Calik Michael W, Carley David W
Center for Sleep and Health Research, University of Illinois Chicago, Chicago, IL, USA.
Department of Biobehavioral Nursing Science, University of Illinois Chicago, Chicago, IL, USA.
J Cannabis Res. 2023 Jul 28;5(1):30. doi: 10.1186/s42238-023-00199-4.
Dimethyl sulfoxide (DMSO) is an amphipathic molecule with innate biological activity that also is used to dissolve both polar and nonpolar compounds in preclinical and clinical studies. Recent investigations of dronabinol, a cannabinoid, dissolved in DMSO demonstrated decreased sleep apnea frequency and time spent in REM sleep in rats. Here, we tested the effects of dronabinol dissolved in 25% DMSO diluted in phosphate-buffered saline (PBS) to rule out potentiating effects of DMSO.
Sprague-Dawley rats were anesthetized and implanted with bilateral stainless steel screws into the skull for electroencephalogram recording and bilateral wire electrodes into the nuchal muscles for electromyogram recording. Each animal was recorded by polysomnography. The study was a fully nested, repeated measures crossover design, such that each rat was recorded following each of 8 intraperitoneal injections separated by three days: vehicle (25% DMSO/PBS); vehicle and CB antagonist (AM 251); vehicle and CB antagonist (AM 630); vehicle and CB/CB antagonist; dronabinol (CB/CB agonist); dronabinol and CB antagonist; dronabinol and CB antagonist; and dronabinol and CB/CB antagonists. Sleep was manually scored into NREM and REM stages, and sleep apneas were quantified.
Dronabinol dissolved in 25% DMSO did not suppress sleep apneas or modify sleep efficiency compared to vehicle controls, in contrast to previously published results. However, dronabinol did suppress REM sleep, which is in line with previously published results.
Dronabinol in 25% DMSO partially potentiated dronabinol's effects, suggesting a concomitant biological effect of DMSO on breathing during sleep.
二甲基亚砜(DMSO)是一种具有固有生物活性的两亲性分子,在临床前和临床研究中也用于溶解极性和非极性化合物。最近对溶解于DMSO中的大麻素屈大麻酚的研究表明,大鼠的睡眠呼吸暂停频率降低,快速眼动睡眠时长减少。在此,我们测试了溶解于磷酸盐缓冲盐水(PBS)中25% DMSO的屈大麻酚的效果,以排除DMSO的增强作用。
将Sprague-Dawley大鼠麻醉,在其颅骨上双侧植入不锈钢螺钉用于脑电图记录,在颈部肌肉中双侧植入线状电极用于肌电图记录。通过多导睡眠图记录每只动物的情况。该研究采用完全嵌套、重复测量交叉设计,使得每只大鼠在8次腹腔注射中的每次注射后进行记录,注射间隔为三天:溶剂(25% DMSO/PBS);溶剂和CB拮抗剂(AM 251);溶剂和CB拮抗剂(AM 630);溶剂和CB/CB拮抗剂;屈大麻酚(CB/CB激动剂);屈大麻酚和CB拮抗剂;屈大麻酚和CB拮抗剂;以及屈大麻酚和CB/CB拮抗剂。睡眠手动分为非快速眼动和快速眼动阶段,并对睡眠呼吸暂停进行量化。
与溶剂对照组相比,溶解于25% DMSO的屈大麻酚并未抑制睡眠呼吸暂停或改变睡眠效率,这与之前发表的结果相反。然而,屈大麻酚确实抑制了快速眼动睡眠,这与之前发表的结果一致。
25% DMSO中的屈大麻酚部分增强了屈大麻酚的作用,表明DMSO对睡眠期间呼吸有伴随的生物学效应。