The Pharmacological Effects of Plant-Derived versus Synthetic Cannabidiol in Human Cell Lines

Q1 Medicine
Ryan. Maguire, D. J. Wilkinson, T. England, S. O’Sullivan
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引用次数: 6

Abstract

Introduction: Cannabidiol (CBD) can be isolated from Cannabis sativa L. or synthetically produced. The aim of this study was to compare the in vitro effects of purified natural and synthetic CBD to establish any pharmacological differences or superiority between sources. Methods: Six purified samples of CBD were obtained, 4 of these were natural and 2 synthetic. The anticancer effects of CBD were assessed in a human ovarian cancer cell line (SKOV-3 cells). The neuroprotective effects of CBD were assessed in human pericytes in a model of stroke (oxygen glucose deprivation [OGD]). The ability of CBD to restore inflammation-induced intestinal permeability was assessed in differentiated human Caco-2 cells (a model of enterocytes). Results: (1) In proliferating and confluent SKOV-3 cells, all CBD samples similarly reduced resazurin metabolism as a marker of cell viability in a concentration-dependent manner (p < 0.001). (2) In pericytes exposed to OGD, all CBD samples similarly reduced cellular damage (measured by lactate dehydrogenase) at 24 h by 31–48% and reduced inflammation (measured by IL-6 secretion) by 30–53%. Attenuation of IL-6 was inhibited by 5HT1A receptor antagonism for all CBD sources. (3) In differentiated Caco-2 cells exposed to inflammation (TNFα and IFNγ, 10 ng/mL for 24 h), each CBD sample increased the speed of recovery of epithelial permeability compared to control (p < 0.05–0.001), which was inhibited by a CB1 receptor antagonist. Conclusion: Our results suggest that there is no pharmacological difference in vitro in the antiproliferative, anti-inflammatory, or permeability effects of purified natural versus synthetic CBD. The purity and reliability of CBD samples, as well as the ultimate pharmaceutical preparation, should all be considered above the starting source of CBD in the development of new CBD medicines.
植物来源与合成大麻二酚在人体细胞系中的药理作用
简介:大麻二酚(CBD)可以从大麻中分离或人工合成。本研究的目的是比较纯化的天然和合成CBD的体外效果,以确定来源之间的任何药理学差异或优势。方法:获得6个CBD纯化样品,其中4个为天然样品,2个为合成样品。在人卵巢癌症细胞系(SKOV-3细胞)中评估CBD的抗癌作用。在中风模型(氧-葡萄糖剥夺[OGD])中评估了CBD在人周细胞中的神经保护作用。在分化的人Caco-2细胞(肠细胞模型)中评估CBD恢复炎症诱导的肠道通透性的能力。结果:(1)在增殖和融合的SKOV-3细胞中,所有CBD样品以浓度依赖的方式类似地降低了作为细胞活力标志的resazulin代谢(p<0.001)。(2)在暴露于OGD的周细胞中,在24小时时,所有CBD样本类似地减少了31-48%的细胞损伤(通过乳酸脱氢酶测量)和30-53%的炎症(通过IL-6分泌测量)。对于所有CBD来源,5HT1A受体拮抗作用抑制IL-6的衰减。(3) 在暴露于炎症(TNFα和IFNγ,10 ng/mL,持续24小时)的分化Caco-2细胞中,与对照组相比,每个CBD样品都提高了上皮通透性的恢复速度(p<0.05–0.001),而对照组被CB1受体拮抗剂抑制。结论:我们的研究结果表明,纯化的天然CBD与合成CBD在体外的抗增殖、抗炎或渗透作用没有药理学差异。在开发新的CBD药物时,CBD样品的纯度和可靠性以及最终的药物制剂都应高于CBD的起始来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medical Cannabis and Cannabinoids
Medical Cannabis and Cannabinoids Medicine-Complementary and Alternative Medicine
CiteScore
6.00
自引率
0.00%
发文量
18
审稿时长
18 weeks
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