首页> 美国卫生研究院文献>Cannabis and Cannabinoid Research >Cannabidiols Upregulation of N-acyl Ethanolamines in the Central Nervous System Requires N-acyl Phosphatidyl Ethanolamine-Specific Phospholipase D
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Cannabidiols Upregulation of N-acyl Ethanolamines in the Central Nervous System Requires N-acyl Phosphatidyl Ethanolamine-Specific Phospholipase D

机译:Cannabidiol在中枢神经系统中对N-酰基乙醇胺的上调需要N-酰基磷脂酰乙醇胺特定的磷脂酶D

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摘要

>Introduction: Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD) are bioactive cannabinoids. We recently showed that acute THC administration drives region-dependent changes in the mouse brain lipidome. This study tested the hypothesis that cell lines representing cell types present in the central nervous system (CNS), neurons (N18 cells), astrocytes (C6 glioma cells), and microglia (BV2 cells) would respond differently to THC, CBD, or their combination. This experimental strategy also allowed us to test the hypothesis that THC and CBD are metabolized differently if presented in combination and to test the hypothesis that responses to CBD are not like the fatty acid amide hydrolase (FAAH) inhibitor URB597. Finally, we tested the hypothesis that CBD's CNS effects would differ in the N-acyl phosphatidyl ethanolamine-specific phospholipase D (NAPE-PLD) knockout (KO) compared to wild-type (WT) mice.>Methods: N18, C6, and BV2 cells were stimulated with 1 μM THC, 1 μM CBD, 1 μM THC:CBD, 1 μM URB597, or vehicle for 2 h and lipids extracted. Adult female WT and NAPE-PLD KO mice were injected with 3 mg/kg CBD or vehicle i.p., brains collected 2 h later, eight brain regions dissected, and lipids extracted. Extracted lipids were characterized and quantified using high-pressure liquid chromatography coupled with tandem mass spectrometry (HPLC/MS/MS).>Results: Lipid levels in each cell type were differentially affected by THC, CBD, or THC:CBD with a few exceptions. In all cell lines, THC increased levels of arachidonic acid and CBD increased levels of N-acyl ethanolamines (NAEs), including N-arachidonoyl ethanolamine. More THC remained when cells were coincubated with CBD; however, levels of THC metabolites were cell-type dependent. CBD and URB597 caused very different lipid profiles in the cell-based assays with the primary similarity being increases in NAEs. CBD increased levels of NAEs in the WT hippocampus, cerebellum, thalamus, cortex, midbrain, and brainstem; however, NAEs did not increase in any brain region after CBD in NAPE-PLD KO mice.>Conclusions: CBD and THC differentially modify the lipidome of the brain and CNS-type cell lines. Increases in NAEs observed after CBD treatment had previously been attributed to FAAH inhibition; however, data here suggest the alternative hypothesis that CBD is activating NAPE-PLD to increase NAE levels.
机译:>简介:Δ 9 -四氢大麻酚(THC)和大麻二酚(CBD)是具有生物活性的大麻素。我们最近显示,急性四氢大麻酚的管理驱动小鼠脑脂质组中的区域依赖性变化。这项研究检验了以下假设:代表中枢神经系统(CNS),神经元(N18细胞),星形胶质细胞(C6胶质瘤细胞)和小胶质细胞(BV2细胞)中存在的细胞类型的细胞系对THC,CBD或其反应的反应不同组合。这种实验策略还使我们能够检验THC和CBD组合使用时代谢不同的假设,并能够检验对CBD的反应不像脂肪酸酰胺水解酶(FAAH)抑制剂URB597的假设。最后,我们检验了以下假设:与野生型(WT)小鼠相比,CBD的CNS效应在N-酰基磷脂酰乙醇胺特异性磷脂酶D(NAPE-PLD)基因敲除(KO)中会有所不同。>方法:用1μMTHC,1μMCBD,1μMTHC:CBD,1μMURB597或溶媒刺激N18,C6和BV2细胞2μh,并提取脂质。给成年雌性WT和NAPE-PLD KO小鼠注射3μg/ kg的CBD或媒介物腹腔注射,2h后收集大脑,解剖八个大脑区域,提取脂质。使用高压液相色谱结合串联质谱(HPLC / MS / MS)对提取的脂质进行表征和定量。>结果:每种细胞类型的脂质水平受THC,CBD或THC的差异影响:CBD,但有一些例外。在所有细胞系中,THC增加了花生四烯酸的水平,而CBD增加了N-酰基乙醇胺(NAE)(包括N-花生四烯酸乙醇胺)的水平。当细胞与CBD共孵育时,仍有更多的四氢大麻酚;但是,THC代谢物的水平取决于细胞类型。 CBD和URB597在基于细胞的测定中引起了非常不同的脂质谱,主要相似之处在于NAE的增加。 CBD增加了野生海马,小脑,丘脑,皮层,中脑和脑干中NAE的水平;然而,NAPE-PLD KO小鼠在CBD后大脑任何区域的NAE都没有增加。>结论: CBD和THC差异性地修饰了大脑脂质体和CNS型细胞系。 CBD治疗后观察到的NAE升高以前归因于FAAH抑制。但是,这里的数据提出了另一种假设,即CBD正在激活NAPE-PLD以增加NAE水平。

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