Amiodarone is a class III antiarrhythmic drug used for treating ventricular arrythmias. It is administered orally or intravenously. Amiodarone targets the cardiac myocytes where it blocks the inward rectifying potassium channels. This potassium is responsible for phase 3 of the action potential. During phase 3, K+ goes out of the cell to allow repolarization. In the presence of amiodarone, K+ accumulates in the cell since the potassium channels are blocked by amiodarone. This causes the repolarization phase, and thus, the action potential duration to be prolonged. The excitability of the cell is reduced and this leads to a slowing of the heart rate. The QRS duration is increased and the QT interval is also prolonged. These effects on the action potentials and the heart rate therefore mean that abnormal heart rhythms like tachyarrhythmias are less likely to occur. Amiodarone may have adverse effects such as thyrotoxicosis or hypothyroidism, tremor, uncontrollable and unusual movement of the body, dizziness, headache, nausea and vomiting, constipation, blurred vision, due to its effects on other targets such as beta-adrenergic receptors, sodium channels, and calcium channels.
References
Amiodarone Pathway (New) References
Wishart, D., Knox, C., Guo, A., Shrivastava, S., Hassanali, M., Stothard, P., . . . Woolsey, J. (2005, June). Amiodarone. Retrieved July 09, 2020, from https://www.drugbank.ca/drugs/DB01118
Florek JB, Girzadas D. Amiodarone. [Updated 2020 May 8]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK482154/
Ritter, James (2020). Rang and Dale’s Pharmacology (9th ed). Retrieved from: https://www-clinicalkey-com.login.ezproxy.library.ualberta.ca/#!/browse/book/3-s2.0-C2016004202X
Koenen, A., Kroemer, H., Grube, M., & Schwabedissen, H. (2011, November 15). Hepatic and Intestinal OATP-mediated Drug-Drug Interactions. Retrieved July 09, 2020, from https://www.medscape.com/viewarticle/752973_15
Dhein S. (2008) Antiarrhythmic Drugs. In: Offermanns S., Rosenthal W. (eds) Encyclopedia of Molecular Pharmacology. Springer, Berlin, Heidelberg
Highlighted elements will appear in red.
Highlight Compounds
Highlight Proteins
Enter relative concentration values (without units). Elements will be highlighted in a color gradient where red = lowest concentration and green = highest concentration. For the best results, view the pathway in Black and White.