IndraLab

Statements


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"In contrast, haloperidol blocked HERG channels potently with an IC50 value of approximately 1 microM."

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"One of these agents, haloperidol, has already been shown to produce a high affinity blockade of HERG K + channels [22] but the effects of the two others still remain poorly investigated."

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"Haloperidol, pimozide, and fluspirilene inhibited HERG current with IC (50) of 1.36, 1.74, and 2.34 microM, and maximal block of 73%, 76% and 65%, respectively."

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"The mechanism of HERG blockade by haloperidol may also involve interaction with the channel in inactivated state [22]."

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"For comparison, haloperidol (30 nM) and olanzapine (300 nM) reduced hERG current amplitude by 44.2 +/-3.9% and 49.7 +/-4.2%, respectively."

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"However, with up to 5 muM testosterone and up to 12 hr of incubation, enough oocytes with acceptable membrane properties (input resistance of no less than 2 x 10 5 Omega at -80 mV) were available.Appl[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"This analysis shows that enhancements of endogenous HF oscillations in HR were also found in beagle dogs with dofetilide and with other hERG blockers such as cisapride, haloperidol, risperidone, DL sotalol, terfenadine and thioridazine."

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"The inactivation attenuated mutant S631A reduces hERG drug block by haloperidol."

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