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.
Authors
- Graeme Henderson (ORCID: https://orcid.org/0000-0001-6050-0048)
- Caroline S. Copeland (ORCID: https://orcid.org/0000-0002-4462-1402)
- Stephen C. Harmer (ORCID: https://orcid.org/0000-0003-3909-6698)
- Jules C. Hancox (ORCID: https://orcid.org/0000-0002-2055-6482)
- Henggui Zhang (ORCID: https://orcid.org/0000-0002-0863-5807)
- Yibo Wang (ORCID: https://orcid.org/0009-0001-3921-4415)
Institutions
- King's College London (GB)
- University of Manchester (GB)
- University of Bristol (GB)
- HM Prison and Probation Service (GB)
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
Funders
- British Heart Foundation