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本文引用的文献

1
'Spice' and other herbal blends: harmless incense or cannabinoid designer drugs?“香料”及其他草药混合物:无害香薰还是大麻素类合成毒品?
J Mass Spectrom. 2009 May;44(5):832-7. doi: 10.1002/jms.1558.
2
Endocannabinoid-mediated control of synaptic transmission.内源性大麻素介导的突触传递调控
Physiol Rev. 2009 Jan;89(1):309-80. doi: 10.1152/physrev.00019.2008.
3
Modulation of excitatory synaptic transmission by Delta 9-tetrahydrocannabinol switches from agonist to antagonist depending on firing rate.δ9-四氢大麻酚对兴奋性突触传递的调节作用会根据放电频率从激动剂转变为拮抗剂。
Mol Pharmacol. 2009 Apr;75(4):892-900. doi: 10.1124/mol.108.051482. Epub 2008 Dec 31.
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.
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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.
6
Genetic dissection of behavioural and autonomic effects of Delta(9)-tetrahydrocannabinol in mice.小鼠中Δ⁹-四氢大麻酚行为和自主神经效应的遗传学剖析
PLoS Biol. 2007 Oct;5(10):e269. doi: 10.1371/journal.pbio.0050269.
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Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940.CP - 47,497和CP - 55,940的1 - 脱氧类似物的合成与药理学
Bioorg Med Chem. 2008 Jan 1;16(1):322-35. doi: 10.1016/j.bmc.2007.09.033. Epub 2007 Sep 22.
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The diverse CB1 and CB2 receptor pharmacology of three plant cannabinoids: delta9-tetrahydrocannabinol, cannabidiol and delta9-tetrahydrocannabivarin.三种植物大麻素:Δ⁹-四氢大麻酚、大麻二酚和Δ⁹-四氢大麻萜酚的不同CB1和CB2受体药理学特性
Br J Pharmacol. 2008 Jan;153(2):199-215. doi: 10.1038/sj.bjp.0707442. Epub 2007 Sep 10.
9
On the pharmacological properties of Delta9-tetrahydrocannabinol (THC).关于Δ9-四氢大麻酚(THC)的药理特性
Chem Biodivers. 2007 Aug;4(8):1664-77. doi: 10.1002/cbdv.200790146.
10
Phytocannabinoids in Cannabis sativa: recent studies on biosynthetic enzymes.大麻中的植物大麻素:生物合成酶的最新研究
Chem Biodivers. 2007 Aug;4(8):1649-63. doi: 10.1002/cbdv.200790145.

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.

DOI:10.1111/j.1476-5381.2009.00582.x
PMID:20100276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2931559/
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。