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选定大麻素对人淋巴母细胞 TK6 细胞的遗传毒性。

Genotoxicity of selected cannabinoids in human lymphoblastoid TK6 cells.

机构信息

Institute of Pharmacology and Toxicology, University of Wuerzburg, 97078, Würzburg, Germany.

出版信息

Arch Toxicol. 2024 Oct;98(10):3439-3451. doi: 10.1007/s00204-024-03826-y. Epub 2024 Aug 22.

Abstract

Natural non-psychoactive cannabinoids such as cannabigerol (CBG), cannabidiol (CBD), cannabichromene (CBC), cannabidivarin (CBDV), and cannabinol (CBN) are increasingly consumed as constituents of dietary products because of the health benefits claims. Cannabinoids may reduce certain types of pain, nausea, and anxiety. Anti-inflammatory and even anti-carcinogenic properties have been discussed. However, there are insufficient data available regarding their potential (geno-)toxic effects. Therefore, we tested CBG, CBD, CBC, CBDV, and CBN for their genotoxic potential and effects on mitosis and cell cycle in human lymphoblastoid TK6 cells. The selected cannabinoids (except CBDV) induced increased micronuclei formation, which was reduced with the addition of a metabolic activation system (S9 mix). CBDV induced micronuclei only after metabolic activation. Mitotic disturbances were observed with all tested cannabinoids, while G1 phase accumulation of cells was observed for CBG, CBD and CBDV. The genotoxic effects occurred at about 1000-fold higher concentrations than are reported as blood levels from human consumption. However, the results clearly indicate a need for further research into the genotoxic effects of cannabinoids. The mechanism of the mitotic disturbance, the shape of the dose-response curves and the possible effects of mixtures of cannabinoids are aspects which need clarification.

摘要

天然非精神活性大麻素,如大麻萜酚 (CBG)、大麻二酚 (CBD)、大麻色烯 (CBC)、大麻素 (CBDV) 和大麻酚 (CBN),由于具有健康益处的说法,越来越多地被用作膳食产品的成分。大麻素可能会减轻某些类型的疼痛、恶心和焦虑。抗炎甚至抗癌特性已被讨论。然而,关于它们的潜在(遗传)毒性作用的数据还不够。因此,我们测试了 CBG、CBD、CBC、CBDV 和 CBN 对人类淋巴母细胞 TK6 细胞的遗传毒性潜力和有丝分裂及细胞周期的影响。所选的大麻素(除了 CBDV)诱导增加了微核的形成,而添加代谢激活系统(S9 混合物)后则减少了微核的形成。CBDV 仅在代谢激活后诱导微核形成。所有测试的大麻素都会导致有丝分裂紊乱,而 CBG、CBD 和 CBDV 则导致细胞 G1 期积累。遗传毒性作用发生在比人类消费报告的血液水平高约 1000 倍的浓度下。然而,这些结果清楚地表明需要进一步研究大麻素的遗传毒性作用。有丝分裂紊乱的机制、剂量反应曲线的形状以及大麻素混合物的可能影响是需要澄清的方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5270/11402852/dc959d9edcc8/204_2024_3826_Fig1_HTML.jpg

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