IndraLab

Statements


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"Raising the extracellular potassium to 10 mmol/l, HERG block by azimilide, dofetilide, quinidine and sotalol was significantly decreased, while the block by amiodarone was unchanged."

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"Dofetilide block involves interactions with open and inactivated states of HERG channels."

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"Dofetilide, bepridil, and cisapride are high or intermediate-proarrhythmic-risk drug that prolongs the QT by blocking hERG."

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"Indeed, the pure hERG channel blocker, dofetilide, was shown to increase both QTc (heart rate-corrected QT) and J-T peak c (heart rate-corrected J-T peak ) intervals, while the strong L-type Ca 2+ and[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"Additional application of dofetilide (500 nmol/L) led to complete suppression of I KCNH2."

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"Chronic administration of the I -blocker dofetilide that prolongs repolarization in larger animals and human subjects by blocking HERG channels on the other hand, lengthen repolarization in mice—at least partly—by increasing I (via phosphoinositide 3-kinase pathway) (Yang et al., 2014)."

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"Another approach to (therapeutically) influence repolarization reserve was introduced in a dofetilide-induced LQT2 rabbit model, in which I Ks current densities were enhanced after immunization with a[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"Dofetilide corrected pentamidine induced hERG, but not K (IR) 2.1 trafficking defects."