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抗氧化剂叔丁基对羟基茴香醚和2,6-二叔丁基对甲酚对前诱变剂激活的抑制作用。

Inhibition of promutagen activation by the antioxidants butylated hydroxyanisole and butylated hydroxytoluene.

作者信息

McKee R H, Tometsko A M

出版信息

J Natl Cancer Inst. 1979 Aug;63(2):473-7.

PMID:287836
Abstract

Butylated hydroxyanisole (BHA) and butylated hydroxytoluene (BHT) exhibited antimutagenic activity in the Salmonella typhimurium reversion test. Both BHA and BHT reduced reversion induced by chemicals requiring metabolic activation for effectiveness. However, they did not affect reversion induced by direct-acting mutagens. These results suggested that BHA and BHT may inhibit the metabolic activation processes and demonstrated that the S. typhimurium reversion test may be used to identify inhibitors of the neoplastic process.

摘要

丁基羟基茴香醚(BHA)和丁基化羟基甲苯(BHT)在鼠伤寒沙门氏菌回复突变试验中表现出抗诱变活性。BHA和BHT均能降低需要代谢激活才能发挥作用的化学物质诱导的回复突变。然而,它们并不影响直接作用诱变剂诱导的回复突变。这些结果表明,BHA和BHT可能抑制代谢激活过程,并证明鼠伤寒沙门氏菌回复突变试验可用于鉴定肿瘤形成过程的抑制剂。

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