Designer Drug Research Unit, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA.
Department of Neurology and Molecular Pharmacology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Neuropharmacology. 2018 May 15;134(Pt A):101-107. doi: 10.1016/j.neuropharm.2017.08.016. Epub 2017 Aug 12.
Novel synthetic opioids (NSO) are increasingly encountered in illicit heroin and counterfeit pain pills. Many NSO are resurrected from older biomedical literature or patent applications, so limited information is available about their biological effects. Here we examined the pharmacology of three structurally-distinct NSO found in the recreational drug market: N-(1-(2-phenylethyl)-4-piperidinyl)-N-phenylbutyramide (butyrylfentanyl), 3,4-dichloro-N-[(1R,2R)-2-(dimethylamino)cyclohexyl]-N-methylbenzamide (U-47700) and 1-cyclohexyl-4-(1,2-diphenylethyl)piperazine (MT-45). Radioligand binding and GTPγS functional assays were carried out in cells transfected with murine mu- (MOR-1), delta- (DOR-1) or kappa-opioid receptors (KOR-1). Antinociceptive effects were determined using the radiant heat tail flick technique in mice, and opioid specificity was assessed with the mu-opioid antagonist naloxone. Butyrylfentanyl, U-47700 and MT-45 displayed nM affinities at MOR-1, but were less potent than morphine, and had much weaker effects at DOR-1 and KOR-1. All NSO exhibited agonist actions at MOR-1 in the GTPγS assay. Butyrylfentanyl and U-47700 were 31- and 12-fold more potent than morphine in the tail flick assay, whereas MT-45 was equipotent with morphine. Analgesic effects were reversed by naloxone and absent in genetically-engineered mice lacking MOR-1. Our findings confirm that butyrylfentanyl, U-47700 and MT-45 are selective MOR-1 agonists with in vitro affinities less than morphine. However, analgesic potencies vary more than 30-fold across the compounds, and in vitro binding affinity does not predict in vivo potency. Taken together, our findings highlight the risks to humans who may unknowingly be exposed to these and other NSO when taking adulterated heroin or counterfeit pain medications. This article is part of the Special Issue entitled 'Designer Drugs and Legal Highs.'
新型合成阿片类药物(NSO)在非法海洛因和假冒止痛药中越来越常见。许多 NSO 是从旧的生物医学文献或专利申请中复活的,因此关于它们的生物学效应的信息有限。在这里,我们研究了在娱乐性药物市场中发现的三种结构不同的 NSO 的药理学:N-(1-(2-苯乙基)-4-哌啶基)-N-苯基丁酰胺(丁酰芬太尼),3,4-二氯-N-[(1R,2R)-2-(二甲氨基)环己基]-N-甲基苯甲酰胺(U-47700)和 1-环己基-4-(1,2-二苯乙基)哌嗪(MT-45)。放射性配体结合和 GTPγS 功能测定在转染了小鼠 μ-(MOR-1)、δ-(DOR-1)或 κ-阿片受体(KOR-1)的细胞中进行。使用放射性热尾闪烁技术在小鼠中确定镇痛作用,并用 μ-阿片受体拮抗剂纳洛酮评估阿片类特异性。丁酰芬太尼、U-47700 和 MT-45 在 MOR-1 上显示出纳摩尔亲和力,但效力低于吗啡,在 DOR-1 和 KOR-1 上的作用较弱。所有 NSO 在 GTPγS 测定中均表现出 MOR-1 的激动作用。在尾巴闪烁试验中,丁酰芬太尼和 U-47700 比吗啡分别强 31 倍和 12 倍,而 MT-45 与吗啡等效。镇痛作用被纳洛酮逆转,在缺乏 MOR-1 的基因工程小鼠中不存在。我们的研究结果证实,丁酰芬太尼、U-47700 和 MT-45 是选择性 MOR-1 激动剂,其体外亲和力小于吗啡。然而,镇痛效力差异超过 30 倍,体外结合亲和力不能预测体内效力。总之,我们的研究结果强调了人类在服用掺假海洛因或假冒止痛药时可能会无意中接触到这些和其他 NSO 的风险。本文是特刊“设计药物和合法兴奋剂”的一部分。