Nitazene opioids and the heart: Identification of a cardiac ion channel target for illicit nitazene opioids

The growing use of nitazene synthetic opioids heralds a new phase of the opioid crisis. However, limited information exists on the toxic effects of these drugs, aside from a propensity for respiratory depression. With restricted research availability of nitazenes, we used machine-learning-based tools to evaluate five nitazene compounds' interaction potential with the hERG potassium channel, a key drug antitarget in the heart. All nitazenes were predicted to inhibit hERG with low μM IC<sub>50</sub> values. These findings indicate a potential for proarrhythmic hERG block by nitazene opioids, warranting detailed cardiac safety evaluations of these drugs.

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Publication Details

Journal
Journal of Molecular and Cellular Cardiology Plus
Published
2024-10-22
DOI
https://doi.org/10.1016/j.jmccpl.2024.100118
Citations
3
Primary Topic
Cardiac electrophysiology and arrhythmias
Type
article
Field-Weighted Citation Impact
1.21

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article

Nitazene opioids and the heart: Identification of a cardiac ion channel target for illicit nitazene opioids

Graeme Henderson, Caroline S. Copeland, Stephen C. Harmer, Jules C. Hancox et al.
3 citations
Journal of Molecular and Cellular Cardiology Plus
Cardiac electrophysiology and arrhythmias
1.21
article

Nitazene opioids and the heart: Identification of a cardiac ion channel target for illicit nitazene opioids

Graeme Henderson, Caroline S. Copeland, Stephen C. Harmer, Jules C. Hancox, Henggui Zhang, Yibo Wang
article en
3 citations

Abstract

The growing use of nitazene synthetic opioids heralds a new phase of the opioid crisis. However, limited information exists on the toxic effects of these drugs, aside from a propensity for respiratory depression. With restricted research availability of nitazenes, we used machine-learning-based tools to evaluate five nitazene compounds' interaction potential with the hERG potassium channel, a key drug antitarget in the heart. All nitazenes were predicted to inhibit hERG with low μM IC<sub>50</sub> values. These findings indicate a potential for proarrhythmic hERG block by nitazene opioids, warranting detailed cardiac safety evaluations of these drugs.

Journal of Molecular and Cellular Cardiology PlusVol. 10
King's College London (GB), University of Manchester (GB), University of Bristol (GB), HM Prison and Probation Service (GB)
British Heart Foundation
Zero hunger
Openalex Percentile: Top 18%
Cardiac electrophysiology and arrhythmias
1.21
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Nitazene opioids and the heart: Identification of a cardiac ion channel target for illicit nitazene opioids — Graeme Henderson, Caroline S. Copeland, et al. · Journal of Molecular and Cellular Cardiology Plus (2024) | TGRS Research Map | TGRS