Suppr超能文献

JWH018 是“香料”草药混合物的常见成分,是一种有效且强效的大麻素 CB 受体激动剂。

JWH018, a common constituent of 'Spice' herbal blends, is a potent and efficacious cannabinoid CB receptor agonist.

机构信息

The Gill Center and the Department of Psychological & Brain Sciences, Indiana University, Bloomington, IN 47405, USA.

出版信息

Br J Pharmacol. 2010 Jun;160(3):585-93. doi: 10.1111/j.1476-5381.2009.00582.x. Epub 2010 Jan 22.

Abstract

BACKGROUND AND PURPOSE

'Spice' is an herbal blend primarily marketed in Europe as a mild hallucinogen with prominent cannabis-like effects and as a legal alternative to cannabis. However, a recent report identified a number of synthetic additives in samples of 'Spice'. One of these, the indole derivative JWH018, is a ligand for the cannabinoid receptor 1 (CB(1)) cannabinoid receptor and inhibits cAMP production in CB(1) receptor-expressing CHO cells. Other effects of JWH018 on CB(1) receptor-mediated signalling are not known, particularly in neurons. Here we have evaluated the signalling pathways activated by JWH018 at CB(1) receptors.

EXPERIMENTAL APPROACH

We investigated the effects of JWH018 on neurotransmission in cultured autaptic hippocampal neurons. We further analysed its activation of ERK1/2 mitogen activated protein kinase (MAPK) and internalization of CB(1) receptors in HEK293 cells stably expressing this receptor.

KEY RESULTS

In cultured autaptic hippocampal neurons, JWH018 potently inhibited excitatory postsynaptic currents (IC(50)= 14.9 nM) in a concentration- and CB(1) receptor-dependent manner. Furthermore, it increased ERK1/2 MAPK phosphorylation (EC(50)= 4.4 nM). We also found that JWH018 potently induced rapid and robust CB(1) receptor internalization (EC(50)= 2.8 nM; t(1/2)= 17.3 min).

CONCLUSIONS AND IMPLICATIONS

JWH018, a prominent component of several herbal preparations marketed for their psychoactivity, is a potent and effective CB(1) receptor agonist that activates multiple CB(1) receptor signalling pathways. Thus, it is likely that the subjective effects of 'Spice' are due to activation of cannabinoid CB(1) receptors by JWH018, added to this herbal preparation.

摘要

背景与目的

“香料”是一种草药混合物,主要在欧洲作为一种轻度致幻剂销售,具有显著的大麻样作用,并作为大麻的合法替代品。然而,最近的一份报告在“香料”样本中发现了一些合成添加剂。其中之一,吲哚衍生物 JWH018,是大麻素受体 1(CB1)大麻素受体的配体,抑制 CB1 受体表达 CHO 细胞中的 cAMP 产生。JWH018 对 CB1 受体介导的信号转导的其他作用尚不清楚,特别是在神经元中。在这里,我们评估了 JWH018 在 CB1 受体上激活的信号通路。

实验方法

我们研究了 JWH018 对培养的自突触海马神经元中神经传递的影响。我们进一步分析了它在稳定表达该受体的 HEK293 细胞中激活 ERK1/2 丝裂原激活蛋白激酶(MAPK)和 CB1 受体内化的作用。

主要结果

在培养的自突触海马神经元中,JWH018 以浓度和 CB1 受体依赖的方式强烈抑制兴奋性突触后电流(IC50=14.9 nM)。此外,它增加了 ERK1/2 MAPK 磷酸化(EC50=4.4 nM)。我们还发现,JWH018 强烈诱导快速和强大的 CB1 受体内化(EC50=2.8 nM;t1/2=17.3 分钟)。

结论和意义

JWH018 是几种以其精神活性销售的草药制剂的主要成分,是一种有效的 CB1 受体激动剂,可激活多种 CB1 受体信号通路。因此,“香料”的主观作用很可能是由于 JWH018 激活了大麻素 CB1 受体,添加到这种草药制剂中。

相似文献

引用本文的文献

5
The State of Synthetic Cannabinoid Medications for the Treatment of Pain.用于治疗疼痛的合成大麻素药物现状
CNS Drugs. 2024 Aug;38(8):597-612. doi: 10.1007/s40263-024-01098-9. Epub 2024 Jul 1.

本文引用的文献

2
4
Guide to Receptors and Channels (GRAC), 3rd edition.《受体与通道指南》(GRAC),第三版。
Br J Pharmacol. 2008 Mar;153 Suppl 2(Suppl 2):S1-209. doi: 10.1038/sj.bjp.0707746.
5
G protein-coupled receptor sorting to endosomes and lysosomes.G蛋白偶联受体向内体和溶酶体的分选
Annu Rev Pharmacol Toxicol. 2008;48:601-29. doi: 10.1146/annurev.pharmtox.48.113006.094646.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验