黄曲霉毒素B1和石蜡毒素在细胞培养中的细胞毒性比较。

Molecular toxicology Pub Date : 1987-04-01
J Gabliks, S Barter
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引用次数: 0

摘要

人类和动物细胞培养物对人类食物中发现的两种环境毒素的易感性进行了评估:黄曲霉毒素B1(一种由霉菌黄曲霉产生的肝毒素)和石蜡毒素(一种由海洋鞭毛菌钩胞Gonyaulax catenella产生的麻痹性神经毒素)。这两种毒素都会导致人类和其他动物食物中毒。两种毒素的急性细胞毒性是通过抑制细胞生长和渐进的细胞致病性导致细胞破坏来测量和比较的。黄曲霉毒素B1对来自易感动物的11个原代肾脏培养物均有细胞毒性。细胞生长抑制10%值(TD10)范围为0.02 ~ 6.0微克/毫升:小鼠(TD10 = 0.02微克)、豚鼠(0.03微克)、大鼠(0.07微克)、仓鼠(0.16微克)、猴(0.1微克)、人(0.7 ~ 1.5微克)、鸡(0.05微克)、鸭(6.0微克)。相应的TD50浓度约为10倍,并在2天内引起细胞破坏。在易感物种(小鼠肾、人癌HeLa系、鸡胚和金鱼鳍(CAR)细胞系)的培养物中,当浓度高达5微克/毫升时,石蛤毒素没有引起细胞毒性表现。当同样的毒素制剂注射到小鼠体内时,只注射1微克,小鼠立即死亡。结果表明,动物细胞培养物可用于研究影响普通基本代谢的一般细胞毒素,但不能用于检测通过干扰器官系统特定生理功能而引起毒性表现的环境毒素。
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Comparative cytotoxicity of aflatoxin B1 and saxitoxin in cell cultures.

Human and animal cell cultures were evaluated for their susceptibility to two environmental toxins found as contaminants in human food supplies: aflatoxin B1, a hepatotoxin produced by the mold Aspergillus flavus, and saxitoxin, a paralytic neurotoxin produced by the marine dinoflagellate Gonyaulax catenella. Both toxins cause food poisoning in humans and other animals. The acute cytotoxicity of both toxins was measured and compared by inhibition of cell growth and by progressive cytopathogenicity resulting in cell destruction. Aflatoxin B1 was cytotoxic to all of the 11 primary kidney cultures derived from susceptible animals. The cell growth inhibition 10% values (TD10) ranged from 0.02 to 6.0 micrograms/ml: mouse (TD10 = 0.02 micrograms), guinea pig (0.03 micrograms), rat (0.07 micrograms), hamster (0.16 micrograms), monkey (0.1 microgram), human (0.7-1.5 micrograms), chick (0.05 micrograms), and duck (6.0 micrograms). The corresponding TD50 levels were about 10 times higher concentrations and caused cell destruction within 2 d. Saxitoxin did not induce cytotoxicity manifestations in cultures derived from susceptible species--mouse kidney, human carcinoma HeLa line, chick embryo, and goldfish fin (CAR) cell line--at high concentration levels up to 5 micrograms/ml. When the same toxin preparation at only 1 microgram was injected into mice, the animals died immediately. The results indicate that animal cell cultures are useful for studies of general cytotoxins that affect common essential metabolism but cannot be used to detect environmental toxins that cause toxic manifestations by an interference with specific physiological functions of organ systems.

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