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大鼠长期暴露于大麻二酚和大麻萜酚后的安全性评估及氧化还原状态

Safety assessment and redox status in rats after chronic exposure to cannabidiol and cannabigerol.

作者信息

Polanska Hana Holcova, Petrlakova Katerina, Papouskova Barbora, Hendrych Michal, Samadian Amir, Storch Jan, Babula Petr, Masarik Michal, Vacek Jan

机构信息

Department of Physiology, Faculty of Medicine, Masaryk University, Kamenice 753/5, 625 00 Brno, Czech Republic; Department of Pathological Physiology, Faculty of Medicine, Masaryk University, Kamenice 753/5, 625 00 Brno, Czech Republic.

Department of Pathological Physiology, Faculty of Medicine, Masaryk University, Kamenice 753/5, 625 00 Brno, Czech Republic.

出版信息

Toxicology. 2023 Apr;488:153460. doi: 10.1016/j.tox.2023.153460. Epub 2023 Feb 14.

Abstract

Cannabidiol (CBD) and cannabigerol (CBG) are the two main non-psychotropic phytocannabinoids with high application potential in drug development. Both substances are redox-active and are intensively investigated for their cytoprotective and antioxidant action in vitro. In this study, we focused on an in vivo safety evaluation and the effect of CBD and CBG on the redox status in rats in a 90-d experiment. The substances were administered orogastrically in a dose of 0.66 mg synthetic CBD or 0.66 mg/1.33 mg CBG/kg/day. CBD produced no changes in the red or white blood count or biochemical blood parameters in comparison to the control. No deviations in the morphology or histology of the gastrointestinal tract and liver were observed. After 90 d of CBD exposure, a significant improvement in redox status was found in the blood plasma and liver. The concentration of malondialdehyde and carbonylated proteins was reduced compared to the control. In contrast to CBD, total oxidative stress was significantly increased and this was accompanied by an elevated level of malondialdehyde and carbonylated proteins in CBG-treated animals. Hepatotoxic (regressive changes) manifestations, disruption in white cell count, and alterations in the ALT activity, level of creatinine and ionized calcium were also found in CBG-treated animals. Based on liquid chromatography-mass spectrometry analysis, CBD/CBG accumulated in rat tissues (in the liver, brain, muscle, heart, kidney and skin) at a low ng level per gram. Both CBD and CBG molecular structures include a resorcinol moiety. In CBG, there is an extra dimethyloctadienyl structural pattern, which is most likely responsible for the disruption to the redox status and hepatic environment. The results are valuable to further investigation of the effects of CBD on redox status and should contribute towards opening up critical discussion on the applicability of other non-psychotropic cannabinoids.

摘要

大麻二酚(CBD)和大麻二醇(CBG)是两种主要的非精神活性植物大麻素,在药物开发中具有很高的应用潜力。这两种物质都具有氧化还原活性,并且因其在体外的细胞保护和抗氧化作用而受到深入研究。在本研究中,我们专注于在一项为期90天的实验中对大鼠进行体内安全性评估以及CBD和CBG对氧化还原状态的影响。这些物质以0.66毫克合成CBD或0.66毫克/1.33毫克CBG/千克/天的剂量经口灌胃给药。与对照组相比,CBD对红细胞或白细胞计数以及血液生化参数没有产生变化。未观察到胃肠道和肝脏的形态或组织学有偏差。在暴露于CBD 90天后,发现血浆和肝脏中的氧化还原状态有显著改善。与对照组相比,丙二醛和羰基化蛋白质的浓度降低。与CBD相反,在CBG处理的动物中总氧化应激显著增加,同时丙二醛和羰基化蛋白质水平升高。在CBG处理的动物中还发现了肝毒性(退行性变化)表现、白细胞计数紊乱以及谷丙转氨酶活性、肌酐水平和离子钙的改变。基于液相色谱 - 质谱分析,CBD/CBG以每克低纳克水平在大鼠组织(肝脏、大脑、肌肉、心脏、肾脏和皮肤)中积累。CBD和CBG的分子结构都包含一个间苯二酚部分。在CBG中,有一个额外的二甲基辛二烯基结构模式,这很可能是导致氧化还原状态和肝脏环境破坏的原因。这些结果对于进一步研究CBD对氧化还原状态的影响具有重要价值,并且应该有助于开启关于其他非精神活性大麻素适用性的关键讨论。

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