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  2. Potassium channel blocker - Wikipedia

    en.wikipedia.org/wiki/Potassium_channel_blocker

    Potassium channel blockers exhibit reverse use-dependent prolongation of the action potential duration. Reverse use dependence is the effect where the efficacy of the drug is reduced after repeated use of the tissue. [11] This contrasts with (ordinary) use dependence, where the efficacy of the drug is increased after repeated use of the tissue.

  3. Drug-induced QT prolongation - Wikipedia

    en.wikipedia.org/wiki/Drug-induced_QT_prolongation

    Class III antiarrhythmic drugs are potassium channel blockers that cause QT prolongation and are associated with TdP. Amiodarone. Amiodarone works in many ways. It blocks sodium, potassium, and calcium channels, as well as alpha and beta adrenergic receptors. Because of its multiple actions, amiodarone causes QT prolongation but TdP is rarely ...

  4. Channel blocker - Wikipedia

    en.wikipedia.org/wiki/Channel_blocker

    Example of voltage-dependent potassium ion channel in relation to changing ion concentrations . To comprehend the mechanism of channel blockers, it is critical to understand the composition of ion channels. Their main function is to contribute to the resting membrane potential of a cell via the flow of ions through a cell membrane.

  5. 4-Aminopyridine - Wikipedia

    en.wikipedia.org/wiki/4-Aminopyridine

    However, the effect of the drug is strongly established for walking capacity only. [26] Common side effects include dizziness, nervousness and nausea, and the incidence of adverse effects was shown to be less than 5% in all studies. [27] [5] 4-AP works as a potassium channel blocker.

  6. Amiloride - Wikipedia

    en.wikipedia.org/wiki/Amiloride

    Because Liddle phenotype usually involves an upregulation of ENaC channels, leading to retention of sodium and water and to hypokalemia, amiloride is useful as an ENaC channel inhibitor due to its promotion of sodium excretion and its potassium-sparing effects, restoring potassium to normal levels. [13]

  7. Quinidine - Wikipedia

    en.wikipedia.org/wiki/Quinidine

    [13] [14] Inhibition of the Na v 1.5 channel is specifically involved in its antiarrhythmic effects as a class I antiarrhythmic agent. [15] Quinidine also blocks certain voltage-gated potassium channels (e.g., K v 1.4 , K v 4.2 , hERG , among others), [ 16 ] [ 17 ] acts as an antimuscarinic and alpha-1 blocker , [ 18 ] and is an antimalarial ...

  8. Cardiovascular agents - Wikipedia

    en.wikipedia.org/wiki/Cardiovascular_agents

    Beta-blockers with intrinsic sympathomimetic activity: acebutolol, pindolol; Some common side effects include increased airway resistance for non-selective beta-blockers, exacerbation of peripheral vascular diseases, and hypotension [15] Beta-blockers are contraindicated in patients with second- or third-degree atrioventricular block.

  9. Potassium-sparing diuretic - Wikipedia

    en.wikipedia.org/wiki/Potassium-sparing_diuretic

    Epithelial sodium channel blockers: [6] Amiloride – better tolerated than triamterene; Triamterene – increased renal side-effects; Aldosterone antagonists, also known as mineralocorticoid receptor antagonists: [7] Spironolactone – most widespread use, inexpensive