The Potential Mechanisms behind Loperamide-Induced Cardiac Arrhythmias Associated with Human Abuse and Extreme Overdose

• Published in: Biomolecules (Basel, Switzerland) Vol. 13; no. 9; p. 1355
• Main Authors: Lu, Hua Rong, Damiano, Bruce P, Kreir, Mohamed, Rohrbacher, Jutta, van der Linde, Henk, Saidov, Tamerlan, Teisman, Ard, Gallacher, David J
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.09.2023; MDPI
• Subjects: Action potential; Arrhythmia; Automation; Cardiac arrhythmia; Cardiotoxicity; Complications and side effects; Conduction; conductions slowing; Development and progression; Diarrhea; Drug abuse; Drug dosages; Drug overdose; Drugs; free therapeutic plasma concentration (FTPC); Heart; HERG current; Investigations; Ions; Loperamide; loperamide overdose/abuse; Narcotics; Overdose; Prescription drugs; Risk factors; Safety; sodium current; Software; Toxicity; Ventricle; ventricular tachycardia (VT) torsade de pointes TdP; Belgium; St Louis Missouri; United States > US; Germany
• ISSN: 2218-273X; 2218-273X
• DOI: 10.3390/biom13091355

Loperamide has been a safe and effective treatment for diarrhea for many years. However, many cases of cardiotoxicity with intentional abuse of loperamide ingestion have recently been reported. We evaluated loperamide in in vitro and in vivo cardiac safety models to understand the mechanisms for this cardiotoxicity. Loperamide slowed conduction (QRS-duration) starting at 0.3 µM [~1200-fold (×) its human Free Therapeutic Plasma Concentration; FTPC] and reduced the QT-interval and caused cardiac arrhythmias starting at 3 µM (~12,000× FTPC) in an isolated rabbit ventricular-wedge model. Loperamide also slowed conduction and elicited Type II/III A-V block in anesthetized guinea pigs at overdose exposures of 879× and 3802× FTPC. In ion-channel studies, loperamide inhibited hERG (IKr), INa, and ICa currents with IC50 values of 0.390 µM, 0.526 µM, and 4.091 µM, respectively (i.e., >1560× FTPC). Additionally, in silico trials in human ventricular action potential models based on these IC50s confirmed that loperamide has large safety margins at therapeutic exposures (≤600× FTPC) and confirmed repolarization abnormalities in the case of extreme doses of loperamide. The studies confirmed the large safety margin for the therapeutic use of loperamide but revealed that at the extreme exposure levels observed in human overdose, loperamide can cause a combination of conduction slowing and alterations in repolarization time, resulting in cardiac proarrhythmia. Loperamide’s inhibition of the INa channel and hERG-mediated IKr are the most likely basis for this cardiac electrophysiological toxicity at overdose exposures. The cardiac toxic effects of loperamide at the overdoses could be aggravated by co-medication with other drug(s) causing ion channel inhibition.