Department of Forensic Medicine, Aarhus University Hospital, Aarhus, Denmark.
Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Addict Biol. 2022 Sep;27(5):e13214. doi: 10.1111/adb.13214.
Fatal opioid poisonings often involve methadone or morphine. This study aimed to elucidate if quetiapine, a widely used sedative antipsychotic medication, may increase the risk of fatal opioid poisoning by additive inhibitory effects on the central nervous system. We used data from 323 cases of fatal methadone or/and morphine poisonings autopsied from 2013 to 2020, a survey of 34 drug users, and performed blinded placebo-controlled studies in 75 Flinders Resistant Line rats receiving three cumulative intraperitoneal doses of vehicle, methadone (2.5, 10 and 15 mg/kg), morphine (3.75, 15 and 22.5 mg/kg), quetiapine (3, 10 and 30 mg/kg) or quetiapine combined with methadone or morphine. Quetiapine was detected in 20.4% of fatal opioid poisonings with a significantly increased frequency over time, primarily in low or therapeutic concentrations, and was not associated with methadone or morphine concentrations. Use of quetiapine, most commonly in low-to-moderate doses to obtain a sleep-inducing or tranquillizing effect, was reported by 67.6% of survey respondents. In the animal studies, a significant impairment of sedation score, performance on the rotarod and open field mobility was observed in all treatment groups compared with vehicle. However, the effect of quetiapine plus the opioid was not significantly different from that of the opioid alone. Thus, no additive sedative effects were observed in rats. Our results suggest that quetiapine is more often an innocent bystander than a contributor to fatal opioid poisoning. However, the combined effects on other parameters, including blood pressure, cardiac rhythm and respiratory rate, need investigation.
致命的阿片类药物中毒通常涉及美沙酮或吗啡。本研究旨在阐明广泛使用的镇静抗精神病药物喹硫平是否通过对中枢神经系统的附加抑制作用增加致命阿片类药物中毒的风险。我们使用了 2013 年至 2020 年 323 例致命美沙酮和/或吗啡中毒尸检病例的数据,对 34 名吸毒者进行了调查,并在 75 只 Flinders 抗性线大鼠中进行了盲法安慰剂对照研究,这些大鼠接受了三种累积剂量的腹腔内给药,分别为载体、美沙酮(2.5、10 和 15mg/kg)、吗啡(3.75、15 和 22.5mg/kg)、喹硫平(3、10 和 30mg/kg)或喹硫平与美沙酮或吗啡联合使用。喹硫平在 20.4%的致命阿片类药物中毒中被检测到,随着时间的推移,其频率显著增加,主要出现在低浓度或治疗浓度,与美沙酮或吗啡浓度无关。调查对象报告,最常见的是低至中等剂量使用喹硫平以获得诱导睡眠或镇静作用,67.6%的调查对象报告了这种情况。在动物研究中,与载体相比,所有治疗组的镇静评分、旋转棒和开放场移动能力均显著受损。然而,喹硫平加阿片类药物的作用与阿片类药物单独使用的作用没有显著差异。因此,在大鼠中没有观察到附加的镇静作用。我们的结果表明,喹硫平更像是一个无辜的旁观者,而不是致命阿片类药物中毒的原因。然而,需要调查其对其他参数的联合作用,包括血压、心律和呼吸频率。