Galzigna L, Zanatta L, Esposito N
Institue of Experimental and Laboratory Medicine, University of Padova, Viale G. Colombo, 3, 35121 Padova, Italy.
Neurotox Res. 1999 Dec;1(2):149-52. doi: 10.1007/BF03033278.
Cultured rat fibroblasts, monkey kidney tumor cells (line Vero) and murine neuroblastoma cells were exposed to dopamine or dopaminochrome in the presence and absence of ascorbic acid. Ascorbic acid is able to potentiate the toxicity of both dopamine and dopaminochrome for all the tested cells. The toxicity of dopaminochrome was higher than that of dopamine. There is a correlation between toxicity and levels of bioreductive defenses of the cells, e.g. DT-diaphorase (NAD(P)H:quinone oxidoreductase EC 1.6.99.2) and glutathione. In general, tumor cells have lower defenses and seem to be more sensitive to the toxic action.
在有和没有抗坏血酸存在的情况下,将培养的大鼠成纤维细胞、猴肾肿瘤细胞(Vero细胞系)和小鼠神经母细胞瘤细胞暴露于多巴胺或多巴色素中。抗坏血酸能够增强多巴胺和多巴色素对所有受试细胞的毒性。多巴色素的毒性高于多巴胺。毒性与细胞的生物还原防御水平之间存在相关性,例如DT-黄递酶(NAD(P)H:醌氧化还原酶,EC 1.6.99.2)和谷胱甘肽。一般来说,肿瘤细胞的防御能力较低,似乎对毒性作用更敏感。