Zimmerman A M, Stich H, San R
Pharmacology. 1978;16(6):333-43. doi: 10.1159/000136789.
Under the specific conditions reported for the separate tests delta9-tetrahydrocannabinol (THC) did not elicit a mutagenic response in microbial and eukaryotic in vitro test systems. THC treatment to histidine auxotrophs of Salmonella typhimurium strains TA 98 (susceptible to frame shift mutation) and TA 100 (susceptible to base pair substitution) were investigated. Analysis for possible revertance in the presence and absence of S9 microsomal activation system indicated an absence of induction of gene mutation. Cultured fibroblasts from healthy individuals and DNA repair deficient Xeroderma pigmentosum patients display similar survival activity upon exposure to THC. There was no observable increase in the number of chromosome breaks or chromatid exchanges following exposure to THC or THC plus S9 microsomal fraction. THC, 11-OHdelta9-THC, cannabinol, and cannabidiol did not induce unscheduled DNA repair synthesis in cultured human fibroblasts. Moreover, THC did not suppress UV-induced DNA repair synthesis.
在针对单独测试报告的特定条件下,Δ⁹-四氢大麻酚(THC)在微生物和真核体外测试系统中未引发诱变反应。研究了用THC处理鼠伤寒沙门氏菌TA 98菌株(易发生移码突变)和TA 100菌株(易发生碱基对替换)的组氨酸营养缺陷型。在有和没有S9微粒体激活系统的情况下分析可能的回复突变,结果表明未诱导基因突变。健康个体和DNA修复缺陷的着色性干皮病患者的培养成纤维细胞在暴露于THC后显示出相似的存活活性。暴露于THC或THC加S9微粒体组分后,染色体断裂或染色单体交换的数量没有明显增加。THC、11-OHΔ⁹-THC、大麻酚和大麻二酚在培养的人成纤维细胞中未诱导非程序性DNA修复合成。此外,THC不抑制紫外线诱导的DNA修复合成。