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一种针对比芬太尼效力更强的苯并咪唑类新型精神活性物质的疫苗。

A Vaccine against Benzimidazole-Derived New Psychoactive Substances That Are More Potent Than Fentanyl.

作者信息

Lee Jinny Claire, Park Hyeri, Eubanks Lisa M, Ellis Beverly, Zhou Bin, Janda Kim D

机构信息

Departments of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute for Research and Medicine (WIRM), The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.

出版信息

J Med Chem. 2022 Feb 10;65(3):2522-2531. doi: 10.1021/acs.jmedchem.1c01967. Epub 2022 Jan 7.

Abstract

New psychoactive substance (NPS) opioids have proliferated within the international drug market. While synthetic opioids are traditionally composed of fentanyl analogues, benzimidazole-derived isotonitazene and its derivatives are the current NPS opioids of concern. Hence, in this study, we implement immunopharmacotherapy wherein antibodies are produced with high titers and nanomolar affinity to multiple benzimidazole-derived NPS opioids (BNO). Notably, these antibodies blunt psychoactive and physiological repercussions from BNO exposure, which was observed through antinociception, whole-body plethysmography, and blood-brain biodistribution studies. Moreover, we detail previously unreported pharmacokinetics of these drugs, which explains the struggle of traditional pharmaceutical opioid antagonists against BNO substances. These findings provide further insight into the effects of BNO drugs and the development of effective broad-spectrum therapeutics against NPS opioids.

摘要

新型精神活性物质(NPS)阿片类药物在国际毒品市场上迅速扩散。传统上,合成阿片类药物由芬太尼类似物组成,而苯并咪唑衍生的异噻嗪及其衍生物是当前令人担忧的NPS阿片类药物。因此,在本研究中,我们实施了免疫药物疗法,即产生对多种苯并咪唑衍生的NPS阿片类药物(BNO)具有高滴度和纳摩尔亲和力的抗体。值得注意的是,这些抗体减轻了BNO暴露引起的精神活性和生理反应,这在抗伤害感受、全身体积描记法和血脑生物分布研究中得到了观察。此外,我们详细介绍了这些药物以前未报道的药代动力学,这解释了传统药物阿片类拮抗剂对抗BNO物质的困难。这些发现为BNO药物的作用以及针对NPS阿片类药物的有效广谱治疗方法的开发提供了进一步的见解。

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