Evidence for enduring cardiac and multiorgan toxicity after repeated exposure to the synthetic cannabinoid JWH-018 in male rats

被引:0
|
作者
Pintori, Nicholas [1 ]
Serra, Maria Pina [1 ]
Carai, Antonio [2 ]
Lobina, Carla [3 ]
Isola, Raffaella [1 ]
Noli, Roberta [1 ]
Piras, Gessica [1 ]
Spano, Enrica [1 ]
Baumann, Michael H. [4 ]
Quartu, Marina [1 ]
De Luca, Maria Antonietta [1 ]
机构
[1] Univ Cagliari, Dept Biomed Sci, Cittadella Univ Monserrato, I-09042 Monserrato, Cagliari, Italy
[2] Univ Cagliari, Dept Med Sci & Publ Hlth, Cittadella Univ Monserrato, I-09042 Monserrato, Cagliari, Italy
[3] Cittadella Univ Monserrato, Neurosci Inst, Natl Res Council Italy, Sect Cagliari, I-09042 Monserrato, Cagliari, Italy
[4] Natl Inst Drug Abuse NIDA, Designer Drug Res Unit, Intramural Res Program, Natl Inst Hlth NIH, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
In silico and in vivo JWH-018 toxicity; Heart mitochondria bioenergetics; Heart histopathology; Kidney; Liver; Lung; MITOCHONDRIAL-FUNCTION; BLOOD-PRESSURE; DRUG; HEART; SUPPLEMENTATION; CARDIOTOXICITY; ABNORMALITIES; SENSORIMOTOR; DYSFUNCTION; WITHDRAWAL;
D O I
10.1016/j.tox.2024.153878
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The use of synthetic cannabinoid receptor agonists (SCRAs) represents a public health concern. Besides abuse liability and cognitive impairments, SCRAs consumption is associated with serious medical consequences in humans, including cardiotoxicity. The precise mechanisms underlying cardiac or other toxicities induced by SCRAs are not well understood. Here, we used in silico, in vivo, and ex vivo approaches to investigate the toxicological consequences induced by exposure to the SCRA JWH-018. Along with in silico predictive toxicological screening of 36 SCRAs by MC4PC software, adult male Sprague-Dawley rats were repeatedly exposed to JWH018 (0.25 mg/kg ip) for 14 consecutive days, with body temperature and cardiovascular parameters measured over the course of treatment. At 1 and 7 days after JWH-018 discontinuation, multiorgan tissue pathologies and heart mitochondria bioenergetics were assessed. The in silico findings predicted risk of cardiac adverse effects specifically for JWH-018 and other aminoalkylindole SCRAs (i.e., electrocardiogram abnormality and QT prolongation). The results from rats revealed that repeated, but not single, JWH-018 exposure induced hypothermia and cardiovascular stimulation (e.g., increased blood pressure and heart rate) which persisted throughout treatment. Post-mortem findings demonstrated cardiac lesions (i.e., vacuolization, waving, edema) 1 day after JWH-018 discontinuation, which may contribute to lung, kidney, and liver tissue degeneration observed 7 days later. Importantly, repeated JWH-018 exposure induced mitochondrial dysfunction in cardiomyocytes, i.e., defective lipid OXPHOS, which may represent one mechanism of JWH-018-induced toxicity. Our results demonstrate that repeated administration of even a relatively low dose of JWH-018 is sufficient to affect cardiovascular function and induce enduring toxicological consequences, pointing to risks associated with SCRA consumption.
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页数:16
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