Department of Neuroscience, The Scripps Research Institute, La Jolla, CA, USA; Department of Psychiatry, University of California, San Diego, La Jolla, CA, USA.
Department of Neuroscience, The Scripps Research Institute, La Jolla, CA, USA; Department of Psychiatry, University of California, San Diego, La Jolla, CA, USA.
Pharmacol Biochem Behav. 2020 Dec;199:173061. doi: 10.1016/j.pbb.2020.173061. Epub 2020 Oct 24.
Over the last two decades the United States has experienced a significant increase in the medical and non-medical use of opioid drugs, resulting in record numbers of opioid-related overdoses and deaths. There was an initial increase in non-medical use of prescription opioids around 2002, followed later by increased heroin use and then most recently fentanyl. Inhalation is a common route of administration for opioids, with a documented history spanning back to Mediterranean antiquity and up through modern use with e-cigarette devices. Unfortunately, preclinical studies using inhalation as the route of administration remain relatively few. This study was conducted to determine the efficacy of e-cigarette vapor inhalation of heroin in rats. Non-contingent exposure to heroin or methadone vapor produced anti-nociceptive efficacy in male and female rats. Female rats were trained to self-administer heroin vapor; the most-preferring half of the distribution obtained more vapor reinforcers when the concentration of heroin was reduced in the vapor vehicle and when pre-treated with the opioid receptor antagonist naloxone. The anti-nociceptive effect of heroin self-administered by vapor was identical in magnitude to that produced by intravenous self-administration. Finally, anxiety-like behavior increased 24-48 h after last heroin vapor access, consistent with withdrawal signs observed after intravenous self-administration. In sum, these studies show that rewarding and anti-nociceptive effects of heroin are produced in rats by vapor inhalation using e-cigarette technology. Importantly, self-administration models by this route can be deployed to determine health effects of inhaled heroin or other opioids.
在过去的二十年中,美国的阿片类药物(包括医疗用和非医疗用)的使用显著增加,由此导致阿片类药物相关的过量用药和死亡人数创下历史新高。大约从 2002 年开始,非医疗用处方类阿片类药物的使用最初有所增加,随后是海洛因使用量的增加,最近则是芬太尼。阿片类药物的常见给药途径是吸入,有记录表明,这种给药途径可追溯到地中海古代,一直延续到现代电子烟装置的使用。不幸的是,作为给药途径的吸入,其临床前研究仍然相对较少。本研究旨在确定电子烟吸入海洛因在大鼠体内的疗效。非条件暴露于海洛因或美沙酮蒸气可产生雄性和雌性大鼠的抗伤害作用。雌性大鼠被训练吸入海洛因蒸气;在蒸气载体中降低海洛因浓度和预先用阿片受体拮抗剂纳洛酮预处理时,获得的分布中更倾向于海洛因蒸气的一半会获得更多的蒸气强化物。通过蒸气自我给药的海洛因的镇痛作用与静脉内自我给药产生的镇痛作用大小相同。最后,在最后一次海洛因蒸气接触后 24-48 小时,焦虑样行为增加,与静脉内自我给药后观察到的戒断迹象一致。总之,这些研究表明,使用电子烟技术通过蒸气吸入,海洛因的奖赏和镇痛作用可在大鼠体内产生。重要的是,通过这种途径的自我给药模型可用于确定吸入海洛因或其他阿片类药物的健康影响。