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大鼠肝脏微粒体制剂对8-甲氧基补骨脂素(8-MOP)的代谢失活作用。

Metabolic inactivation of 8-methoxypsoralen (8-MOP) by rat-liver microsomal preparations.

作者信息

Schimmer O, Fischer K

出版信息

Mutat Res. 1980 Dec;79(4):327-30. doi: 10.1016/0165-1218(80)90156-1.

Abstract

A modified Ames assay was developed that used an arginine-requiring mutant of Chlamydomonas reinhardii as an indicator organism. By counting the numbers of colonies formed and Arg+ revertants, we studied the influence of a rat-liver S9 mix (S9 fraction plus co-factors) on the toxic and mutagenic activities of 8-MOP plus black light. Both activities were decreased after pre-incubation of 5 micrograms 8-MOP/ml with S9 mix at 37 degrees C. S9 fractions without co-factors were almost completely inactive.

摘要

开发了一种改良的艾姆斯试验,该试验使用莱茵衣藻的精氨酸需求突变体作为指示生物。通过计算形成的菌落数和精氨酸阳性回复突变体数量,我们研究了大鼠肝脏S9混合液(S9组分加辅助因子)对8-甲氧基补骨脂素加黑光的毒性和诱变活性的影响。在37℃下将5微克/毫升的8-甲氧基补骨脂素与S9混合液预孵育后,两种活性均降低。不含辅助因子的S9组分几乎完全无活性。

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