Vandeputte Marthe M, Krotulski Alex J, Walther Donna, Glatfelter Grant C, Papsun Donna, Walton Sara E, Logan Barry K, Baumann Michael H, Stove Christophe P
Laboratory of Toxicology, Department of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium.
Center for Forensic Science Research and Education, Fredric Rieders Family Foundation, Willow Grove, PA, 19090, USA.
Arch Toxicol. 2022 Jun;96(6):1845-1863. doi: 10.1007/s00204-022-03276-4. Epub 2022 Apr 28.
Novel synthetic opioids continue to emerge on recreational drug markets worldwide. In response to legislative bans on fentanyl analogues, non-fentanyl structural templates, such as 2-benzylbenzimidazoles ('nitazenes'), are being exploited to create new μ-opioid receptor (MOR) agonists. Here, we pharmacologically characterize an emerging cyclic analogue of etonitazene, called N-pyrrolidino etonitazene (etonitazepyne), using in vitro and in vivo methods. A series of analytically confirmed fatalities is described to complement preclinical findings. Radioligand binding assays in rat brain tissue revealed that N-pyrrolidino etonitazene has high affinity for MOR (Ki = 4.09 nM) over δ-opioid (Ki = 959 nM) and κ-opioid (Ki = 980 nM) receptors. In a MOR-β-arrestin2 activation assay, N-pyrrolidino etonitazene displayed high potency (EC = 0.348 nM), similar to etonitazene (EC = 0.360 nM), and largely exceeding the potencies of fentanyl (EC = 14.9 nM) and morphine (EC = 290 nM). When administered s.c. to male Sprague Dawley rats, N-pyrrolidino etonitazene induced opioid-like antinociceptive, cataleptic, and thermic effects. Its potency in the hot plate test (ED = 0.0017 mg/kg) was tenfold and 2,000-fold greater than fentanyl (ED = 0.0209 mg/kg) and morphine (ED = 3.940 mg/kg), respectively. Twenty-one overdose fatalities associated with N-pyrrolidino etonitazene were found to contain low blood concentrations of the drug (median = 2.2 ng/mL), commonly in the context of polysubstance use. N-Pyrrolidino etonitazene was reported as a cause of death in at least two cases, demonstrating toxicity in humans. We demonstrate that N-pyrrolidino etonitazene is an extremely potent MOR agonist that is likely to present high risk to users. Continued vigilance is required to identify and characterize emergent 2-benzylbenzimidazoles, and other non-fentanyl opioids, as they appear in the marketplace.
新型合成阿片类药物在全球娱乐性毒品市场上不断涌现。为应对对芬太尼类似物的立法禁令,非芬太尼结构模板,如2-苄基苯并咪唑(“硝氮烯类”),正被用于制造新的μ-阿片受体(MOR)激动剂。在此,我们使用体外和体内方法对一种新出现的依托尼达唑环类似物N-吡咯烷基依托尼达唑(依托尼达唑炔)进行了药理学特征分析。描述了一系列经分析确认的死亡案例以补充临床前研究结果。大鼠脑组织中的放射性配体结合试验表明,N-吡咯烷基依托尼达唑对MOR具有高亲和力(Ki = 4.09 nM),而对δ-阿片受体(Ki = 959 nM)和κ-阿片受体(Ki = 980 nM)的亲和力较低。在MOR-β-抑制蛋白2激活试验中,N-吡咯烷基依托尼达唑显示出高效能(EC = 0.348 nM),与依托尼达唑(EC = 0.360 nM)相似,且大大超过芬太尼(EC = 14.9 nM)和吗啡(EC = 290 nM)的效能。当对雄性Sprague Dawley大鼠皮下给药时,N-吡咯烷基依托尼达唑可诱导阿片样镇痛、僵住和体温变化效应。其在热板试验中的效能(ED = 0.0017 mg/kg)分别比芬太尼(ED = 0.0209 mg/kg)和吗啡(ED = 3.940 mg/kg)高10倍和2000倍。发现21例与N-吡咯烷基依托尼达唑相关的过量用药死亡案例中,该药物的血药浓度较低(中位数 = 2.2 ng/mL),通常发生在多药合用的情况下。至少有两例报告称N-吡咯烷基依托尼达唑是死亡原因,证明其对人类具有毒性。我们证明N-吡咯烷基依托尼达唑是一种极其强效的MOR激动剂,可能对使用者构成高风险。随着市场上出现新的2-苄基苯并咪唑和其他非芬太尼类阿片类药物,需要持续保持警惕以识别和表征它们。