Eisenstadt E, Gold A
Proc Natl Acad Sci U S A. 1978 Apr;75(4):1667-9. doi: 10.1073/pnas.75.4.1667.
A polycyclic aromatic hydrocarbon recently isolated from carbon black and identified as cyclopenta[c,d]pyrene (CPP) is highly mutagenic. By the criteria of the Salmonella/mammalian-microsome mutagenicity test, the mutagenic potency of CPP is equalled by only two other naturally occurring polycyclic aromatic hydrocarbons--benzo[a]pyrene and dibenz[a,c]anthracene. The potent mutagenicity of CPP is noteworthy for two reasons: (i) CPP is a mutagenic polycyclic aromatic hydrocarbon without a "bay-region" and (ii) there is evidence that it is distributed widely in the environment. On the basis of experimental observations and perturbational molecular orbital calculations we propose that a mutagenic metabolite of CPP will be the 3,4-oxide. The carbonium ion derived from opening of CPP 3,4-oxide is identical to that derived from opening of benzo[a]pyrene 7,8-diol-9,10-oxide, the metabolite now thought to be an ultimate mutagenic and carcinogenic species.
最近从炭黑中分离出来并被鉴定为环戊[c,d]芘(CPP)的一种多环芳烃具有高度致突变性。根据沙门氏菌/哺乳动物微粒体诱变性试验的标准,CPP的诱变效力仅与另外两种天然存在的多环芳烃——苯并[a]芘和二苯并[a,c]蒽相当。CPP的强致突变性值得关注有两个原因:(i)CPP是一种没有“湾区”的诱变多环芳烃,(ii)有证据表明它在环境中广泛分布。基于实验观察和微扰分子轨道计算,我们提出CPP的诱变代谢产物将是3,4-氧化物。由CPP 3,4-氧化物开环产生的碳正离子与由苯并[a]芘7,8-二醇-9,10-氧化物开环产生的碳正离子相同,现在认为该代谢产物是一种最终的诱变和致癌物质。