, 4 mm MgCl, 0.33 mm NaH2
, 0.015 mm CaCl2
, 10 mm glucose, and 238 mm mannitol, titrated to pH 7.40 with NaOH. For patch clamp experiments, myocytes were bathed in modified Tyrode solution containing 138 mm NaCl, 4 mm KCl, 1 mm MgCl2
, 0.33 mm NaH2
, 2 mm CaCl2
, 10 mm glucose, and 10 mm HEPES, titrated to pH 7.30 with NaOH. The pipette solution contained 120 mm K-glutamate, 10 mm KCl, 2 mm MgCl2
, 10 mm EGTA, 10 mm HEPES, and 2 mm Na2
-ATP, titrated to pH 7.20 with KOH. Droperidol (Sigma, Deissenhofen, Germany) was dissolved in dimethyl sulfoxide. The maximal concentration of dimethyl sulfoxide in the respective extracellular solution was 1%, whereas the concentration used for kinetic analysis was less than 0.1%. At these concentrations, dimethyl sulfoxide did not by itself inhibit currents (data not shown), and its effect on HERG channel gating is negligible.22
Molecular Biology, cRNA Preparation
The HERG mutants T623A, S624A, V625A, Y652A, and F656A were created by site directed mutagenesis.23
All constructs were cloned in the pGEM expression vector for complementary RNA (cRNA) synthesis. The cRNA was synthesized in vitro
with the mMESSAGE mMACHINE Kit (Ambion, Austin, TX) according to the manufacturer's protocol. The cRNA was purified with a phenol/chloroform extraction. The integrity of the cRNA was analyzed in a denaturating gel. The concentration was determined with the RiboGreen method (RiboGreen RNA Quantification Reagent; Molecular Probes, Eugene, OR). For preparation of oocytes, female Xenopus laevis
frogs (n = 37) were anesthetized with tricaine solution, and ovarian lobes were surgically removed. Oocytes were isolated by enzymatic digestion using collagenase A (Roche, Mannheim, Germany; Serva, Heidelberg, Germany) for 2–4 h. Enzymatic digestion was stopped by incubation in Ringer's or NaCl-95 solution. Defolliculated oocytes (stages V and VI) were injected with cRNA of HERG, HERG mutants, or KCNQ1/KCNE1 (in a ratio of 1:1).
Two-electrode Voltage Clamp
Whole cell currents were measured 2–7 days after cRNA injection with the two-electrode voltage clamp technique using an Oocyte-Clamp OC-725C amplifier (Warner Instrument Corporation, Hamden, CT) or a TurboTec 05 amplifier (npi electronic, Tamm, Germany), both controlled by Pulse software (HEKA Elektronik, Lambrecht, Germany). Sharp electrodes were pulled from borosilicate glass capillary tube (World Precision Instruments, Sarasota, FL or Clark Electromedical Instruments, Reading, United Kingdom) and filled with 3 m KCl and 3% agar. Whole cell currents were measured at room temperature (21°–24°C) while oocytes were superfused at a constant rate.
Isolation of Guinea Pig Ventricular Myocytes and Patch Clamp Experiments
For isolation of cardiomyocytes, male Dunkin-Hartley guinea pigs (n = 12; 350–450 g) were deeply anesthetized by thiopental-Na+
(200 mg/kg body weight), and hearts were excised and quickly placed into cold (4°C) cardioplegic solution. Myocytes of the center part of the left ventricular free wall were enzymatically isolated as previously described using a Langendorff apparatus.24,25
Single myocytes were stored at room temperature in Ca2+
free modified Tyrode solution. Only single rod-shaped cells with clear cross-striations and no spontaneous contractions were used for experiments within 12 h after isolation. The ruptured-patch whole cell configuration was used as previously described26
using an EPC-9 amplifier controlled by the Pulse software. Membrane voltages were recorded in the zero current clamp mode. Pipette potentials were corrected online for liquid junction potentials. APs were elicited at 0.2 Hz by depolarizing current injections of 5 or 10 ms in duration. All experiments were performed at room temperature (21°–24°C) while cells were superfused at a constant rate.
Data were analyzed using PulseFit software (HEKA Elektronik), Igor (WaveMetrics, Lake Oswego, OR), and KaleidaGraph software (Synergy Software, Reading, PA). The normalized tail currents during the activation protocol were fitted by a modified Boltzmann equation: I = Imax
/[1 + exp((V0.5
)/k)], where V0.5
is the membrane potential of half-maximal activation, Vm
is the membrane potential, and k is the slope factor. For the analysis of the steady state inactivation, maximal current amplitudes during the tail were corrected for the closing during the hyperpolarizing step at very negative potentials as described previously.27
The corrected curves were fitted by a Boltzmann function. The inhibition of currents by droperidol was quantified by the reduction of the maximal current during the test pulse. The fractional block f was calculated by the following formula: f = 1 − (Imax, drug
). Concentration-response curves were fitted by a Hill equation: f = 1/[1 + (IC50
], where c is the concentration of droperidol and h is the Hill coefficient. The impact of droperidol on the APD at 90% repolarization (APD90
) was quantified by the following formula: y = (APD90, drug
+ APD90, washout
)/2), where APD90, control
is the APD90
before application, APD90, drug
is the APD90
in the presence of droperidol, and APD90, washout
is the APD90
after maximal possible washout of the drug.
All data are given as mean ± SD; n values indicate the number of experiments. When only two groups were compared, statistical significance was calculated by the Student t test, otherwise by one-way analysis of variance (ANOVA) followed by Bonferroni post hoc test using Excel (Microsoft, Redmond, WA) or PRISM (GraphPad Software Inc., San Diego, CA). Where appropriate, paired t tests were performed. Statistical significance was defined as P < 0.05.
Computer Simulations of Cardiac Action Potentials
Computer simulations were conducted using a modified version of the Luo-Rudy dynamic model as previously described.28–30
The influence of droperidol on the AP was simulated assuming a reduction of IKr
by 50% and by variable degrees of ICaL
inhibition. Simulations were performed with a basic cycle length of 1,000 ms for 500 cycles.
Effects of Droperidol on HERG and KCNQ1/KCNE1 Currents
The effect of droperidol on HERG and KCNQ1/KCNE1 currents was studied in oocytes injected with corresponding cRNA. Throughout all experiments, the holding potential was −80 mV, and repetitive pulses were applied to ensure steady state conditions.
Different pulse protocols were employed to assess the effect of droperidol on HERG currents: The ramp protocol was used to elicit a HERG current similar to that during a normal AP.20,31
Oocytes were depolarized to +60 mV and repolarized to −80 mV within 1 s, and the maximal current Imax
was determined. Using square pulses, the cells were depolarized to +0 mV for 2 s, and tail currents were then recorded at −40 mV (Itail −40
) or at −120 mV (Itail −120
). Figure 1A
shows representative current traces elicited by the different pulse protocols under control conditions and after application of 1 μm droperidol. A strong suppression of HERG currents could be detected with each pulse protocol. The concentration dependent fractional inhibition of Imax
, Itail −40
, and Itail −120
were described by Hill equations (fig. 1B
and table 1
). The IC50
was in the range of 0.6–0.9 μm. The inhibition at a concentration of 1 μm droperidol did not significantly differ between the applied pulse protocols (statistically not significant; ANOVA). Therefore, this concentration was chosen to further analyze the effect of droperidol on channel gating properties. The Hill coefficients of all Hill equations were comparable.
To investigate the effect of droperidol on KCNQ1/KCNE1 currents, oocytes were depolarized to +60 mV for a duration of 5 s (Itest
). Tail currents were recorded at −60 mV (Itail −60
). Figure 1C
shows representative current traces under control conditions and after application of 10 μm droperidol. Whereas 1 μm droperidol did not influence the current amplitude of Itest
(n = 4), 10 μm droperidol reduced Itest
in two of five experiments by 3% and 5%. Itail −60
was not affected by either concentration.
Effects of Droperidol on HERG Channel Gating
To analyze the influence of droperidol on the activation of HERG currents, the pulse protocol shown in figure 2A
was used. Depolarizing steps between −70 mV and +80 mV activated time-dependent outward currents. The amplitude of the outward currents at the end of the depolarizing pulse (Itest
) increased with more positive voltage steps and reached a maximum value at approximately 0 mV. Depolarization to more positive values caused a current decrease. To visualize the current inhibition by droperidol, Itest
was normalized to the maximum control current and plotted against the activation potential under control conditions and in the presence of 1 μm droperidol (fig. 2B
). Whereas droperidol strongly inhibited the amplitude of Itest
, no influence on the voltage-dependence of activation was detected.
After the depolarizing step, the tail current Itail
was elicited by a repolarization to −40 mV. The amplitude of Itail
increased with depolarizing steps from −70 to +20 mV and reached a current plateau upon further depolarization (fig. 2C
was normalized to the maximum Itail
of each cell and plotted against the depolarizing membrane potential. The resulting current-voltage curves (fig. 2C
) were described by Boltzmann equations (see table 2
for details). Droperidol significantly shifted the membrane potential of half-maximal activation (V0.5
) toward negative potentials (P
< 0.001) and decreased the slope factor (P
< 0.001). The inhibition of Itail
by droperidol significantly increased with depolarization of the membrane potential (P
< 0.001, ANOVA, n = 8; fig. 2D
The influence of droperidol on the steady state inactivation was assessed by a three-step protocol (fig. 3A
): The membrane was depolarized for 2 s to +40 mV, then pulses from −120 to +60 mV in steps of 10 mV were applied for 50 ms, and finally the membrane potential was kept at +40 mV for 1 s. Figure 3A
shows representative current traces under control conditions and after application of 1 μm droperidol. The magnitude of the resulting tail current at +40 mV was normalized to the maximum tail current and was plotted against the depolarizing voltage steps (fig. 3B
). The parameters of the corresponding Boltzmann functions are given in table 2
. Whereas droperidol caused a significant left shift of the inactivation midpoint (P
< 0.001), the slope factor was not influenced. The fractional inhibition of Itail
significantly depended on the membrane potential (P
< 0.001, ANOVA, n = 7; fig. 3C
). The inactivation time constants were analyzed using a three-step pulse protocol (data not shown): depolarization to 0 mV (2 s) followed by a repolarization to −80 mV for 50 ms and recording of the tail currents between −80 and +40 mV. The time constants of the monoexponential fits of the current decay under control conditions were similar to the ones found after application of 1 μm droperidol (droperidol, 18.0 ± 5.7 ms; control, 20.1 ± 6.2 ms at a pipette potential of 0 mV; n = 7).
The influence of droperidol on HERG deactivation was investigated using the following pulse protocol: depolarization to +60 mV (2 s) followed by repolarization steps to −120 to −50 mV (2 s). The current decay was best described by exponential functions with one or two time constants, respectively. There was no significant difference between the time constants under control conditions and in the presence of 1 μm droperidol (n = 8 oocytes investigated; ANOVA: statistically not significant; data not shown).
Time Dependence of Droperidol Inhibition.
The time dependence of HERG block was investigated with an “envelope of tails” protocol (fig. 4
). The pulse protocol as well as representative current traces are depicted in figure 4A
. After a depolarization to +40 mV for a duration (Δt) of 100–700 ms, tail currents were recorded at −40 mV. Fractional inhibition of the tail currents was calculated for each depolarization (fig. 4B
). The time-dependent increase of inhibition followed a monoexponential function with a time constant of 186 ± 36 ms.
Frequency Dependence of Droperidol Inhibition.
The frequency dependence of HERG current inhibition by droperidol was investigated after the drug was allowed to wash in for 10 min at −80 mV (fig. 4C
). HERG currents were activated by repetitive current pulses (depolarization to +20 mV of 300 ms duration, followed by a subsequent repolarization to −40 mV for 300 ms) at a basic cycle length of 1 s (n = 5), 2 s (n = 4), 4 s (n = 4), or 10 s (n = 4). After exposure to 1 μm droperidol, application of the pulse train at the different basic cycle lengths decreased tail current amplitude by 47 ± 5, 43 ± 10, 46 ± 12, or 44 ± 5% at a basic cycle length of 1, 2, 4, or 10 s, respectively. The time course of the inhibition was described by monoexponential functions with time constants of 1.2 ± 0.4, 1.9 ± 0.3, 4.3 ± 0.3, or 7.9 ± 1.3 s at a basic cycle length of 1, 2, 4, or 10 s, respectively. Although the development of block was faster at higher stimulation frequencies (P
< 0.001, ANOVA), the extent of steady state inhibition did not depend on the stimulation frequency.
Interaction Sites of Droperidol
The inhibitions of mutated HERG constructs (Y652A, F656A, T623A, S624A, and V625A) by droperidol were established to identify the molecular sites of interaction with HERG channels. The mutants S624A and Y652A show similar gating behavior as wild-type HERG channels. Inhibition by 1 μm droperidol was assessed using the three pulse protocols shown in figure 1A
. The mutants T623A, V625A, and F656A gave rise to only small currents in response to either the ramp protocol or the protocol eliciting tail currents at −40 mV. Therefore, these mutants were investigated by assessing the inhibition of tail currents at −120 mV. Representative current recordings of wild-type HERG and mutant channels under control conditions and in the presence of 1 μm droperidol are shown in figure 5A
. The residual tail currents at −120 mV are depicted in figure 5B
. Inhibition of all mutants by 1 μm droperidol was significantly smaller than inhibition of wild-type channels (see also table 3
Influence of Droperidol on APD of Guinea Pig Cardiac Myocytes
Figures 6A and B
show representative APs recorded from isolated guinea pig left ventricular myocytes under control condition and in the presence of droperidol after an incubation time of 3 min. APs were elicited at 0.2 Hz by short depolarizing currents under steady state conditions. Figure 6C
visualizes the influence of droperidol on APD90
, and table 4
summarizes AP details. Droperidol influenced neither the resting membrane potential nor the AP overshoot. At low concentrations (5–100 nm), droperidol increased APD in a concentration-dependent manner with a maximal prolongation of 17 ± 5% observed at a concentration of 100 nm. At a concentration of 300 nm, the AP prolongation was abolished, whereas even higher concentrations of up to 10 μm shortened APD compared with control.
In the current study, the molecular mechanisms underlying inhibition of HERG channels by droperidol were characterized. The role in drug channel interaction of several amino acid residues located in the S6 domain and within the channel pore were established. Furthermore, possible consequences of this interaction for the excitability of isolated ventricular cardiomyocytes were elucidated.
Droperidol blocked HERG currents in Xenopus
oocytes with an IC50
value between 0.6 and 0.9 μm. This value is well within the range of that reported for other high-affinity blockers such as dofetilide and E-4031 (0.4 and 0.6 μm, respectively).19
The difference between the value reported in the current study and the value reported by Drolet et al.12
(approximately 0.03 μm in HEK293 cells) is most likely caused by differences in the expression systems.30
Droperidol did not significantly influence KCNQ1/KCNE1 currents, which confirms that droperidol specifically interacts with IKr
but not with IKs
. Whereas droperidol potently inhibited the amplitude of HERG currents, it had only small effects on channel gating. Channel activation and steady state inactivation were slightly shifted toward negative potentials, whereas deactivation was not influenced. Current inhibition by droperidol significantly increased with the membrane potential and with increasing duration of current activation. Furthermore, the development of block depended on the stimulation frequency. These results indicate that the inhibition by droperidol may be state dependent, with a preference for open channels. Therefore, droperidol acts similarly to other high-affinity blockers of HERG channels.19,21
Several residues located in the S6 domain (Tyr652, Phe656) and within the channel pore (Thr623, Ser624, Val625) are important for the interaction of high-affinity blockers with HERG channels.16,17,19,32
In the current study, these amino acid residues were identified to also mediate inhibition of HERG channels by droperidol. However, these mutations are known to alter channel gating behavior.16,20
Whereas S624A slows and V625A abolishes channel inactivation, the other mutants accelerate inactivation. Moreover, all mutations shift the voltage dependence of activation and/or inactivation. Although it cannot be excluded that the reduced inhibition by droperidol is related to changes in channel gating, this seems less likely. The reduction in inhibition is similar for all mutations despite the changes in gating being qualitatively different. The role of inactivation in HERG channel block is controversial: Abolishing C-type inactivation by introducing the double mutant HERGG628C/S631C
reduces inhibition of HERG channel by blockers such as dofetilide33
However, other mutations affecting HERG inactivation yield inconsistent results regarding the role of inactivation for the inhibition by high-affinity blockers.35,36
Our results demonstrate that inhibition of HERG channels by droperidol is reduced to a similar extend by a mutation that accelerates inactivation (T623A) and by a mutation that abolishes inactivation (V625A). Reduced droperidol affinity of noninactivating HERG mutant channels may thus result from inactivation gating-associated reorientation of residues in the S6 domain that comprise the droperidol binding site rather than resulting from a direct effect of the inactivation. Taken together, our findings may, therefore, suggest that inactivation is neither a sufficient nor a necessary prerequisite for high-affinity block of HERG channels by droperidol.
Consistent with its potency to inhibit IKr
, droperidol prolonged the APD in guinea pig cardiomyocytes. At concentrations between 5 and 100 nm, droperidol increased APD in a concentration-dependent manner with a maximal increase of approximately 20% at 100 nm. Further increases of the droperidol concentration of 300 nm or greater, however, attenuated the AP prolongation and reversed the effect at even higher concentrations. This dual concentration-dependent effect on APD of ventricular cardiomyocytes may explain why some authors found AP shortening,8,9
whereas others found AP prolongation11,12
or no effect on APD.10
The potency of droperidol to prolong APD and to induce EADs is a matter of debate.8–12
Droperidol at antiemetic concentrations is estimated to reach free plasma concentrations of approximately 30 nm.37–39
At this concentration, IKr
would be inhibited by a maximum of 50%.12
Assuming that droperidol at these plasma concentrations exclusively inhibits HERG currents, computational modeling based on the Luo-Rudy dynamic model would predict APD prolongation and induction of EADs (fig. 7A
). However, EADs were not observed in our experiments with ventricular cardiomyocytes. Furthermore, EADs and severe ventricular arrhythmias have not been reported during the antiemetic application of droperidol.2,4
Our results may, therefore, suggest that despite being a high-affinity blocker of HERG channels, additional pharmacologic effects of droperidol may counterbalance these proarrhythmic effects.
It is well known that several HERG blockers exhibit additional effects on Ca2+
is involved in the development of EADs,44–48
blockade of this current has repeatedly been suggested to diminish the proarrhythmic effects induced by inhibition of HERG channels.42,49,50
The calcium channel antagonist verapamil also is a highly potent inhibitor of IKr
and specifically interacts with HERG channels.40
Despite its specific effects on HERG channels, verapamil abolishes EADs and does not induce torsades de pointes ventricular arrhythmia.41–43,45,51–54
Although direct effects of droperidol on ICaL
are unknown, indirect evidence suggests that droperidol interacts with ICaL
Droperidol has recently been reported to decrease the potassium chloride-induced increase of Ca2+
concentration in myocytes, indicative of an interaction with ICaL
Inhibition of ICaL
would explain the AP shortening by droperidol reported in the current study and previous studies.8,9
Therefore, we simulated 50% IKr
block with different degrees of ICaL
block. Computational modeling indicates that inhibition of ICaL
by 40% would prevent the occurrence of EADs (fig. 7B
). It may, therefore, be hypothesized that concomitant inhibition of IKr
prevents induction of EADs by droperidol in cardiomyocytes. Such a dual mechanism has been established for verapamil and also for the neuroleptic agent risperidone.43,50
Furthermore, this dual effect may offer an explanation why severe ventricular cardiac arrhythmia have not been reported after application of droperidol at antiemetic doses.2,4
In conclusion, this study provides evidence that droperidol is a high-affinity blocker of HERG channels causing only minor alterations of channel gating. The residues Thr623, Ser624, Val625, Tyr652, and Phe656 are important for the drug effect. Despite this molecular mode of interaction, droperidol does not induce EADs in ventricular cardiomyocytes. Computational modeling allows us to hypothesize that interaction with other depolarizing currents such as ICaL may explain why droperidol at antiemetic concentrations prolongs the APD without inducing EADs. This hypothesis warrants further investigation.
The authors thank Olaf Pongs, Ph.D. (Director of the Institute of Neural Signal Transduction, University Medical Center, Hamburg-Eppendorf, Germany), for his continuous support.
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†† US Food and Drug Administration strengthens warnings for droperidol. Available at: http://www.fda.gov/bbs/topics/ANSWERS/2001/ANS01123.html
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