Waters M D, Stack H F, Jackson M A, Brockman H E, De Flora S
U.S. Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
Mutat Res. 1996 Feb 19;350(1):109-29. doi: 10.1016/0027-5107(95)00097-6.
In this review, retinol, chlorophyllin, and N-acetylcysteine are examined and compared with regard to their antimutagenic activity against some promutagens and a group of direct-acting alkylating agents. The promutagens included aflatoxin B1, certain polycyclic aromatic hydrocarbons (e.g., benzo[a]pyrene), and certain heterocyclic amines (e.g., food pyrolysates). Results of antimutagenicity testing selected from data surveyed in the published literature are displayed graphically as activity profiles of antimutagens showing both the doses tested and the extent of inhibition or enhancement of mutagenic activity. All three antimutagens are discussed in terms of their putative mechanisms of action in vitro and in vivo with emphasis on the xenobiotic metabolizing enzyme systems.
在本综述中,对视黄醇、叶绿酸和N-乙酰半胱氨酸针对某些前诱变剂和一组直接作用的烷基化剂的抗诱变活性进行了研究和比较。前诱变剂包括黄曲霉毒素B1、某些多环芳烃(如苯并[a]芘)和某些杂环胺(如食物热解产物)。从已发表文献中调查的数据中选取的抗诱变测试结果以抗诱变剂的活性曲线形式直观呈现,显示了所测试的剂量以及诱变活性的抑制或增强程度。从体外和体内的推定作用机制方面对所有三种抗诱变剂进行了讨论,重点是外源性物质代谢酶系统。