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4,4'-DMAR in-vivo acute cardiotoxicity: differences between (±)cis-4,4'-DMAR and its coadministration with the
Giorgia Corli1, Elisa Roda2, Beatrice Marchetti1
1Department of Translational Medicine, Section of Legal Medicine, LTTA Center and University Center of Gender Medicine, University of Ferrara, Ferrara, Italy.
Backgrounds/Aims:
Synthetic stimulants represent the largest group of new psychoactive substances and include the aminorex class, which possess anorectic properties and a pharmacological profile similar to that of amphetamine. Among these, 4,4'-dimethylaminorex (4,4'-DMAR) is one of the best-known synthetic stimulants with a chiral structure, which gives rise to two stereoisomers [(±)cis-4,4'-DMAR and (±)trans-4,4'-DMAR] with distinct pharmacological and toxicological characteristics. This substance has been detected in cases of intoxication and deaths among adults and adolescents. Although 4,4'-DMAR can also induce respiratory impairments, tachycardia, and sudden cardiac death/arrest, clinical and preclinical investigations of its cardiorespiratory toxicity remain limited. Thus, this study aimed to investigate the cardiorespiratory effects of (±)cis-4,4'-DMAR (1, 3, and 10 mg/kg) administration and the coadministration of 1 mg/kg (±)cis-4,4'-DMAR and 30 mg/kg (±)trans-4,4'-DMAR in awake CD-1 male mice.
Methods:
We evaluated heart rate, breathing rate, and cardiac (ECG) and respiratory (plethysmography) electrical parameters. The most severe effects were observed after administration of 10 mg/kg (±)cis-4,4'-DMAR and coadministration of 1 mg/kg (±)cis-4,4'-DMAR and 30 mg/kg (±)trans-4,4'-DMAR.
Results:
These treatments induced tachycardia and narrow-QRS arrhythmias, characterized by an increase in the corrected QT/QT interval, tachypnea, and a decrease in relaxation time, with varying degrees of intensity, probably due to differences in metabolism. Moreover, immunohistochemical analysis of the heart specimens revealed significant alterations in inflammation/oxidative stress markers in cardiomyocytes and blood vessel walls, accompanied by cytoarchitectural changes.
Conclusions:
These findings provide the first evidence of the severe toxicity of 4,4'-DMAR to the cardiac and respiratory systems, highlighting the importance of dosage and stereoisomer coadministration. This serves as a warning of the complex nature and potential dangers of intoxication.
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