首页> 美国卫生研究院文献>Cannabis and Cannabinoid Research >Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ9-THC at Human CB1 and CB2 Receptors
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Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ9-THC at Human CB1 and CB2 Receptors

机译:缺少随行人员:在大麻中常见的萜类化合物不能调节人CB1和CB2受体对Δ9-THC的功能活性

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摘要

>Introduction: Compounds present in Cannabis sativa such as phytocannabinoids and terpenoids may act in concert to elicit therapeutic effects. Cannabinoids such as Δ9-tetrahydrocannabinol (Δ9-THC) directly activate cannabinoid receptor 1 (CB1) and cannabinoid receptor 2 (CB2); however, it is not known if terpenoids present in Cannabis also affect cannabinoid receptor signaling. Therefore, we examined six common terpenoids alone, and in combination with cannabinoid receptor agonists, on CB1 and CB2 signaling in vitro.>Materials and Methods: Potassium channel activity in AtT20 FlpIn cells transfected with human CB1 or CB2 receptors was measured in real time using FLIPR® membrane potential dye in a FlexStation 3 plate reader. Terpenoids were tested individually and in combination for periods up to 30 min. Endogenous somatostatin receptors served as a control for direct effects of drugs on potassium channels.>Results: α-Pinene, β-pinene, β-caryophyllene, linalool, limonene, and β-myrcene (up to 30–100 μM) did not change membrane potential in AtT20 cells expressing CB1 or CB2, or affect the response to a maximally effective concentration of the synthetic cannabinoid CP55,940. The presence of individual or a combination of terpenoids did not affect the hyperpolarization produced by Δ9-THC (10 μM): (CB1: control, 59%±7%; with terpenoids (10 μM each) 55%±4%; CB2: Δ9-THC 16%±5%, with terpenoids (10 μM each) 17%±4%). To investigate possible effect on desensitization of CB1 responses, all six terpenoids were added together with Δ9-THC and signaling measured continuously over 30 min. Terpenoids did not affect desensitization, after 30 min the control hyperpolarization recovered by 63%±6% in the presence of the terpenoids recovery was 61%±5%.>Discussion: None of the six of the most common terpenoids in Cannabis directly activated CB1 or CB2, or modulated the signaling of the phytocannabinoid agonist Δ9-THC. These results suggest that if a phytocannabinoid–terpenoid entourage effect exists, it is not at the CB1 or CB2 receptor level. It remains possible that terpenoids activate CB1 and CB2 signaling pathways that do not involve potassium channels; however, it seems more likely that they may act at different molecular target(s) in the neuronal circuits important for the behavioral effect of Cannabis.
机译:>简介:存在于大麻中的化合物,例如植物大麻素和萜类化合物可能会协同发挥作用,以产生治疗效果。诸如Δ 9 -四氢大麻酚(Δ 9 -THC)之类的大麻素可直接激活大麻素受体1(CB1)和大麻素受体2(CB2)。但是,尚不知道大麻中存在的萜类化合物是否也会影响大麻素受体的信号传导。因此,我们在体外分别检测了六种常见的萜类化合物,并与大麻素受体激动剂结合使用,对CB1和CB2信号进行了研究。在FlexStation 3读板器中使用FLIPR ®膜电势染料实时测量。萜类化合物可以单独或组合测试长达30分钟。内源性生长抑素受体可以控制药物对钾通道的直接作用。>结果:α-P烯,β-pine烯,β-石竹烯,芳樟醇,mon烯和β-月桂烯(最多30- 100μM)不会改变表达CB1或CB2的AtT20细胞的膜电位,也不会影响对最大有效浓度的合成大麻素CP55,940的响应。单独或组合的萜类化合物的存在不影响Δ 9 -THC(10μm)产生的超极化:(CB1:对照,59%±7%;萜类化合物(各10μm)) 55%±4%; CB2:Δ 9 -THC 16%±5%,萜类化合物(每个10μm)17%±4%)。为了研究对CB1应答脱敏的可能影响,将全部六个萜类化合物与Δ 9 -THC一起添加,并在30分钟内连续测量信号传导。萜类化合物不影响脱敏,​​30分钟后,在存在萜类化合物的情况下,对照超极化的恢复率为63%±6%。>讨论:最常见的六种方法都不是大麻酚类化合物直接激活CB1或CB2,或调节植物大麻素激动剂Δ 9 -THC的信号传导。这些结果表明,如果存在植物大麻素-萜类化合物的伴生作用,则不是在CB1或CB2受体水平。萜类化合物仍可能激活不涉及钾通道的CB1和CB 2 信号通路。但是,它们似乎更有可能作用于对大麻的行为作用重要的神经元回路中的不同分子靶标。

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