口服大麻和腹腔注射 THC:CBD 会导致小鼠大脑和血浆中的神经化学物质和内源性大麻素发生变化。

IF 4.1 Q1 PHARMACOLOGY & PHARMACY
Nichole Reisdorph, Katrina Doenges, Cassandra Levens, Jon Manke, Michael Armstrong, Harry Smith, Kevin Quinn, Richard Radcliffe, Richard Reisdorph, Laura Saba, Kristine A Kuhn
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引用次数: 0

摘要

背景:虽然口服大麻、大麻二酚(CBD)和含四氢大麻酚(THC)的产品(即 "食用食品")的使用在不断扩大,但其对健康的影响在很大程度上仍然未知。本研究探讨了口服整株大麻和复方大麻提取物对小鼠神经化学物质、内源性大麻素(eCB)和生理参数(体温、心率)的影响:在这项试验性研究中,C57BL/6 J 小鼠每隔一天接受一次以下其中一种药物的治疗,为期 2 周:灌胃复合大麻提取物;通过自由喂食将整株大麻与营养凝胶混合;或通过腹腔注射纯化的 THC/CBD。采用4种剂量进行治疗,CBD剂量为0-100毫克/千克/天,自由喂食和灌胃的THC水平为≤1.2毫克/千克/天,腹腔注射的THC水平为10毫克/千克/天。最后一次治疗 48 小时后,使用质谱法测量神经化学物质、eCB、四氢大麻酚、CBD 和 11-OH-THC 的水平。采用方差分析和 t 检验进行统计比较:结果:发现经静脉注射治疗的小鼠大脑和血浆中的神经化学物质(如多巴胺、P 结论)之间存在差异:无论治疗类型如何,神经化学物质和 eCBs 在所有剂量下都有明显变化。神经化学物质的水平似乎因复合大麻提取物的存在而变化,这表明在反复口服后,四氢大麻酚和神经化学物质之间会产生非线性反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral Cannabis consumption and intraperitoneal THC:CBD dosing results in changes in brain and plasma neurochemicals and endocannabinoids in mice.

Background: While the use of orally consumed Cannabis, cannabidiol (CBD) and tetrahydrocannabinol (THC) containing products, i.e. "edibles", has expanded, the health consequences are still largely unknown. This study examines the effects of oral consumption of whole Cannabis and a complex Cannabis extract on neurochemicals, endocannabinoids (eCB), and physiological parameters (body temperature, heart rate) in mice.

Methods: In this pilot study, C57BL/6 J mice were treated with one of the following every other day for 2 weeks: a complex Cannabis extract by gavage, whole Cannabis mixed with nutritional gel through free feeding, or purified THC/CBD by intraperitoneal (i.p.) injection. Treatments were conducted at 4 doses ranging from 0-100 mg/kg/day of CBD with THC levels of ≤ 1.2 mg/kg/day for free feeding and gavage and 10 mg/kg/day for i.p. Body temperature and heart rate were monitored using surgically implanted telemetry devices. Levels of neurochemicals, eCB, THC, CBD, and 11-OH-THC were measured using mass spectrometry 48 h after the final treatment. Statistical comparisons were conducted using ANOVA and t-tests.

Results: Differences were found between neurochemicals in the brains and plasma of mice treated by i.p. (e.g. dopamine, p < 0.01), gavage (e.g., phenylalanine, p < 0.05) and in mice receiving whole Cannabis (e.g., 3,4-dihydroxyphenylacetic DOPAC p < 0.05). Tryptophan trended downward or was significantly decreased in the brain and/or plasma of all mice receiving Cannabis or purified CBD/THC, regardless of dose, compared to controls. Levels of the eCB, arachidonoyl glycerol (2-AG) were decreased in mice receiving lowest doses of a complex Cannabis extract by gavage, but were higher in mice receiving highest doses compared to controls (p < 0.05). Plasma and brain levels of THC and 11-OH-THC were higher in mice receiving 1:1 THC:CBD by i.p. compared to those receiving 1:5 or 1:10 THC:CBD. Nominal changes in body temperature and heart rate following acute and repeated exposures were seen to some degree in all treatments.

Conclusions: Changes to neurochemicals and eCBs were apparent at all doses regardless of treatment type. Levels of neurochemicals seemed to vary based on the presence of a complex Cannabis extract, suggesting a non-linear response between THC and neurochemicals following repeated oral dosing.

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