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2C-B-Fly-NBOMe对雄性Wistar大鼠的急性药理学特征——药代动力学、对行为和体温调节的影响

Acute pharmacological profile of 2C-B-Fly-NBOMe in male Wistar rats-pharmacokinetics, effects on behaviour and thermoregulation.

作者信息

Syrová Kateřina, Šíchová Klára, Danda Hynek, Lhotková Eva, Jorratt Pascal, Pinterová-Leca Nikola, Vejmola Čestmír, Olejníková-Ladislavová Lucie, Hájková Kateřina, Kuchař Martin, Horáček Jiří, Páleníček Tomáš

机构信息

Psychedelics Research Centre, National Institute of Mental Health, Prague, Czechia.

Third Faculty of Medicine, Charles University, Prague, Czechia.

出版信息

Front Pharmacol. 2023 Mar 9;14:1120419. doi: 10.3389/fphar.2023.1120419. eCollection 2023.

Abstract

-2-methoxy-benzylated ("NBOMe") analogues of phenethylamine are a group of new psychoactive substances (NPS) with reported strong psychedelic effects in sub-milligram doses linked to a number of severe intoxications, including fatal ones. In our present work, we provide a detailed investigation of pharmacokinetics and acute behavioural effects of 2C-B-Fly-NBOMe (2-(8-bromo-2,3,6,7-tetrahydrobenzo [1,2-b:4,5-b']difuran-4-yl)-[(2-methoxybenzyl]ethan-1-amine), an analogue of popular psychedelic entactogen 2C-B (4-Bromo-2,5-dimethoxyphenethylamine). All experiments were conducted on adult male Wistar rats. Pharmacokinetic parameters of 2C-B-Fly-NBOMe (1 mg/kg subcutaneously; s. c.) in blood serum and brain tissue were analysed over 24 h using liquid chromatography-mass spectrometry (LC/MS). For examination of behavioural parameters in open field test (OFT) and prepulse inhibition (PPI) of acoustic startle reaction (ASR), 2C-B-Fly-NBOMe (0.2, 1 and 5 mg/kg s. c.) was administered in two temporal onsets: 15 and 60 min after administration. Thermoregulatory changes were evaluated in individually and group-housed animals over 8 h following the highest dose used in behavioural experiments (5 mg/kg s. c.). Peak drug concentrations were detected 30 and 60 min after the drug application in serum (28 ng/ml) and brain tissue (171 ng/g), respectively. The parental compound was still present in the brain 8 h after administration. Locomotor activity was dose-dependently reduced by the drug in both temporal testing onsets. ASR was also strongly disrupted in both temporal onsets, drug's effect on PPI was weaker. 2C-B-Fly-NBOMe did not cause any significant thermoregulatory changes. Our results suggest that 2C-B-Fly-NBOMe penetrates animal brain tissue in a relatively slow manner, induces significant inhibitory effects on motor performance, and attenuates sensorimotor gating. Its overall profile is similar to closely related analogue 2C-B and other NBOMe substances.

摘要

苯乙胺的 -2-甲氧基苄基化(“NBOMe”)类似物是一类新型精神活性物质(NPS),据报道,亚毫克剂量就能产生强烈的迷幻效果,与包括致命中毒在内的多种严重中毒事件有关。在我们目前的工作中,我们对2C-B-Fly-NBOMe(2-(8-溴-2,3,6,7-四氢苯并[1,2-b:4,5-b']二呋喃-4-基)-[(2-甲氧基苄基]乙胺)进行了详细的药代动力学和急性行为效应研究,它是流行的致幻性促智药2C-B(4-溴-2,5-二甲氧基苯乙胺)的类似物。所有实验均在成年雄性Wistar大鼠身上进行。使用液相色谱-质谱联用(LC/MS)分析了2C-B-Fly-NBOMe(1毫克/千克皮下注射;s.c.)在血清和脑组织中的药代动力学参数,持续时间为24小时。为了检测旷场试验(OFT)中的行为参数和听觉惊吓反应(ASR)的前脉冲抑制(PPI),2C-B-Fly-NBOMe(0.2、1和5毫克/千克s.c.)在两个时间点给药:给药后15分钟和60分钟。在行为实验中使用的最高剂量(5毫克/千克s.c.)给药后8小时内,对单独饲养和群居的动物进行体温调节变化评估。给药后30分钟和60分钟分别在血清(28纳克/毫升)和脑组织(171纳克/克)中检测到药物浓度峰值。给药8小时后,母体化合物仍存在于脑中。在两个时间测试点,药物均剂量依赖性地降低了运动活性。在两个时间点,ASR也受到强烈干扰,药物对PPI的影响较弱。2C-B-Fly-NBOMe没有引起任何显著的体温调节变化。我们的结果表明,2C-B-Fly-NBOMe以相对缓慢的方式穿透动物脑组织,对运动性能产生显著抑制作用,并减弱感觉运动门控。其总体特征与密切相关的类似物2C-B和其他NBOMe物质相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfdb/10033663/89cb35be99a7/fphar-14-1120419-g001.jpg

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