Yan L S
Carcinogenesis. 1985 Jan;6(1):1-6. doi: 10.1093/carcin/6.1.1.
With the help of results on the metabolism and the carcinogenic activities of polycyclic aromatic hydrocarbons (PAH), the comprehensive metabolic process in vivo is discussed. It is thought that the carcinogenic activity exhibited by a PAH is determined by the competition between the carcinogenesis and detoxification in which it participates. It is suggested that the essential agent of carcinogenesis should be, as a rule, the highest delocalization energy (beta unit) of the carbonium ion at the aromatic angular ring (A region), which is obtained by the pertubational molecular orbit (PMO) method. Since there are no essential distinctions in the molecular geometry and delocalization energy states between two carbonium ions of the aromatic angular ring and of the bay region, the A region can be looked upon as the extended bay region. On the basis of discussion of the overall metabolism, evaluation of the detoxification efficacy of each kind of the competing carcinogenic factors, including the biological factor B and three structural factors of the PAH molecule: K, A and L, was made. After making necessary approximation, K = 0.228, A = 0.5, L = 1.22 and B = 0.7 are obtained. It can be seen from these values that the L region plays the most important role in detoxification processes, and the K region plays the least important role. The effect of biological factor B is approximately the sum of the K region and the A region. This paper suggests the concept of a carcinogenic constant. For the PAHs with the same number of aromatic rings (N), C is a constant. The curve of function C = f(N), including the extensional line, is an isosceles triangle. The author suggests that it should be called the 'Pyramid Rule'. The final form of the quantitative equation is log R = C[delta E3deloc/(0.7 + 0.228nk + 0.5na + 1.22n1)]. The values for 50 PAHs which had been tested by animal experiments were calculated. Of these, 92% of the PAHs are in agreement with experiments on carcinogenic activities.
借助多环芳烃(PAH)的代谢及致癌活性研究结果,探讨了其在体内的综合代谢过程。人们认为,PAH所表现出的致癌活性取决于其参与的致癌作用与解毒作用之间的竞争。有人提出,致癌作用的关键因素通常应是通过微扰分子轨道(PMO)方法得到的芳香角环(A区)碳正离子的最高离域能(β单位)。由于芳香角环的碳正离子与湾区的碳正离子在分子几何结构和离域能状态上并无本质区别,所以A区可视为扩展的湾区。在讨论整体代谢的基础上,对包括生物因素B以及PAH分子的三个结构因素K、A和L在内的各种竞争性致癌因素的解毒功效进行了评估。经过必要的近似处理,得到K = 0.228、A = 0.5、L = 1.22和B = 0.7。从这些数值可以看出,L区在解毒过程中起最重要作用,K区起最不重要作用。生物因素B的作用约为K区和A区作用之和。本文提出了致癌常数的概念。对于具有相同芳香环数(N)的PAH,C为常数。函数C = f(N)的曲线(包括延长线)是一个等腰三角形。作者建议将其称为“金字塔规则”。定量方程的最终形式为log R = C[δE3deloc/(0.7 + 0.228nk + 0.5na + 1.22n1)]。计算了经动物实验测试的50种PAH的值。其中,92%的PAH与致癌活性实验结果相符。