Concentration-dependent effect of delta-9-tetrahydrocannabinol on epigenetic DNA modifiers in human peripheral blood mononuclear cells.

IF 5.8 1区 医学 Q1 PSYCHIATRY
Kerda Pulk, Kelli Somelar-Duracz, Mikk Rooden, Kaili Anier, Anti Kalda
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Abstract

Cannabis is among the most used illicit substances in the world, and approximately 10% of regular cannabis users are estimated to be susceptible to developing cannabis use disorder (CUD). We examined the effect of different concentrations of delta-9-tetrahydrocannabinol (THC) on the epigenetic DNA modifiers DNA methyltransferases (DNMTs) and ten-eleven translocation enzymes (TETs); cannabinoid CB1 and CB2 receptors; and the cytokines IL-1β, IL-6, IL-10, and TNF-α. We used two in vitro study designs on human peripheral blood mononuclear cells (PBMCs) collected from healthy donors: (a) repeated THC incubations and (b) repeated THC incubations followed by an "abstinence" period and a THC challenge incubation. We observed no significant effects on DNMTs and TETs mRNA levels, enzymatic activity, or CB1 and CB2 mRNA levels at an average THC concentration (50 ng/ml, n = 8 donors). However, repeated incubations at a high THC concentration (200 ng/ml, n = 16 donors) significantly downregulated DNMTs and upregulated TETs, CB1, and CB2 mRNA levels. Both THC concentrations upregulated the gene expression of IL-1β, IL-6, and IL-10, but had no effect on TNF-α gene expression. At the genome-wide level, repeated THC incubations resulted in a significant number of differentially hydroxymethylated genes being hyperhydroxymethylated. An additional THC challenge shifted the hyperhydroxymethylated state to hypohydroxymethylation. The genes with the strongest associations with THC exposure were found to be functionally significant for various signaling pathways. These findings suggest that repeated incubations with high concentrations of THC may affect the expression of genes critical for the development of CUD through aberrant demethylation.

δ -9-四氢大麻酚对人外周血单核细胞表观遗传DNA修饰因子的浓度依赖性影响。
大麻是世界上使用最多的非法物质之一,据估计,大约10%的经常使用大麻的人容易患上大麻使用障碍。研究了不同浓度的δ -9-四氢大麻酚(THC)对表观遗传DNA修饰因子DNA甲基转移酶(dnmt)和10 - 11易位酶(TETs)的影响;大麻素CB1和CB2受体;以及细胞因子IL-1β、IL-6、IL-10和TNF-α。我们采用了两种体外研究设计,对从健康供体收集的人外周血单个核细胞(PBMCs)进行:(a)重复四氢大麻酚孵育,(b)重复四氢大麻酚孵育,然后是“戒断”期和四氢大麻酚激发孵育。我们观察到平均四氢大麻酚浓度(50 ng/ml, n = 8个供体)对dnmt和TETs mRNA水平、酶活性或CB1和CB2 mRNA水平没有显著影响。然而,在高THC浓度(200 ng/ml, n = 16个供体)的重复孵育下,dnmt显著下调,tet、CB1和CB2 mRNA水平上调。两种THC浓度均上调IL-1β、IL-6和IL-10基因表达,但对TNF-α基因表达无影响。在全基因组水平上,重复四氢大麻酚孵育导致大量差异羟甲基化基因被超羟甲基化。另外的THC刺激将高羟甲基化状态转变为低羟甲基化。发现与四氢大麻酚暴露最强相关的基因在各种信号通路中具有重要的功能。这些发现表明,高浓度四氢大麻酚的反复培养可能会通过异常去甲基化影响CUD发展的关键基因的表达。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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